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C: Plasmonics; Optical, Magnetic, and Hybrid Materials
A Novel and Sensitive Chemiluminescence Sensor Based on 2DMOFs Nanosheets for One-Step Detection of Glucose in Human Urine Nuanfei Zhu, Lantian Gu, Jin Wang, Xuesong Li, Guo-Xi Liang, Jinhui Zhou, and Zhen Zhang J. Phys. Chem. C, Just Accepted Manuscript • DOI: 10.1021/acs.jpcc.9b00671 • Publication Date (Web): 13 Mar 2019 Downloaded from http://pubs.acs.org on March 14, 2019
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A Novel and Sensitive Chemiluminescence Sensor Based on 2D-MOFs Nanosheets for One-Step Detection of Glucose in Human Urine
Nuanfei Zhu1, Lantian Gu1, Jin Wang1,2, Xuesong Li1, Guoxi Liang1, Jinhui Zhou3*, Zhen Zhang1*
1School
of the Environment and Safety Engineering, Jiangsu University,
Zhenjiang 212013, China
2Institute
3Institute
of Life Sciences, Jiangsu University, Zhenjiang 212013, China
of Apicultural Research, Chinese Academy of Agricultural Sciences,
Beijing 100093, PR China
*Corresponding authors: E-mail:
[email protected],
[email protected]. Tel.: +86-511-88790955, 86-10 62596429;
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ABSTRACT The development of a simple and sensitive method for glucose determination is significant in the early diagnosis and treatment of diabetes. However, current analytical approaches have various defects in their applications. Here, an attractive chemiluminescence-based sensor is developed for one-step and rapid detection of glucose in human urine. In this work, a 2D-MOFs nanosheet with peroxidase activity was firstly synthesized, which could catalyze the decomposition of hydrogen peroxide (H2O2) and further oxidize luminol to produce strong chemiluminescence signal. Then, luminol and glucose oxidase (GOD) were successively labeled on the 2D-MOFs nanosheet, obtaining a simple chemiluminescence-functionalized sensor (Co-TCPP(Fe)@luminol@GOD). When the Co-TCPP(Fe)@luminol@GOD was introduced to the detection system containing glucose, substantial H2O2 was released under the catalysis of GOD on the Co-TCPP(Fe). Then, the produced H2O2 was decomposed
by
the
2D-MOFs
nanosheet
and
the
luminol
on
the
Co-TCPP(Fe)@luminol@GOD further oxidized, generating chemiluminescence signal, finally achieving a rapid determination for glucose. Under the optimized condition, fabrication of 2D-MOFs nanosheet as a sensitive glucose sensor exhibited a good performance during the process: (i) good sensitivity (LOD, 10.667 μg/L) with a wide linear range (32-5500 μg/L); (ii) satisfactory accuracy (recoveries, 89-121.2%; CV, 3.5-7.4%); (iii) low cost; (iv) simple operation. And our proposed method here has the potential for screening the glucose in various human urines from hospitals.
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INTRODUCTION The diabetes is a kind of public health problem in the world, characterized by hyperglycemia with the high mortality and morbidity 1. For diabetics, the long-term hyperglycemia easily leads to the chronic damage and dysfunction of their tissues, especially eyes, kidneys, heart, blood vessels and nerves 2. What's worse, the disease can result in other complications of diabetes, like blindness and kidney failure, all of which are due to the excessed concentration of glucose in human blood 3. Previous research have shown that the early diagnosis of diabetics can protect the function of islet P cells and improve the insulin sensitivity, delaying and preventing diabetes-related complications4-5. Therefore, as a common indicator, the rapid and real-time determination of blood glucose is very necessary for the early diagnosis and the diagnosis/adjuvant treatment of diabetes. At present, various available strategies have been applied for detection of glucose from human body fluid or other samples, including colorimetric methods, chemical sensors and so on
6-8.
For example, Wu et al. established a novel and
sensitive electrochemical biosensor based on the co-catalysis effect of glucose oxidase (GOD) and nanoporous gold (NPG) for the glucose detection 9. This biosensor has a very low detection limit of 1.02 μM and the results are in good agreement with those produced by an automatic biochemical analyzer. Besides, Ji et al. reported a smartphone-based cyclic voltammetry (CV) electrochemical devices used to determine glucose in different simples, showing excellent linear and specific responses to the targets
10.
Although these methods have wider liner ranges, high
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sensitivity and low detection of limit, they always suffer from high expenses, cumbersome operation and complex synthesis or modification process. Nanozymes, a kind of nanomaterials with enzyme-mimic activity, have caught great attention over the past decades owing to their great catalytic efficiency, massive active sites and high stability in a wide range of temperatures or pH
11-12.
Currently,
various nanozymes have been used in many fields including biosensor, immunoassay, cancer diagnosis and treatment, neuroprotection
13-15.
For example, Md. N. Karim et
al. developed a rapid and colorimetric method based on a novel 3D matrix of a cotton fabric to detect the glucose from complex biological fluids
16.
In this work, Ag
nanoparticles were embedded within the 3D matrix of a cotton fabric, obtaining a kind of enzyme-mimicking catalytic nanoparticles- Ag@Fabric with the excellent peroxidase-like activity. Furthermore, many nanozymes were also applied in electrochemical sensors for the glucose determination, such as ammoniadoped-prGO/CuO 17, CuONW/CC 8, Cu3P NW/CF 1 and so on. Herein, inspired by these studies, a novel 2D metal-organic frameworks (2D MOFs)- Co-TCPP(Fe) was synthesized and applied in a sensitive chemiluminescence sensor for one-step detection of glucose from human urine samples (shown in Scheme 1). In this work, the GOD and luminol were modified on the Co-TCPP (Fe) to form a simple chemiluminescence-functional sensor, in which the Co-TCPP(Fe) has a high catalysis for the H2O2 produced by the reaction between GOD and glucose, further triggering the chemiluminescence signal of luminol, achieving the quantitative analysis for the glucose.
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MATERIALS AND METHOD Materials
and
Apparatus.
Cobaltous
nitrate
hexahydrate,
pyrazine,
polyvinylpyrrolidone (PVP), luminol, glucose, GOD, NH2-PEG-COOH, ethanol, NaCl, KH2PO4, KCl, 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide (EDC), N-hydroxysuccinimide (NHS), NaH2PO4•12H2O, and H2O2 were obtained from the Sinopharm Chemical Reagent Co. Ltd. (Shanghai, China). Horseradish peroxidase (HRP) and 3, 3’, 5, 5’ -tetramethylbenzidine dihydrochloride (TMB) was purchased from Aladdin (USA). N, N-dimethylformamide (DMF), TCPP(Fe) were provided by J&K Scientific. All chemicals and materials were used without further purification. Synthesis of Co-TCPP(Fe). The Co-TCPP (Fe) was synthesized according to the previous literature 18. Preparation of the Co-TCPP(Fe)@luminol. Firstly, 1 mg Co-TCPP(Fe) in 0.1 M PBS (1 mL, pH 7.0) were dispersed by ultrasonic for 20 min. Then, 2 mg EDC/NHS (1:1) was added into the mixed solution, maintaining at 37ºC for 5 h. After that, 2 mg NH2-PEG-COOH was mixed with the above product under vigorous stirring for 12 h at 37ºC. Finally, the obtained product was centrifuged and washed using anhydrous ethanol. Afterwards, the resulting solid was dissolved in 1 mL 0.1 M PBS (pH 7.0). 20 min ultrasound later, the same processing mode was carried out by using 2 mg EDC/NHS (1:1) at 37 ºC for 5 h. Then, 2 mg luminol was added into the above solution and kept reacting 12 h at 37 ºC. After a similar centrifugation and washing step, the Co-TCPP(Fe)@luminol was successfully synthesized and stored at 4 ºC for
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further use. Preparation of Co-TCPP(Fe)@luminol@GOD. First of all, the obtained Co-TCPP(Fe)@luminol was dispersed in 0.1 M PBS (pH 7.0) with ultrasonic waves for
20
min.
Subsequently,
2
mg
EDC/NHS
was
dissolved
into
the
Co-TCPP(Fe)@luminol solution under 37ºC for 5 h. Through the activation, 1 mg GOD was mixed with the above solution. 12 hours later, another centrifugation and washing step were implemented for removing the extra GOD to get the pure Co-TCPP(Fe)@luminol@GOD. RESULTS AND DISCUSSION Synthesis of Co-TCPP(Fe)@luminol and Co-TCPP(Fe)@luminol@GOD. In this
paper,
the
synthesis
of
Co-TCPP(Fe)@luminol
and
Co-TCPP(Fe)@luminol@GOD were the key steps in the preparation of the proposed chemiluminescence sensor. Therefore, several critical factors during the procedure were investigated to achieve the optimal performance, including the concentrations of Co-TCPP(Fe), luminol and GOD, the reaction times of Co-TCPP(Fe)/luminol and Co-TCPP(Fe)@luminol/GOD. As shown in Figure 1, three conditions was optimized for the preparation of Co-TCPP(Fe)@luminol (A. the concentration of Co-TCPP(Fe); B. the concentration of luminol; C. The mixture time of luminol /Co-TCPP(Fe)). Seen from Figure 1A, with the increasing of Co-TCPP(Fe), the chemiluminescence intensity (CL) enhanced initially, following an obvious decrease, achieving the highest peak at 2 mg/L. Therefore, 2 mg/L was selected as the optimum concentration for Co-TCPP(Fe) in
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this reaction. In addition, a similar trend for luminol was observed (Figure 1B), suggesting that the optimized concentration of luminol was 2 mg/L. Besides, according to the results in Figure 1C, 6 h was thought as the most suitable reaction time during the process. The synthesis conditions for Co-TCPP(Fe)@luminol@GOD also were studied. Displayed by Figure 2A, the highest CL value was observed under the reaction time of 8 h, illustrating that was the optimum reactive time. Meanwhile, Figure 2B showed that when GOD was 2 mg/L, the highest CL value was generated, obtaining the best performance for the glucose determination. The
Characterization
of
Co-TCPP(Fe),
Co-TCPP(Fe)@luminol
and
Co-TCPP(Fe)@luminol@GOD. The luminol and GOD were modified on the surface of Co-TCPP(Fe) step by step. And the product and its intermediates were characterized by transmission electron microscope (TEM), Fourier transform infrared spectrometer and UV-visible spectrophotometer. The TEM images of Co-TCPP(Fe) showed an obvious and uniform 2D sheet structure (Figure 3), implying that the material was successfully synthesized. To further test the change of functional groups, the FTIR of Co-TCPP(Fe), Co-TCPP(Fe)@luminol and Co-TCPP(Fe)@luminol@GOD were carried out, and the detailed information was shown in Figure 4A. Seen from the spectrum, a distinct peak (line c) at a wave number of 1600 cm-1 was represented, indicating there were a large number of carboxyl groups in the Co-TCPP(Fe), which was ascribed to the modification of other reagents. After the addition of luminol and GOD, due to that
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numerous carboxyl groups on the surface of Co-TCPP(Fe) were consumed, the peaks of Co-TCPP(Fe)@luminol (line b) and Co-TCPP(Fe)@luminol@GOD (line a) at 1600 (cm-1) had a significant reduction. The above characterization showed that the Co-TCPP(Fe)@luminol@GOD had been successfully prepared. Figure 4B indicated that Co-TCPP(Fe)@luminol was produced as expectation, because its three characteristic absorption peaks (line c, at 301, 348, 407 nm) were consistent with these corresponding peaks of the luminol solution (line a, 303, 350 nm) and Co-TCPP(Fe) (line b, 409 nm). After the modification of GOD, except for the characteristic absorption peak of luminol, the other two peaks at 390 nm and 458 nm could be observed in the spectrum of Co-TCPP(Fe)@luminol@GOD, which was similar with the GOD solution (line e, 382, 455 nm), meaning that the Co-TCPP(Fe)@luminol@GOD was obtained. The Peroxidase-like Activity of Co-TCPP(Fe). In order to systematically study the peroxidase-like activity of Co-TCPP(Fe), the 3,3',5,5'-tetramethylbenzidine (TMB) was set as a model substrate in the presence of H2O2, and the absorbance was recorded by an UV-visible spectroscopy. Revealed by Figure 5A, a significant enhancement could be observed in present of Co-TCPP(Fe), which meant the substance had a good performance in peroxidase-like catalysis. Besides, the reaction conditions of the Co-TCPP(Fe) had also been investigated, including the pH (Figure 5B) and temperature (Figure 5C). As shown in Figure 5B, the relative activity of Co-TCPP(Fe) kept increasing with the pH firstly and then decreased, the peak reached at pH=7.0, which was considered as the appropriate pH value in this system.
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Meanwhile, the optimal temperature of Co-TCPP(Fe) was chosen at 37°C. Furthermore, compared with the natural enzyme (HRP as a model), the Co-TCPP(Fe) had greater advantages in tolerance, showing a higher resistance to a strong acid or base and the extreme temperature. The
Optical
Properties
of
Co-TCPP(Fe)@luminol
and
Co-TCPP(Fe)@luminol@GOD. 5 parallel tests were carried out to study the chemiluminescent effect of Co-TCPP(Fe)@luminol with or without H2O2. Seen from Figure
6A,
the
chemiluminescence
enhancement
only
occurred
when
Co-TCPP(Fe)@luminol was mixed with H2O2, proving the luminol had been coupled to the Co-TCPP(Fe). In addition, an obvious increase in chemiluminescence was observed after the glucose solution was added in the Co-TCPP(Fe)@luminol@GOD (Figure
6B).
The
above
evidences
demonstrated
that
the
obtained
Co-TCPP(Fe)@luminol@GOD can be applied in the further detection for glucose as a chemiluminescence sensor. And the selectivity of this chemiluminescence sensor was investigated in a series of experiments and the results showed that the proposed sensor had a high selectivity for glucose (in Figure S1). The Method Validation and Samples Analysis. Under the above optimized conditions, the standard curve for glucose detection was established and shown in Figure 7. The detection range was 32-5500 μg/L with a limit of detection (10.667 μg/L), which was lower than that using other methods (Table S1). In order to evaluate the accuracy and precision of this chemiluminescence sensor, different simples (milk, pure water, tea and energy drink) spiked with a series
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concentration of glucose were measured (Table 1). The results showed satisfactory recoveries (89-121.2%) and the good intra-assay coefficient of variation (CV) ranged from 3.5% to 7.4% (under 3 replicates), indicating this proposed sensor could be used as an effective tool for high- throughput analysis of glucose from various samples. This established method was applied to detect the concentration of glucose in human urines that were collected from different population including diabetic patients and health persons, and the results were shown in Table 2. CONCLUSION Herein, based on the catalysis of a novel 2D-MOFs nanosheet, we developed a simple and sensitive chemiluminescence sensor for quick, high-throughput analysis of glucose. After optimized the conditions, this established method displayed a low limit of detection (10.667 μg/L) with a wider detection range (32-5500 μg/L), good accuracy and precision (recoveries, 89-121.2%; CV, 3.5-7.4%), illustrating great potential in the detection of glucose from human blood or urine and other samples. Supporting Information Available The Supporting Information is available free of charge on the ACS Publications website, including the comparisons of different methods and the selectivity of this method. ACKNOWLEDGEMENT The present work was supported by the National Natural Science Foundation of China (Grants 21577051, 21876067) and the Jiangsu Collaborative Innovation Center for Technology and Water Treatment.
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REFERENCES 1.
Xie, L.; Asiri, A. M.; Sun, X., Monolithically Integrated Copper Phosphide Nanowire: An
Efficient Electrocatalyst for Sensitive and Selective Nonenzymatic Glucose Detection. Sensors and Actuators B: Chemical 2017, 244, 11-16. 2.
Balasubramanian, P.; Balamurugan, T. S. T.; Chen, S.-M.; Chen, T.-W., Facile Synthesis of
Orthorhombic Strontium Copper Oxide Microflowers for Highly Sensitive Nonenzymatic Detection of Glucose in Human Blood. Journal of the Taiwan Institute of Chemical Engineers 2017, 81, 182-189. 3.
Gokoglan, T. C.; Soylemez, S.; Kesik, M.; Dogru, I. B.; Turel, O.; Yuksel, R.; Unalan, H. E.;
Toppare, L., A Novel Approach for the Fabrication of a Flexible Glucose Biosensor: The Combination of Vertically Aligned Cnts and a Conjugated Polymer. Food. Chem. 2017, 220, 299-305. 4.
Ornatska, M.; Sharpe, E.; Andreescu, D.; Andreescu, S., Paper Bioassay Based on Ceria
Nanoparticles as Colorimetric Probes. Anal. Chem. 2011, 83, 4273. 5.
Radhakumary, C.; Sreenivasan, K., Naked Eye Detection of Glucose in Urine Using Glucose
Oxidase Immobilized Gold Nanoparticles. Anal. Chem. 2011, 83, 2829. 6.
Samphao, A.; Butmee, P.; Jitcharoen, J.; Svorc, L.; Raber, G.; Kalcher, K., Flow-Injection
Amperometric Determination of Glucose Using a Biosensor Based on Immobilization of Glucose Oxidase onto Au Seeds Decorated on Core Fe(3)O(4) Nanoparticles. Talanta 2015, 142, 35-42. 7.
Shen, X. W.; Huang, C. Z.; Li, Y. F., Localized Surface Plasmon Resonance Sensing Detection of
Glucose in the Serum Samples of Diabetes Sufferers Based on the Redox Reaction of Chlorauric Acid. Talanta 2007, 72, 1432-7. 8.
Zhong, Y.; Shi, T.; Liu, Z.; Cheng, S.; Huang, Y.; Tao, X.; Liao, G.; Tang, Z., Ultrasensitive
Non-Enzymatic Glucose Sensors Based on Different Copper Oxide Nanostructures by in-Situ Growth. Sensors and Actuators B: Chemical 2016, 236, 326-333. 9.
Wu, C.; Sun, H.; Li, Y.; Liu, X.; Du, X.; Wang, X.; Xu, P., Biosensor Based on Glucose
Oxidase-Nanoporous Gold Co-Catalysis for Glucose Detection. Biosens. Bioelectro. 2015, 66, 350-355. 10. Lei, Y.; Tang, L.; Xie, Y.; Xianyu, Y.; Zhang, L.; Wang, P.; Hamada, Y.; Jiang, K.; Zheng, W.; Jiang, X., Gold Nanoclusters-Assisted Delivery of Ngf Sirna for Effective Treatment of Pancreatic Cancer. Nat. Commun. 2017, 8, 15130. 11. Cheng, H., et al., Monitoring of Heparin Activity in Live Rats Using Metal-Organic Framework Nanosheets as Peroxidase Mimics. Anal. Chem. 2017, 89, 11552-11559. 12. Wang, Y., et al., Bioinspired Design of Ultrathin 2d Bimetallic Metal-Organic-Framework Nanosheets Used as Biomimetic Enzymes. Adv. Mater. 2016, 28, 4149-55. 13. Fu, S.; Zhu, C.; Song, J.; Engelhard, M.; Xia, H.; Du, D.; Lin, Y., Pdcupt Nanocrystals with Multibranches for Enzyme-Free Glucose Detection. ACS Appl. Mater. Inter. 2016, 8, 22196-200. 14. Liu, C.; Sheng, Y.; Sun, Y.; Feng, J.; Wang, S.; Zhang, J.; Xu, J.; Jiang, D., A Glucose Oxidase-Coupled Dnazyme Sensor for Glucose Detection in Tears and Saliva. Biosens. Bioelectron. 2015, 70, 455-61. 15. Wang, Q.; Zhang, X.; Huang, L.; Zhang, Z.; Dong, S., One-Pot Synthesis of Fe3o4 Nanoparticle Loaded 3d Porous Graphene Nanocomposites with Enhanced Nanozyme Activity for Glucose Detection. ACS Appl. Mater. Inter. 2017, 9, 7465-7471. 16. Karim, M. N.; Anderson, S. R.; Singh, S.; Ramanathan, R.; Bansal, V., Nanostructured Silver Fabric as a Free-Standing Nanozyme for Colorimetric Detection of Glucose in Urine. Biosens.
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Bioelectron. 2018, 110, 8-15. 17. Maaoui, H.; Singh, S. K.; Teodorescu, F.; Coffinier, Y.; Barras, A.; Chtourou, R.; Kurungot, S.; Szunerits, S.; Boukherroub, R., Copper Oxide Supported on Three-Dimensional Ammonia-Doped Porous Reduced Graphene Oxide Prepared through Electrophoretic Deposition for Non-Enzymatic Glucose Sensing. Electrochimica. Acta. 2017, 224, 346-354. 18. Feng, D.; Chung, W.-C.; Wei, Z.; Gu, Z.-Y.; Jiang, H.-L.; Chen, Y.-P.; Darensbourg, D. J.; Zhou, H.-C., Construction of Ultrastable Porphyrin Zr Metal–Organic Frameworks through Linker Elimination. J. Am. Chem. Soc. 2013, 135, 17105-17110.
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Scheme 1. The principle of the novel chemiluminescence sensor for one-step ultrasensitive glucose detection (A. The preparation of the chemiluminescence sensorCo-TCPP(Fe)@luminol@GOD; B. The process of one-step detection for glucose).
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Tables Table 1. Analysis of glucose-spiked samples using our established method. Background
Added
Found
Recover
CV
(μg/L)
(μg/L)
(μg/L)
(%)
(%)
100
93.00
93.00
3.5
1000
1212
121.2
4.2
3000
2954
98.47
3.7
100
89.00
89.00
5.2
1000
972.0
97.20
4.8
3000
3135
104.5
3.9
100
112.0
112.0
4.6
1000
983.0
98.30
3.7
3000
2893
96.43
5.3
100
107.0
107.0
4.2
1000
982.0
98.20
6.7
3000
2973
99.10
7.4
Sample
Pure water
Milk
Tea
ND
ND
ND
Energy ND drink
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Table 2. The detection of human urine samples using our established method. Found Samples (μg/L) Sample 1
1350
Sample 2
720.0
Sample 3
560.0
Sample 4
1140
Sample 5
3260
Sample 6
3180
Sample 7
4210
Sample 8
3520
Sample 9
2930
Simple 10
4670
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Figure captions Figure 1. The optimization for the synthesis of Co-TCPP(Fe)@luminol (A. The concentration of Co-TCPP(Fe); B. The concentration of luminol; C. The mixture time of luminol and Co-TCPP(Fe)). Figure 2. The optimization for the synthesis of Co-TCPP(Fe)@luminol@GOD (A. The
concentration
of
GOD;
B.
The
mixture
time
between
GOD
and
Co-TCPP(Fe)@luminol@GOD. Figure 3. The TEM images of Co-TCPP(Fe). Figure 4. A. The FTIR spectrum of
(a) Co-TCPP(Fe)@lumino@GOD, (b)
Co-TCPP(Fe)@luminol and (c) Co-TCPP(Fe); B. The UV absorption spectrum of (a) luminol
solution,
(b)
Co-TCPP(Fe),
(c)
Co-TCPP(Fe)@luminol,
(d)
Co-TCPP(Fe)@luminol@GOD and (e) GOD solution. Figure 5. A. The absorbance of TMB-H2O2 substrates with Co-TCPP(Fe) or without; B. The relative activity of Co-TCPP(Fe) and HRP in different pH; C. The relative activity of Co-TCPP(Fe) and HRP at different temperatures. Figure 6. The optical properties of (A) Co-TCPP(Fe)@luminol and (B) Co-TCPP(Fe)@luminol@GOD. Figure 7. The calibration curves of the chemiluminiscence versus glucose concentrations with a LOD of 10.667 μg/L. The error bars represent the standard deviation of three replicates.
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Figure 1. The optimization for the synthesis of Co-TCPP(Fe)@luminol (A. The concentration of Co-TCPP(Fe); B. The concentration of luminol; C. The mixture time of luminol and Co-TCPP(Fe)).
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Figure 2. The optimization for the synthesis of Co-TCPP(Fe)@luminol@GOD (A. The
concentration
of
GOD;
B.
The
mixture
Co-TCPP(Fe)@luminol@GOD.
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time
between
GOD
and
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The Journal of Physical Chemistry
Figure 3. The TEM images of Co-TCPP(Fe).
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Figure 4. A. The FTIR spectrum of
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(a) Co-TCPP(Fe)@lumino@GOD, (b)
Co-TCPP(Fe)@luminol and (c) Co-TCPP(Fe); B. The UV absorption spectrum of (a) luminol
solution,
(b)
Co-TCPP(Fe),
(c)
Co-TCPP(Fe)@luminol,
Co-TCPP(Fe)@luminol@GOD and (e) GOD solution.
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(d)
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The Journal of Physical Chemistry
Figure 5. A. The absorbance of TMB-H2O2 substrates with Co-TCPP(Fe) or without; B. The relative activity of Co-TCPP(Fe) and HRP in different pH; C. The relative activity of Co-TCPP(Fe) and HRP at different temperatures.
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Figure 6. The optical properties of (A) Co-TCPP(Fe)@luminol and (B) Co-TCPP(Fe)@luminol@GOD.
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The Journal of Physical Chemistry
Figure 7. The calibration curves of the chemiluminiscence versus glucose concentrations with a LOD of 10.667 μg/L. The error bars represent the standard deviation of three replicates.
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The Journal of Physical Chemistry 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
TOC Graphic
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