Marine Toxins: Origin, Structure, and Molecular Pharmacology

Marine Toxins: Origin, Structure, and Molecular Pharmacology. Anal. Chem. , 1990, 62 (13), pp 720A–720A. DOI: 10.1021/ac00212a731. Publication Date:...
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INSTRUMENTATION tion while being swept slowly toward the mass spectrometer by the bulk electroosmotic flow within the capil­

lary. As the separated bands of analyte elute from the CE column, they are car­ ried through the liquid junction to the

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Marine Toxins: Origin, Structure, and Molecular Pharmacology

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ringing together research from many disciplines, this comprehensive volume reports the latest results in the study of marine toxins. This unique book covers the en­ tire range of source organisms and toxins while focusing on the structure and metabolic origin of toxins and the molecular basis of tox­ icity. In addition, this volume discusses con­ temporary molecular pharmacology and con­ formational chemistry as well as the traditional structural studies. Divided into four sections, the 27 chapters cover the following areas:

Figure 6. L C / M S / M S analysis of a tryptic digest of hemoglobin normal β chain, (a) Full-scan micro LC/MS/MS TIC chromatogram for the same sample shown in Figure 5a. The doubly charged ion (signal at m/z 658) was focused into the collision cell, which was charged with argon gas; CID was carried out with a collision energy of 50 eV. (b) Full-scan CID product ion mass spectrum for the ion (signal at m/z 658) of the tryptic fragment eluting at 12 min in Figure 5a. The retention times in Fig­ ures 5a and 6a differ somewhat because of minor variations in HPLC reproducibility; micro LC conditions were the same as described in Figure 5.

• General considerations • Polyether toxins • Palytoxin • Peptide toxins

The scope of the book goes slightly beyond the title and includes cyanophytes that occur in fresh or brackish waters. Also, an examina­ tion of the interactions between toxins and their primary sites of action is provided. Sherwood Hall, Editor, U.S. Food and Drug Administration Gary Strichartz, Editor, Harvard Medical School Developed from a symposium held under the auspices of the Commission on Food Chemistry. Applied Chem­ istry Division, International Union of Pure and Applied Chemistry." ACS Symposium Series No. 418 390 pages (1989) Clothbound ISBN 0-8412-1733-5 LC 89-18505 $74.95 0

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Figure 7 . C E / S I M M S total selected ion current electropherogram for 4 0 0 - 5 0 0 pg of synthetic sulfonylurea herbicides using the ion spray L C / M S interface. Conditions: 50:50 CH.,CN/10 mM NH4OAc (pH = 5.5), 17 kV (13 mA); samples injected for 30 s at 5 cm hydrostatic head (injection volume of 6-7 nL); 100 ^m X 100 cm fused-silica column; and the ion spray interface held at 3 kV. The elution order is 1, bensulfuron methyl; 2, sulfometuron methyl; 3, tribenuron methyl; 4, chlorimuron ethyl; and 5, thifensulfuron methyl. (Separation and samples kindly provided by G. Sherwood, E. I. du Pont de Nemours & Co., Wilmington, DE.)

720 A • ANALYTICAL CHEMISTRY, VOL. 62, NO. 13, JULY 1, 1990