20 Ascorbic A c i d Technology i n Agricultural, Pharmaceutical, Food, and Industrial
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Applications J. CHRISTOPHER BAUERNFEIND Gainesville, FL 32605
Ascorbic acid, as well as its salts and esters, has many useful applications. In plants L-ascorbic acid has been reported to promote germination of seeds, growth of plants, and growth of roots on cuttings. Spraying of plants such as lettuce, celery, spinach, petunias, and roses with ascorbic acid or sodium ascorbate solutions enabled those plants to better withstand damage from ozone and smog exposure. Spraying tree or bush fruits with ascorbic acid solution syn chronizes maturation and causes fruit to fall more easily in mechanical harvesting. In some instances ascorbic acid application has been cited to improve the defense mechnism of plants to attack by disease agents. Fish require a dietary source of vitamin C, without which they grow poorly and develop fracture dislocations of the spine, distortions of cartilage, and other deficiency signs. In some instances, ruminants and monogastric animals appear to benefit from administration of L-ascorbic acid under stress. Animals with viral disease, such as canine or feline distemper, have responded to treatment with high levels of ascorbic acid. Solid and liquid forms constitute a substan tial pharmaceutical market for manufactured ascorbic acid. Tableting techniques have been devised to prepare a wide array of swallowable or chewable tablets with an assured vitamin C content after manufacture and prolonged storage. L-Ascorbic acid may be added to foods or food ingredients as a nutrient to fortify natural or fabricated foods having little or no vitamin C, to restore losses, and to standardize a given class of food products with a preselected quantity of 0065-2393/82/0200-0395$26.75/0 © 1982 American Chemical Society In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
396
ASCORBIC
the vitamin.
ACID
Factors that must be considered with appro-
priate technology before adding ascorbic acid are the following: (i) cost of the specific food; (ii) convenience (iii) relationship of the food in question
of use;
to normal food
selection or to replacement or supplemental food products; (iv) stability of the vitamin in the food during slielf life and home preparation;
(v) public
health considerations;
and
(vi) special food needs, such as infant, geriatric, and mili-
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tary. In addition to serving as an added nutrient in food, L-ascorbic acid is often used as a processing aid or as a preservative in certain foods or food ingredients. include preventing
enzymatic
Examples
browning of cut fruit, scav-
enging oxygen in beer, fruit, or vegetable products, inhibiting oxidative rancidity in frozen fish, stabilizing the color and flavor in cured meats, maturing of wheat flour and improving of dough, and acting as a reducing agent in wine. An extensive list of patents and scientific papers exists on proposed industrial uses of ascorbic
acid.
The greatest
interest appears to be in the synthetic polymer industry, in photoprocessing,
and in metal technology.
Miscellaneous
uses have been proposed in cosmetics, tobacco, fibers, preservation
of
blood, preservation
of
cut
plants,
cleaning
agents, and in assay reagents.
p p r o x i m a t e l y 50 years a g o L - a s c o r b i c a c i d h a d its b e g i n n i n g as a 1
x
p u r e c h e m i c a l c o m p o u n d . I n t h e 1928-1931 p e r i o d S z e n t - G y o r g y i
(1,2)
e x t r a c t e d f r o m a d r e n a l g l a n d s , c a b b a g e , oranges, a n d p a p r i k a , a
substance h e n a m e d h e x u r o n i c a c i d .
I n 1932 W a u g h a n d K i n g
(3,4)
reported hexuronic a c i d was identical w i t h v i t a m i n C that they isolated f r o m l e m o n s a n d oranges.
Subsequently Svirbely and Szent-Gyorgyi
( 5 - 8 ) i n 1932-1933 d e m o n s t r a t e d a n t i s c o r b u t i c a c t i v i t y f o r the substance. T h e s t r u c t u r a l f o r m u l a ( F i g u r e 1) w a s d e t e r m i n e d i n 1933 b y s e v e r a l investigators
(9-12).
CH OH 2
Figure I .
CH OH 2
Structural formulas of L-ascorbic acid (reductant) (right) and L-denydroascorbic acid (oxidant) (left).
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
397
Ascorbic Acid Technology
BAUERNFEIND
L - A s c o r b i c a c i d w a s s y n t h e s i z e d i n 1933 b y R e i c h s t e i n a n d c o w o r k e r s (13)
i n S w i t z e r l a n d a n d also i n d e p e n d e n t l y
by Ault
et a l . (14)
in
E n g l a n d . I n d u s t r i a l synthesis l a r g e l y f o l l o w s t h e L - s o r b o s e process ( F i g ure 2)
of
starting
Reichstein.
with
Continuous improvements
D-glucose have
feasible process.
made
i n the various
this a p p r o a c h
the
steps
commercially
C o m m e r c i a l p r o d u c t i o n has b e e n c o n t i n u o u s since 1933
a n d is c u r r e n t l y p r a c t i c e d i n several c o u n t r i e s . I n one l a r g e f a c t o r y a b o u t 30 tons of p u r e L - a s c o r b i c a c i d is p r o d u c e d d a i l y , a n a m o u n t e q u i v a l e n t
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to t h a t c o n t a i n e d i n 1 / 2 b i l l i o n (500,000,000) large oranges.
Today, an
i n c r e a s i n g tonnage of this v e r s a t i l e substance is p r o d u c e d a n n u a l l y a n d a v e r y w i d e r a n g e of a p p l i c a t i o n s has b e e n f o u n d for i t i n t h e
food
i n d u s t r y . It o c c u p i e s a n e s t a b l i s h e d p o s i t i o n as a n essential n u t r i e n t a n d as a p h a r m a c e u t i c a l agent i n h u m a n n u t r i t i o n (915) use as a n a d d i t i v e to a n i m a l feeds is g r o w i n g .
and medicine.
Its
Applications on plants
a n d c r o p s as w e l l as i n v a r i o u s i n d u s t r i e s h a v e b e e n i n d i c a t e d . L - A s c o r b i c acid, a six-carbon, water-soluble, white, crystalline c o m p o u n d is v i t a m i n C ( t h e a n t i s c o r b u t i c v i t a m i n ) a n d has also b e e n c a l l e d L - x y Z o - a s c o r b i c a c i d , h e x u r o n i c a c i d , or c e v i t a m i c a c i d . L - A s c o r b i c a c i d ( C H 0 ) resembles the sugars i n s t r u c t u r e a n d reacts l i k e sugars u n d e r 6
8
6
some c h e m i c a l c o n d i t i o n s . T h e u n u s u a l p r o p e r t i e s of t h e m o l e c u l e
(mol.
w t . 176.13) are d u e to t h e e n e - d i o l g r o u p i n g . O t h e r p r o p e r t i e s a r e : m e l t i n g p o i n t of 1 9 0 ° - 1 9 2 ° C w i t h d e c o m p o s i t i o n ; p K i of 4.17 a n d a p K
2
[«]
D
2 0
+
23° i n w a t e r ; a
of 11.57. I t is a m o d e r a t e l y s t r o n g r e d u c i n g a g e n t
a n d is sufficiently a c i d i c to f o r m n e u t r a l salts w i t h bases.
L-Ascorbic acid
( 1 g ) dissolves i n a b o u t 3 m L of w a t e r , or 50 m L of a b s o l u t e e t h a n o l , or 100 m L of g l y c e r o l .
T h e p H of a 1 0 % a q u e o u s s o l u t i o n is
2.1-2.5;
f o r a 1 0 % a q u e o u s s o l u t i o n of s o d i u m ascorbate i t is 7.4—7.9. D e s c r i p t i o n , i d e n t i f i c a t i o n , specifications, a n d tests of L - a s c o r b i c a c i d a n d s o d i u m L - a s c o r b a t e are g i v e n i n the U . S . P h a r m a c o p o e i a
(15)
the F o o d
palmitoyl
Chemicals
Codex
(16).
Similar
information
on
L - a s c o r b i c a c i d ( a s c o r b y l p a l m i t a t e ) is c o n t a i n e d i n t h e C o d e x .
and
Sodium
ascorbate is t w i c e as s o l u b l e i n w a t e r as a s c o r b i c a c i d . A s c o r b y l p a l m i tate is s o l u b l e i n e t h a n o l ( 2 5 ° C ) p r o p y l e n e g l y c o l , or d e c a g l y c e r o l ( 2 5 ° C ) at 0 . 0 1 - 0 . 1 %
at 1 2 . 5 % , i n h o t octaoleate
(80°C)
glycerin,
to 1 0 % , i n vegetable
oils
a n d i n w a t e r ( 7 0 ° C ) at 0 . 2 % .
C r y s t a l structures of L - a s c o r b i c a c i d v a r y i n g f r o m coarse to u l t r a f i n e p o w d e r constitute t h e m a j o r c o m m e r c i a l p r o d u c t forms of t h e c o m p o u n d , f o l l o w e d b y s p e c i a l c o a t e d a n d g r a n u l a t e d forms. also p r o d u c e d
i n granular and powder
other forms s u c h as c a l c i u m ascorbate
forms.
S o d i u m L - a s c o r b a t e is Limited production
and ascorbyl palmitate
of
depend
o n d e m a n d of these p r o d u c t s i n s p e c i a l t y use a p p l i c a t i o n s . H u n d r e d s of d e r i v a t i v e s of L - a s c o r b i c a c i d h a v e b e e n r e p o r t e d i n t h e l i t e r a t u r e , some of w h i c h are as f o l l o w s : m e t a l c o m p l e x e s or salts of
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
398
ASCORBIC
2
2
2
CO I HOCH I HCOH I HO 2.5 cm in May 1979 from Young Pecan Trees Treated with Dikegulac on October 4, 1978 in Three Georgia Orchards New
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Dosage (g Active/L)
Control (no s p r a y ) 1.07 1.60 2.14
Living
Law Orchard* (Tifton)
Shoots/Terminal
Shoot
a
Garrison Orchard (Ray City)
Rigdon Orchard (Tifton)
5.3 a
3.8 a
5.8 a
6.4 a 5.6 a 6.8 a
5.3 b 6.1c 6.0 be
8.4 b 8.9 b 9.5 b
M e a n separation b y D u n c a n ' s m u l t i p l e range test, 5% l e v e l . C u l t i v a r s i n the L a w orchard were " C h e r o k e e " and " C h i c k a s a w " . T h e R i g d o n orchard was " D e s i r a b l e " and the G a r r i s o n orchard was " S t u a r t " . Source: R e p r o d u c e d , w i t h permission, f r o m R e f . 112. C o p y r i g h t 1980, A m e r i c a n Society for H o r t i c u l t u r a l Science. a
6
Animal Applications A s stated b y C h a t t e r j e e et a l . (116,918),
the a b i l i t y to
L - a s c o r b i c a c i d is absent i n insects, invertebrates, a n d t h e t i c c a p a c i t y started p h y l o g e n e t i c a l l y
synthesize
fish.
The biosyn
i n the k i d n e y of
amphibians,
r e m a i n e d i n t h a t of reptiles, b e c a m e t r a n s f e r r e d to the l i v e r of m a m m a l s , a n d finally d i s a p p e a r e d f r o m the g u i n e a p i g , some flying m a m m a l s , t h e m o n k e y , a n d h u m a n s . T h e o v e r a l l p a t t e r n of a s c o r b i c a c i d synthesis b y different species of a n i m a l s is c o r r e l a t e d to t h e i r p h y l o g e n y ( F i g u r e 3 ) . T r a d i t i o n a l l y , f a r m a n i m a l s d o not r e q u i r e a s c o r b i c a c i d i n t h e i r diets since this v i t a m i n is p r o d u c e d w i t h i n t h e i r bodies.
H o w e v e r , i t has l o n g
b e e n t h o u g h t t h a t the c a p a c i t y of the e n z y m e system i n v o l v e d c o u l d b e o v e r t a x e d or i m p a i r e d u n d e r stress c o n d i t i o n s s u c h as h i g h t e m p e r a t u r e a n d disease.
It is also c o n c e i v a b l e
t h a t i n b r e e d i n g a n i m a l s for h i g h
planes of p r o d u c t i v i t y , the rate of synthesis c o u l d b e i n a d e q u a t e .
De
p e n d i n g u p o n c i r c u m s t a n c e s a n d species, s u p p l e m e n t a r y L - a s c o r b i c a c i d i n the d i e t of some a n i m a l s has h a d a b e n e f i c i a l effect. Fish.
F i s h f a r m i n g or a q u a c u l t u r e , as i t is m o r e l i k e l y t o b e c a l l e d
t o d a y , has b e e n a t i m e - h o n o r e d p r a c t i c e g o i n g b a c k o v e r a t h o u s a n d years.
U n t i l m o r e r e c e n t l y , fish f a r m i n g w a s p r a c t i c e d o n a s m a l l scale
basis as m o r e or less a c o m p l e m e n t to other a g r i c u l t u r a l or m a r i n e p u r suits.
L i t t l e or n o t e c h n o l o g y
w a s i n v o l v e d ; b r e e d i n g stock w a s i n t r o
d u c e d i n t o a s u i t a b l e p o n d or f e n c e d off estuary, a n d n a t u r e p e r f o r m e d t h e rest. H a r v e s t i n g was d o n e b y h o o k i n g , n e t t i n g , or d r a i n i n g . W i t h i n t h e past t w o decades a n e w a p p r o a c h w a s i n t r o d u c e d , n a m e l y the l a r g e scale, e n v i r o n m e n t a l l y c o n t r o l l e d , r e s e a r c h - g u i d e d a q u a c u l t u r e w i t h a n expectancy
of l a r g e v o l u m e p r o d u c t i o n of h u m a n f o o d .
Growing
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
fish
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20.
BAUERNFEIND
407
Ascorbic Acid Technology
BIRDS
H I G H E R OROffft)
Figure 3. Schematic of ascorbic acid synthesizing abilities of various species of animals in relation to their phytogeny. (Reproduced, with permission, from Ref. 918. Copyright 1973, American Association for the Advancement of Science.)
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
408
ASCORBIC
ACID
confined i n tanks w i t h water temperature, acidity, a n d salinity controlled, f e d a r t i f i c i a l l y f o r m u l a t e d diets, a n d t r e a t e d w i t h p r o p h y l a c t i c
drugs
a n d p e s t i c i d e s b r o u g h t f o r t h p r o b l e m s absent i n t h e o l d s t y l e p r a c t i c e s . A s e a r l y as 1933, M c C a y a n d T u n i s o n (117) h a d n o t e d t h a t b r o o k t r o u t f e d f o r m a l i n - p r e s e r v e d m e a t d e v e l o p e d lordosis a n d scoliosis
(Fig
u r e 4 ) , b u t t h e c a u s a t i v e agent w a s u n k n o w n u n t i l t h e m i d - s i x t i e s w h e n K i t a m u r a et a l . ( 1 1 8 ) , N a k a g a w a (119), a n d P o s t o n (120) d e m o n s t r a t e d t h a t these d i s t o r t i o n s of t h e v e r t e b r a l c o l u m n w e r e t h e s y m p t o m s of a
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d i e t a r y d e f i c i e n c y of L - a s c o r b i c a c i d ( v i t a m i n C ) . O t h e r d e f i c i e n c y s y m p toms a r e f r a c t u r e d i s l o c a t i o n of t h e s p i n e , b i z a r r e d i s t o r t i o n of c a r t i l a g e , impaired
collagen
formation,
depigmented
areas,
poor
growth, a n d
m o r t a l i t y . T h e d e f i c i e n c y is c o m m o n l y r e f e r r e d t o as t h e " b r o k e n b a c k " syndrome.
A s c o r b i c a c i d deficient t r o u t h a v e a l o w h e m a t o c r i t a n d h i g h
p l a s m a levels of t r i g l y c e r i d e s a n d c h o l e s t e r o l
(121).
B y 1972 i t w a s
k n o w n (122) t h a t s a l m o n , t r o u t , c h a r , c a r p , a q u a r i u m fish, a n d p r o b a b l y many
more
k i n d s of
fish
d e v e l o p specific
avitaminosis C
symptoms
( F i g u r e 4 ) w h e n d e n i e d d i e t a r y sources of a s c o r b i c a c i d . H i l t o n (123) r e p o r t e d t h a t t h e r a i n b o w t r o u t has v i r t u a l l y n o a b i l i t y t o s y n t h e s i z e a s c o r b i c a c i d . W h i l e c l i n i c a l aspects a r e d r a m a t i c , t h e s u b c l i n i c a l m a n i festations of t h e d e f i c i e n c y m a y p l a y a n e v e n m o r e i m p o r t a n t r o l e i n resistance t o b a c t e r i a l or v i r a l infections a n d the r e p a i r of tissue d a m a g e d
Figure 4. Ascorbic acid deficiency in fish. Coho salmon fed diet devoid of ascorbic acid and showing spinal curvatures typical of scoliosis (upper). Normal coho fed complete test diet containing 100 mg vitamin C/100 g dry ration (middle). Coho on same diet as upper fish and showing spinal curvature typical of lordosis (bottom). (Reproduced, with permission, from Ref. 130. Copyright 1969, American Fisheries Society.)
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
Ascorbic Acid Technology
b y p a r a s i t i c i n v a s i o n o r b y p h y s i c a l means.
409
B l a c k d e a t h is r e g a r d e d as
a n a s c o r b i c a c i d d e f i c i e n c y disease i n p e n a e i d s h r i m p ( 1 2 4 ) .
I n large-
scale a q u a c u l t u r a l field p r a c t i c e , v i t a m i n C deficiency w a s one of t h e u n a p p r e c i a t e d d i e t a r y aspects d u r i n g t h e late sixties a n d t h e seventies. C h a n n e l catfish f r o m i n t e n s i v e c u l t u r e s r a i s e d b y l o c a l fish f a r m e r s a n d showing skeletal deformities stimulated L o v e l l
( 1 2 5 ) i n 1973 t o
d e m o n s t r a t e e x p e r i m e n t a l l y t h a t these s y m p t o m s w e r e t h e result of a deficiency
of L - a s c o r b i c a c i d .
I n addition to the physical deformities,
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w e i g h t gains of t h e g r o w i n g fish a n d f e e d c o n v e r s i o n w e r e
adversely
i n f l u e n c e d . W i l s o n a n d P o e (126) i n t h e same y e a r i n d u c e d the s c o r b u t i c c o n d i t i o n i n c h a n n e l catfish r e a r e d i n floating cages. T h e L - a s c o r b i c a c i d r e q u i r e m e n t w a s d e t e r m i n e d t o b e a b o u t 50 m g / k g of d i e t
(127,128).
W h i l e i n t h e past catfish a p p a r e n t l y w e r e a b l e t o o b t a i n a significant a m o u n t of a s c o r b i c a c i d f r o m organisms s u c h as insects, l a r v a e , a n d a l g a e w h e n r a i s e d i n e a r t h e n p o n d s , L o v e l l a n d L i m ( 1 2 9 ) i n 1978 s h o w e d that additional ascorbic a c i d was beneficial. Ascorbic a c i d supplemented diets a r e n e e d e d
f o r t r o u t (118-121, 130,131,132),
salmon
(119,130,
132), c a r p (133), a n d eels (134). A t t e m p t s h a v e b e e n m a d e to d e v e l o p m o r e stable forms of v i t a m i n C f o r fish feeds. (135)
A s c o r b a t e - 2 - s u l f a t e has b e e n p r o p o s e d
as a stable f o r m
of v i t a m i n C . A s a d i e t a r y c o m p o n e n t i t has b e e n r e p o r t e d to c u r e
scorbutic
signs i n s a l m o n o i d
fish
(136), to p r e v e n t
s c u r v y i n catfish
(137) b u t n o t t o possess a n t i s c o r b u t i c a c t i v i t y f o r e i t h e r t h e g u i n e a p i g (138) o r t h e rhesus m o n k e y
(139).
A n interesting pesticide-ascorbic
a c i d i n t e r a c t i o n i n fish h a s b e e n
s t u d i e d b y M a y e r a n d c o w o r k e r s (140-143).
S e v e r a l species of fish w e r e
c o n t i n u o u s l y e x p o s e d t o t o x a p h e n e o n diets w i t h a n d w i t h o u t
ascorbic
a c i d . T h e t o x a p h e n e r e d u c e d t h e a s c o r b i c a c i d content of t h e v e r t e b r a e b u t n o t of the l i v e r , l e a d i n g the investigators t o b e l i e v e t h a t this r e d u c t i o n u n f a v o r a b l y affects c o l l a g e n f o r m a t i o n . D i e t s c o n t a i n i n g t h e h i g h e r levels of L - a s c o r b i c a c i d r e d u c e d t o x a p h e n e residues a n d i n c r e a s e d t h e t o l e r a n c e t o t h e c h r o n i c effect of t o x a p h e n e o n g r o w t h , b o n e
development,
a n d s k i n lesions. Poultry.
M o r e t h a n 100 papers h a v e b e e n p u b l i s h e d o n t h e v a l u e
of s u p p l e m e n t i n g diets of f a r m a n i m a l s w i t h L - a s c o r b i c a c i d . T h e o v e r a l l results a r e at times c o n t r o v e r s i a l . E n h a n c e m e n t of p o u l t r y g r o w t h h a s b e e n r e p o r t e d b y s e v e r a l w o r k e r s u s i n g p u r i f i e d (144,145) a n d p r a c t i c a l (146,147,148)
rations a n d n o t b y others (149), t h e g e n e r a l i n t e r p r e t a
t i o n b e i n g t h a t t h e a s c o r b i c a c i d does n o t f u n c t i o n d i r e c t l y b u t i n d i r e c t l y , i n v o l v i n g a p r o t e c t i v e a c t i o n o r i m p r o v e d u t i l i z a t i o n of nutrients.
other
A d d e d d i e t a r y a s c o r b i c a c i d has b e e n r e p o r t e d t o s t i m u l a t e
synthesis o r l i b e r a t i o n of f o l i c a c i d b y i n t e s t i n a l b a c t e r i a , t o a i d i n its c o n v e r s i o n to f o l a c i n (146,150,151,152),
to reinforce antibiotics i n h i g h
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
410
ASCORBIC
energy feeds a n d t o i m p r o v e i r o n a b s o r p t i o n .
ACID
H i g h environmental tem
peratures r e d u c e t h e thickness ( 1 5 3 ) of eggshells of hens, thus l o w e r i n g the b r e a k i n g s t r e n g t h of t h e eggs ( 1 5 4 ) as w e l l as l o w e r i n g , e g g p r o d u c tion.
H i g h concentrations
of a s c o r b i c a c i d a r e f o u n d n o r m a l l y i n t h e
b i r d ' s tissues, e s p e c i a l l y i n t h e k i d n e y s a n d adrenals, gonads, a n d i n t h e bursa (155).
N e a r significant c o r r e l a t i o n has b e e n f o u n d b e t w e e n t h e
a s c o r b i c a c i d content of t h e a d r e n a l g l a n d a n d e g g p r o d u c t i o n i n t h e d u c k (156).
T h o r t o n a n d D e e b (157) noted that w h i l e ascorbic
acid
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synthesis i n t h e k i d n e y s of l a y i n g hens w a s sufficient f o r p h y s i o l o g i c a l needs at n o r m a l e n v i r o n m e n t a l temperatures, i t w a s n o t w h e n t e m p e r a tures w e r e i n c r e a s e d f r o m 2 1 ° t o 31 ° C as b l o o d a s c o r b i c decreased.
N e s t o r et a l . ( 1 5 8 ) d e m o n s t r a t e d
a c i d levels
that ascorbic
acid (330
m g / k g ) a d d e d to t h e r a t i o n p r e v e n t e d a d e c l i n e i n b l o o d ascorbic levels that o c c u r r e d i n t u r k e y s c o n s u m i n g t h e u n s u p p l e m e n t e d
acid
ration
during w a r m weather ( 3 0 ° C ) . I n a trial during hot weather ( 3 5 - 4 0 ° C ) , P e r e k a n d K e n d l e r (159) o b t a i n e d significant i m p r o v e m e n t in egg production
a n d eggshell
weight when
ascorbic
m g / k g ) w a s a d d e d to t h e r a t i o n of L e g h o r n l a y i n g hens.
(Table V )
acid
(25-400
A subsequent
r e p o r t o n a s c o r b i c a c i d a p p l i c a t i o n ( 2 5 - 4 0 0 m g / k g ) b y t h e same w o r k e r s (160) c o n f i r m e d increases i n e g g p r o d u c t i o n ( 1 1 - 2 4 % ) , b u t e g g w e i g h t differences w e r e e q u i v o c a l .
S u p p l e m e n t a t i o n of diets w i t h a s c o r b i c a c i d
c o u n t e r a c t i n g h i g h e n v i r o n m e n t a l temperatures f o r p o u l t r y w e r e c l a i m e d b y A h m a d et a l . (161) a n d P a s u a l et a l . (162).
Under practical condi
tions of t h e r m a l stress ( 2 2 . 8 - 3 6 . 9 ° C ) a n d h u m i d i t y some benefit i n e g g p r o d u c t i o n has b e e n n o t e d f o l l o w i n g t h e f e e d i n g of a s p i r i n a n d a s c o r b i c acid
(163). S i n c e there is a n a b n o r m a l i t y of c a l c i u m m e t a b o l i s m i n s c u r v y , i t has
b e e n reasoned that s u p p l e m e n t a r y a s c o r b i c a c i d i n t h e h e n r a t i o n m i g h t h e l p t o resolve t h e p r o b l e m of t h i n e g g s h e l l d u r i n g s u m m e r heat.
Some
reports s h o w i m p r o v e d s h e l l soundness d u r i n g h i g h e n v i r o n m e n t a l t e m p e r a t u r e s ; others d o n o t . A c c o r d i n g t o T h o r t o n (164,165) a n d T h o r t o n
Table V .
Effect of Feeding L - A s c o r b i c A c i d to Hens Ascorbic Acid in Feed
Criteria
0
25
75
C u l l i n g a n d m o r t a l i t y (% of groups) E g g production (total eggs/hen) F e e d efficiency (average g / e g g ) E g g weights (average g/egg) E g g s h e l l w e i g h t (average % of whole egg)
31.5 80.0 232.2 60.1 9.05
7.4 102.7 210.4 60.9 9.87
20.3 90.6 206.7 61.3 9.25
(mg/kg)
400 12.9 103.5 202.8 62.7 9.47
Source: Reproduced, with permission, from Ref. 159. Copyright 1962, Poultry Science Association.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
411
Ascorbic Acid Technology
a n d M o r e n g (166), a s c o r b i c a c i d ( 2 2 m g / k g ) a d d e d t o t h e f e e d w a s of v a l u e d u r i n g t h e h o t s u m m e r m o n t h s ( 2 9 ° C ) f o r t h e m a i n t e n a n c e of e g g s h e l l s t r e n g t h a n d thickness. I t w a s b e l i e v e d t h a t t h e a d d e d a s c o r b i c a c i d i n the feed increased feed consumption a n d oxygen consumption i n hens d u r i n g h o t w e a t h e r a n d t h a t a s c o r b i c a c i d counters t h e n o r m a l d e c l i n e i n t h y r o i d a c t i v i t y d u r i n g the h o t s u m m e r m o n t h s (167). A n o t h e r e x p l a n a t i o n offered f o r t h e h i g h t e m p e r a t u r e effect is a p o s s i b l e d e f o r m a t i o n i n t h e s t r u c t u r e of t h e i n n e r layers of t h e s h e l l u p o n w h i c h c a l c i u m Downloaded by UCSF LIB CKM RSCS MGMT on November 18, 2014 | http://pubs.acs.org Publication Date: June 1, 1982 | doi: 10.1021/ba-1982-0200.ch020
is d e p o s i t e d d u r i n g t h e e g g l a y i n g process as w e l l as t h e m i c r o s t r u c t u r e of the outer s h e l l (168,169).
A s n o t e d b y L y l e a n d M o r e n g (153), u n d e r
i n c r e a s e d t e m p e r a t u r e s , t h e a d d i t i o n of a s c o r b i c a c i d ( 4 4 m g / k g ) t o t h e d i e t p r e v e n t e d the b o d y t e m p e r a t u r e increase a n d the associated decrease i n e g g s h e l l t h i c k n e s s . S u l l i v a n a n d c o w o r k e r s (170,171) a n d E l - B o u s h y a n d c o w o r k e r s (168,172,173)
p u b l i s h e d c o n f i r m a t o r y results i n d i c a t i n g
significant i m p r o v e m e n t i n e g g q u a l i t y u n d e r h i g h e n v i r o n m e n t a l t e m peratures.
F o r example
(168),
the shell percentage
of t h e e g g w a s
significantly i m p r o v e d w h e n ascorbic a c i d ( 5 0 m g / k g ) was incorporated into the diet under a hot environmental temperature ( F i g u r e 5 ) . I n this r e p o r t , t h e a s c o r b i c a c i d a d d e d to t h e f e e d w a s s h o w n t o b e present. Changes
1 control
in shell
percentage
2 3 acclima. acclima. tization 1 tization 2
4 transition
5 stress
6 7 Months vitamin C vitaminC addition 1 addition 2 Experimental periods
Figure 5. Changes in eggshell percentage during the course of environmental temperature changes and vitamin C additions. Key: control, cold; O , treated, cold; A , control, hot; •, treated, hot; , vitamin C addition. (Reproduced, with permission, from Ref. 168. Copyright 1966, H. Veenman ir Zonen NV.)
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
412
ASCORBIC
ACID
K i v i m a e (174) o b t a i n e d i m p r o v e m e n t i n t h e q u a l i t y of t h e e g g s h e l l w i t h supplementary dietary ascorbic acid (100 m g / k g ) .
O t h e r w o r k e r s (160,
175-185) h a v e n o t b e e n a b l e t o s h o w i m p r o v e m e n t i n s h e l l t h i c k n e s s of eggs p r o d u c e d u n d e r t h e stress of h i g h t e m p e r a t u r e e n v i r o n m e n t s . Some
c r i t i c s c o n t e n d t h a t past e x p e r i m e n t a l studies d i d n o t i n v o l v e
c u r r e n t l y u s e d , h i g h - p r o d u c i n g genetic strains of p o u l t r y a n d t h e better f o r m u l a t e d rations c u r r e n t l y i n c o m m e r c i a l use. A g e n e r a l c r i t i c i s m l e v e l e d at m a n y of t h e studies o n a s c o r b i c a c i d a d d i t i o n t o t h e d i e t is
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t h a t s t a b i l i t y d a t a a r e n o t r e p o r t e d a n d , d u e to t h e w e l l - k n o w n l a b i l i t y of the c o m p o u n d , i t m a y n o t h a v e b e e n a l w a y s present i n t h e f e e d a t t h e t i m e of c o n s u m p t i o n as d e c l a r e d . A n o t h e r i n d e x of e g g q u a l i t y , n a m e l y t h e t h i c k n e s s or v i s c o s i t y of the a l b u m e n s u r r o u n d i n g t h e y o l k , m e a s u r e d i n H a u g h u n i t s , w a s f o u n d to b e s u p e r i o r b y M o s t e r t (186), H e r r i c k a n d N o c k e l s (187), a n d C h e n a n d N o c k e l s (188) w i t h a s c o r b i c a c i d s u p p l e m e n t a t i o n of t h e hen's d i e t , b u t R a u c h ( 1 8 9 ) r e p o r t e d n o effect. S t i m u l a t e d spermatogenesis i n c o c k erels w a s i n d i c a t e d b y t h e e a r l y observations of W a w r z y n i a k (190) a n d Zanelli
(191).
T h e s e observations w e r e c o n f i r m e d b y t h e studies o f
Perek a n d Snapir (192).
W h e n ascorbic a c i d (100-200 m g / k g ) w a s
f e d i n t h e d i e t over some m o n t h s , t h e d a t a s h o w e d a significant i n c r e a s e of s p e r m a t o z o a n p r o d u c t i o n f o r the t r e a t e d groups over the c o n t r o l g r o u p . A n o t h e r t y p e of stress, " l a y i n g cage f a t i g u e , " w h e r e i n t h e l a y i n g h e n h a s difficulty i n s t a n d i n g o n t h e w i r e floor, has r e s p o n d e d t o a d m i n i s t r a t i o n of a s c o r b i c a c i d b y injections ( 1 0 0 m g ) a c c o r d i n g t o P o l s t e r (193). T h e r o l e of v i t a m i n C i n t h e p h y s i o l o g y a n d n u t r i t i o n of p o u l t r y h a s b e e n r e v i e w e d b y T a g w e r k e r (194). Swine.
I t is g e n e r a l l y a c c e p t e d that pigs d o n o t n e e d a s u p p l e m e n
t a r y s u p p l y of L - a s c o r b i c a c i d i n t h e i r r a t i o n u n d e r field o r p e n confine ment management practices.
Some f e e d i n g trials w h e r e a d d e d
ascorbic
a c i d w a s tested r e s u l t e d i n n e g a t i v e r e p o r t i n g s u c h as those of B a r b e r et a l . ( 1 9 5 ) , B o w l a n d (196), a n d T r a v n i c e k et a l . (197). I n others s u c h as C r o m w e l l et a l . ( 1 9 8 ) a v a r i a b l e g r o w t h response w a s r e p o r t e d a n d D v o r a k (199) r e p o r t e d e q u i v o c a l d a t a . B r o w n et a l . (200) f e d g r o w i n g pigs supplementary ascorbic a c i d (0-1000 m g p e r head d a i l y ) i n feed w i t h different levels of energy ( 1 4 0 - 3 4 0 k c a l X k g W °
7 5
per head d a i l y ) .
Increases i n g r o w t h o b s e r v e d w e r e i n a n i n c r e a s i n g o r d e r w i t h i n c r e a s i n g ascorbic
acid intake a n d a decreasing increment w i t h the rising
e n e r g y i n t a k e . B u r n s i d e (201) r e p o r t e d some g a i n i n f e e d efficiency w i t h a s c o r b i c a c i d ( 1 0 0 m g / k g ) , a n d V a l d m a u i s (202) a n d A n d r e s e n (203) d e m o n s t r a t e d i n c r e a s e d v i a b i l i t y i n b a b y p i g s . O t h e r s suggested L - a s c o r b i c a c i d as a s u p p l e m e n t f o r p i g l e t feeds (204) o r as p r o t e c t i o n a g a i n s t stress c o n d i t i o n s (205). iron availability:
T h e state of a s c o r b i c a c i d a d e q u a c y
Dvorak
(206) r e p o r t e d i r o n d e f i c i e n c y
influences
anemic
pigs
to h a v e l o w e r e d p l a s m a levels of a s c o r b i c a c i d , a n d G i p p et a l . (207)
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
observed
413
Ascorbic Acid Technology
BAUERNFEIND
i n c r e a s e d p l a s m a v a l u e s of i r o n w h e n a s c o r b i c a c i d
(0.5%)
w a s a d d e d to f e e d of the p i g l e t s . Ruminants.
T r e a t m e n t of r u m i n a n t s w i t h L - a s c o r b i c a c i d has m e r i t
i n u n u s u a l c i r c u m s t a n c e s r a t h e r t h a n a n y t y p e of r o u t i n e p r a c t i c e since these species synthesize t h e i r r e q u i r e m e n t s i n t h e i r n o r m a l l i f e
cycle
p a t t e r n . T h e d i g e s t i v e system of t h e y o u n g c a l f or l a m b f u n c t i o n s s i m i l a r l y to t h a t of m o n o g a s t r i c a n i m a l s f o r t h e e a r l y w e e k s of l i f e u n t i l t h e r u m i n a t i n g process is i n i t i a t e d .
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Phillips a n d coworkers sin recommended
of t h e U n i v e r s i t y of W i s c o n
(208,209,210)
L-ascorbic a c i d (250 m g ) , v i t a m i n A (5000 I U ) , a n d
n i a c i n ( 5 0 m g ) as a d a i l y s u p p l e m e n t f o r t h e first 1 0 - 2 1 days of l i f e f o r the c a l f as p r o p h y l a x i s a n d c o n t r o l of e a r l y c a l f h o o d diseases.
Subsequent
reports b y N o r t o n et a l . (211) a n d N e v i n s et a l . (212) d i d n o t c o n f i r m the d e c l a r e d
benefits
of s u p p l e m e n t a r y
v i t a m i n feedings.
I n 1944 a
strange e c z e m a t o i d disease of calves w i t h c o n c o m i t a n t v e r y l o w p l a s m a a s c o r b i c a c i d values o c c u r r i n g o n d a i r y f a r m s i n M i c h i g a n w a s r e p o r t e d b y C o l e et a l . (213). T h e c o n d i t i o n r e s p o n d e d to a s c o r b i c a c i d t h e r a p y . B e t w e e n 1951 a n d 1961 a b o u t 4 % of t h e y o u n g calves i n a S c o t t i s h l a r g e h e r d of F r i e s i a n cattle w e r e n o t e d w i t h a n i n h e r i t e d d e r m a t o l o g i c a l c o n d i t i o n a n d other disorders w i t h l o w l i v e r , b l o o d a n d u r i n e a s c o r b i c a c i d values.
Calves treated w i t h ascorbic
acid produced
sponse (214) a n d r e l a p s e d after t h e r a p y Olson a n d Tammeus
a spectacular r e
ceased.
( 2 1 5 ) r e p o r t e d a s y n d r o m e of s u b p e r i o s t e a l
h e m o r r h a g e s , progressive stiffness, a n d e v e n t u a l i m m o b i l i t y i n a h e r d of H e r e f o r d cattle that r e s p o n d e d t o L - a s c o r b i c a c i d t r e a t m e n t b u t r e l a p s e d w h e n t r e a t m e n t ceased.
M i c h i g a n w o r k e r s (216) also o b s e r v e d a s c u r v y
like condition, a dermatitis, l o w hemoglobin
a n d ascorbic
acid
blood
v a l u e s , a n d d e a t h ( 3 5 a n i m a l s ) i n a h e r d of S h o r t h o r n cattle. S o m e decades a g o i t h a d b e e n f o u n d t h a t a s c o r b i c a c i d injections i m p r o v e d a large percentage
of sterile o r p a r t i a l l y sterile b u l l s
(217).
I n very h i g h p r o d u c i n g m i l k cows, w h i c h have difficulty b e c o m i n g
preg
n a n t , c e r t a i n breeders h a v e f o u n d , b y p r a c t i c a l experience, t h a t a s c o r b i c a c i d injected intravenously (2 g ) a n d intramuscularly ( 2 g ) before breed i n g w i t h t h e b u l l o n t h e same d a y or t h e f o l l o w i n g d a y i m p r o v e s c e p t i o n , e v e n t h o u g h , i n l a r g e h e r d s , i t is a b u r d e n s o m e P h i l l i p s et a l . (218), as e a r l y as 1941, i n observations " h a r d t o settle" c o w s , i n d i c a t e d that c e r t a i n cases
con
procedure.
a n d trials w i t h
(Table
V I ) were
a m e n a b l e t o a s c o r b i c a c i d t h e r a p y (0.5 g i n t r a v e n o u s l y a n d 2 g s u b c u taneously).
T h e vitamin A adequacy
of these a n i m a l s is n o t r e p o r t e d
a n d , hence, c o u l d b e a n i n f l u e n c i n g factor as i n v i t a m i n A synthesis of v i t a m i n C is d e c r e a s e d Disease Therapy.
deficiency,
(219).
I n a c t i v a t i o n of viruses b y L - a s c o r b i c a c i d w a s
r e p o r t e d i n 1935 t o o c c u r r a t h e r q u i c k l y u n d e r i n v i t r o c o n d i t i o n s
(220)
a n d s o m e w h a t l a t e r b y J u n g e b l u t (221) w i t h l i m i t e d c o n f i r m a t i o n in v i v o .
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
414
ASCORBIC
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Table V I .
D a t a Showing the Effect of A s c o r b i c
Cow
Before Treatment (Number of Times Bred)
Type of Case
427
4
r e g u l a r e s t r u m — f a i l e d to settle
455
7
s k i p s 1 or 2 periods after service
437
6
s k i p s 1 or 2 periods after service
17
8
r e g u l a r e s t r u m — f a i l e d to settle
16
9
r e g u l a r e s t r u m — f a i l e d to settle
29
4
s k i p s 1 or 2 periods after service
33
5
s k i p s 1 or 2 periods after service
1W
6
r e g u l a r e s t r u m — f a i l e d to settle
9W
5
r e g u l a r e s t r u m — f a i l e d to settle
4W
4
r e g u l a r e s t r u m — f a i l e d to settle
1450
many
u t e r u s — n o tone
1479
many
u t e r u s — n o tone
B
4
65
many
cystic ovary
404
many
cystic ovary
662
7
cystic ovary
D
many
ACID
r e g u l a r e s t r u m — f a i l e d to settle
Source: Reproduced, with permission, from Ref. 218. Copyright 1941, American Dairy Science Association. I n t h e c h i c k e n , t h e presence of i n c r e a s e d a s c o r b i c a c i d i n t a k e h a s b e e n r e p o r t e d t o l o w e r t h e response
to a T - i n d e p e n d e n t
antigen,
Brucella
abortus, a n d t o raise t h e response i n a d u l t s ( 2 2 2 ) , a n d t o i n h i b i t r e p l i c a t i o n a n d i n e f f e c t i v i t y of t h e a v i a n R N A t u m o r v i r u s ( 2 2 3 ) . reports b y others
(224r-230) s h o w e d
Subsequent
e n c o u r a g i n g results f o r a s c o r b i c
a c i d t r e a t m e n t i n t h e i n a c t i v a t i o n or a l l e v i a t i o n of c e r t a i n v i r a l a n d b a c t e r i a l diseases. N u n g e s t e r a n d A m e s ( 2 3 1 ) n o t e d t h a t a c t i v i t y o f p h a g o cytes w a s s i g n i f i c a n t l y i n c r e a s e d w i t h h i g h e r a s c o r b i c a c i d c o n c e n t r a tions i n t h e a m b i e n t m e d i u m .
I n 1971 a b i o c h e m i c a l m e c h a n i s m o f
a c t i o n i n p h a g o c y t o s i s w a s offered b y D e C h a t e l e t et a l . (232,919) i n volving L-ascorbic acid.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
415
Ascorbic Acid Technology
A c i d T h e r a p y u p o n H a r d to Settle C o w s
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After Treatment Services
Result
Method of Treating
1
pregnancy
injections 8 weeks before b r e e d i n g — w e e k l y , subcutaneous
pregnancy
6 i n j e c t i o n s over 5 weeks, b e g i n n i n g w i t h b r e e d i n g
pregnancy
6 injections over 30 d a y s p r i o r t o b r e e d i n g
pregnancy
i n t r a v e n o u s a n d subcutaneous i n j e c t i o n a t t i m e of heat
pregnancy
4 doses over 10 d a y s after b r e e d i n g
pregnancy
4 doses over 10 d a y s after b r e e d i n g
pregnancy
4 doses over 10 d a y s after b r e e d i n g
pregnancy
3 doses over 12 d a y s before b r e e d i n g
pregnancy
3 doses over 12 d a y s before b r e e d i n g
pregnancy
3 doses over 12 d a y s before b r e e d i n g
many
no help
subcutaneous a n d i n t r a v e n o u s
many
no help
subcutaneous a n d i n t r a v e n o u s
3
?
subcutaneous
many
no help
subcutaneous
many
no help
subcutaneous
several
no help
subcutaneous subcutaneous a n d i n t r a v e n o u s dosage too low
In
1967
Belfield
(233)
introduced a therapeutic program
L - a s c o r b i c a c i d i n the t r e a t m e n t against d i s t e m p e r of canines
using
(2000mg
i n t r a v e n o u s l y d a i l y ) a n d of felines (cats a n d t o y b r e e d s of dogs, 1000 mg)
w i t h s u p p o r t i v e t h e r a p y w i t h a r e s u l t a n t h i g h d e g r e e of
success.
C o n f i r m a t i o n o f the t r e a t m e n t w a s r e p o r t e d b y E d w a r d s (234)
i n the
t r e a t m e n t of cats w i t h f e l i n e r h i n o t r a c h e i t i s a n d b y B r a n d t ( 2 3 5 )
i n the
t r e a t m e n t of f e l i n e d i s t e m p e r a n d p n e u m o n i t i s i n cats. successful w i t h dogs. L e v e q u e (236)
B r a n d t w a s less
t r e a t e d dogs ( 6 7 a n i m a l s ) o v e r a
22-month p e r i o d w i t h canine distemper w i t h ascorbic a c i d a n d raised h i s r e c o v e r y rate of a n i m a l s to 7 2 % ( T a b l e V I I ) f r o m 5 - 1 0 % experienced.
W a r d (237)
previously
i n d i c a t e d t h a t h e h a d success i n a s c o r b i c a c i d
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
416
ASCORBIC
ACID
Table VII. Recovery Rates Among Dogs Treated with Ascorbic A c i d for Canine Distemper Complex Number Treated
Number Recovered
Recovery Rate (%)
A l l dogs t r e a t e d
67
48
71.6
Cases showing C N S disturbance
16
7
43.8
4
3
75.0
T y p i c a l cases w i t h c o n v u l s i o n s
12
4
33.3
Cases without C N S disturbance
51
41
80.4
T y p i c a l cases w i t h c o n v u l s i o n s a n d g i v e n 3 or fewer doses of ascorbic a c i d
7
1
14.3
T y p i c a l cases w i t h c o n v u l s i o n s a n d g i v e n more t h a n 3 doses of ascorbic acid
5
3
60.0
T y p i c a l cases w i t h o u t c o n v u l s i o n s a n d g i v e n more t h a n 3 doses of ascorbic acid
14
11
78.6
Patient Group
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A t y p i c a l cases w i t h C N S d i s t u r b a n c e but no c o n v u l s i o n s
Source: Reproduced, with permission, from Ref. 236. Copyright 1969, Veterinary Medicine Publishing Company.
t r e a t m e n t of c a n i n e a n d f e l i n e d i s t e m p e r over a p e r i o d of years.
Other
v i r a l diseases s u c h as v i r a l e n c e p h a l i t i s ( 2 3 8 ) , for w h i c h there is a l a c k of effective t h e r a p y , m a y r e s p o n d to t r e a t m e n t w i t h h i g h levels of a s c o r b i c acid. Administration Methods.
I n a d m i n i s t e r i n g L - a s c o r b i c a c i d to a n i
m a l s , there are several feasible routes, d e p e n d i n g
o n the size of
the
a n i m a l a n d its c h a r a c t e r i s t i c s . F o r s m a l l a n i m a l s s u c h as c h i c k e n s , i t is p o s s i b l e to a d d the L - a s c o r b i c a c i d to t h e a u t o m a t i c w a t e r s u p p l y , p r o v i d i n g d i s s o l v e d trace m i n e r a l s s u c h as c o p p e r a n d i r o n c a n b e a v o i d e d or m i n i m i z e d , for e x a m p l e b y i n c o r p o r a t i o n of a c h e l a t i n g agent w i t h t h e a s c o r b i c a c i d . T h i s route w o u l d o n l y b e c o n s i d e r e d for a short p e r i o d or as a n e m e r g e n c y measure since s t a b i l i t y of aqueous solutions e x p o s e d to a i r is poor.
F o r l a r g e a n i m a l s , p a r e n t e r a l a d m i n i s t r a t i o n is t h e m o s t
r a p i d a n d effective
r o u t e for short p e r i o d s of n e e d .
F o r longer term
a d m i n i s t r a t i o n t h e f e e d r o u t e is p r e f e r r e d , a s s u m i n g a d e q u a t e
stability
exists for the t i m e p e r i o d of i n t e n d e d use. H i g h m o i s t u r e content i n feeds or exposure of f e e d to h i g h h u m i d i t y , h i g h t e m p e r a t u r e storage is d e t r i m e n t a l to a d d e d a s c o r b i c a c i d . P e l l e t i n g of f e e d , w h i c h i n c l u d e s exposure to steam or h o t w a t e r a n d s u b s e q u e n t storage, also destroys ( 3 0 - 6 0 % )
a s c o r b i c a c i d . A t t e m p t s to o v e r c o m e
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
Ascorbic Acid Technology
All
t h i s d e s t r u c t i v e a c t i o n i n c l u d e t h e use of c o a t e d a s c o r b i c a c i d p r o d u c t f o r m s a n d t h e a p p l i c a t i o n of a s c o r b i c a c i d to t h e p e l l e t f e e d f o l l o w i n g t h e p e l l e t i z i n g process. L - A s c o r b i c a c i d c o a t e d w i t h e t h y l c e l l u l o s e ( 4 % ) a n d finely p o w d e r e d a s c o r b i c a c i d u n i f o r m l y b l e n d e d i n t o a w a r m e d i b l e h y d r o g e n a t e d fat ( 5 0 % )
and immediately sprayed i n chilled air into
s m a l l b e a d l e t f o r m are t w o m e t h o d s
that have improved stability i n
a n i m a l feeds ( T a b l e V I I I ) . E v e n w i t h these p r o d u c t s , a n excess o v e r c l a i m values must be added.
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If s o l i d fat is a n i n g r e d i e n t of t h e f e e d as a n e n e r g y source, p r a c t i c a l w a y of a d d i n g a s c o r b i c a c i d is to u n i f o r m l y s u s p e n d t h e powdered
product into the liquified hydrogenated
one finely
fat a n d s p r a y
the
s u s p e n s i o n onto t h e c o o l e d p e l l e t e d f e e d i n a t u m b l e r or o n a m o v i n g belt conveyor.
A n d r e w s a n d D a v i s (239)
f e a s i b l e for p e l l e t e d fish f e e d .
r e p o r t e d this m e t h o d to
be
H e a t - e x p a n d e d c o m m e r c i a l catfish f e e d
( 3 2 % p r o t e i n ) w a s s p r a y e d w i t h a w a r m fat suspension of a s c o r b i c a c i d to 2, 5, a n d 1 0 % fat c o a t i n g o n the feed. A f t e r d r y i n g , t h e w a t e r s t a b i l i t y ( w a t e r l e a c h i n g of a s c o r b i c a c i d ) of t h e p r o d u c t w a s e v a l u a t e d
(Table
I X ) as fish f e e d is n o r m a l l y cast o n w a t e r f o r fish c o n s u m p t i o n . A p r o b l e m arose as h o w to a d d L - a s c o r b i c a c i d to b a k e d
monkey
b i s c u i t s since b a k i n g is q u i t e d e s t r u c t i v e to a s c o r b i c a c i d . A f t e r some trial work it was discovered that ascorbic a c i d ( 1 0 - 2 0 % ) i n concentrated
Table VIII.
Ascorbic A c i d Stability in Unpelleted Feed Storage Condition 3 Weeks/45°C 100% Humidity
(% Retention Ascorbic Acid)
Type Product Ascorbic acid, crystalline E t h o c e l coated, A A F a t ( 5 0 % ) beadlets, A A
Table IX.
90 197 379
0 0 78-84
40-80 84-87 91-99
Retention of Ascorbic Acid° in Fabricated Fish Feeds
i ' A 'J T 7 Ascorbic Acid Level mg/kg Diet A
6 Weeks/45°C Room Humidity
Ascorbic Acid (%) Remaining in Feed Particles Alter Water Exposure 1 Minute
5 Minutes
10 Minutes
96 86 83
74 67 67
50 42 36
° Ascorbic acid in a warm fat suspension sprayed on feed after pelleting. Source: Reproduced, with permission, from Ref. 239. Copyright 1979, Miller Publishing Company.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
418
ASCORBIC
ACID
sucrose s y r u p ( 5 0 - 6 0 % ) c o u l d b e b r u s h e d , s p r a y e d , o r d r o p p e d o n t o the b i s c u i t s after b a k i n g w i t h f a i r l y g o o d s t a b i l i t y p e r f o r m a n c e .
Ascorbic
a c i d is q u i t e stable i n h i g h sugar c o m p o s i t i o n s u c h as c a n d y , a d d e d a t the last stage of p r o c e s s i n g b e c a u s e of t h e dense n a t u r e of t h e h i g h sucrose p r o d u c t s a n d r e l a t i v e f r e e d o m f r o m
oxygen.
I n m i s c e l l a n e o u s a n i m a l a p p l i c a t i o n s r e l a t i n g to t h e
Miscellaneous.
use of a s c o r b i c a c i d , i n t e r a c t i o n s w i t h t o x i c levels of m i n e r a l s h a v e b e e n observed.
H i l l (240) f o u n d i n c r e a s e d d i e t a r y a s c o r b i c a c i d i n c h i c k e n s
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w a s specific i n c o u n t e r a c t i n g m e t a l t o x i c i t y i n cases of s e l e n i u m a n d v a n a d i u m . T h i s w a s also n o t e d b y B e r g et a l . (241).
C a d m i u m toxicity
i n t h e r a t (242) a n d i n Japanese q u a i l (243,244) has b e e n r e v e r s e d o r counteracted.
Ascorbic acid (500 m g / k g )
given intraperitoneally before
or s i m u l t a n e o u s l y w i t h a n o r a l dose of p a r a q u a t a l t e r e d t h e a c t i v i t y of p a r a q u a t i n d i c a t i n g a s c o r b i c a c i d to b e a n effective
detoxifying
agent
(245). K a l l i s t r a t o s a n d F a s s k e (246) n o t e d i n h i b i t i o n of b e n z o [ a ] p y r e n e carcinogenesis i n rats w i t h a s c o r b i c a c i d t r e a t m e n t . T h e r e is a d e c r e a s e d l e v e l of a s c o r b i c a c i d i n l u n g tissue of m i c e f o l l o w i n g exposure t o o z o n e , a n d K r a t z i n g a n d W i l l i s (247) p r o p o s e t h a t one f u n c t i o n of tissue ascor b i c a c i d m a y b e a n e x t r a c e l l u l a r a n t i o x i d a n t i n t h e l u n g s . U s e of ascor b i c a c i d a n d m i n e r a l s u p p l e m e n t s i n t h e detoxification of n a r c o t i c a d d i c t s (248,920)
has b e e n
discussed.
W h i l e not a practical approach, the
i n j e c t i o n of y o u n g c h i c k e n s w i t h s o d i u m ascorbate has b e e n r e p o r t e d to h e a l bruises at a faster rate t h a n i n n o n t r e a t e d a n i m a l s (249).
Pharmaceutical
Applications
L - A s c o r b i c a c i d ( v i t a m i n C ) is a n a c t i v e i n g r e d i e n t i n a v a r i e t y of p h a r m a c e u t i c a l dosage forms s u c h a s : h i g h - p o t e n c y m u l t i v i t a m i n s u p p l e ment;
high-potency
multivitamin supplement w i t h iron;
high-potency
multivitamin supplement w i t h minerals; vitamin B complex; v i t a m i n B c o m p l e x w i t h v i t a m i n E ; p e d i a t r i c d r o p s ; tablets of a r a n g e of p o t e n c i e s ; i n j e c t a b l e s ; a n d s y r u p s a n d elixirs. A n a l t e r n a t i v e list of p h a r m a c e u t i c a l dosage forms c o n t a i n i n g a s c o r b i c a c i d w o u l d b e : tablets w i t h a w i d e r a n g e of potencies, d r o p s ( e s p e c i a l l y f o r p e d i a t r i c u s e ) , injectables, s y r u p s a n d elixirs, effervescent tablets, a n d m u l t i v i t a m i n p r e p a r a t i o n s . M a n y v i t a m i n s a r e q u i t e stable u n d e r n o r m a l p r o c e s s i n g tions a n d present l i t t l e o r n o s t a b i l i t y p r o b l e m s ceutical products.
in
finished
condi
pharma
These include biotin, niacin, niacinamide, pyridoxine,
r i b o f l a v i n , a n d a - t o c o p h e r y l acetate.
O t h e r s t h a t c a n present
problems
are a s c o r b i c a c i d , c a l c i f e r o l , c a l c i u m p a n t o t h e n a t e , c y a n o c o b a l a m i n , f o l a c i n , a n d r e t i n y l esters.
Overages
above label c l a i m are customarily
a d d e d t o v i t a m i n f o r m u l a t i o n s as a means of m a i n t a i n i n g t h e c l a i m e d l e v e l of e a c h v i t a m i n f o r t h e e x p e c t e d shelf l i f e of t h e p r o d u c t s . T h e p e r c e n t o v e r a g e f o r a p a r t i c u l a r v i t a m i n s u c h as L - a s c o r b i c a c i d w i l l v a r y
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
419
Ascorbic Acid Technology
BAUERNFEIND
a c c o r d i n g t o its p e r f o r m a n c e p a t t e r n . I n g e n e r a l , p r o b l e m s of i n s t a b i l i t y of v i t a m i n s are m u c h m o r e acute i n m u l t i v i t a m i n l i q u i d s t h a n i n s i n g l e v i t a m i n f o r m u l a t i o n s or i n s o l i d dosage forms. L - A s c o r b i c a c i d tablets constitute one of t h e
Solid Dosage Forms.
m a j o r uses i n p h a r m a c e u t i c a l a p p l i c a t i o n s . T a b l e t s m a y b e of t h e c o a t e d or u n c o a t e d t y p e , i n v a r i o u s potencies a n d sizes, a n d also s w a l l o w a b l e o r chewable.
These
s o l i d dosage forms
are p r e p a r e d
either b y
c o m p r e s s i o n or s l u g g i n g , b y w e t g r a n u l a t i o n , or b y d i r e c t
double
compression.
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I n t h e u s u a l process of t a b l e t p r e p a r a t i o n a s c o r b i c a c i d i n p o w d e r
or
fine g r a n u l a r f o r m together w i t h s u i t a b l e d i l u e n t s of lactose, sucrose, o r s t a r c h w i t h l u b r i c a n t is s l u g g e d a n d r e d u c e d t o g r a n u l e s , t h e n
recom-
p r e s s e d i n t o tablets of t h e d e s i r e d size. A n alternate m e t h o d consists of m a k i n g a m o i s t paste of lactose, s t a r c h , a n d sucrose, w h i c h is screened, d r i e d , a n d r e d u c e d t o granules, t h e n m i x e d w i t h a s c o r b i c a c i d i n coarse crystalline form
a n d lubricant a n d compressed
i n t o tablets.
Special
L - a s c o r b i c a c i d a p p l i c a t i o n forms are a v a i l a b l e that p e r m i t d i r e c t c o m pression i n t o t a b l e t f o r m .
C h e w a b l e tablets c o n t a i n s o d i u m ascorbate i n
a d d i t i o n t o a s c o r b i c a c i d a n d flavoring agents t o p r o v i d e a m o r e p l e a s a n t taste. A n o t h e r s p e c i a l t y p e of s o l i d dosage f o r m is t h e effervescent t a b l e t , u s u a l l y of h i g h e r p o t e n c y
( 0 . 5 - 2 . 0 g ) t h a t is c o n s u m e d
when
added
w a t e r converts t h e t a b l e t to a l i q u i d p r e p a r a t i o n . T h e r e are a n u m b e r of scientific papers facture
(250-257)
(258-266), bility
a n d patents d e t a i l i n g t h e f o r m u l a t i o n a n d m a n u of s o l i d a s c o r b i c
a c i d dosage f o r m s , t h e i r s t a b i l i t y
i n v i t r o release of n u t r i e n t s (267,268,269),
(270-275).
Data (Table
X ) collected
a n d bioavaila
on commercial
ascorbic
a c i d tablets stored at r o o m t e m p e r a t u r e ( 2 5 ° C ) d e m o n s t r a t e f u l l l a b e l p o t e n c y over a shelf l i f e p e r i o d of m a n y years.
U n d e r n o r m a l storage
c o n d i t i o n s , c o m m e r c i a l t y p e a s c o r b i c a c i d tablets are stable f o r over 5 years
( > 9 5 % potency
products
retention).
(dehydroascorbic
T h e a m o u n t of three
acid, diketogulonic
breakdown
acid, a n d oxalic
acid)
f o r m e d u n d e r v a r i o u s storage c o n d i t i o n s constitutes a s m a l l p e r c e n t a g e of t h e a s c o r b i c a c i d content a n d poses n o d i e t a r y h a z a r d (276).
I n the
a p p l i c a t i o n of sugar c o a t i n g to m u l t i v i t a m i n tablets, c a r e f u l t e c h n i q u e is r e q u i r e d t o p r e v e n t excessive p e n e t r a t i o n of m o i s t u r e i n t o t h e t a b l e t core, w h i c h c a n l e a d to h i g h losses of v i t a m i n s sensitive to m o i s t u r e a n d p H influences. L i q u i d Dosage Forms.
I n d r y f o r m a n d at v e r y l o w m o i s t u r e c o n
tent, L - a s c o r b i c a c i d is v e r y stable, b u t i n s o l u t i o n e x p o s e d t o a i r o r o x y g e n i t is subject to o x i d a t i o n a c c e l e r a t e d b y d i s s o l v e d t r a c e m i n e r a l s ( c o p p e r a n d i r o n ) a n d l i g h t exposure.
L - A s c o r b i c a c i d is a r e d u c i n g
agent a n d is subject t o o x i d a t i v e d e c o m p o s i t i o n
i n solution. T h i s pro
ceeds first to d e h y d r o a s c o r b i c a c i d , w h i c h has f u l l v i t a m i n C a c t i v i t y , b u t continues t o d i k e t o g u l o n i c a c i d a n d v a r i o u s other b r e a k d o w n
products.
T h e d e g r a d a t i o n reactions are c o m p l e x a n d v a r y w i t h a e r o b i c o r a n a e r o b i c
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
420
ASCORBIC
Table X .
ACID
S t a b i l i t y of
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Analysis of Ascorbic Acid, 100-mg Tablets, After Long-Term Storage at 25°C Lot Number
Storage Time (months)
V-418 KRK-202-66I KRK-202-65-III KRK-202-65-IV KRK-202-66-II DMS-289-II L o t 2082 L o t 2964B L o t 002-0B097A
103 103 103 103 103 90 120 240 96
Assay (% of claim)'
Initial Assay of claim) 103 107 110 110 111 102
99 104 106 106 105 104 111 101 98
— — —
* Assay by iodoraetric and 2,6-dichloroindophenol titrations.
situations, the n a t u r e of the f o r m u l a t i o n , a n d the t y p e of stress to w h i c h p h a r m a c e u t i c a l solutions are subjected. p H dependent.
A s c o r b i c a c i d d e g r a d a t i o n is also
U n d e r a e r o b i c c o n d i t i o n s , the rate of o x i d a t i o n
shows
m a x i m a at p H 5, c o r r e s p o n d i n g to r e a c t i o n w i t h 1 e q u i v a l e n t of
base,
a n d at p H 11.5, c o r r e s p o n d i n g to r e a c t i o n w i t h 2 e q u i v a l e n t s of
base.
A p H - l o g rate profile ( p H r a n g e of 3.5-7.2) for rate of a e r o b i c o x i d a t i o n of aqueous
a s c o r b i c a c i d solutions ( 6 7 ° C ) w a s d e t e r m i n e d b y
and Hajratwala (277). and Yacomeni solutions
(278)
A
first-order
degradation was observed.
Blaug Rogers
also s t u d i e d the effect of p H o n a s c o r b i c
acid
(25°C).
Under
anaerobic
c o n d i t i o n s , the
dependency
of
the s t a b i l i t y of
a s c o r b i c a c i d i n aqueous solutions o n p H is r e l a t i v e l y l o w , b u t t h e r e is a m a x i m u m rate of d e g r a d a t i o n , w h i c h is e q u a l to the p K ^ i of a c i d , at a p H of a b o u t 4.1.
ascorbic
S t a b i l i t y of a s c o r b i c a c i d i n m u l t i v i t a m i n
d r o p s has b e e n s t u d i e d at v a r i o u s p H levels. M a x i m u m losses o c c u r i n the p H range of 3.3 to 4.5 a n d s m a l l e r losses are f o u n d at h i g h e r p H ( u p to 5.5).
F i g u r e 6 shows s t a b i l i t y d a t a f o r a s c o r b i c a c i d i n m u l t i v i t a
m i n e l i x i r p r e p a r a t i o n s for teaspoon dosage for storage at 4 5 ° C . of s u c h solutions has a m o r e p r o n o u n c e d drops.
The p H
effect t h a n i n m u l t i v i t a m i n
Losses at p H 3.5 are as h i g h as 4 0 % i n 6 weeks at 4 5 ° C .
Rate
studies o n the a n a e r o b i c d e g r a d a t i o n of a s c o r b i c a c i d as i n f l u e n c e d b y m e t a l ions, F i n h o l t et a l . (279,280), h a v e i n d i c a t e d the i n v o l v e m e n t of s a l t - a c i d a n d metal complex formations. D u r i n g the past t w o decades a s c o r b i c a c i d free r a d i c a l s h a v e b e c o m e recognized
a n d their kinetics studied
(281-287)
i n the oxidation
of
a s c o r b i c a c i d . I n t e r a c t i o n s b e t w e e n c e r t a i n of the v i t a m i n s or i n g r e d i e n t s
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
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Ascorbic Acid Technology
Vitamin C Tablets Analysis of Ascorbic After Long-Term
Acid, 100-mg Tablets, Storage at 25°C
Diketogulonic
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Acid
4 3 4 4 6
Oxalic
(%)
Acid (%)
1.0 2.0 1.0 1.0 2.0 0.5
0.5 0.5 0.5 0.5 1.0 0.5 0.2 0.4
S o u r c e : R e p r o d u c e d , w i t h permission, from R e f . 276. Pharmaceutical Association.
Dehydroascorbic Acid
(%)
0.5 0.2 0.2 0.4 2.4 0.3 0.4 2.3 1.3 C o p y r i g h t 1976, A m e r i c a n
are of great interest to the p h a r m a c e u t i c a l c h e m i s t b o t h f r o m the t h e o r e t i c a l a n d the p r a c t i c a l v i e w p o i n t s . 1.
H a n d , G u t h r i e , a n d S h a r p (288) r e p o r t e d t h a t r i b o f l a v i n catalyzes the p h o t o c h e m i c a l o x i d a t i o n of a s c o r b i c a c i d t h a t occurs i n t h e presence of o x y g e n o n exposure to l i g h t . C o n v e r s e l y , a s c o r b i c a c i d exerts a r e d u c i n g effect o n r i b o flavin, w h i c h is v e r y l i k e l y i n v o l v e d i n the f o r m a t i o n of c h l o r o f l a v i n i n B - c o m p l e x solutions c o n t a i n i n g a s c o r b i c acid.
2.
A y e l l o w c o m p l e x of 1 m o l e c u l e of n i a c i n a m i d e w i t h 1 m o l e c u l e of a s c o r b i c a c i d also forms r e a d i l y i n s o l u t i o n b y w h a t appears to b e a charge-transfer r e a c t i o n . T h e c o m p l e x has b e e n p r e p a r e d i n s o l i d f o r m . I t has b e e n c l a i m e d that the p r e f o r m i n g of this c o m p l e x presents difficulties w i t h t h i c k e n i n g a n d h a r d e n i n g of m i x t u r e s e m p l o y e d i n soft g e l a t i n capsules. G u t t m a n a n d B r o o k e ( 2 8 9 ) f o u n d the extent of association b e t w e e n n i a c i n a m i d e a n d a s c o r b i c a c i d to b e p H d e p e n d e n t w i t h m a x i m u m a d s o r b a n c e at p H 3.8.
3.
I n a c i d m e d i u m the f o l i c a c i d m o l e c u l e is c l e a v e d b y r e d u c i n g agents s u c h as a s c o r b i c a c i d . T h i s r e a c t i o n occurs i n t w o stages: ( i ) cleavage to the p t e r i d i n e m o i e t y p l u s p - a m i n o b e n z o y l g l u t a m i c a c i d , a n d ( i i ) d e s t r u c t i o n of t h e free a m i n o g r o u p of the p - a m i n o b e n z o y l g l u t a m i c a c i d . T h e d e c o m p o s i t i o n of f o l i c a c i d is m o r e r a p i d at p H 3 t h a n at p H 6.5.
4.
S t a b i l i z a t i o n of v i t a m i n B solutions i n the presence of t h i a m i n e , n i a c i n a m i d e , a n d a s c o r b i c a c i d has b e e n the s u b ject of a n u m b e r of patents. N e w m a r k (290) has d e s c r i b e d i 2
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
Figure 6.
Ascorbic acid in multivitamin preparations for teaspoon dosage. Left, 3 weeks/45°C ucts); right, 6 weeks/45°C (4 products).
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(5 prod-
o > o 8
M
W W
o o
>
to to
20.
423
Ascorbic Acid Technology
BAUERNFEIND
the effective s t a b i l i z a t i o n of B i i n s u c h solutions b y v a r i ous i r o n c o m p o u n d s a n d salts.
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2
5.
A s c o r b i c a c i d w i l l destroy m a n y of t h e F D & C a z o colors i n s o l u t i o n , so stable colorants m u s t b e chosen.
6.
T h e d e c o m p o s i t i o n of a s c o r b i c a c i d is c a t a l y z e d b y trace m e t a l ions i n s o l u t i o n , h e n c e t h e a d d i t i o n of s e q u e s t e r i n g agents s u c h as E D T A a n d its salts has b e e n s h o w n t o e n h a n c e t h e s t a b i l i t y of a s c o r b i c a c i d (291,292,293).
A r e v i e w of s u c h i n t e r a c t i o n s w a s p u b l i s h e d b y S c h e i n d l i n ( 2 9 4 ) i n 1958.
P o r i k h a n d L o f g r e n ( 2 9 5 ) d e m o n s t r a t e d i n c r e a s e d s t a b i l i t y of
a s c o r b i c a c i d , c o n f i r m e d b y K a t o (296), w h e n g l y c e r i n a n d / o r p r o p y l e n e g l y c o l t y p e p r o d u c t s w e r e s u b s t i t u t e d f o r p a r t of t h e w a t e r i n a n o r a l multivitamin findings
liquid.
B a u d e l i n a n d Tuschhoff
(297)
reported
similar
o n a s c o r b i c a c i d a n d , i n a d d i t i o n , f o u n d t h a t e t h a n o l o r sugars
s u c h as sucrose, c o r n s y r u p , a n d dextrose also p r o v i d e a s t a b i l i z i n g effect o n a s c o r b i c a c i d . P a u s t a n d C o l i a z z i ( 2 9 8 ) a n d F a b r i z i et a l . ( 2 9 9 ) f o u n d t h a t t h e first-order rate constants f o r o x i d a t i v e d e c o m p o s i t i o n of a s c o r b i c a c i d decrease as a f u n c t i o n of p o l y s o r b a t e 80 c o n c e n t r a t i o n u p t o 3 0 % at 3 0 ° C .
Similar
findings
w e r e o b s e r v e d b y N i x o n a n d C h a w l a (300)
w i t h p o l y s o r b a t e 20. O t h e r reports (301-309) d e a l w i t h factors i n f l u e n c i n g f o r m u l a t i o n a n d s t a b i l i t y of l i q u i d dosage forms of a s c o r b i c a c i d . Sterile a q u e o u s solutions p r e p a r e d w i t h h i g h p u r i t y a s c o r b i c a c i d and
pyrogen-free distilled water i n glass-lined equipment under absolute
sanitary operations a n d filled i n t o a m p u l e s a r e necessary f o r i n j e c t a b l e solutions f o r p a r e n t e r a l use i n h u m a n s a n d a n i m a l s . F o r a l l i n j e c t a b l e p r o d u c t s , i t is i m p o r t a n t t o select c o n t a i n e r , stopper, p r e s e r v a t i v e , a n d other i n g r e d i e n t s t h a t are c o m p a t i b l e . T h e f o r m u l a t o r of l i q u i d m u l t i v i t a m i n p h a r m a c e u t i c a l p r o d u c t s s u c h as b a b y d r o p s , s y r u p s , elixirs, a n d injectables encounters n u m e r o u s p r o b lems i n a t t e m p t i n g to d e v e l o p p r o d u c t s h a v i n g a d e q u a t e p h y s i c a l a n d c h e m i c a l s t a b i l i t y as w e l l as s u i t a b l e taste, o d o r , color, a n d f r e e d o m f r o m b a c t e r i a l c o n t a m i n a t i o n . M a n y of these p r o b l e m s arise f r o m t h e d i f f e r i n g s o l u b i l i t y a n d s t a b i l i t y c h a r a c t e r i s t i c s of t h e i n d i v i d u a l v i t a m i n s , p a r t i c u l a r l y as these relate t o t h e p H of t h e solutions a n d p o t e n t i a l i n t e r a c t i o n s . D e s p i t e these n u m e r o u s p r o b l e m s , v a r i o u s w a y s h a v e b e e n d e v i s e d f o r producing multivitamin combinations i n liquid form containing L-ascorbic a c i d that have acceptable stability characteristics. Successful
develop
m e n t of s u c h p r o d u c t s r e q u i r e s a k n o w l e d g e o f : ( i ) t h e f u n d a m e n t a l aspects of t h e p h y s i c a l a n d c h e m i c a l p r o p e r t i e s of t h e v i t a m i n
forms
a v a i l a b l e ; ( i i ) t h e use of a d e q u a t e t e c h n i q u e s of m a n u f a c t u r e ; a n d ( h i ) t h e e m p l o y m e n t of s u i t a b l e overages b a s e d o n c r i t i c a l s t a b i l i t y studies.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
424
ASCORBIC
ACID
Food Applications L - A s c o r b i c a c i d m a y b e a d d e d to foods or f o o d i n g r e d i e n t s as a n u t r i e n t to f o r t i f y n a t u r a l foods h a v i n g l i t t l e or n o v i t a m i n C , to restore losses, to s t a n d a r d i z e a g i v e n class of f o o d p r o d u c t s to h a v i n g a p r e selected q u a n t i t y , a n d to e n d o w or e n r i c h s y n t h e t i c foods w i t h n u t r i t i o n a l value.
T h e t e r m n u t r i f i c a t i o n is u s e d to c o v e r a l l t h e a b o v e situations
f o r a d d i n g a n u t r i e n t to a f o o d p r o d u c t .
T o n u t r i f y a f o o d o r to m a k e
it a n u t r i f i e d f o o d i m p l i e s a n act to m a k e the f o o d m o r e n u t r i t i o u s .
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Adding
m i c r o n u t r i e n t s s u c h as v i t a m i n s , m i n e r a l s , a m i n o
acids,
and
v i t a m i n A a c t i v e c a r o t e n o i d colorants to a f o o d at l o w cost for n u t r i t i o n a l i m p r o v e m e n t is not a n e w c o n c e p t . I o d i n e w a s a d d e d to salt i n t h e 19th c e n t u r y i n S o u t h A m e r i c a . N u t r i f i c a t i o n is a most r a p i d , most e c o n o m i c a l , most
flexible, a n d most
socially acceptable
method
of
changing
the
n u t r i e n t i n t a k e of a g i v e n p o p u l a t i o n (310). N e w t e c h n o l o g i c a l a d v a n c e s e n a b l e the f o o d p r o c e s s i n g i n d u s t r y t o m a r k e t m a n y m o r e f o o d p r o d u c t s t h a n decades past. F a c t o r s t h a t m u s t be considered i n conjunction w i t h appropriate technology before a d d e d a s c o r b i c a c i d is c o n s i d e r e d a r e : cost of the specific f o o d ; c o n v e n i e n c e
of
use; r e l a t i o n s h i p of the n u t r i e n t to the u s u a l f o o d selection p a t t e r n o r other r e p l a c e m e n t or s u p p l e m e n t a l f o o d p r o d u c t s ; s t a b i l i t y of the n u t r i ent i n the f o o d d u r i n g m a r k e t shelf l i f e a n d h o m e p r e p a r a t i o n ; s p e c i a l f o o d needs,
for
e x a m p l e , i n f a n t , g e r i a t r i c , or m i l i t a r y ; p u b l i c h e a l t h
considerations. L - A s c o r b i c a c i d is also a d d e d to f o o d i n essentially a n o n - n u t r i e n t c a p a c i t y s u c h as a p r e s e r v a t i v e or o x y g e n acceptor, as a n a c i d u l a n t , as a s t a b i l i z e r of c u r e d m e a t color, or as a flour i m p r o v e r .
B e c a u s e of t h e
e n e - d i o l g r o u p , i t has a m a r k e d i n h i b i t o r y influence o n the o x i d a t i o n r e d u c t i o n reactions r e s p o n s i b l e for u n d e s i r a b l e color, development.
flavor,
and
odor
Its m e c h a n i s m of a c t i o n is d e p e n d e n t u p o n the c h a r a c t e r
istics of the f o o d or f o o d i n g r e d i e n t , the associated e n v i r o n m e n t s , t h e p r o c e s s i n g t e c h n o l o g y , a n d the storage e x p e c t a n c y of the p r o d u c t . T h e food processing industry can obtain L-ascorbic a c i d a n d sodium ascorbate c o m m e r c i a l l y i n a v a r i e t y of m e s h sizes to meet the r e q u i r e ments of v a r i o u s k i n d s of f o o d p r o d u c t s .
These crystalline compounds
are stable f o r years w h e n s t o r e d u n d e r c o o l , d r y c o n d i t i o n s i n containers.
closed
E s t e r s of a s c o r b i c a c i d s u c h as a s c o r b y l p a l m i t a t e are also
available. A d d i t i o n Methods.
T h e f o u r b a s i c technologies d e v e l o p e d for a d d
i n g a s c o r b i c a c i d to foods a r e : 1.
Tablets or wafers. C o m p r e s s e d s o l u b l e discs c o n t a i n i n g inert, e d i b l e carriers a n d sufficient a s c o r b i c a c i d to m e e t the ascorbic a c i d regulatory a n d (or) processing require ments of a g i v e n q u a n t i t y of f o o d . T h e t a b l e t a d d e d t o
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
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the c o n t a i n e r p r i o r t o filling a n d s e a l i n g of l i q u i d foods dissolves i m m e d i a t e l y , o r m a y b e d i s s o l v e d a n d a d d e d t o s e m i s o l i d foods o r d r y foods at a late stage of f o o d preparation. 2.
Dry premixes. A u n i f o r m m i x t u r e of a k n o w n a m o u n t of a s c o r b i c a c i d a n d a d r y c a r r i e r , u s u a l l y a constituent of t h e f o o d . T h e p r e m i x b l e n d e d w i t h a p r e s c r i b e d q u a n t i t y of d r y f o o d p r o d u c t gives a greater assurance of p r o d u c t u n i f o r m i t y since t h e q u a n t i t y of t h e p u r e v i t a m i n m a y b e small.
3.
Liquid sprays. S p r a y s of a s c o r b i c a c i d solutions o r s u s p e n sions t h a t m a y b e c o n s i d e r e d l i q u i d p r e m i x e s . T h e sprays are d i r e c t e d onto t h e surface of a f o o d o r i n j e c t e d i n t o l i q u i d f o o d p r o d u c t s t o c i r c u m v e n t difficult o r c o n t i n u o u s p r o c e s s i n g c o n d i t i o n s . F o r e x a m p l e , toasted ready-to-eat cereals a r e f o r t i f i e d b y s p r a y i n g a s o l u t i o n onto flakes s t i l l w a r m f r o m t h e t o a s t i n g process.
4.
Pure compound. C r y s t a l l i n e a s c o r b i c a c i d , s o d i u m ascor bate o r s p e c i a l c o a t e d p r o d u c t forms a r e w i d e l y a d d e d d i r e c t l y to f o o d o r p r e d e t e r m i n e d q u a n t i t i e s often i n t h e f o r m of p r e w e i g h e d packets f o r c o n v e n i e n c e . A d d i t i o n is a c c o m p a n i e d b y m i x i n g t o ensure u n i f o r m i t y .
H u n d r e d s , i f n o t t h o u s a n d s , of reports h a v e b e e n p u b l i s h e d o n t h e a p p l i c a t i o n of a s c o r b i c a c i d t o f o o d p r o d u c t s f o r either n u t r i t i o n a l objec tives o r i m p r o v e m e n t i n f o o d q u a l i t y . B a u e r n f e i n d r e v i e w e d t h e use of a s c o r b i c a c i d (311,312) i n p r o c e s s i n g f o o d i n 1953 ( 4 0 6 references) a n d a g a i n i n 1970 ( 5 2 0 r e f e r e n c e s ) ; other r e v i e w s (313-332) o n f o o d a p p l i cations of a s c o r b i c a c i d h a v e a p p e a r e d p r i o r t o a n d f o l l o w i n g these dates. T h e s t a b i l i t y of a s c o r b i c a c i d is i n f l u e n c e d b y a t m o s p h e r i c
oxygen,
water activity, oxidative enzymes, pasteurization methods, metal con t a m i n a t i o n , a n d s u l f u r d i o x i d e content. T h e d e g r a d a t i o n of a s c o r b i c a c i d i n foods h a s b e e n w i d e l y s t u d i e d . I t is c o m p l e x
i n nature a n d depends
presence of other substances.
o n specific c o n d i t i o n s a n d t h e
W h i l e d e g r a d a t i o n is n o t a t o p i c of this
r e v i e w a f e w f o o d r e l a t e d references a r e i n c l u d e d as a n i n t r o d u c t i o n t o t h e l i t e r a t u r e o n this subject.
A s c o r b i c a c i d has t h e a b i l i t y t o scavenge
s u p e r o x i d e a n d h y d r o x y l r a d i c a l s as w e l l as singlet o x y g e n (333).
In a
1975 r e p o r t o n t h e d e s t r u c t i o n of a s c o r b i c a c i d as a f u n c t i o n of w a t e r a c t i v i t y b y L e e a n d L a b u z a ( 3 3 4 ) , t h e h a l f - l i f e of a s c o r b i c a c i d ( F i g u r e 7)
is w e l l i l l u s t r a t e d as a f u n c t i o n of m o i s t u r e content.
Degradation
compounds formed b y heating ascorbic a c i d i n solution were identified b y T a t u m et a l . ( 3 3 5 ) a n d K a m i y a (337)
(336).
Thompson and Fennema
o b s e r v e d differences i n t h e effect of f r e e z i n g o n t h e rate of o x i
d a t i o n of a s c o r b i c a c i d i n foods as c o m p a r e d w i t h d i l u t e s i m p l e solutions. T i m b e r l a k e (338) f o u n d t h e o x i d a t i o n of a s c o r b i c a c i d i n t h e presence of metals w a s significant a n d c o u l d b e i n f l u e n c e d b y m e t a l c h e l a t i n g
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
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426
ASCORBIC A C I D
MOISTURE CONTENT (g H 0/IOOg SOLIDS) 2
Figure 7. Half-life for ascorbic acid as a function of moisture content. Key: %, DM; O, DH. (Reproduced, with permission, from Ref. 334. Copyright 1975, Institute of Food Technologists.) agents i n b l a c k c u r r a n t juice. I n t h e last d e c a d e m o r e a t t e n t i o n h a s b e e n g i v e n t o k i n e t i c s of q u a l i t y d e g r a d a t i o n i n c l u d i n g a s c o r b i c a c i d o x i d a t i o n i n food products
or model
systems.
E x a m p l e s are m o i s t u r e - s e n s i t i v e
p r o d u c t s (339), a s c o r b i c a c i d o x i d a t i o n i n i n f a n t f o r m u l a d u r i n g storage (340), a s c o r b i c a c i d s t a b i l i t y of t o m a t o j u i c e as f u n c t i o n s of t e m p e r a t u r e , p H , a n d m e t a l c a t a l y s t (341), t h e d e g r a d a t i o n of a s c o r b i c
acid i n a
d e h y d r a t e d f o o d system (342), a n d t h e o x y g e n effect o n t h e d e g r a d a t i o n of a s c o r b i c a c i d i n a d e h y d r a t e d f o o d system ( 3 4 3 ) . T h e p o i n t i n t h e f o o d m a n u f a c t u r i n g process a t w h i c h a s c o r b i c a c i d is i n t r o d u c e d is i m p o r t a n t . I d e a l l y , i t is a d d e d as close t o t h e t e r m i n a l process stage as p o s s i b l e , w h e n c o n d i t i o n s a l l o w . T o m a x i m i z e t h e sta b i l i t y a n d efficacy of a s c o r b i c a c i d a d d e d t o foodstuffs, precautions are recommended
the following
f o r p r a c t i c a l success a c c o r d i n g t o K l a e u i
(317): 1.
D i r e c t contact of t h e f o o d p r o d u c t o r its i n g r e d i e n t s w i t h brass, b r o n z e , m o n e l , steel, a n d i r o n m u s t b e a v o i d e d .
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
2.
T h e e q u i p m e n t u s e d s h o u l d b e of stainless steel, a l u m i n u m , e n a m e l , glass, c h i n a , or a p p r o v e d p l a s t i c . W h e r e v e r possible, deaeration should precede processing, w h i c h s h o u l d b e c a r r i e d out u n d e r i n e r t gas o r i n a vacuum. D u r i n g mixing, emulsification, homogenization, a n d the l i k e , o x y g e n or a i r s h o u l d n o t b e i n t r o d u c e d i n t o t h e product. W h e r e possible, food product should be protected f r o m l i g h t a n d other r a d i a n t energy. C o n t a i n e r s s h o u l d b e filled to m a x i m u m c a p a c i t y , t h a t i s , t h e h e a d s p a c e s h o u l d b e k e p t as s m a l l as p o s s i b l e . A f t e r h e a t p r o c e s s i n g of sealed containers, r a p i d c o o l i n g s h o u l d f o l l o w a n d the p r o d u c t s s h o u l d be s t o r e d at c o o l temperatures.
3.
4.
5.
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427
Ascorbic Acid Technology
6. 7.
8.
If p r a c t i c a b l e , s e q u e s t e r i n g agents s u c h as citrates, E D T A , or cysteine m a y b e a d d e d .
phosphates,
9.
A l l a u t o x i d i z a b l e i n g r e d i e n t s , s u c h as flavoring oils, a d d e d to the f o o d p r o d u c t s h o u l d h a v e a l o w p e r o x i d e v a l u e .
10.
W h e n e v e r feasible, a s h o r t - t i m e heat t r e a t m e n t of f r e s h f o o d p r o d u c t s s h o u l d b e e m p l o y e d to i n a c t i v a t e e n z y m e s before a d d i n g ascorbic acid.
11.
W h e r e feasible, m i c r o o r g a n i s m s m a y b e r e m o v e d b y fil t r a t i o n or i n a c t i v a t e d b y heat t r e a t m e n t a n d , i f p o s s i b l e , p r o c e s s i n g m a y b e c o n t i n u e d u n d e r aseptic c o n d i t i o n s .
12.
P r e f e r a b l y , some a s c o r b i c a c i d s h o u l d b e present p r i o r to b o t t l i n g or c a n n i n g ( 1 m L of r e s i d u a l a i r reacts, t h e o r e t i c a l l y , w i t h 3.3 m g of a s c o r b i c a c i d ) .
L - A s c o r b i c a c i d is f o u n d i n a l l l i v i n g tissues, b o t h a n i m a l a n d p l a n t m a t t e r , a n d as s u c h has b e e n c o n s u m e d b y h u m a n s for t h o u s a n d s
of
years, thus g i v i n g e n c o u r a g e m e n t t h a t the c o m p o u n d is p h y s i o l o g i c a l l y a c c e p t a b l e a n d safe.
F u r t h e r m o r e , extensive t e s t i n g of L - a s c o r b i c a c i d
p r e p a r e d b y c h e m i c a l synthesis confirms its r e l a t i v e safety.
Large-scale
m a n u f a c t u r e , c o u p l e d w i t h h i g h standards of p u r i t y a n d r e l a t i v e l y l o w cost, makes a p p l i c a t i o n to f o o d p r o d u c t s e c o n o m i c a l l y feasible. Use as a Nutrient. complete
P r o c e s s i n g n e v e r makes a f o o d p r o d u c t
more
than the o r i g i n a l fresh product nor can it compensate
for
nature's i d i o s y n c r a s i e s i n c o n t e n t of o r i g i n a l n u t r i e n t s . H o w e v e r ,
the
p r e s e r v a t i o n , p r o c e s s i n g , a n d storage of f o o d are necessary to p r o v i d e p a l a t a b i l i t y , safety to h e a l t h , v a r i e t y of selection, a n d p r o v i s i o n for f u t u r e use. I n t h e p r o d u c t i o n , h a n d l i n g , p r e s e r v i n g , p r o c e s s i n g , a n d storage of f o o d , some n u t r i e n t s are lost or s i g n i f i c a n t l y l o w e r e d . N o t o n l y does t h e n u t r i e n t content v a r y i n the n a t u r a l w h o l e - p l a n t f o o d — b e c a u s e of v a r i e t y , c l i m a t e , h a r v e s t i n g m e t h o d s , s t o r a g e — b u t p r o c e s s i n g ( b e c a u s e of e x p o sure to heat, o x y g e n , metals, a n d so f o r t h , a n d f o o d - f r a c t i o n a t i o n
proc
esses ) modifies t h e n u t r i e n t content. O n e n u t r i e n t e s p e c i a l l y sensitive to
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
428
ASCORBIC
ACID
some of the factors m e n t i o n e d is L - a s c o r b i c a c i d . F u r t h e r m o r e , n o t o n l y are the t r a d i t i o n a l n a t u r a l a n d p r o c e s s e d but
also n e w
"convenience,"
" d i e t e t i c or l o w - c a l o r i e " foods. foods.
or r e f i n e d foods s o l d
"semblance,"
"fabricated,"
today,
"novel,"
and
S o m e of these p r o d u c t s s i m u l a t e k n o w n
O t h e r s h a v e n o p a s t c o u n t e r p a r t a n d m a y h a v e l o w levels
of
m i c r o n u t r i e n t s s u c h as L - a s c o r b i c a c i d , w h i c h c a n b e c o r r e c t e d b y n u t r i fication.
M a n y countries ( 3 4 4 ) h a v e e s t a b l i s h e d a r e c o m m e n d e d
daily
a l l o w a n c e or i n t a k e of a s c o r b i c a c i d f o r h u m a n s ( T a b l e X I ) .
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FRUIT
L - A s c o r b i c a c i d has b e e n associated w i t h
BEVERAGE PRODUCTS.
f r u i t a n d f r u i t juices since 1 7 5 3 w h e n C a p t a i n James L i n d , p h y s i c i a n t o t h e B r i t i s h F l e e t , d e m o n s t r a t e d the successful t r e a t m e n t of s c u r v y i n c o r p o r a t i n g c i t r u s juices i n t h e d i e t . consumption
has u n d e r g o n e
a
T h e p a t t e r n of f r u i t
gradual change
d e c l i n e of w h o l e f r e s h f r u i t a n d v e g e t a b l e
over
the
consumption
years. is
by
products The
correlated
w i t h i n c r e a s e d use of f r o z e n or c a n n e d f r u i t s , vegetables, a n d juices a n d , m o r e r e c e n t l y , r e c o n s t i t u t e d f r u i t - f l a v o r e d beverages.
F r u i t a n d vege
t a b l e p r o d u c t s are the p r i m a r y sources of L - a s c o r b i c a c i d i n this d i e t . A p p l e , g r a p e , p i n e a p p l e , p r u n e , a n d c r a n b e r r y juices a n d p e a c h
and
a p r i c o t nectars c o n t a i n l i t t l e or n o a s c o r b i c a c i d unless n u t r i f i e d . O t h e r juices m a y b e v a r i a b l e sources.
F r u i t juices l o w i n a s c o r b i c a c i d a r e
u s e d i n t e r c h a n g e a b l y w i t h those of h i g h a s c o r b i c a c i d content.
Table X I .
International Dietary Allowances
Country Australia Canada Columbia Finland East Germany West Germany INCAP India Indonesia Japan Malaysia Netherlands Philippines Thailand Turkey United Kingdom U n i t e d States*
Adult Male 30 30 50 30 70 75 55 ( 5 0 ) ' 50 60 60 (50)• 30 50 75 ( 7 0 ) ' 30 50 30 60
It is t h e
for Vitamin C
Pregnancy
Lactation
60 40 65 50 100 100 60 50 90 60 60 75 100 50 70 60 80
60 50 65 90 100 120 60 80 90 90 60 75 150 50 80 60 100
Note: Values are given in milligrams per day. ° Female. * NRC-1980 allowance. Source. Reproduced, with permission, from Ref. 844- Copyright 1975, Common Agricultural Bureaux.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
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429
Ascorbic Acid Technology
c o n t e n t i o n of some g r o u p s t h a t i t is d e s i r a b l e t o n u t r i f y those juices t o m a k e t h e m m o r e c o m p a r a b l e w i t h t h e l a t t e r f r o m a s t a n d p o i n t of n u t r i t i v e v a l u e , h e n c e , l e a v i n g c h o i c e of s e l e c t i o n b a s e d o n flavor preferences. A s c o r b i c a c i d levels of 3 0 - 6 0 m g / 1 0 0 - 2 0 0 m L a r e m e a n i n g f u l c o n centrations.
F o r example, D e l M o n t e (345) began a d d i n g L-ascorbic
a c i d t o t o m a t o j u i c e ( 6 0 m g / 1 8 0 m L ) o n a c o m m e r c i a l basis i n 1974. T h i s c o n f o r m s t o U . S . F D A r e g u l a t i o n s . T h e effect of p r o c e s s i n g v a r i a b l e s a n d p r o d u c t storage i n a s c o r b i c n u t r i f i e d t o m a t o j u i c e has b e e n s t u d i e d
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b y F l i n n (346) a n d b y P o p e a n d G o u l d ( 3 4 7 ) . I n a d d i t i o n t o t h e s t r a i g h t f r u i t juices, different b e v e r a g e - b a s e d
products have
been
s t u d i e d as
a s c o r b i c a c i d n u t r i f i e d foods; s u c h p r o d u c t s i n c l u d e a c h o c o l a t e - f l a v o r e d p o w d e r (348), a w h e y - s o y drink m i x (349), malt lemonades (350), a n d f r u i t j u i c e c a r b o n a t e d beverages (351,352).
L - A s c o r b i c a c i d s t a b i l i t y , its
i n f l u e n c e o n q u a l i t y d u r i n g storage, a n d its influence o n p r o c e s s i n g f r u i t juices a n d beverages r e m a i n a subject of a c t i v e s t u d y
(353-359).
T h e a c i d - t y p e f r u i t a n d v e g e t a b l e juices a r e g o o d carriers of a s c o r b i c a c i d , t h u s p r o v i d i n g a r e l a t i v e l y stable e n v i r o n m e n t .
G r e s s w e l l (322)
a n d others i n t h e past (311, 312,318) h a v e r e v i e w e d t h e use of L - a s c o r b i c a c i d i n beverages a n d f r u i t juices. I n a d d i n g a s c o r b i c a c i d t o juices a n d beverages,
a decision must be made about the nutrient level to b e
c l a i m e d for the product i n the market place plus that expected to b e d e s t r o y e d i n p r o c e s s i n g a n d d u r i n g shelf l i f e . It m u s t b e r e c o g n i z e d t h a t o x i d a t i v e e n z y m e s ( a s c o r b i c a c i d oxidase, p e r o x i d a s e s ) exist i n f r u i t a n d n e e d t o b e h e a t i n a c t i v a t e d . R e m o v a l of o x y g e n
or a i r b y v a c u u m
d e a e r a t i o n a n d r e p l a c e m e n t b y n i t r o g e n or c a r b o n d i o x i d e o r
flushing
h e a d s p a c e w i t h i n e r t gas w i l l r e d u c e a s c o r b i c a c i d d e s t r u c t i o n . I n some instances t h e a d d i t i o n of glucose oxidase a n d catalase is u s e f u l i n r e m o v i n g dissolved a n d headspace oxygen, w h i c h minimizes required ascorbic a c i d a d d i t i o n . U s e of m i n i m u m a m o u n t s of s u l f u r d i o x i d e (insufficient to cause
flavor
changes)
c a n b e h e l p f u l i n some p r o d u c t s f o r b e t t e r
ascorbic a c i d retention values. E x p o s u r e of a s c o r b i c a c i d n u t r i f i e d juices a n d beverages t o d i r e c t sunlight, d e p e n d i n g o n the l i q u i d formulation, c a n accelerate destruction of a s c o r b i c a c i d a n d b r i n g a b o u t flavor changes.
If the product w i l l be
e x p o s e d , c h o i c e of p a c k a g i n g m a y m i n i m i z e l i g h t influences.
Oxygen
p e r m e a b i l i t y of p a c k a g i n g m a t e r i a l s h o u l d n o t b e o v e r l o o k e d .
In any
n e w p r o d u c t t o b e n u t r i f i e d , p i l o t - s i z e p r o d u c t i o n batches ( T a b l e X I I ) s h o u l d b e r u n w i t h t h e best selected v a r i a n t s a n d storage d a t a o b t a i n e d b e f o r e c o m m e r c i a l p r o d u c t i o n is c o m m e n c e d .
A d d e d L-ascorbic acid i n
d r y , f r u i t - f l a v o r e d p o w d e r e d p r o d u c t s t o b e r e c o n s t i t u t e d is q u i t e stable i f m o i s t u r e levels a r e k e p t l o w a n d i f t h e y a r e p a c k e d i n l a m i n a t e d , moisture-resistant packets. I t has b e e n r e c o g n i z e d t h a t t h e e l d e r l y (360) d o n o t a l w a y s c o n s u m e sufficient L - a s c o r b i c a c i d d u e , i n p a r t , t o l a c k of s e l e c t i o n of a p p r o p r i a t e
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
430
ASCORBIC
Table X I I .
ACID
S t a b i l i t y of A d d e d After Processing
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Product A p p l e juice A p p l e juice A p p l e juice A p p l e juice A p p l e juice A p p l e juice A p p l e juice A p p l e juice Apple cherry A p p l e orange A p p l e orange A p p l e orange Applesauce A p r i c o t nectar A p r i c o t nectar A p r i c o t nectar A p r i c o t pineapple Apricot drink Apricot drink A p r i c o t orange Cereals, d r y Cereals, dry Cereals, d r y C o c o a powders C o c o a powders C o c o a powders C o c o a powders C o c o a powders C r a n b e r r y juice C r a n b e r r y juice C r a n b e r r y juice C r a n b e r r y juice C r a n b e r r y orange Cranberry apricot F r u i t punch F r u i t punch
Ascorbic Acid
Vitamin C
30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 1 0 fl oz 30 m g / 4 fl oz 30 m g / 8 fl oz 35 m g / 1 0 0 m L 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 4 fl oz 40 m g / 1 0 0 m L 40 m g / 1 0 0 m L 30 m g / 1 0 0 g 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 6 fl oz 30 m g / 4 fl oz 30 m g / 4 fl oz 10 m g / o z 10 m g / o z 10 m g / o z 25 m g / 1 0 0 g 120 m g / l b 75 m g / 2 0 g 15 m g / 0 . 7 5 oz 15 m g / o z 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 4 fl oz 30 m g / 6 fl oz 30 m g / 6 fl oz 30 m g / 6 fl oz 30 m g / 8 fl oz 30 m g / 1 0 fl oz
40 38 38 38 35 35 38 42 53 66 62 61 69 57 35 39 69 47 49 47 10.3 11.4 10.5 34 180 78 14.1 18 39 60 42 38 59 38 44 67
44 41 49 43 47 41 45 49 54
c a n , 1 2 oz c a n , 1 2 oz c a n , 1 2 oz
30 m g / 1 2 fl oz 30 m g / 1 2 fl oz 30 m g / 1 2 fl oz
42 44 40
46 46 50
p a c k a g e , 3 oz envelope
30 m g / 3 oz 30 m g / 4 fl oz
82 78
87 79
Packaging glass, 1 q t glass, 1 q t glass, 1 q t glass, 1 q t glass, 24 oz c a n , 2 0 oz c a n , 1 8 oz glass, 1 q t glass, 1 q t glass, 4 oz glass, a m b e r can can, 1 lb c a n , 4 oz c a n , 1 8 oz
—
can, 4 oz can, 6 oz c a n , 1 2 oz c a n , 1 2 oz box, l i n e r box, l i n e r box, l i n e r envelope f o i l bags box, 1 lb can, 0.5 lb package glass, 16 oz glass, 16 oz glass, 16 oz glass, 16 oz glass, 1 q t glass, 1 q t c a n , 4 6 oz glass, 0.5 g a l
Goal
a
—
63 62 74 59 40
—
70 48 53 49
— — —
48 214 80
— —
39 61 49 41 61 49 48 68
F r u i t c a r b o n a t e d beverages grape orange root beer F r u i t p o w d e r mixes orange orange
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
Ascorbic A c i d i n Food
Products Storage, 70-75°F
(23°C)
6 Months Ascorbic Acid 31 29
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Vitamin C 6
— 33
31 35 31 28 35 56 (85) 46 49 59 61 31 37 (95) 53 40 48 43 8.3 (80)
—8.0
12 Months
40 ( 8 0 ) 33 (80)
— 29
(76)
34 166 76 13.0 (92) 15.8 (88) 30 51 -7 33 47 35 31 54
431
Ascorbic Acid Technology
(77) 34 (72)
— 33
(73) 30 (61) 44 (81)
— 48 53 62 62 46
— 56
(76) (85) (84) (100) (100)
(80) 46 (95) 49 (92) 43 (88) 9.7 12.5 10.7 45 (94) 194 (90) 87 (100) 14.0
— 35
Ascorbic Acid
Vitamin C
— — 25 — 28
— — 37 — 32
26 26 25 31 54 (82) 37 39 56 45 29 32 (82) 52 29 37
31 26 31 34
—7.2
—9.9
(70) 9.9 (87) 7.0 (67) 28 137 77 11.4 (81) 16.5 (91)
— 40 48 56 50 32
(76) (68) (76) (58) (63) (63) (64) (77) (76) (84) (80)
— 59
(84) 40 (83) 41 (77)
10.3 9.1 39 (81) 171 (80) 82 (100) 12.9
— — — 38
(90) (94) (80) (86) (87) (82) (73) (85)
— — 32
— 38 — —
— 40 — —
30 30 31
35 (76) 35 (76) 41 (82)
26 22 28
28 (61) 25 (54) 32 (64)
75 71
80 (92) 77 (97)
73 68
79 (91) 76 (96)
57 39 35 53 40 35 58
32
(78) 34 (83) (82)
Continued on next page.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
432
ASCORBIC
ACID
Table
XII.
After Processing
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Product F r u i t p o w d e r mixes orange orange lemon fruit gelatin fruit gelatin F r u i t lollipops lemon pineapple G r a p e juice C ' Grape drink Grape drink Grape drink Grape drink Grape drink Grape drink Grapefruit juice G r a p e f r u i t juice Grapefruit juice Grapefruit juice Grapefruit juice G r a p e f r u i t juice C° Lemonade drink
Goal
Packaging glass, 7 oz c a n , 4 oz glass, 7 oz c a n , 2 4 oz c a n , 2 4 oz
136 m g / o z 75 m g / 4 fl oz 60 m g / 2 5 g 15 m g / 3 oz 15 m g / 4 oz
c a n , 6 oz can c a n , 12 oz c a n , 46 oz. can,1 qt glass, 0.5 g a l glass, 0.5 g a l glass, 17 oz c a n , 1 8 oz c a n , 18 oz c a n , 1 8 oz c a n , 6 oz c a n , 6 oz c a n , 4 6 oz
30 30 15 30 30 30 30 30 30 30 30 30 30 30 30 30
L o w - c a l o r i e d r i n k powders vanilla c a n , 8 oz chocolate c a n , 8 oz
mg/pop mg/pop m g / 1 oz m g / 8 fl oz m g / 6 fl oz m g / 6 fl oz m g / 6 fl oz m g / 8 fl oz m g / 8 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 8 fl oz
136 144 75 17.5 63 29 30 13 31 44 43 36 26 30 68 56 63 57 74 44* 76 d
Vitamin C a
—
122
—
18.2 68
— —
14* 33 48 46 40 35 41 71 58 69 57 76 47 78 d
188 180
100 m g / q t 100 m g / q t
148 140
50 m g / c a n 50 m g / c a n
54 99 94 57 63 136 157 184
63 79 200 188 200
47 33 67 28 53 40 37 79
50 39 88 28 56 44 44 82
M i l k products liquid formula liquid formula evaporated m i l k dry formula dry formula dry m i l k , whole dry m i l k , whole dry m i l k , whole
c a n , 13 oz c a n , 1 3 oz c a n , 13 oz c a n / g gas can/g vacuum can, air can, air c a n , gas
60 m g / 1 1 2 g 60 m g / 1 1 2 g 100 m g / l b 100 m g / l b 100 m g / l b
Orange Orange Orange Orange Orange Orange Orange Orange
c a n , 4 6 oz c a n , 1 2 oz c a n , 1 2 oz glass, 1 q t glass, 1 q t glass, 1 q t c a n , 46 oz glass, 0.5 g a l
30 30 60 15 30 30 30 30
drink drink drink drink drink drink drink drink
Ascorbic Acid
m g / 8 fl oz m g / 6 fl oz m g / 1 2 fl oz m g / 4 fl oz m g / 8 fl oz m g / 8 fl oz m g / 8 fl oz m g / 1 0 fl oz
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
56
— —
20.
BAUERNFEIND
433
Ascorbic Acid Technology
Continued Storage, 70-75°F
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6 Months Ascorbic Acid Vitamin C 139 (100) 144 71 (95) 16.8 62 — — 12" 31 33 37 35 23 28 _ 48 56 50 (88) 68 43" 69
— 121 (99) — 17.9 (98) 68 (100) — — 14" (100) 34 (100) 39 (81) 39 (85) 41 (100) 27 (80) 31 (76) — 51 (88) 61 (90) — 69 (90) 4 8 " (100) 77 (99)
(23°C)
12 Months Ascorbic Acid Vitamin C 166 (85) 106 71 (95) 15.5 61 30 (100) 30 (100) 11" 18 — 26 24 — — 51 46 53 49 60 — 60
— 119 (97) — 16.6 (91) 66 (97) — — 1 2 " (86) 31 (94) — 32 (70) 26 (65) — — 52 (73) 48 (83) 57 (83) 4 9 (86) 63 (83) — 67 (86)
141 136
168 (90) 160 (90)
100 129
121 (64) 143 (80)
27 49 (50) 62 (64) — — 147 115 184 37 27 62 25 50 36 31 71
34 — — — — 195 158 189 41 30 81 27 54 40 37 73
— 49(50) — 58 63 138 133 188 — — — 16 32 31 27 66
— — — 61 76 168 122 186 — — — 23 46 33 34 68
(60)
(98) (84) (95) (82) (77) (92) (99) (96) (91) (84) (89)
(97) (96) (84) (65) (93)
(82) (82) (75) (77) (83)
Continued on next page.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
434
ASCORBIC
ACID
Table X I I . After
Processing
Ascorbic
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Goal
Packaging
Product
Orange drink C° Orange drink C Orange drink C Pineapple juice Pineapple juice Pineapple juice Pineapple juice Pineapple juice Pineapple juice C Pineapple grapefruit Pineapple grapefruit Pineapple grapefruit Pineapple orange Pineapple orange Pineapple orange Potato flakes Potato flakes Potato flakes c
0
c
Soybean products liquid formula dry powder Tomato juice Tomato juice Tomato juice Tomato juice Tomato juice Tomato juice Vegetable juice Vegetable juice Vegetable juice
can, can, can, can, can, can, can,
6 oz 6 oz 6 oz 11 oz 18 oz 46 oz 46 oz
can, can, can, can, can, can, can, can can, can,
6 oz 12 oz 46 oz 46 oz 46 oz 46 oz 12 oz air gas
can, 13 oz can, l i b can, 18 oz can, 46 oz can, 18 oz can, 46 oz glass jar can, 46 oz can, 46 oz can 6 oz glass jar
Acid
Vitamin C a
30 30 30 30 30 30 30 30 30 30 30 30 30 30 30 60 60 60
m g / 4 fl oz m g / 4 fl oz m g / 8 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 4 fl oz m g / 6 fl oz m g / 6 fl oz m g / 8 fl oz m g / 8 fl oz m g / 6 fl oz m g / 6 fl oz m g / 3 oz mg/100 g mg/100 g
53 68 39 47 44 43 39 69 79' 40 59 39 36 43 42 48 51 70
57* 71 51 48 44 47 39
50 60 30 30 30 30 30 30 30 30 30
mg/can m g / 4 oz mg/100 m L mg/100 m L m g / 4 fl oz m g / 4 fl oz m g / 6 fl oz m g / 6 fl oz m g / 6 fl oz m g / 4 fl oz m g / 4 fl oz
45 62 52 39 40 41 55 72 53 36 45
—
d
d
d
d
d
—
88 42 60 40 37 45 49 59 65 79
d
62 54
—
41 44 59 75 58 42
—
° Vitamin C equals ascorbic acid plus dehydroascorbic acid. Values in parentheses are percent retention during storage. Concentrate. 0°F. Source: Reproduced, with permission, from Ref. 312. Copyright 1970, Academic Press, Incorporated. b
c
d
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
435
Ascorbic Acid Technology
Continued Storage, 70-75°F
(23°C) 12 Months
6 Months
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Ascorbic Acid 55" 62" 40" 43 38 42 36 63 (91) 78" 35 50 36 32 38 36 30 40 68 47 49 45 35 37 41 51 57 40 32 42
Vitamin C 57"(100) 6 6 " (94) 47"(92) 43 (90) 45 (100) 42 (89) 36 (92) 82"(93) 39 (93) 54 (90) 38 (95) 32 (82) 41 (91) 41 (84) 43 (73) 60 (92) 71 (90)
(100) 60 (97) 45 (83) (90) (93) 50 56 63 43 34 (93)
(100) (95) (84) (74) (81)
Ascorbic Acid
Vitamin C
61" 41" 38 (81) 35 35
65"(91) 4 6 " (90) 36 (82) 35 (74)
55 (80)
38
4 3 (95) 48 44 27 (70) 34 32 39 45 32 29 41 (91)
46 (92)
61 44 30 37 35 47 48 38 29
(98) (81) (93) (80) (80) (64) (66) (69)
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
436
ASCORBIC
f o o d s b e c a u s e of d e n t i t i o n p r o b l e m s .
ACID
F r u i t purees s u c h as a p p l e sauce
(361) h a v e b e e n o v e r l o o k e d p r o d u c t s .
L i k e d b y t h e e l d e r l y as a b r e a k
fast f r u i t , as a d i n n e r dessert, as a t o p p i n g f o r i c e c r e a m , these w o u l d b e one w a y of g e t t i n g m o r e a s c o r b i c a c i d t o t h e e l d e r l y i f t h e y w e r e n u t r i fied.
Ascorbic acid ( T a b l e X I I ) c a n feasibly a n d economically be a d d e d
to a p p l e
sauce.
C a n c e l et a l . (362)
reported
favorable
retention of
L - a s c o r b i c a c i d a d d e d t o c i t r o n slices p a c k e d i n s y r u p a n d to c i t r o n b a r s . A C I D - F E R M E N T E D
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of
A c i d f e r m e n t a t i o n is a v e r y a n c i e n t a r t
PRODUCTS.
p r e s e r v i n g a n d s t o r i n g foods s u c h as c a b b a g e a n d p i c k l e s
retaining their nutritive value.
while
A l t h o u g h cabbage has been k n o w n for
centuries as a v a l u a b l e a n t i s c o r b u t i c v e g e t a b l e , s a u e r k r a u t m a n u f a c t u r i n g , p a c k a g i n g , a n d storage c a n affect a s c o r b i c a c i d levels. D u r i n g a c t i v e a c i d f e r m e n t a t i o n , there is l i t t l e loss, b u t i n t a n k storage a n d t h e c a n n i n g process losses of v i t a m i n C c a n occur.
I n a s t u d y of 217 samples of
c a n n e d k r a u t , v a r i a t i o n s of 1 - 2 5 m g / 1 0 0
g were found.
T h e canned
p r o d u c t c o u l d b e m o d i f i e d to c o n t a i n a g i v e n a m o u n t of a d d e d acid, p r o d u c i n g a more u n i f o r m product POTATO
PRODUCTS.
ascorbic
(363).
I n some countries, potatoes c o n t r i b u t e a n a p p r e
c i a b l e p r o p o r t i o n of t h e d a i l y L - a s c o r b i c a c i d needs.
D u r i n g t h e last
d e c a d e a n d f o r e s h a d o w i n g t h e t r e n d i n t h e d e c a d e a h e a d , m o r e of t h e annual potato
c r o p is b e i n g c o n v e r t e d
to processed
potato
products,
particularly i n the developed countries. Average ascorbic a c i d values for varieties of potatoes t h a t a r e c o m m e r c i a l l y i m p o r t a n t r a n g e f r o m
about
10 t o 33 m g p e r 100 g of t h e f r e s h l y d u g t u b e r s , w i t h a n o v e r a l l v a l u e of 26 m g . Losses d u r i n g storage a p p r o x i m a t e o n e - f o u r t h of t h e a s c o r b i c a c i d c o n t e n t after 1 m o n t h , o n e - h a l f after 3 m o n t h s a n d t h r e e - f o u r t h s after 9 m o n t h s (364). A f u r t h e r d e g r a d a t i o n of a b o u t 4 0 % occurs d u r i n g w a s h i n g a n d c o o k i n g , a loss t h a t m a y increase i f t h e c o o k e d p r o d u c t is h e l d o n steamtables
before serving.
ascorbic a c i d has been observed
F o r f r e n c h fries, a loss of 6 5 % A n ever-increasing
(365).
percentage
of t h e p o t a t o c r o p is p r o c e s s e d i n t o p r o d u c t s s u c h as d e h y d r a t e d flakes,
granules, chips
o r crisps, a n d f r o z e n
sticks.
potato
D e h y d r a t i o n of
potatoes t o flakes, g r a n u l e s , o r slices i n d u c e s losses of 3 0 - 8 9 %
of t h e
natural
i n the
ascorbic
acid
L - a s c o r b i c a c i d content
content
(365-373).
of t h e p o t a t o
Interest
a n d potato
continues
products
(365-377)
w i t h a t t e n t i o n g i v e n t o assay m e t h o d s t h a t s p e c i f i c a l l y m e a s u r e a c i d i n processed potato products
ascorbic
(365).
C o n c e r n has b e e n s h o w n f o r t h e r e s t o r a t i o n of L - a s c o r b i c a c i d losses i n p o t a t o p r o d u c t s o r its a d d i t i o n f o r p r o d u c t i m p r o v e m e n t 367,371,372,373,378).
(317,366,
R e s t o r a t i o n m a y n o t b e a s i m p l e process, d e
p e n d i n g o n t h e specific p r o d u c t .
M e c h a n i c a l m i x i n g of t h e p o t a t o p r o d
u c t , g r a n u l e s , o r flakes w i t h c r y s t a l l i n e L - a s c o r b i c a c i d w i l l n o t y i e l d a u n i f o r m product, a n d mechanical m i x i n g breaks d o w n the potato particle.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
437
Ascorbic Acid Technology
BAUERNFEIND
P o w d e r e d ascorbic a c i d suspended i n an antioxidant-treated, saturated v e g e t a b l e o i l m a y b e s p r a y e d o n t h e d r i e d flakes, i f t h e p h y s i c a l a p p e a r a n c e of
the n u t r i f i e d p r o d u c t
is n o t
influenced.
W i t h potato
chips,
a s c o r b i c a c i d c a n b e a d d e d i n a salt p r e m i x . A d d i t i o n of a s c o r b i c a c i d t o the l i q u i d p o t a t o m a s h m a y b e p r a c t i c a l i f significant r e c y c l i n g of t h e h e a t e d p r o d u c t t h r o u g h the d r y i n g process is n o t excessive.
I n one s t u d y
( 3 6 7 ) , a s c o r b i c a c i d has b e e n a d d e d to c o o k e d p o t a t o m a s h , w h i c h w a s t h e n d r u m - d r i e d i n t o flakes, p a c k a g e d Downloaded by UCSF LIB CKM RSCS MGMT on November 18, 2014 | http://pubs.acs.org Publication Date: June 1, 1982 | doi: 10.1021/ba-1982-0200.ch020
n i t r o g e n gas. 70 ° F
i n t o cans, a n d sealed i n a i r o r
Storage r e t e n t i o n values i n t h e p r o d u c t after 7 m o n t h s at
approximated
nitrogen-packed.
75%
for a i r - p a c k e d containers
I n another
m a n u f a c t u r i n g of
potato
study
flakes
and 9 0 %
for
the
(372), extrusion variables i n the
were
noted
to s i g n i f i c a n t l y a l t e r
the
a s c o r b i c a c i d l e v e l of the e x t r u d e d p r o d u c t ( T a b l e X I I I ) . Klaeui
(317)
i n d i c a t e s some success has b e e n a t t a i n e d i f s u l f u r
d i o x i d e at levels w i t h i n l e g a l l i m i t s a n d a s m a l l a m o u n t of s o d i u m p y r o p h o s p h a t e a c t i n g as a sequestrant are a d d e d w i t h a s c o r b i c a c i d to p o t a t o Table XIII. Percent Vitamin C Retention in Potato Flakes Influenced by Extrusion Variables in Their Production Extrusion lemperature (°C)
J
RPM
/
t
S
(
r
e
w
g
/
1
g
c
r
e
as
w
Small Die
Large Die
Small Die
Large Die
135
40 80 120 160 200
94.3 90.1 85.2 81.9 80.7
96.5 95.1 91.9 86.8 82.9
90.2 84.7 80.5 80.1 76.1
91.5 90.2 85.8 82.8 79.4
149
40 80 120 160 200
90.4 82.5 80.6 77.1 76.5
92.4 91.0 87.3 82.5 80.6
87.2 80.1 75.2 70.7 64.2
90.5 86.2 83.3 74.0 70.1
163
40 80 120 160 200
88.9 83.5 77.6 70.2 63.5
91.1 88.2 80.3 75.6 72.1
83.1 80.8 75.2 68.3 60.2
87.2 83.3 76.2 72.4 67.9
177
40 80 120 160 200
87.2 81.5 67.4 50.7 46.2
90.2 89.4 73.2 60.0 53.7
83.0 77.2 65.1 48.3 42.6
85.0 80.8 68.9 52.4 44.5
Source: Reproduced, with permission, from Ref. 872. Copyright, 1978, ForsterVerlag AG.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
438
ASCORBIC
ACID
m a s h , t o a i d i n g o o d a s c o r b i c a c i d r e t e n t i o n a n d u n i f o r m i t y of c o l o r . U s i n g s o d i u m ascorbate ( 4 0 0 fig/g)
a n d ascorbyl palmitate (300 /*g/g)
i n p l a c e of a s c o r b i c a c i d p r o v i d e d a n t i o x i d a n t v a l u e a n d i m p r o v e d t e x t u r e d u r i n g t h e r e c o n s t i t u t i o n of t h e d r y p r o d u c t i n a d d i t i o n t o i m p r o v e d v i t a m i n v a l u e . I f n i t r o g e n p a c k i n g is n o t u s e d t o d e l a y d e t e r i o r a t i o n i n d r y p o t a t o p r o d u c t s d u r i n g p a c k a g i n g a n d storage, a n t i o x i d a n t s m a y b e incorporated
to retard oxidative
rancidity.
M o i s t u r e content
of t h e
p r o d u c t s h o u l d b e k e p t as l o w as is t e c h n i c a l l y f e a s i b l e ( p r e f e r a b l y
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than
less
6-8%). PRODUCTS.
C E R E A L - G R A I N
Cereal
grain products
contribute i m
m e a s u r a b l y t o t h e h u m a n d i e t a r y state (379, 380) a r o u n d the w o r l d . H o w ever, b a k e d goods s u c h as b r e a d , b u n s , a n d rolls a r e n o t g o o d carriers for a d d e d ascorbic a c i d w h e n the expectancy c l a i m is to b e m a d e .
of a specific
nutritional
A s c o r b i c a c i d f u n c t i o n s as a w h e a t flour i m p r o v e r ,
d e c o m p o s i n g t o a l a r g e extent i n its i m p r o v i n g a c t i o n d u r i n g t h e b a k i n g process; therefore l i t t l e r e m a i n s t o m e e t a c l a i m e d a s c o r b i c a c i d v a l u e i n the b a k e d p r o d u c t .
I f situations d e v e l o p w h e r e b y i t is d e s i r a b l e t o h a v e
a s c o r b i c a c i d i n a b a k e d i t e m , i t s h o u l d b e a p r o d u c t of t h e fast heat t y p e s u c h as d o n u t s (381) o r a c a k e o r c o o k i e f o r m u l a t i o n w h e r e a s c o r b i c a c i d is p u t i n a c r e a m filling o r i n a n i c i n g (382).
added
Stable deriva
tives ( 3 8 3 , 384) of a s c o r b i c a c i d t h a t w i l l s u r v i v e t h e b a k i n g process a r e known
b u t have
not been
demonstrated
as b i o l o g i c a l l y a v a i l a b l e t o
humans. A b l e n d of c o r n , soy, a n d m i l k i n a d r y m e a l n u t r i f i e d w i t h m i n e r a l a n d v i t a m i n s , t e r m e d C S M , has b e e n d e s i g n e d as a n u t r i t i o u s f o o d f o r human
consumption.
O n e of t h e a d d e d
Vojnovich a n d Pfeifer ( 3 8 5 ) conducted
v i t a m i n s is L - a s c o r b i c a c i d .
some trials w i t h a s c o r b i c
n u t r i f i e d C S M a n d p r e c o o k e d d r y i n f a n t cereals.
acid
Stability data revealed
t h a t d e s t r u c t i o n of t h e a d d e d a s c o r b i c a c i d w a s a first-order r e a c t i o n a n d that moisture content
w a s a c r i t i c a l issue i n a s c o r b i c
acid retention
( F i g u r e 8 ) . N o t more than 9 % moisture was shown to provide storage r e t e n t i o n v a l u e s .
good
E t h y l cellulose coated ascorbic a c i d was pre
f e r r e d over r e g u l a r c r y s t a l l i n e a s c o r b i c a c i d i n this c e r e a l p r o d u c t a p p l i cation. dry
L i n k o (386) n o t e d s t a b i l i t y of a s c o r b i c a c i d a d d e d t o F i n n i s h
r o l l e d oats w a s excellent
d u r i n g storage
cooking ( 9 2 % , 5 m i n boil i n water).
(88-96%)
and during
I n the U . S . , vitamins have
been
a d d e d t o d r y b r e a k f a s t cereals (387,388,389)
f o r some t i m e , a n d t e c h
nologies f o r a d d i n g t h e m h a v e b e e n d e v e l o p e d .
T h e effects of p r o c e s s i n g
a n d storage of cereals w i t h a d d e d m i c r o n u t r i e n t s , i n c l u d i n g L - a s c o r b i c a c i d , w e r e i n v e s t i g a t e d b y A n d e r s o n et a l . (390), a n d a s l i g h t loss a t 4 0 ° C w a s e x p e r i e n c e d f o r a s c o r b i c a c i d i n some cereals b u t n o t i n others. T h e l o w m o i s t u r e c o n t e n t of this class of p r o d u c t s a n d use of m o i s t u r e resistant p a c k a g i n g m a k e t h e m a g o o d c a r r i e r . K l a e u i (314)
conducted
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
439
Ascorbic Acid Technology
—
^^CC^TI
26 C , 8.0% H 0 f
2
— 37°C , 8 0% H 0 2
H0 2
4 5 ° C . 8.0% H 0 2
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2
^37C.
10.4% H 0 2
3
2 4 5 Stotage. Months Figure 8. Storage of CSM containing brand a: effect of moisture content and temperature on retention of ascorbic acid. (Reproduced, with permission, from Ref. 385. Copyright 1970, American Association of Cereal Chemists, Incorporated.)
a s t u d y i n c l u d i n g a s c o r b i c a c i d , s o d i u m ascorbate, a n d a s c o r b y l p a l m i t a t e i n v a r i o u s m i x t u r e s t h a t illustrates t h e s i g n i f i c a n t i n f l u e n c e of t h e t y p e o f carrier o n stability performances ( T a b l e X I V ) .
G a g e (391) has exam
i n e d snack foods i n c l u d i n g those t h a t m a y b e s u i t a b l e f o r n u t r i f i c a t i o n w i t h ascorbic acid. IRON UTILIZATION.
I r o n deficiency, a m a j o r cause o f a n e m i a i n
h u m a n s , is a w o r l d - w i d e p r o b l e m
(392,893,394)
a n d t h e search f o r
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
440
ASCORBIC
ACID
Table X I V . Stability of Various Vitamin C Forms in Some Edible Carriers ( A f t e r 1 Year Storage in Closed Bottles)
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Vitamin
Vitamin
Tem-
Added
perature
Wheat Starch
C-Retention
in Percent Skimmed Milk Powder
Wheat Flour
of Initial
Glucose Monohydrate
Value Glucose Anhydrous
Ascorbic acid
R T
97.8
71.2
83.7
68.5
70.7 70.2
76.8 74.2
97.2
45°C
Sodium ascorbate
R T 45°C
97.5 81.4
70.4 70.2
81.3 72.1
84.5 74.5
94.8 74.2
Ascorbyl palmitate
95.8 85.4
69.3 43.4
86.0
90.1
45°C
81.8
55.3
85.9 80.4
12.0%
12.5%
R T
W a t e r content of carrier material
75.8
0.1%
9.1%
3.5%
Source: Reproduced, with permission, from Ref. 31^. Copyright 1 9 7 4 , Applied Science Publishers Limited. effective s u p p l e m e n t s
(392,394) is a n e v e r e n d i n g o n e . O n e p r e v a i l i n g
approach gaining momentum
( 3 9 2 ) is t o i m p r o v e t h e b i o l o g i c a l a v a i l a
b i l i t y of e x i s t i n g d i e t a r y i r o n s u p p l i e s o r a d d e d i r o n b y also i n c o r p o r a t i n g some f a c i l i t a t i n g substance i n t h e d i e t s u c h as L - a s c o r b i c a c i d
(395-404).
C e r e a l g r a i n meals
(396,397),
sugar (399,407,408),
( 3 9 5 , 3 9 8 ) , soy b e a n
meal
( 3 9 5 ) , salt
M S G , coffee, t e a , a n d m i l k
(401-404)
are some
p o t e n t i a l f o o d c a r r i e r s . I n instances, b o t h a n i r o n s o u r c e a n d a s c o r b i c a c i d are added.
S o m e investigators b e l i e v e t h a t i n h i g h c e r e a l
ascorbic a c i d m a y be needed. dependent.
A s l i t t l e as 2 5 m g , as a m e a l i n t a k e , m a y b e significant (400),
b u t intakes of 1 0 0 m g o r m o r e d a i l y m a y b e t h e g o a l sought. been proposed prospect sodium
as a n i r o n c a r r i e r (405,406) w o u l d prevent
Coffee has
a n d L e e (409) raises t h e
of i n s t a n t coffee as a c a r r i e r f o r L - a s c o r b i c ascorbate
whitener.
diets
T h e e n h a n c i n g b y a s c o r b i c a c i d is d o s e -
acid.
c u r d l i n g of a d d e d
T h e use of
cream
o r coffee
Beverages n u t r i f i e d w i t h a d d e d a s c o r b i c a c i d a n d c o n t a i n i n g
i r o n a r e c l a i m e d t o b e s t a b i l i z e d b y t h e a d d i t i o n of cysteine
according
to M o r s e a n d H a m m e s ( 4 1 0 ) . I N F A N T
MILKS.
T h e effect o f p r e p a r a t i o n , t e c h n o l o g y ,
a n d storage
c o n d i t i o n s of a s c o r b i c a c i d n u t r i f i e d e v a p o r a t e d m i l k i n f a n t f o r m u l a t i o n s has b e e n s t u d i e d b y s e v e r a l investigators (411,412,413) has b e e n r e v i e w e d b y others.
a n d i n the past
It is e c o n o m i c a l l y a n d n u t r i t i o n a l l y s o u n d
t o n u t r i f y e v a p o r a t e d m i l k w i t h 5 0 - 1 0 0 m g of a s c o r b i c a c i d p e r 1 3 fl o z (384.5 m L ) , for future reconstitution to a quart or liter, i n vacuum-sealed c o n t a i n e r s a c c o r d i n g t o P e n n s y l v a n i a State U n i v e r s i t y researchers. T h e s o d i u m salt is p r e f e r r e d t o a v o i d a p o t e n t i a l d e s t a b i l i z a t i o n effect o n t h e
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
Ascorbic Acid Technology
BAUERNFEIND
m i l k p r o t e i n s d u r i n g the s t e r i l i z a t i o n process.
441
W h e n 50 a n d 100 m g w a s
a d d e d , 35 a n d 71 m g of a s c o r b i c a c i d p e r l i t e r , r e s p e c t i v e l y , w e r e present o n a r e c o n s t i t u t e d basis after p r o c e s s i n g a n d 12 m o n t h s ' storage at r o o m temperature ( 2 5 ° C ) .
I n the U . S . e v a p o r a t e d m i l k - b a s e i n f a n t foods are
m a r k e t e d c o n t a i n i n g 50 m g of a d d e d a s c o r b i c a c i d p e r 13-fl-oz c a n , w h i c h is d i l u t e d to a q u a r t b e f o r e c o n s u m p t i o n .
Some dry-formulated infant
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foods are l i k e w i s e f o r t i f i e d w i t h a s c o r b i c a c i d . D r y , l o w - c a l o r i e d i e t foods i n t e n d e d for t h e o l d e r a d u l t m a r k e t also c o n t a i n a d d e d a s c o r b i c
acid;
these p r o d u c t s are to be r e c o n s t i t u t e d i n w a t e r or m i l k b e f o r e use.
Many
cereals a n d m i l k p o w d e r s for infants are r o u t i n e l y n u t r i f i e d w i t h one of t h e v a r i o u s a c c e p t a b l e forms of i r o n . T h e b i o a v a i l a b i l i t y of s u c h i r o n is s t r i k i n g l y i m p r o v e d w h e n a s c o r b i c a c i d is also present ( 4 1 4 ) . A r a t i o b y w e i g h t of at least 1:5 i r o n to a s c o r b i c a c i d is H e a d a n d H a n s e n (415)
recommended.
a d d e d L - a s c o r b i c a c i d (42.3
mg/L)
to
w h o l e , chocolate, a n d l o w fat ( 1 % ) fluid m i l k s to increase t h e a s c o r b i c a c i d i n t a k e of s c h o o l c h i l d r e n .
T h r e e m i l k treatments w e r e
examined
( C ) p a s t e u r i z e d m i l k , ( E ) p a s t e u r i z a t i o n ( 7 4 ° C f o r 16 s) after a s c o r b i c a c i d a d d i t i o n , a n d ( F ) a s c o r b i c a c i d a d d i t i o n after p a s t e u r i z a t i o n . S t o r age ( 4 ° C )
r e t e n t i o n of a s c o r b i c a c i d ( F i g u r e 9 ) w a s g o o d , a n d t h e taste
reactions of c h i l d r e n w e r e f a v o r a b l e . a n d A n d e r s o n et a l . (417)
P r e v i o u s l y W e i n s t e i n et a l .
(416)
h a d reported on ascorbic a c i d nutrified fluid
m i l k to w h i c h a s c o r b i c a c i d w a s a d d e d at 50 a n d 200 m g / L , r e s p e c t i v e l y . Infant milks nutrified w i t h ascorbic a c i d were investigated b y C a m e r o n (418)
d u r i n g t h e p r e p a r a t o r y p r o c e d u r e s p r i o r to i n f a n t f e e d i n g . Use as a Processing A i d .
I n a d d i t i o n to s e r v i n g as a n a d d e d n u t r i
ent i n f o o d , L - a s c o r b i c a c i d has the u n u s u a l p r o p e r t y , b e c a u s e of
its
s t r u c t u r e a n d c h e m i c a l n a t u r e , to act as a p r o c e s s i n g a i d for c e r t a i n foods or food ingredients. usually foregoing
I n this r o l e i t is a d d e d for a n i n t e n d e d
nutritional considerations
purpose,
since m u c h of t h e
added
a s c o r b i c a c i d u n d e r g o e s d e g r a d a t i o n to p r o t e c t the q u a l i t y of t h e f o o d product.
O n l y s m a l l a m o u n t s i n some a p p l i c a t i o n s m a y r e m a i n of u n -
reacted ascorbic
acid.
E x a m p l e s of its i m p r o v i n g agent r o l e a r e :
an
o x y g e n s c a v e n g i n g agent i n b o t t l e d a n d c a n n e d f o o d p r o d u c t s ; a n i n h i b i t o r of o x i d a t i v e r a n c i d i t y i n f r o z e n fish; a s t a b i l i z e r of c o l o r a n d flavor i n c u r e d meats; a m a t u r i n g agent for
flour;
an oxygen
acceptor i n beer
p r o d u c t i o n ; a n d a r e d u c i n g agent i n w i n e . FRUIT
A N D
VEGETABLES.
F r u i t s can be
d i v i d e d into two
classes:
those t h a t s h o w d i s c o l o r a t i o n o n c u t t i n g or i n j u r y , s u c h as t h e a p p l e , a p r i c o t , b a n a n a , c h e r r y , n e c t a r i n e , p e a c h , a n d p e a r ; a n d others t h a t d o not, s u c h as c i t r u s f r u i t .
F o r this t y p e of d i s c o l o r a t i o n or b r o w n i n g t o
o c c u r i n c u t f r u i t , three c o m p o n e n t s — s u b s t r a t e , are b r o u g h t together.
oxygen, a n d
enzymes—
I f one of the three is r e m o v e d or p r e v e n t e d f r o m
r e a c t i n g , b r o w n i n g does not t a k e p l a c e .
H e a t i n g w o u l d destroy
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
the
442
ASCORBIC
ACID
9 Or-
eo -
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70 -
01 0
i
i
i
i
4
8
12
i
i
i i
16 20 DAYS OF STORAGE
i
i
i
24
28
32
i 36
Figure 9. Ascorbic acid changes during storage of whole milk ( ), chocolate-flavored whole milk (•---), and 1% fat milk (' ' ') with three treatments ( A , C , O , E; F). (Reproduced, with permission, from Ref. 415. Copyright 1979, American Dairy Science Association.) e n z y m e b u t w o u l d result i n a c o o k e d f r u i t flavor a n d a texture c h a n g e . F r u i t tissues t h a t d i s c o l o r h a v e a c o m b i n a t i o n of l o w c o n c e n t r a t i o n of a s c o r b i c a c i d a n d h i g h l y a c t i v e phenolases, a c t i n g o n o r t h o p h e n o l i c strates t o f o r m t h e c o l o r e d o r t h e q u i n o n e c o m p o u n d s .
sub
L-Ascorbic acid
inhibits the phenolase action or the enzymatic b r o w n i n g sequence b y reducing orthoquinone
products
respective orthophenols.
of t h e e n z y m e
reaction back to the
I f t h e a s c o r b i c a c i d content b e c o m e s e x h a u s t e d ,
b r o w n i n g a g a i n c o m m e n c e s . U s e of a s c o r b i c a c i d i n this a p p l i c a t i o n has b e e n p r e v i o u s l y r e v i e w e d (311,312,321,323,332,
419).
S e l e c t e d g r a d e d f r u i t is p e e l e d a n d s l i c e d o r d i c e d , a n d
sugar i s
a d d e d e i t h e r as sugar s y r u p c o n t a i n i n g a s c o r b i c a c i d o r d r y s u g a r p r e v i ously blended w i t h crystalline ascorbic compactly
a c i d , after w h i c h t h e f r u i t is
p a c k a g e d , q u i c k l y f r o z e n , a n d h e l d i n a f r o z e n state u n t i l
t h a w e d b y the consumer.
T h e a d d i t i o n of 3 0 0 - 5 0 0 m g of L - a s c o r b i c a c i d
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
443
Ascorbic Acid Technology
BAUERNFEIND
p e r k g of f r u i t s u g a r p a c k is a d e q u a t e f o r t h e p r o t e c t i o n of t h e p a c k d u r i n g p r o c e s s i n g , storage, a n d t h a w i n g . W h i l e a h i g h p e r c e n t a g e of a s c o r b i c a c i d is c o n v e r t e d to t h e r e v e r s i b l e o x i d a t i o n p r o d u c t , d e h y d r o a s c o r b i c a c i d ( 4 2 0 ) , d u r i n g t h e t h a w i n g of t h e f r u i t ( T a b l e X V ) , t h e latter is f u l l y b i o l o g i c a l l y a c t i v e ( 9 1 5 ) a n d is also c o n s i d e r e d as v i t a m i n C.
S i n c e fresh a p p l e tissue contains e x t r a c e l l u l a r o x y g e n , slices m u s t b e
c u t t h i n l y ( 6 m m ) or a v a c u u m s y r u p step m u s t b e u s e d o n c o n v e n t i o n a l slices t o get a s c o r b i c a c i d p e n e t r a t i o n (421).
Certain additives w i t h
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a s c o r b i c a c i d s u c h as N a C l (421), cysteine (422), s u l f u r d i o x i d e
(423),
a n d c i t r i c a c i d (424) h a v e b e e n d e c l a r e d to h a v e some m e r i t . I n a s t u d y of s l i c e d a p p l e t r e a t m e n t b e f o r e f r e e z i n g , P o n t i n g a n d J a c k s o n (425) f a v o r e d s o a k i n g slices i n a 2 0 - 3 0 %
sugar solution containing 0 . 2 - 1 %
ascorbic acid, 0 . 2 - 4 % calcium, a n d 0 . 0 2 % sulfur dioxide, f o l l o w i n g b y r a p i d freezing. T h e a s c o r b i c a c i d t r e a t m e n t process has b e e n u s e d f o r h o l d i n g c u t f r u i t at r e f r i g e r a t e d t e m p e r a t u r e s (426, 427,428, 432, 434), f o r f r u i t t o b e f r o z e n (426, 429, 430), a n d i n some instances t o reverse i n i t i a l b r o w n i n g of c u t f r u i t (431).
H e a t o n et a l . (427) r e p o r t e d s l i c e d peaches t r e a t e d
w i t h ascorbic a c i d (0.15% ) a n d sodium benzoate (0.066% for m i c r o b i a l c o n t r o l ) t o h o l d u p w e l l stored f o r 12 m o n t h s at 0 ° C .
E i d and Holfelder
(432) i m m e r s e d ( 2 0 s ) p e e l e d , c o r e d apples i n a s c o r b i c a c i d solutions ( 5 - 1 5 % ) a n d s t o r e d ( 9 d ) t h e m at c o o l t e m p e r a t u r e s ( 4 - 6 ° C ) p a c k a g e d i n p o l y e t h y l e n e bags, w i t h some v a r i a t i o n i n p e r f o r m a n c e b a s e d o n a p p l e variety.
T h e a s c o r b i c a c i d d i p p i n g a p p r o a c h has also b e e n u s e d (433)
p r i o r t o d r y i n g a p p l e slices.
O t h e r reports d e a l i n g w i t h a s c o r b i c a c i d
a p p l i c a t i o n i n v o l v e p i n e a p p l e s ( 4 3 4 ) , a v o c a d o p u r e e (435), pears (436), s t r a w b e r r i e s (437), a n d a p r i c o t j u i c e (438). Table X V .
Vitamin C Content of Thawed Frozen Sliced Peaches Packed with Sugar S y r u p 0
Pack Number
Percent Sugar in Syrup
1 2 3 4 5
65 65 65 35 35
Added Ascorbic Acid
0 150 200 0 150
Assayed Immediately After Thawing
Assayed After Holding 24 Hours at 22°C (72°F) Thawed
Ascorbic Acid Content
Ascorbic Acid Content
9 140 178 4 36
Total Vitamin C Content
11 146 188 7 141
Total Vitamin C Content
2 76 88 1 79
9 154 190 11 156
° Hale Haven, yellow-fleshed, freestone sliced peaches (3 parts) packed in sugar syrup (1 part by weight). Source: Reproduced, with permission, from Ref. J$0. Copyright 1946, A V I P u b lishing Company.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
444
ASCORBIC
ACID
I n h e a t p r o c e s s i n g , t h e oxidases ( a s c o r b i c a c i d oxidase, p o l y p h e n o l oxidase, p e r o x i d a s e )
n a t u r a l l y present i n t h e p r o d u c t
e i t h e r d u r i n g t h e b l a n c h i n g stage o r s e a l e d containers.
finally
C o l o r a n d flavor changes
are destroyed,
d u r i n g s t e r i l i z a t i o n of t h e of f r u i t s a n d vegetables
d u r i n g h e a t p r o c e s s i n g a n d storage, i n p a r t , r e s u l t f r o m o x i d a t i o n b y oxygen w i t h i n the product a n d headspace. helps to protect
aromatic components
u n d e r g o i n g flavor a n d c o l o r changes.
T h e a d d i t i o n of a s c o r b i c a c i d a n d phenolic
substrates
from
C o m b i n e d w i t h deaerating,
filling,
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a n d s c a l i n g t e c h n i q u e s , a s c o r b i c a c i d a d d i t i o n efficiently h e l p s t o create a n d m a i n t a i n a n a n a e r o b i c a t m o s p h e r e w i t h i n t h e c o n t a i n e r . I n t h e past this g e n e r a l subject has b e e n
reviewed
(311,319,323,419,439)
i n v o l v e s heat p r o c e s s e d f r u i t s a n d vegetables.
as i t
A s a n e x a m p l e of o n e of
t h e e a r l i e r trials (440), a d d e d a s c o r b i c a c i d a p p r e c i a b l y i m p r o v e d t h e a p p e a r a n c e a n d flavor of h o m e - c a n n e d s l i c e d a p p l i e s ( T a b l e X V I ) . I n a s u b s e q u e n t s t u d y b y H o p e (441) t h e a d d i t i o n of a s c o r b i c a c i d ( 5 0 0 - 6 0 0 m g / k g of f r u i t ) t o a p p l e h a l v e s ( c a n n e d w i t h o u t d e a e r a t i o n , t h e h e a d space c o n t a i n i n g 1 0 - 1 2 v o l u m e s p e r c e n t o x y g e n ) c o n t r o l l e d b r o w n i n g , reduced headspace oxygen, protected the container from corrosion, pro t e c t e d flavor, a n d i n c r e a s e d t h e r e s i d u a l a s c o r b i c a c i d content. A l i g h t c o l o r e d p e a r j u i c e w a s p r e p a r e d b y t h e use of a s c o r b i c a c i d to r e t a r d b r o w n i n g w h i l e t h e p u l p o r j u i c e w a s h e a t e d to i n a c t i v a t e t h e p o l y p h e n o l oxidase
(442).
B i r c h et a l . (319)
have examined
flavor
changes d u r i n g f r u i t j u i c e p r o c e s s i n g b o t h f r o m a m e c h a n i s m c o n c e p t and from practical and deoxygenation flavor."
finding.
T h e y conclude that ascorbic a c i d a d d i t i o n
p r i o r to p a s t e u r i z a t i o n helps to r e d u c e
"processed
T h e a m o u n t of a s c o r b i c a c i d r e q u i r e d t o e l i m i n a t e flavor c h a n g e
Table X V I .
Effect of Added Ascorbic A c i d on Canned Sliced Apples 0
After Canning Pack Number
Added Ascorbic Acid*
Ascorbic Acid
Total Vitamin C
After 6 Months' Storage at 21>°C (75°F) Ascorbic Acid
Total Vitamin C
Appearance of Pack
5 22 74
5 15 33 82
dark throughout slightly dark normal normal
mg/pt Jar 1 2 3 4
0 67 135 200
0.1 15 57 118
3 18 59 118
° Mcintosh apples peeled and sliced, cooked 3 to 4 min to soften, hot-packed with 50% syrup in Ball Ideal pint jars, 5/16-in. headspace, processed 10 min in boiling water. Ascorbic acid added in aqueous solution before sealing jar. Source: Reproduced, with permission, from Ref. 440. Copyright 1947, Ogden Publishing Company. b
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
445
Ascorbic Acid Technology
BAUERNFEIND
is p r o p o r t i o n a l t o t h e glucose c o n c e n t r a t i o n .
These workers
find
that
g r a p e f r u i t , l e m o n , a n d orange j u i c e a p p e a r t o c o n t a i n sufficient a s c o r b i c a c i d t o exert t h e necessary
p r o t e c t i v e effect.
A p p l e , pineapple, a n d
tomato juice m a y require ascorbic a c i d addition. A d d e d ascorbic a c i d m a y also i m p r o v e j u i c e color, b u t this d e p e n d s p r o c e s s i n g m e t h o d s s t u d i e d (443-448).
on the product a n d
B a s e d u p o n p r a c t i c a l experience
a n d s u p p o r t e d b y t h e o r y , a sufficient l e v e l of a s c o r b i c a c i d m u s t b e present, i f t h e p r o d u c t is subject t o o x i d a t i v e d e t e r i o r a t i o n , t o s u r v i v e Downloaded by UCSF LIB CKM RSCS MGMT on November 18, 2014 | http://pubs.acs.org Publication Date: June 1, 1982 | doi: 10.1021/ba-1982-0200.ch020
p r o c e s s i n g , storage, a n d h o m e p r e p a r a t i o n f o r c o n s u m p t i o n as a n a i d t o m a i n t e n a n c e of p r o d u c t characteristics. E v e n w i t h o x y g e n e x h a u s t i o n , subsequent loss of a s c o r b i c a c i d m a y o c c u r d u e to a n a e r o b i c d e c o m p o sition
(449).
Ascorbic acid w i l l not prevent the non-oxidative
type
b r o w n i n g (sugars a n d nitrogeneous c o m p o u n d s ) a n d m a y e v e n p r o m o t e this t y p e of r e a c t i o n . I n a n y n e w c o m m e r c i a l p r o d u c t i o n v e n t u r e , p i l o t scale studies ( T a b l e X I I ) a r e a d v i s a b l e t o d e t e r m i n e results b a s e d o n t h e specific project d e t a i l t o b e e n c o u n t e r e d .
A s i n f r u i t juices a n d c a n n e d
f r u i t , s i m i l a r b e n e f i c i a l effects c a n result w h e n a s c o r b i c a c i d is u s e d as a p r o c e s s i n g a i d f o r c e r t a i n vegetables, f o r e x a m p l e , olives i n b r i n e ( 4 5 0 ) , s a u e r k r a u t i n b r i n e (311), p i c k l e d c a u l i f l o w e r (456), c a n n e d ( 4 5 7 ) o r g l a s s - p a c k e d ( 4 5 1 ) a n d freeze
d r i e d ( 4 5 2 ) carrots, m u s h r o o m s
454,455), h o r s e r a d i s h p o w d e r (458), a n d c o l e s l a w FISH.
ponent
Fish
fillets,
steaks, a n d some shellfish h a v i n g a f a t t y
u n d e r g o i n g o x i d a t i v e r a n c i d i t y i n f r o z e n storage
f r o m a s c o r b i c a c i d a p p l i c a t i o n (311,312). 461) w e r e
(453,
(459). com
m a y benefit
T a r r a n d coworkers
t h e e a r l y i n v e s t i g a t i v e t e a m t h a t r e s e a r c h e d this
(460,
subject.
A s c o r b i c a c i d ( 0 . 5 - 3 . 0 % ) m a y b e a p p l i e d b y either a d i p p i n g o r a s p r a y i n g t e c h n i q u e . T o ensure a n even a n d a sufficiently t h i c k c o a t i n g , t h i c k e n i n g agents m a y b e a d d e d t o t h e s o l u t i o n . T h e f r o z e n
storage
shelf l i f e of t h e fish m a y b e e x t e n d e d several m o n t h s b y t h e a s c o r b i c a c i d treatment. A s a n e x a m p l e , n e w l y c a u g h t h e r r i n g w e r e filleted, d i p p e d i n a s o l u t i o n o f a s c o r b i c a c i d ( 0 . 5 % ) w i t h a t h i c k e n i n g agent, p a c k e d i n a w a x e d c a r d b o a r d b o x , f r o z e n ( — 4 0 ° C ) , a n d stored ( — 2 0 ° C ) . w e r e t h a w e d m o n t h l y a n d e v a l u a t e d (462).
Samples
U n t r e a t e d samples b e c a m e
r a n c i d after 2 m o n t h s of storage, w h e r e a s t r e a t e d samples r e m a i n e d p a l a t a b l e f o r 11 m o n t h s j u d g e d b y taste p a n e l ( F i g u r e 10) a n d T B A values ( F i g u r e 1 1 ) . J a d h a v a n d M a g a r (463) a p p l i e d a n a s c o r b i c a c i d glaze, w h i c h delayed the yellow discoloration a n d allied organoleptic
changes, t o
f r o z e n w h i t e p o m f r e t , s u r m a i , a n d m a c k e r e l fish. U s e of phosphates i n c o m b i n a t i o n w i t h ascorbate esters has b e e n d e c l a r e d t o i m p r o v e the c o l o r and
flavor
of fish p r o d u c t s
(464).
Shellfish
(465,466,467)
including
prawns a n d breaded shrimp, have been ascorbic a c i d treated, the latter in combination w i t h citric acid.
F o r m a t i o n of d i m e t h y l n i t r o s a m i n e i n
A l a s k a n p o l l a c k r o e (468) w a s i n h i b i t e d w h e n a s c o r b i c a c i d w a s i n -
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
446
ASCORBIC
ACID
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Taste score
Storage
time-months
Figure 10. Results from organoleptic evaluation of untreated herring samples (M) and samples treated with ascorbic acid (O) after different times of storage. (Reproduced, with permission, from Ref. 462. Copyright 1961, Institute of Food Technolgists.) eluded w i t h a nitrite treatment.
Alaskan pollack muscle treated w i t h
a s c o r b i c a c i d w a s i n v e s t i g a t e d b y Y o s h n a k a et a l . (469). M o l e d i n a et a l . (470), w o r k i n g w i t h m e c h a n i c a l l y d e b o n e d
flounder
meat, o b s e r v e d a n
i m p r o v e m e n t i n c o l o r a n d flavor ( F i g u r e 12) w h e n t r e a t e d w i t h a c o m b i n a t i o n of a s c o r b i c a c i d ( 0 . 5 % ) , c i t r i c a c i d ( 0 . 5 % ) , N a E D T A ( 0 . 2 % ) 2
a n d phosphates
( K E N A , 0.2%).
A n u m b e r of p a p e r s (468-A74)
have
r e c e n t l y d i s c u s s e d t h e p r o c e s s i n g of m u l l e t i n c l u d i n g a s c o r b i c a c i d a p p l i c a t i o n . T h e t r e a t m e n t appears m o r e effective f o r fish i n t h e r o u n d a n d i n fillets t h e n i n m i n c e d tissue. MEAT.
F o r p r e s e r v a t i o n purposes, m e a t has b e e n c u r e d w i t h a d d e d
salt ( N a C l ) a n d nitrates ( s a l t p e t e r ) since a n c i e n t times. W i t h t h e r e c o g n i t i o n t h a t n i t r a t e w a s r e d u c e d b y m i c r o b i a l a c t i o n , a b o u t 60 years a g o , a d d e d n i t r i t e b e g a n to r e p l a c e n i t r a t e . T h e t y p i c a l r e d c o l o r of c u r e d m e a t results f r o m t h e r e a c t i o n of n i t r i c o x i d e w i t h m y o g l o b i n t o f o r m nitrogen monoxide
myoglobin,
more
frequently
r e f e r r e d t o as n i t r o -
s o m y o g l o b i n , a n d w i t h heat, n i t r o s o m y o c h r o m e . F o r n e a r l y 3 0 years (327,475,478) fixation,
flavor,
i t has been k n o w n that
color
a n d odor were greatly i m p r o v e d w h e n ascorbic a c i d was
i n c l u d e d i n t h e f o r m u l a t i o n of c o o k e d , n i t r i t e d , g r o u n d p o r k a n d t h a t f r a n k f u r t e r s c o n t a i n i n g ascorbate
h a d a more
products
desirable a n d
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
447
Ascorbic Acid Technology
BAUERNFEIND
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TBA
O
1
O
1
2
1
400 > 400 28.5 4.3 2.4
Source: Reproduced, with permission, from Ref. 641. Copyright 1973, Verlag Hans Huber.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
460
ASCORBIC
Table X X I I I .
Comparative Antioxidant
ACID
Activity"
Days to Reach 20meq/kg PV
b
Concentration
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Antioxidant
Chicken Fat
(%)
None DL-a-Tocopherol DL-a-Tocopherol DL-a-Tocopherol DL-a-Tocopherol DL-a-Tocopherol DL-a-Tocopherol DL-y-Tocopherol DL-y-Tocopherol DL-y-Tocopherol Butylated hydroxyanisole DL-a-Tocopherol Ascorbyl palmitate DL-y-Tocopherol Ascorbyl palmitate Ascorbyl palmitate
Beef Fat 10 24
0.02 0.05 0.2 0.02 0.05 0.2 0.02 0.05 0.2 0.02
8 13 13 10 13 13 11 29 40 46 20
3 15 15 15 15 15 15 37 58 61 28
0.02 each
28
28
38
0.02 each 0.02
53 10
67 9
70 12
° Schaal oven, thin layer, 45°C. * Peroxide value. Source: Reproduced, with permission, from Ref. Oil Chemists Society.
T h e development
Pork Fat
6J+2.
— — — — — 40
— — 36
Copyright 1974, American
is i n f l u e n c e d , a m o n g o t h e r t h i n g s , b y o x y g e n
of t h e m i l k , o x i d a t i v e e n z y m e
activity, oxidation-reduction
exposure of t h e m i l k to l i g h t , presence of d i s s o l v e d c o p p e r ,
content
potential, tocopherol
content, a n d a s c o r b i c a c i d content of t h e m i l k . W h e n m i l k is t a k e n f r o m t h e c o w it c o n t a i n s l i t t l e or n o o x y g e n ; h o w e v e r , w h e n i t comes i n c o n tact w i t h the a i r i t absorbs m o r e o x y g e n .
Freshly d r a w n cows' milk may
c o n t a i n as m u c h as 30 m g of a s c o r b i c a c i d i n the r e d u c e d f o r m p e r l i t e r or p e r q u a r t . C u s t o m a r y h a n d l i n g m e t h o d s , p a s t e u r i z a t i o n , a n d t h e l o n g t i m e i n t e r v a l necessary for s h i p m e n t , storage, a n d d e l i v e r y b e t w e e n m i l k i n g a n d c o n s u m p t i o n c a n destroy 7 0 - 8 0 % o r i g i n a l l y present. delays
flavor
of t h e n a t u r a l a s c o r b i c a c i d
K e e p i n g milk deaerated
and from
light
exposure
changes.
T h e p r a c t i c a l use of a d d e d a s c o r b i c a c i d has p r o v e d to b e of benefit to t h e d a i r y i n d u s t r y (311, 321).
T h e a m o u n t s of a s c o r b i c a c i d or s o d i u m
ascorbate u s e d v a r y b e t w e e n t w e n t y a n d s e v e r a l h u n d r e d m i l l i g r a m s p e r l i t e r , 3 0 - 5 0 m g u s u a l l y b e i n g sufficient for f r e s h fluid m i l k . i n t h e results of
some w o r k e r s
Discrepancies
a t t e m p t i n g to e l u c i d a t e t h e v a l u e
of
a s c o r b i c a c i d i n the d e v e l o p m e n t of off-flavor m a y b e d u e to t h e i r e x a m i n a t i o n of a n i n c o m p l e t e system of o x i d a t i v e reactions.
I t has b e e n
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
dem-
20.
461
Ascorbic Acid Technology
BAUERNFEIND
Table X X I V .
O x i d a t i o n of
Soybean O i l Days to Reach 72 meq/kg PV
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Antioxidant None 0.01% A P 0.02% A P 0.05% A P 0.2% A P 0.02% B H A 0.02% B H T 0.02% T D P A 0.01% P G 0.02% P G 0.02% N D G A 0.02% T B H Q 0.02% Ascorbic A c i d 0.2% Ascorbic A c i d 0.01% A P + 0.01% P G 0.01 % A P + 0.01 % T D P A 0.01 % A P + 0.01 % B H A 0.01% A P + 0.01% B H T 0.01 % A P + 0.01 % N D G A 0.01% A P + 0.01% Tocopherol A P at 0 . 0 5 % , P G , T D P A a t 0 . 0 1 % A P at 0.05%, B H A , T D P A at 0.01% A P a t 0 . 0 5 % , B H A , P G at 0 . 0 1 % A P at 0 . 0 5 % , B H T , T D P A a t 0 . 0 1 %
7 16 19 21 25 9 10 15 20 20 21 26 12 17 27 21 18 17 28 16 42 30 31 31
"Heated at 45°C. A P = ascorbyl palmitate, B H A = butylated hydroxyanisole, B H T = butylated hydroxytoluene, T D P A = thiodipropionic acid, P G = propyl gallate, N D G A = nordihydroguaiaretic acid, T B H Q = 2-ter£-butylhydroquinone. Source: Reproduced, with permission, from Ref. 642. Copyright 1974, American Oil Chemists Society. b
o n s t r a t e d t h a t the t o c o p h e r o l
content of m i l k also p l a y s a r o l e i n t h e
o x i d a t i v e processes. R e p o r t s c l a i m a s y n e r g i s t i c effect of t o c o p h e r o l
and
a s c o r b i c a c i d to b e b e n e f i c i a l i n p r e v e n t i n g o x i d a t i v e off-flavor i n d a i r y products.
T h e a - t o c o p h e r o l c o n t e n t of c o w s m i l k , as r e c e n t l y
reviewed
( 6 4 7 ) , varies w i t h season a n d f e e d i n g p r a c t i c e s , r a n g i n g f r o m 4 - 3 0 ju,g/g fat.
Tocopherol
removes
the
is i n the fat a n d r e m o v a l of fat f r o m m i l k
tocopherol.
Hence,
both
tocopherol
and
obviously
ascorbic
acid
should be considered equally important i n m i l k a n d dairy product
flavor
s t a b i l i z a t i o n . T h e s e observations c o n f i r m t h e d a t a o n b u t t e r r e p o r t e d i n a n y e a r l i e r section. L i t e r a t u r e reports since the 1970 r e v i e w interest i n s t a b i l i z a t i o n of d a i r y p r o d u c t s
(312)
c o n t i n u e to
show
s u c h as use of a s c o r b i c
a n d t o c o p h e r o l i n c o n t r o l l i n g o x i d i z e d flavor i n s t e r i l i z e d c r e a m
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
acid
(648).
462
ASCORBIC
ACID
U s e of a d d e d a s c o r b i c a c i d d e l a y e d flavor d e v e l o p m e n t i n p a c k a g e d m i l k concentrates ( 6 4 9 ) , i n m i l k f a t ( 6 5 0 ) , i n goat m i l k c u r d ( 6 5 1 ) , i n b u t t e r f r o m buffalo m i l k
(652), i n y-irradiated skim-milk powder
(653), i n
l o w - f a t d a i r y spreads ( 6 5 4 ) , a n d i n k h o a p r o d u c t s ( 6 5 5 ) . E x p e r i e n c e i n y o g u r t , cheese, a n d i c e c r e a m has b e e n p r e v i o u s l y r e v i e w e d
(311,312).
F o r n e a r l y 3 0 years a d d e d a s c o r b i c a c i d has b e e n
recognized
BEER.
(312,656,657,658)
i n beer processing
as a n o x y g e n
scavenger,
thus
p r e v e n t i n g changes i n flavor a n d color, r e d u c i n g c h i l l a n d o x i d a t i o n h a z e ,
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a n d , t h e r e b y , e x t e n d i n g shelf l i f e . T o a c h i e v e o p t i m u m s t a b i l i t y i n beer, d i s s o l v e d a n d c o n t a i n e r h e a d s p a c e a i r s h o u l d b e k e p t as l o w as p o s s i b l e , a n d levels of trace metals s h o u l d b e k e p t as l o w as p o s s i b l e .
I t has b e e n
o b s e r v e d that t h e a m o u n t of ascorbic a c i d r e q u i r e d to t a k e u p 1 m L of o x y g e n f r o m b o t t l e d b e e r varies b e t w e e n 8 a n d 15 m g . T h e a m o u n t of a d d e d a s c o r b i c a c i d f o u n d to b e effective u n d e r most p r a c t i c a l c o n d i t i o n s is 2 0 - 4 0 m g / L , 2 - 4 g / h L , 2.4-4.8 g / b a r r e l , o r 0.54-1.08 l b / 1 0 0 b a r r e l s . M o r e m a y b e h e l p f u l o n l y w h e n there is p o o r a i r c o n t r o l . W h e r e b r e w s h a v e b e e n p r e v i o u s l y t r e a t e d w i t h sulfites t h a t h a v e c o n t r i b u t e d t o a s p e c i a l taste c h a r a c t e r , i t is n o t necessary t o r e m o v e a l l t h e sulfite w h e n ascorbates a r e a d d e d since ascorbates a r e c o m p a t i b l e w i t h sulfite. A s c o r b i c a c i d m a y b e a d d e d as a f r e s h l y p r e p a r e d s o l u t i o n a t a n y b r e w i n g stage after f e r m e n t a t i o n i n r o o m t e m p e r a t u r e w a t e r o r b e e r [100 g p e r 1 (or more) L ] . A proportioning device c a n be used to introduce the a s c o r b i c a c i d s o l u t i o n w h i l e t h e b e e r is t r a n s f e r r e d d u r i n g
processing
for u n i f o r m d i s t r i b u t i o n w i t h o u t i n c o r p o r a t i o n of a i r . R e p o r t s c o n t i n u e i n t h e 1970s o n t h e a s c o r b i c a c i d t r e a t m e n t of b e e r (658-669).
U s e of ascorbic a c i d w i t h sulfites shows f a v o r a b l e results o n
b e e r q u a l i t y as d e s c r i b e d b y S c r i b a n a n d S t i e n n e (662) a n d M a s t o r et a l . (669).
A n a l y s e s of i m p o r t e d b e e r i n d i c a t e a d d i t i o n of ascorbates
i f n o t so l a b e l e d ( 6 6 5 ) .
even
Kormornicka (667) reported 3 g / h L addition
of a s c o r b i c a c i d e x t e n d e d b e e r q u a l i t y 89 d a y s ; 5 g / h L , 108 d a y s . B a e t s l e (666), o n a n i n d u s t r i a l scale, f o u n d 2 g / h L p r e s e r v e d c o l o r a n d flavor of b e e r d u r i n g storage f o r 66 d a y s . WINE.
I n 1948 F r a n z y (670) p u b l i s h e d his observations, i n process
i n g of grapes i n t o sweet w i n e s , o n a d d e d L - a s c o r b i c a c i d ( 1 0 0 m g / L ) as a r e p l a c e m e n t c o m p o u n d
for sulfurous a c i d i n protecting the color
of w i n e f r o m o x i d a t i v e changes a n d p r o m o t i n g f r e s h a r o m a .
About a
decade later ascorbic
to be a
acid became quite widely understood
valuable processing a i d i n w i n e production: flavor;
(a) t o preserve taste a n d
(b) t o p r o m o t e c l a r i t y b y p r e v e n t i n g f e r r i c p h o s p h a t e p r e c i p i t a t i o n
or b y c l a r i f y i n g t u r b i d w i n e s ; (c) to r e m o v e excess s u l f u r d i o x i d e s ; a n d (d)
to reduce
t h e a m o u n t of r e q u i r e d s u l f u r o u s a c i d w h e n
ascorbic
s u l f u r o u s a c i d a p p l i c a t i o n is c h o s e n i n w i n e t r e a t m e n t . T o d a y t h e use of a s c o r b i c a c i d a l o n e o r c o m b i n e d w i t h s u l f u r o u s a c i d t r e a t m e n t is l e g a l l y p e r m i t t e d or tolerated i n m a n y countries.
Reviews, wherein
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
ascorbic
20.
463
Ascorbic Acid Technology
BAUERNFEIND
a c i d a p p l i c a t i o n t o w i n e a r e d i s c u s s e d , c a n b e c o n s u l t e d f o r past p u b l i cations o n this subject
(312,321,671,672, 673, 921).
T h e q u a n t i t y of L - a s c o r b i c a c i d n a t u r a l l y present i n grapes is r e l a t i v e l y l o w a n d is m o s t l y d e s t r o y e d d u r i n g f e r m e n t a t i o n . M o r e f r e q u e n t l y than not ascorbic together
a c i d a n d sulfurous a c i d
advantages.
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are used unique
S u l f u r d i o x i d e has a n t i s e p t i c , f u n g i c i d a l , a n t i d i a s t a s e , a n d
antioxidant properties. potentiates
(sulfur dioxide)
since b o t h c o m p o u n d s c o n t r i b u t e
(671,674,675-678)
A s c o r b i c a c i d is a stronger r e d u c i n g agent a n d
t h e l o w r e d u c i n g c a p a c i t y of s u l f u r d i o x i d e a n d , t h e r e b y ,
makes i t p o s s i b l e t o m i n i m i z e t h e c o n c e n t r a t i o n of this necessary b u t headache-related
s u l f u r a d d i t i v e (673,674).
A l o w v a l u e of t h e r e d o x
p o t e n t i a l i n w i n e is m o r e f a v o r a b l e f o r f u l l
flavor
development,
and it
w o u l d t a k e a p r o l o n g e d t i m e to a c h i e v e this w i t h o u t a s c o r b i c a c i d (672). I n Swiss p r a c t i c e , i t has b e e n f o u n d t h a t 5 0 - 1 0 0 m g / L of a s c o r b i c a c i d i n w i n e c o n t a i n i n g 1 5 - 2 0 m g S O ^ / L , w h e n a d d e d a t t h e stage w h e n t h e wine was ready for bottling, generally resulted i n a fruitier bouquet a n d lighter color
(673).
Peynaud
(679),
i n r e p o r t i n g o n 3 years use of
a s c o r b i c a c i d i n w i n e , suggests a d d i t i o n b e m a d e i m m e d i a t e l y b e f o r e o r after a e r a t i o n or, best, just b e f o r e b o t t l i n g . M a x i m u m a d d i t i o n a l l o w e d i n F r a n c e is 10 g / 1 0 0 L ; i n I t a l y , 12 g / 1 0 0 L . M o r e recent studies c o n f i r m t h e v a l u e of a d d e d w i n e f o r i m p r o v e m e n t of q u a l i t y (680-683),
ascorbic
i n champagne
acid i n
production
(684), i n c o n v e r t i n g o r d i n a r y w i n e i n t o s h e r r y w i n e (685), i n e l i m i n a t i n g the n e e d f o r heat s t e r i l i z a t i o n of s u l f u r d i o x i d e (686), a n d i n t h e p r o d u c t i o n of h o t b o t t l e d M o s e l l e w i n e (687).
R e p o r t s o n c o m b i n e d use of
a s c o r b i c a c i d a n d s u l f u r d i o x i d e i n d i c a t e its c o n t i n u e d p r a c t i c a l s i g n i f i cance
(688-691).
COLORS.
T h e m a j o r i t y of t h e F D A certified f o o d colors
display
i n s t a b i l i t y ( 6 9 2 ) w h e n b r o u g h t i n t o contact w i t h r e d u c i n g agents, h e n c e these a z o a n d t r i p h e n y l m e t h a n e colorants m a y f a d e o r b e c o m e colorless b y t h e r e d u c i n g a c t i o n of a s c o r b i c a c i d (692-695).
D e c o l o r i z a t i o n of
these c o a l t a r dyes c a n o c c u r i n c a r b o n a t e d a n d s t i l l beverages i n t h e p r e s e n c e of a s c o r b i c a c i d (696) d e p e n d i n g o n : (a) t h e specific r e a c t i o n t o r e d u c i n g agents;
(b)
t h e a m o u n t of a s c o r b i c
acid
color's added;
(c) t h e o x y g e n a n d d i s s o l v e d m e t a l content; a n d (d) t h e exposure of t h e b o t t l e d beverages t o s u n l i g h t . S o m e c o n t r o l over this aspect c a n b e exer c i s e d b y r e d u c i n g m e t a l content w i t h t h e use of E T D A a n d l i m i t e d e x p o sure of b o t t l e d p r o d u c t s to l i g h t , s u c h as w i t h t h e use of cans or o p a q u e containers ( 6 9 2 ) . A n o t h e r p o s s i b i l i t y t o a v o i d c o l o r f a d i n g is t h e use of nonabsorbable, are r e p o r t e d
p o l y m e r i c c o a l t a r dyes as c o l o r a d d i t i v e s since to be more
stable
t o r e d u c i n g agents
(697)
these
than the
unbound dye. A n t h o c y a n i n s (698,699,700)
a r e s o m e w h a t m o r e stable t o a s c o r b i c
a c i d , b u t beverages n a t u r a l l y c o l o r e d w i t h a n t h o c y a n i n s o r w i t h
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
added
464
ASCORBIC
ACID
a n t h o c y a n i n s s h o u l d s t i l l b e d e a e r a t e d t o b r i n g o x y g e n levels t o a m i n i m u m (701). S t a r r a n d F r a n c i s h a v e i n v e s t i g a t e d t h e i n f l u e n c i n g f a c t o r s , o x y g e n (702) a n d trace m i n e r a l s ( 7 0 3 ) , o n t h e a n t h o c y a n i n - a s c o r b i c a c i d i n t e r r e l a t i o n s h i p . T h e effect of heat, l i g h t , a n d storage c o n d i t i o n s observed
b y S e g a l a n d D i m a (704)
o n five f r u i t juices
with
were added
a s c o r b i c a c i d . I k a w a ( 7 0 5 ) , i n h i s i n v e s t i g a t i o n of t h e n a t u r a l colors a n d t h e influence of a n t i o x i d a n t s , r e p o r t e d t h a t a s c o r b i c a c i d ( 5 0 - 1 0 0 m g / 100 g ) s t a b i l i z e d b e t a n i n e , a n d h a d n o effect o n c a n t h a x a n t h i n , c o c h i n e a l ,
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l a c c a i c , a n d p a p r i k a . O t h e r reports c o n f i r m t h e b e t a n i n e
observation
(706,707,708). T h e naturally occurring carotenoids,
some of w h i c h a r e c o m m e r
c i a l l y a v a i l a b l e i n p u r e f o r m , a r e n o t o n l y resistant t o c o l o r f a d i n g b u t are s t a b i l i z e d b y a s c o r b i c a c i d (709,710,711).
T h e added
carotenoid
f o o d colors a r e stable w h e n r e t o r t e d w i t h p r o t e i n m a t e r i a l a n d a r e s t a b l e w h e n c o m b i n e d w i t h r e d u c i n g agents.
A d d e d ^-carotene e m u l s i o n s p r o
v i d e t h e o r a n g e j u i c e c o l o r h u e ; /?-apocarotenal, t h e d e e p o r a n g e h u e associated w i t h orange beverages.
color
B y p r e l i m i n a r y trials, t h e b e v e r
age m a n u f a c t u r e r c a n choose a n a d d e d c o l o r source, a m o n g t h e colors d i s c u s s e d a n d associated c o n d i t i o n s , t h a t w i l l a l l o w p r o p e r
color h u e
a n d s t a b i l i t y of L - a s c o r b i c a c i d i n t h e l i q u i d p r o d u c t . D r i e d coffee extracts are s t a b i l i z e d i f a d d e d ascor
MISCELLANEOUS.
b i c a c i d is i n c o r p o r a t e d
d u r i n g their processing
Ascorbic
(712,713).
a c i d has also b e e n s t u d i e d i n t h e t e a f e r m e n t a t i o n process (714). C o n fectionaries (715-721)
c a n be a good vehicle for ascorbic acid, p a r t i c u
l a r l y , h a r d c a n d y (311) b e c a u s e of t h e p r e s e n c e of f r u i t acids a n d l o w o x y g e n p e r m e a b i l i t y . A l s o , a s c o r b i c a c i d has b e e n a d d e d successfully t o caramels
(312,721),
chocolates
(312), m a r r o n glaces
and ice
(715),
c a n d i e s (716). A s y n t h e t i c c a v i a r has b e e n d e v e l o p e d a n d p a t e n t e d , t h e f o r m u l a t i o n of w h i c h c a l l s f o r a d d e d a s c o r b i c a c i d Patents have
also b e e n
obtained
o n ascorbic
p r i n c i p l e f o r t h e r e m o v a l of c h l o r i n e f r o m palatable for drinking
(723,724,725).
(722). a c i d as t h e a c t i v e
water, m a k i n g the water
T h e a d d i t i o n of a s c o r b i c
acid
(1 g ) a n d sodium bicarbonate (0.5 g ) to chlorinated water (15 L ) w i l l r e s u l t i n a p a l a t a b l e w a t e r a c c o r d i n g t o a U . S . p a t e n t (723).
City tap
water treated w i t h
t o cause
chlorine-ammonia
(726)
was observed
h e m o l y t i c a n e m i a i n p a t i e n t s i n d i a l y s i s u n i t s of a h o s p i t a l . C o n f i r m a t i o n of this c o n d i t i o n w a s o b t a i n e d i n i n v i t r o tests i n w h i c h t h e s u s p e c t e d water damaged r e d blood
cells.
A s c o r b i c a c i d a d d i t i o n to t h e t r e a t e d
water reduced the anemia p r o b l e m i n the patients i n subsequent
time
periods. L - A s c o r b i c a c i d is n o t n o r m a l l y c o n s i d e r e d
a bacteriostat, y e t i n
aqueous solution at the higher concentrations used i n the aqueous phase of a s c o r b i c a c i d t r e a t e d f o o d s , i t appears t h a t i t c a n c o n f e r some l i m i t e d antimicrobial activity.
Arafa and Chen
(727),
increased
refrigerated
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
shelf l i f e of
465
Ascorbic Acid Technology
BAUERNFEIND
cut-up broiler parts previously d i p p e d
i n ascorbic
acid
s o l u t i o n over w a t e r d i p p e d controls w i t h o u t adverse effects i n t h e c o n sumed product.
Svorcova
(728), investigating ascorbic acid, potassium
sorbate, a n d p H levels i n c a r b o n a t e d beverages, n o t e d some influence of a s c o r b i c a c i d f o r c o n t r o l of n o n s p o r e - f o r m i n g b a c t e r i a . O t h e r instances h a v e b e e n c i t e d for l i m i t e d a n t i m i c r o b i a l a c t i v i t y (729-732) of
ascorbic
acid. Legal Aspects.
T h e use of a s c r o b i c a c i d as a n u t r i e n t or as a f o o d
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p r o c e s s i n g a i d is subject to g o v e r n m e n t T h e status of a s c o r b i c
regulation i n many
countries.
a c i d a d d i t i o n i n e a c h instance of d e s i r e d
use
s h o u l d b e d e t e r m i n e d b y c o n s u l t i n g the p e r t i n e n t r e g u l a t i o n s o r p e r t i n e n t g o v e r n m e n t a l a g e n c y of the c o u n t r y . A s c o r b i c a c i d is " g e n e r a l l y r e g a r d e d as safe,"
U N I T E D STATES.
T H E
G R A S , f o r use i n f o o d as a n u t r i e n t or f o o d p r o c e s s i n g a i d p r o v i d e d t h a t a s t a n d a r d has not b e e n e s t a b l i s h e d b y t h e F o o d a n d D r u g A d m i n i s t r a t i o n f o r t h e f o o d w h e r e i n t h e use of a s c o r b i c a c i d is e x c l u d e d or p e r m i t t e d w i t h i n t h e l i m i t a t i o n s specified b y t h e s t a n d a r d . U n d e r G R A S c o n d i t i o n s , t h e q u a n t i t y a d d e d "does n o t e x c e e d t h e a m o u n t r e a s o n a b l y r e q u i r e d to a c c o m p l i s h its i n t e n d e d p h y s i c a l , n u t r i t i o n a l , or other t e c h n i c a l effect o n f o o d , " a n d the q u a n t i t y of
ascorbic
a c i d " b e c o m e s a c o m p o n e n t of f o o d as a r e s u l t of its use i n the m a n u f a c t u r i n g , p r o c e s s i n g , or p a c k a g i n g of f o o d , a n d w h i c h is n o t i n t e n d e d to a c c o m p l i s h a n y p h y s i c a l or other t e c h n i c a l effect o n the f o o d itself, s h a l l b e r e d u c e d to t h e extent r e a s o n a b l y p o s s i b l e " ; a n d t h e a s c o r b i c a c i d "is of a p p r o p r i a t e f o o d g r a d e a n d is p r e p a r e d a n d h a n d l e d as a f o o d i n g r e d i e n t " ; a n d t h e i n c l u s i o n of a s c o r b i c a c i d " i n t h e list of n u t r i e n t s does not constitute a finding o n t h e p a r t of t h e D e p a r t m e n t t h a t ' a s c o r b i c acid* is u s e f u l as a s u p p l e m e n t to t h e d i e t for h u m a n s . " W h e n a s t a n d a r d for a f o o d p r o d u c t has b e e n e s t a b l i s h e d w h e r e i n t h e use of a s c o r b i c a c i d is p e r m i t t e d , t h e s t a n d a r d s h o u l d b e
consulted
to ensure that the l a b e l i n g of t h e f o o d p r o d u c t conforms w i t h the l a b e l i n g specifications of t h e s t a n d a r d . I n a d d i t i o n to t h e r e g u l a t i o n s e s t a b l i s h e d b y t h e F o o d a n d D r u g A d m i n i s t r a t i o n , t h e U n i t e d States D e p a r t m e n t of A g r i c u l t u r e has p r o m u l g a t e d r e g u l a t i o n s p e r t a i n i n g to the use of
ascorbic
acid in
meat
p r o c e s s i n g a n d t h e A l c o h o l a n d T o b a c c o T a x D i v i s i o n of t h e U n i t e d States D e p a r t m e n t of the T r e a s u r y has e s t a b l i s h e d a r e g u l a t i o n p e r t a i n i n g to t h e use of a s c o r b i c a c i d i n w i n e . these r e g u l a t o r y agencies X X V I , and X X V I I .
T h e r e are also F e d e r a l a n d M i l i t a r y
i n t h e U n i t e d States for XXVIII). O T H E R
T h e standards e s t a b l i s h e d
by
as t h e y exist are d e s c r i b e d i n T a b l e s X X V , food procured
by
Specifications
F e d e r a l agencies
(Table
Regulations change a n d must be monitored frequently. COUNTRIES.
M a n y countries h a v e r e g u l a t i o n s c o n c e r n i n g t h e
a d d i t i o n of L - a s c o r b i c a c i d to foods, some of w h i c h are g e n e r a l a n d others
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
466
ASCORBIC
ACID
Table X X V . U.S. Standards or Regulations of Foods to Which Ascorbic A c i d M a y Be A d d e d 0
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Food
Purpose of Ascorbic Acid
Quantity
Permitted
A r t i f i c i a l l y sweetened fruit jelly
preservative
not more t h a n 0 . 1 % b y w e i g h t of finished food
A r t i f i c i a l l y sweetened f r u i t preserves a n d j a m s
preservative
not m o r e t h a n 0 . 1 % b y w e i g h t of f i n i s h e d food
C a n n e d applesauce
preservative, nutrient
not more t h a n 150 p p m , a n a m o u n t to p r o v i d e 60 m g / 4 oz (113 g)
C a n n e d apricots
preservative
a n a m o u n t no greater t h a n necessary to preserve color
Canned artichokes ( p a c k e d i n glass)
preservative
not m o r e t h a n 32 m g / 1 0 0 g of finished food
preservative
a m o u n t no greater t h a n necessary to preserve color
C a n n e d f r u i t nectars
preservative, nutrient
not more t h a n 150 p p m , a m o u n t s to p r o v i d e n o t less t h a n 30 m g or m o r e t h a n 60 m g / 4 fl oz
Canned mushrooms
preservative
n o t more t h a n 37.5 m g / o z of d r a i n e d w e i g h t of mushrooms
C a n n e d peaches
preservative
a m o u n t n o t greater t h a n necessary to preserve color
C a n n e d pineapple juice
nutrient
a m o u n t s to p r o v i d e n o t less t h a n 30 m g or more t h a n 60 m g / 4 fl oz
Canned pineapple grape fruit juice d r i n k
nutrient
a m o u n t s t o p r o v i d e n o t less t h a n 30 m g or more t h a n 60 m g / 4 fl oz
C a n n e d prune juice
nutrient
a m o u n t s to p r o v i d e n o t less t h a n 30 m g or more t h a n 60 m g / 4 fl oz
C r a n b e r r y juice cocktail
nutrient
a m o u n t s to p r o v i d e not less t h a n 30 m g or more t h a n 60 m g / 4 fl oz
F l o u r (white, whole wheat, plain)
dough conditioner
not to exceed 200 p p m
Canned fruit cocktail
F r o z e n r a w breaded s h r i m p p r e s e r v a t i v e
sufficient to r e t a r d d e v e l o p ment of d a r k spots
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
Table X X V .
Continued
Purpose of Ascorbic Acid
Food
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467
Ascorbic Acid Technology
BAUERNFEIND
Quantity Permitted
Ice c r e a m (the f r u i t therein)
acidulant
such q u a n t i t y as seasons t h e finished p r o d u c t a n d meets the s t a n d a r d s for ice c r e a m
Margarine
preservative
ascorbyl palmitate a n d / o r a s c o r b y l stearate 0 . 0 2 %
N o n f r u i t w a t e r ices
acidulant
s u c h q u a n t i t y as seasons the finished p r o d u c t
T o m a t o juice
nutrient
a m o u n t to p r o v i d e 10 m g / f l oz ( t o t a l v i t a m i n C )
W a t e r ices (the f r u i t therein)
acidulant
such q u a n t i t y as seasons the finished p r o d u c t
F o o d s for w h i c h s t a n d a r d s are established a n d i n w h i c h p r e s e r v a t i v e s m a y be o p t i o n a l ingredients a r e :
nonspecified
dry whole m i l k dry cream breads, r o l l s , buns
dough c o n d i t i o n e r s not referred to i n s t a n d a r d i f the t o t a l q u a n t i t i e s are not m o r e t h a n 0.5 p a r t for each 100 p a r t s b y w e i g h t of flour used
frozen r a w breaded shrimp
a n t i o x i d a n t p r e s e r v a t i v e — m a y be used t o r e t a r d d e v e l o p m e n t of r a n c i d i t y of the f a t content
° Compiled by D. M . Pinkert. Consult regulations for current status and inter pretation. v e r y specific. It w o u l d take a n u m b e r of pages to d e t a i l s u c h i n f o r m a t i o n for e a c h f o o d p r o d u c t for e a c h c o u n t r y h a v i n g r e g u l a t i o n s . F o r e x a m p l e , i n c o n s i d e r i n g a s c o r b i c a c i d as a flour i m p r o v e r , the l e v e l of p e r m i s s i b l e a d d i t i o n ranges f r o m 50 m g to 10 g / k g of flour ( T a b l e X X I X ) . C e r t a i n countries s u c h as A u s t r a l i a , C a n a d a , C h i l e , H o l l a n d , J a p a n , K e n y a , N e w U n i t e d States, U r u g u a y , a n d Z a m b i a p e r m i t
both
L - a s c o r b i c a c i d a n d b r o m a t e as flour i m p r o v e r w h i l e a n u m b e r of
Zealand,
Sweden,
other
countries o n l y a l l o w L - a s c o r b i c a c i d . I n t h e E C C c o u n t r i e s p e r m i s s i b l e L - a s c o r b i c a c i d levels f o r t e c h n i c a l a p p l i c a t i o n to f o o d v a r y f r o m
100
m g / k g to 2 g / k g of f o o d p r o d u c t . T H E
JOINT
FAO/WHO
Joint F A O / W H O was
C O D E X
ALIMENTARIUS
Codex Alimentarius Commission
COMMISSION.
(the
e s t a b l i s h e d to i m p l e m e n t t h e J o i n t F A O / W H O
Program.
Membership
of
the
C o m m i s s i o n comprises
The
Commission)
Food
Standards
those
Member
N a t i o n s a n d A s s o c i a t e M e m b e r s of F A O a n d / o r W H O t h a t h a v e n o t i f i e d
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
468
ASCORBIC
Table X X V I .
U.S. Regulations on Ascorbic A c i d Addition to Meat
Food Ascorbic acid i n : cured p o r k a n d beef cuts, c u r e d comminuted meat food p r o d u c t
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ACID
Purpose
Quantity Permitted
t o accelerate color f i x i n g
70 oz per 100 g a l p i c k l e a t 1 0 % p u m p l e v e l ; 0.75 oz per 100 l b m e a t or m e a t b y p r o d u c t ; 1 0 % s o l u t i o n to surfaces of cured cuts p r i o r to p a c k a g i n g (the use of such s o l u t i o n s h a l l not r e s u l t i n the a d d i t i o n of a s i g n i f i c a n t a m o u n t of m o i s t u r e to t h e product)
S o d i u m ascorbate to accelerate i n : cured p o r k a n d color f i x i n g beef cuts, cured comminuted meat food p r o d u c t
87.5 oz per 100 g a l p i c k l e a t 1 0 % p u m p l e v e l ; 0.88 oz per 100 l b m e a t or m e a t b y p r o d u c t ; 1 0 % s o l u t i o n to surfaces of cured cuts p r i o r to p a c k a g i n g (the use of such s o l u t i o n s h a l l n o t r e s u l t i n the a d d i t i o n of a s i g n i f i c a n t a m o u n t of m o i s t u r e t o the product)
Table X X V I I . U.S. Regulations on Ascorbic A c i d Addition to Alcoholic Beverages Alcohol and Tobacco Tax Div., U.S. Dept. of Treasury Regulations Food
Purpose of Ascorbic Acid
Wine
to p r e v e n t d a r k e n i n g of color a n d d e t e r i o r a t i o n of flavor, a n d o v e r oxidation
w i t h i n l i m i t a t i o n s w h i c h do not a l t e r the class or t y p e of the w i n e (use need not be d e c l a r e d on the l a b e l )
Beer
antioxidant and bio logical stabilization
to be used o n l y b y agreement between U . S . D e p t . of T r e a s u r y a n d the brewer
Quantity Permitted
the O r g a n i z a t i o n s of t h e i r w i s h to b e c o n s i d e r e d as M e m b e r s . B y F e b r u a r y 1979, 117 countries h a d b e c o m e M e m b e r s of the C o m m i s s i o n . O t h e r countries p a r t i c i p a t i n g i n the w o r k of the C o m m i s s i o n or its s u b s i d i a r y b o d i e s i n a n observer c a p a c i t y are e x p e c t e d to b e c o m e M e m b e r s i n t h e near future. T h e p u r p o s e of the J o i n t F A O / W H O F o o d S t a n d a r d s P r o g r a m is t o e l a b o r a t e i n t e r n a t i o n a l standards for foods a i m e d at p r o t e c t i n g t h e h e a l t h of t h e c o n s u m e r , to ensure f a i r p r a c t i c e s i n the f o o d t r a d e , a n d to f a c i l i tate i n t e r n a t i o n a l t r a d e . I n a d d i t i o n to c o m p o s i t i o n a l c r i t e r i a a n d l a b e l i n g , f o o d s t a n d a r d s i n c o r p o r a t e p r o v i s i o n s i n respect to f o o d
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
hygiene,
20.
469
Ascorbic Acid Technology
BAUERNFEIND
Table X X V I I I . A r m e d Forces Regulations on Ascorbic A c i d Addition to F o o d a
Purpose of Ascorbic Acid
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Food
Quantity
Permitted
B e v e r a g e base powders p r e pared from dehydrated f r u i t juices ( T y p e I I )
nutrient
2 0 - 3 0 m g / 1 2 fl oz of recon stituted powder
C o c o a beverage p o w d e r
nutrient
N o t less t h a n 25 m g / o z b y weight
Coffee, i n s t a n t , T y p e I
nutrient
N o t less t h a n 15 m g / 2 . 5 g
D e h y d r a t e d w h i t e potatoes
nutrient
N o t less t h a n 50 m g / o z of dehydrated product
M i l k , non-fat dry (Type II, Style B)
nutrient
20 m g / o z
Peanut butter, v i t a m i n fortified
nutrient
37.5 m g / 1 . 5 oz of p r o d u c t
8
Compiled by N. E . Harris.
f o o d a d d i t i v e s , p e s t i c i d e residues, other c o n t a m i n a n t s , a n d m e t h o d s
of
analysis a n d s a m p l i n g . L - A s c o r b i c a c i d a n d certain derivatives ( T a b l e X X X ) have d e s i g n a t e d t o x i c o l o g i c a l l y as c a t e g o r y A ( 1 ) C A C / F A L 5-1979.
Category A (1)
been
i n the release d e s i g n a t e d
a d d i t i v e s are those t h a t h a v e b e e n
fully cleared b y the Joint F A O / W H O E x p e r t C o m m i t t e e on F o o d A d d i tives a n d e i t h e r h a v e b e e n g i v e n a n " a c c e p t a b l e d a i l y i n t a k e " ( A D I )
or
h a v e n o t b e e n l i m i t e d t o x i c o l o g i c a l l y . A p p r o v e d uses of L - a s c o r b i c a c i d h a v e b e e n i n d i c a t e d , m a x i m u m levels ( M L ) h a v e b e e n s h o w n , a n d g o o d m a n u f a c t u r i n g p r a c t i c e ( G M P ) has b e e n e s t a b l i s h e d . A D I is expressed as m i l l i g r a m s p e r k i l o g r a m b o d y w e i g h t ; M L is expressed as w e i g h t p e r k i l o g r a m of p r o d u c t .
G M P refers to the l i m i t a t i o n of f o o d a d d i t i v e i n
s p e c i f i e d foods. I t means t h a t t h e a d d i t i v e i n q u e s t i o n is s e l f - l i m i t i n g i n f o o d for t e c h n o l o g i c a l , o r g a n o l e p t i c , or other reasons a n d t h a t , therefore, t h e a d d i t i v e n e e d n o t b e subject to l e g a l m a x i m u m l i m i t s . I t also means t h a t the f o o d a d d i t i v e m u s t b e u s e d a c c o r d i n g to g o o d m a n u f a c t u r i n g p r a c t i c e , a n d i n a c c o r d a n c e w i t h the G e n e r a l P r i n c i p l e s for the U s e of F o o d Additives.
Industrial Applications A n extensive list of patents a n d scientific p a p e r s exists o n p r o p o s e d uses of a s c o r b i c a c i d i n v a r i o u s i n d u s t r i e s ; h o w e v e r , t h e a m o u n t of c o m -
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
470
A S C O R B I C ACED
Table X X I X . Legal Status of L-Ascorbic A c i d as a Flour Improver
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Country
Maximum
Australia Austria Belgium Brazil Canada Chile Cyprus Denmark England Finland France Germany Greece Holland Italy Japan Kenya N e w Zealand Norway Portugal South A f r i c a Spain Sweden Switzerland Uruguay U n i t e d States Zambia
Level Permitted
GMP 200 m g / k g 50 m g / k g 2 g/kg 200 m g / k g 20-50 m g / k g 75 m g / k g 200 m g / k g GMP 200 m g / k g 500 m g / k g GMP° GMP° 50 m g / k g 200 m g / k g GMP 200 m g / k g GMP° GMP 8-10 g / k g 200 m g / k g 200 m g / k g GMP° GMP 20 m g / k g 200 m g / k g 200 m g / k g a
a
b
a
a
a
° G M P = Good Manufacturing Practice. May only be added by the baker. b
p o u n d u s e d i n the i n d u s t r i a l a p p l i c a t i o n s is s m a l l r e l a t i v e to p h a r m a ceutical and food applications.
W h i l e ascorbic a c i d m a y be
declared
to b e f u n c t i o n a l w i t h m e r i t o r i o u s advantages, there is a s t r o n g p r e f e r e n c e to f i n d a n d use m o r e e c o n o m i c a l c h e m i c a l aids, e v e n t h o u g h t h e y m a y n o t b e q u i t e as effective.
T h e greatest a c t i v i t y i n p u r s u i n g uses appears t o
b e f o r p o l y m e r i z a t i o n reactions i n the plastics i n d u s t r y , for uses i n p r i n t i n g inks, i n photoprocessing, i n metal technology, a n d i n miscellaneous areas, i n c l u d i n g cosmetics, t o b a c c o , fibers, a n a l y t i c a l assays, p r e s e r v a t i o n of b l o o d , p r e s e r v a t i o n of c u t p l a n t s , a n d c l e a n i n g agents. Polymerization
Reactions.
Polymerization
reactions
take
place
u n d e r h i g h a n d l o w t e m p e r a t u r e s . W h e r e a n aqueous p h a s e exists s u c h as i n e m u l s i o n s , or i f a p o l a r solvent is i n v o l v e d , a s c o r b i c a c i d is s o l u b i l i z e d a n d m a y h a v e m e r i t , b e c a u s e of its r e d u c i n g p o w e r , i n f a c i l i t a t i n g t h e p o l y m e r i z a t i o n w i t h a t e m p e r a t u r e a d v a n t a g e , a rate of better control, or a superior e n d product.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
reaction,
20.
471
Ascorbic Acid Technology
BAUERNFEIND
Table X X X .
Antioxidants and Antioxidant
Synergists
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NumAdditive
Evaluation
and Maximum
Limit
ber
List
.230
A(l)
ascorbic a c i d (Syn: L ascorbic acid)
A D I : 0 - 1 5 m g / k g b o d y w e i g h t , s u m of ascorbic a c i d a n d ascorbates f r o m a l l sources ( R e f . : T o x . 29, 30, 3 2 ; Spec. 47 T e c h n . EfT. 28) C o d e x S p e c i f i c a t i o n : A L I N O R M 76/41
.231
A(l)
ascorbate, potassium
A D I : 0 - 1 5 m g / k g b o d y w e i g h t , s u m of ascorbic a c i d a n d ascorbates f r o m a l l sources ( R e f . : T o x . 29, 30, 3 2 ; Spec. 1; T e c h n . EfT. 28)
.232
A(l)
ascorbate, sodium
A D I : 0 - 1 5 m g / k g b o d y w e i g h t , s u m of ascorbic a c i d a n d ascorbates f r o m a l l sources ( R e f . : T o x . 29, 30, 3 2 ; Spec. 47 T e c h n . E f f . 28) C o d e x S p e c i f i c a t i o n : A L I N O R M 76/41
Approved
Uses of .230 in:
Evaluation
Canned tropical fruit salad C a n n e d peaches C a n n e d applesauce E d i b l e f u n g i a n d fungus products A p r i c o t , peach a n d pear n e c t a r s Apple juice Q u i c k frozen s t r a w b e r r i e s C a n n e d mushrooms C a n n e d asparagus Concentrated apple j u i c e T a b l e olives Q u i c k frozen peaches Canned fruit cocktail J a m s a n d jellies B l a c k currant j a m Citrus marmalade Grape juice C o n c e n t r a t e d grape j u i c e Sweetened concentrated L a b r u s c a t y p e grape j u i c e Q u i c k frozen s h r i m p s a n d p r a w n s 0
0
0
0
0
0
Approved
ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML: ML:
and Maximum
Limit
700 m g / k g 550 m g / k g 150 m g / k g limited by G M P limited by G M P limited by G M P limited by G M P limited by G M P limited by G M P limited by G M P 200 m g / k g 750 m g / k g limited by G M P 500 m g / k g 750 m g / k g 500 m g / k g 400 m g / k g 400 m g / k g
M L : 400 m g / k g M L : limited by G M P
Uses of .230 and .232 in:
C a n n e d corned beef Luncheon meat C o o k e d cured chopped m e a t C o o k e d cured p o r k shoulder C o o k e d cured h a m C a n n e d b a b y foods C e r e a l - b a s e d processed foods infants and children
I / \ /
M L : 500 m g / k g , expressed as the a c i d M L : 500 m g / k g , s i n g l y o r i n c o m b i n a t i o n w i t h isoascorbic a c i d , i s o ascorbate, expressed as ascorbic acid M L : limited by G M P
for M L : limited by G M P Continued on next page.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
472
ASCORBIC
Table X X X .
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Approved uses of .231 and .232 in: Q u i c k frozen lobsters Q u i c k frozen fillets of ocean p e r c h Q u i c k frozen fillets o f c o d a n d haddock Q u i c k frozen fillets of flat fish Q u i c k frozen fillets of h a k e Number
List
Additive
.236
A(l)
.237
A(l)
ascorbyl palmitate , , ascorbyl stearate
ACID
Continued
M L : 1 g / k g , expressed as the a c i d M L : 1 g / k g , expressed as t h e a c i d M L : 1 g / k g , expressed as t h e a c i d M L : 1 g / k g , expressed as the a c i d M L : 1 g / k g , expressed as the a c i d
Evaluation
and Maximum
Limit
\ A D I : 0-1.25 m g / k g body weight, singly I or i n c o m b i n a t i o n ( R e f . : T o x . 2 9 , 3 0 ; ) Spec. 4 7 ; T e c h n . EfT. 28) C o d e x S p e c i f i I . A L I N O R M 76/41 c
a
t
i
Approved Uses of .236 in: Infant formula C a n n e d b a b y foods C e r e a l - b a s e d processed foods for infants and children
o
n
M L : limited by G M P M L : limited by G M P M L : limited by G M P
Approved Uses of .236 and .237 in: E d i b l e fats a n d oils
M L : 200 m g / k g , s i n g l y o r i n c o m b i nation
Margarine
M L : 200 m g / k g , s i n g l y o r i n c o m b i nation
° Preserved exclusively by physical means. In products intended for vending machines only. b
I n v i n y l c o m p o u n d p o l y m e r i z a t i o n of v i n y l acetate, a l c o h o l , b r o m i d e , c h l o r i d e , or c a r b o n a t e , a s c o r b i c a c i d c a n b e a c o m p o n e n t of t h e p o l y m e r i z a t i o n m i x t u r e (733-749).
Activators for the polymerization have
b e e n a c r i f l a v i n e ( 7 3 4 ) , other p h o t o s e n s i t i v e d y e c o m p o u n d s hydrogen
peroxides
(740,741,742),
(737,738),
potassium peroxydisulfate
ferrous sulfate, a n d a c y l s u l f o n y l p e r o x i d e s
(747).
(743),
Nagabhooshanam
a n d S a n t a p p a (748) r e p o r t e d o n d y e s e n s i t i z e d p h o t o p o l y m e r i z a t i o n o f v i n y l m o n o m e r s i n t h e presence of a s c o r b i c a c i d - s o d i u m h y d r o g e n o r t h o phosphate complex.
A n o t h e r c o m b i n a t i o n is v i n y l c h l o r i d e w i t h
cyclo-
h e x a n e s u l f o n y l a c e t y l p e r o x i d e w i t h a s c o r b i c a c i d , i r o n sulfate, a n d a n a l c o h o l ( 7 4 9 ) . U s e of l o w t e m p e r a t u r e c o n d i t i o n s i n e m u l s i o n p o l y m e r i z a t i o n , w i t h a s c o r b i c a c i d , is m e n t i o n e d (750,751).
C l a r i t y of c o l o r is
i m p o r t a n t a n d i m p a c t - r e s i s t a n t , clear, m o l d a b l e p o l y v i n y l c h l o r i d e c a n b e p r e p a r e d w i t h a s c o r b i c a c i d as a n a c i d c a t a l y s t (752) i n t h e f o r m u lation.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
Ascorbic Acid Technology
BAUERNFEIND
473
S i m i l a r reports h a v e a p p e a r e d i n t h e t e c h n o l o g y acrylic monomers
s u c h as a c r y l o n i t r i l e (753-759)
of p o l y m e r i z i n g
or acrylamide
(760-
763). K o r o l e v et a l . (764) h a v e u s e d a s c o r b i c a c i d as a r e d u c i n g agent i n t h e m i x t u r e t o increase t h e p o l y m e r i z a t i o n rate. p o l y m e r i z a t i o n i n t h e presence c o n t a i n i n g a s c o r b i c a c i d (765).
T h e k i n e t i c s of
of o x y g e n has b e e n s t u d i e d i n systems R e c e n t patents (766,767)
have
been
i s s u e d w i t h a s c o r b i c a c i d i n t h e d i s p e r s i o n of a c r y l i c aqueous resins. A t h i r d t y p e of p o l y m e r s is p o l y m e r i z e d m e t h y l m e t h a c r y l a t e o r Downloaded by UCSF LIB CKM RSCS MGMT on November 18, 2014 | http://pubs.acs.org Publication Date: June 1, 1982 | doi: 10.1021/ba-1982-0200.ch020
m e t h a c r y l a m i d e (768-773).
S t r u b e l l (768) has c a r r i e d o u t p o l y m e r i z a
t i o n of m e t h y l m e t h a c r y l a t e w i t h a n a s c o r b i c system.
I n a n aqueous
acid-benzoyl
peroxide
p o l y m e r i z a t i o n of m e t h y l m e t h a c r y l a t e ,
Misra
a n d G u p t a (770) u s e d the r e d o x system of p o t a s s i u m p e r o x y d i s u l f a t e a n d a s c o r b i c a c i d . A s i m i l a r system w a s r e p o r t e d b y P a t t n a i k et a l . ( 7 7 3 ) . A s c o r b i c a c i d is d e c l a r e d t o f u n c t i o n as a n a n t i o x i d a n t f o r p o l y e t h y l e n e (774), f o r l i g h t - s e n s i t i v e p o l y m e r mass ( 7 7 5 ) , f o r clear t h e r m o p l a s t i c s (776), a n d f o r colorless s y n t h e t i c r u b b e r (777).
I t is l i s t e d as
a n accelerator f o r c u r i n g a n a e r o b i c resins (778) a n d f o r h a r d e n i n g p r o c esses of u n s a t u r a t e d p o l y e s t e r resins (779—783). A s c o r b i c a c i d is a n a d d i t i v e w i t h s y n e r g i s t i c effect u p o n other c o m p o u n d s
i n stabilized pre
mixes f o r p o l y u r e t h a n e f o a m (784) a n d as a s t a b i l i z e r f o r polyesters t o b e u s e d as a n l u b r i c a n t a d d i t i v e s or p l a s t i c i z e r s (785).
Ascorbic acid
triggers p o l y m e r i z i n g r e s i n - f o r m i n g m a t e r i a l s u s e d i n w e l l b o r e as d r i l l i n g fluids (786) a n d i n fire-resistant p o l y m e r c o m p o s i t i o n s Ferrocene-containing polymers a n d their photooxidation-reduction t i o n (788,789),
holes (787). reac
a n d synthesis a n d reactions of p o r p h y r i n a n d m e t a l l o -
p o r p h y r i n p o l y m e r s ( 7 9 0 ) are other systems f o r u t i l i t y of a s c o r b i c a c i d . I n plastics a n d p o l y m e r i z a t i o n reactions there appears t o b e m u c h art w i t h i n t h e s y s t e m s — w h a t m a y w o r k i n o n e case or w h a t m a y b e a p l u s feature i n o n e m a y b e u n d e s i r a b l e i n another.
Trials must be r u n
to substantiate w h e r e a n d h o w m u c h of t h e m o r e expensive
ascorbic
a c i d has m e r i t over e c o n o m i c a l i n o r g a n i c a n d o r g a n i c substitutes. A s c o r b i c a c i d m a y h a v e a better o p p o r t u n i t y w h e r e color, o d o r , or safety a r e important i n the e n d product. Photographic Developing and Printing.
T h e association of ascor
b i c a c i d a n d d e r i v a t i v e s w i t h t h e p h o t o g r a p h i c i n d u s t r y is n o t a n e w r e l a t i o n s h i p ; i t goes b a c k over 4 5 years w h e n a s c o r b i c a c i d w a s first p r o d u c e d c o m m e r c i a l l y b y c h e m i c a l synthesis. D u r i n g this
four-decade
p e r i o d m a n y patents h a v e b e e n i s s u e d a r o u n d t h e w o r l d . Some w i l l b e m e n t i o n e d i n this r e v i e w . material development,
Basically, i n the technology
of film emulsions a n d i n film developers white photography.
of p h o t o g r a p h i c
a s c o r b i c a c i d has b e e n c o n s i d e r e d a
component
both i n color a n d black a n d
I t has b e e n s t u d i e d as a n i n v e s t i g a t i o n a l m a t e r i a l ,
a n d w h i l e m e r i t m a y b e s h o w n f o r its i m a g e q u a l i t y o r f o r f u n c t i o n a l
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
474
ASCORBIC
ACID
q u a l i t i e s i n t h e d e v e l o p i n g s o l u t i o n , its i n s t a b i l i t y , r a p i d i t y of e x h a u s t i o n i n a c t i o n , o r h i g h e r cost a r e d i s a d v a n t a g e o u s
considerations
that keep
its usage i n this i n d u s t r i a l a p p l i c a t i o n at a l o w e r l e v e l t h a n its p o t e n t i a l . A s c o r b i c a c i d has b e e n d e c l a r e d as a u s e f u l o p t i o n a l i n g r e d i e n t i n d e v e l o p e r c o m p o s i t i o n s (791-799).
Ascorbic acid c a n be used
without
sulfite a d d i t i o n a n d i t has n o solvent effect o n s i l v e r h a l i d e s ( 7 9 3 ) . Its a d d i t i o n increases t h e a c t i v i t y of c e r t a i n d e v e l o p e r c o m p o n e n t s
(800)
a n d m a y s t a b i l i z e the i m a g e (801-804) o r i n t e n s i f y i t ( 8 0 5 ) . I n a B e l g i a n
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p a t e n t (806) b o t h L - a s c o r b i c a c i d a n d a 2 , 3 - d i p h e n y l - L - a s c o r b i c
acid are
c i t e d as a d d i t i v e s . F o r d e v e l o p e r s f u n c t i o n i n g at a n a l k a l i n e p H , a s c o r b i c a c i d b o r a t e (807) w a s d e c l a r e d t o b e stable w h i l e a c t i n g as a r e d u c i n g agent.
A s c o r b i c a c i d is u s e f u l i n b l e a c h i n g processes (808,809,810):
in
the b l e a c h i n g of p h o t o g r a p h s o b t a i n e d b y t h e s i l v e r salt d i f f u s i o n process (808), i n b l e a c h - f i x b a t h d e s i l v e r i n g (809), a n d as a c o l o r
photography
b l e a c h i n g agent (810). T h e k i n e t i c s of d e v e l o p m e n t a n d silver f o r m a t i o n h a v e b e e n i n v e s t i g a t e d b y W i l l i s et a l . (811) a n d P o n t i u s et a l . (812). Applications for ascorbic acid have been considered tography
where
i n color pho
i t m a y b e a c o m p o n e n t of t h e d e v e l o p e r f o r s p e c i a l
p u r p o s e s u c h as t o r e d u c e f r o t h (813,814), o r i n i m a g e s t a b i l i z a t i o n i n color photographic
m a t e r i a l (815,816).
in
processes
image
emulsions
transfer
Ascorbic acid may be involved
(817,818),
direct
positive
photographic
(819), one-step d i f f u s i o n processes (820) i n a
photographic
p r o d u c t i n c o r p o r a t i n g a d e v e l o p e r y i e l d i n g images b y s i m p l e
treatment
w i t h w a t e r (821), o r as a b i n d e r f o r p h o t o g r a p h i c m a t e r i a l s (822). I n t h e p r e p a r a t i o n of l i t h o g r a p h i c m a t e r i a l s a n d i n t h e l i t h o g r a p h i c process, a s c o r b i c a c i d m a y b e u s e f u l .
T h e production
of l i t h o g r a p h i c
masters is i m p r o v e d b y i n c l u s i o n of a s c o r b i c a c i d i n t h e h a r d e n e r a n d r e c e i v i n g sheet (823) a n d , i n g e n e r a l , i n p r o c e s s i n g
silver halide litho
g r a p h i c m a t e r i a l s (824).
A s c o r b i c a c i d has b e e n c o n s i d e r e d
investigations
as a c o m p o n e n t of t h e d e v e l o p e r s u s e d i n
lithography.
(825-828)
i n several
I n offset p r i n t i n g plates b y c o l l o i d transfer (829), a s c o r b i c
acid a n d l-phenyl-3-pyrazolidinone
are used
as n o n h a r d e n i n g
agents.
I n k w i t h h i g h p o w e r to a b s o r b l i g h t (830) is benefited b y a s c o r b i c a c i d a d d i t i o n . O t h e r a p p l i c a t i o n s i n v o l v e l i g h t - s e n s i t i v e c o p y m a t e r i a l (831), h e a t - d e v e l o p a b l e i m a g i n g systems (832,833), p o w d e r l e s s e t c h i n g a n d various recording a n d print-out papers T h e r e is a m e t a l aspect of p h o t o g r a p h y be i n v o l v e d .
(834),
(835-838). where ascorbic acid m a y
S e v e r a l patents c l a i m a s c o r b i c a c i d u s e f u l as a sequestering
or c h e l a t i n g a g e n t (839,840), g r a p h i c m a t e r i a l (841,842).
or, t o p r e v e n t
i r o n s p o t t i n g of p h o t o
I t is i n c l u d e d i n a t w o - s t a g e c o p p e r d e v e l
o p m e n t of a s i l v e r latent i m a g e i n s e m i c o n d u c t o r
photographic
layers
(843), a n d i n a s t u d y of silver-free p h y s i c a l d e v e l o p m e n t process b y electrochemical
m e t h o d s , a s c o r b i c a c i d acts as a p h y s i c a l d e v e l o p e r i n
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
20.
BAUERNFEIND
the
form
lesions)
475
Ascorbic Acid Technology
of c u p r i a s c o r b i c
acid
(844).
Chromate
dermatitis
(hand
is a n o c c u p a t i o n a l h e a l t h p r o b l e m i n t h e p r i n t i n g a n d l i t h o
g r a p h i c i n d u s t r i e s . A p r e v e n t i v e r e g i m e n ( 8 4 5 ) i n v o l v i n g use of a 1 0 % ascorbic
a c i d s o l u t i o n is b e n e f i c i a l i n p r e v e n t i n g o r c o n t r o l l i n g t h e
occurrence. Metal Technology.
T h e p a t e n t a n d scientific l i t e r a t u r e reveals some
p o t e n t i a l uses f o r a s c o r b i c a c i d i n m e t a l l i c r e d u c t i o n s , c o a t i n g tions, e l e c t r o p l a t i n g processes, a n d o x i d a t i o n c o n t r o l .
composi
Metal ion and
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m e t a l c o m p l e x c a t a l y z e d reactions (846) a n d t h e s t r u c t u r e of ascorbate complexes
of metals (847) h a v e b e e n i n v e s t i g a t e d .
T h e kinetics a n d
m e c h a n i s m of t h e r e d u c t i o n of p l a t i n u m ( 8 4 8 ) , v a n a d i u m ( 8 4 9 ) , c e r i u m ( 8 5 0 ) , m o l y b d e n u m ( 8 5 1 ) , g o l d ( 8 5 2 ) , a n d s i l v e r (853,854) b y a s c o r b i c a c i d h a v e b e e n e x a m i n e d . O t h e r topics of a s c o r b i c a c i d i n v o l v e m e n t a r e p r o v i d i n g resistance t o m e t a l surfaces (855, 8 5 6 ) , m e t a l l i z i n g n o n m e t a l l i c substrates (857), o x i d a t i o n - r e s i s t a n t c o a t i n g f o r c o p p e r a n d c o p p e r alloys (858), c o p p e r p l a t i n g (859), n i c k e l p l a t i n g (860,861), of n i c k e l a l l o y films (862-865),
electrodeposition
of z i n c alloys (866,867),
of t i n a l l o y s
(868), e l e c t r o d e p o s i t i o n of a l u m i n u m (869,870), a n d a c t i v a t i o n of z i n c p h o s p h a t e c o m p o s i t i o n s f o r steel (871). R u s t r e m o v e r c o m p o s i t i o n (872) for steels, rust i n h i b i t i n g uses (873,874), a n d r u s t p r o o f i n g agents
(875)
f o r ferrous a n d nonferrous metals a n d alloys a r e other c i t e d a p p l i c a t i o n s .
Miscellaneous
Applications
A s c o r b i c a c i d a n d d e r i v a t i v e s are c i t e d as p o t e n t i a l i n g r e d i e n t s i n c o s m e t i c f o r m u l a t i o n s (876-879). Specific uses i n v o l v e cosmetic c o m p o sitions f o r t h e r m a l d i s p e n s i n g
(880),
d e n t i f r i c e tablets
(881),
bath
p r e p a r a t i o n s (882), deodorants a n d m o u t h w a s h e s (883-886), s k i n p r e p a rations s u c h as s k i n l i g h t e n i n g p r e p a r a t i o n s (887) o r p r o t e c t i v e
creams
(888-890).
T h e m o r e a c t i v e areas h a v e b e e n h a i r a n d scalp p r e p a r a t i o n s
(891,892),
h a i r setting c o m p o s i t i o n s
(893), h a i r b l e a c h i n g
programs
(894, 895), a n d h a i r d y e i n g p r e p a r a t i o n s (896, 897, 898). A s c o r b i c a c i d has b e e n d e c l a r e d u s e f u l i n i n t r a v a g i n a l c o n t r a c e p tives i n r e d u c i n g s p e r m m o t i l i t y (899,900).
T h e p r e s e r v a t i o n of h u m a n
b l o o d b y t h e a d d i t i o n of s o d i u m ascorbate ( 9 0 1 ) has b e e n f o u n d t o h a v e some m e r i t . T h e usefulness of a s c o r b i c a c i d i n the t r e a t m e n t of i n d u s t r i a l c h e m i c a l t o x i c i t y (902,903), i n t h e p r e s e r v a t i o n of c u t - b l o o m s i n w a t e r (904,905), i n w a t e r t r e a t m e n t of the f e r r u g i n o u s t y p e (906), i n i n h i b i t i n g c o r r o s i o n (907), i n t r e a t m e n t f o r t h e p r o d u c t i o n of d u r a b l e creases i n c l o t h (908), a n d i n b r i g h t e n e d y a r n s w i t h h i g h l i g h t fastness ( 9 0 9 ) is mentioned.
Adhesive compositions
(910) a n d s p e c i a l cleansers
912) a r e other p o t e n t i a l a p p l i c a t i o n s .
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.
(911,
476
ASCORBIC
ACID
T h e p u r g i n g o f n i t r o g e n oxides f r o m exhaust gases (913) a n d treat m e n t of s m o k i n g m a t e r i a l s (914) w i t h ascorbates a r e o f interest, p a r t i c u l a r l y t h e latter, w h e r e i n a l o w e r p r o d u c t i o n of p o t e n t i a l l y
carcinogenic
nitrosated compounds m a y result i f the application were to b e p u t into effect. A n extensive l i t e r a t u r e exists o n t h e use o f a s c o r b i c a c i d i n c h e m i c a l a n a l y t i c a l assays.
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20. BAUERNFEIND Ascorbic Acid Technology
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Received for review April 16, 1981. Accepted June 27, 1981.
In Ascorbic Acid: Chemistry, Metabolism, and Uses; Seib, P., et al.; Advances in Chemistry; American Chemical Society: Washington, DC, 1982.