Improved method for preparation and use of 9-anthryldiazomethane for derivatization of hydroxycarboxylic acids Application to diarrhetic shellfish poisoning toxins

被引:21
作者
Quilliam, MA
Gago-Martínez, A
Rodríguez-Vázquez, JA
机构
[1] Natl Res Council Canada, Inst Marine Biosci, Halifax, NS B3H 3Z1, Canada
[2] Univ vigo, Fac Ciencias, Dpto Quim Analit & Alimentaria, Vigo 36200, Spain
关键词
diarrhetic shellfish poisoning; derivatization; LC; anthryldiazomethane; hydroxycarboxylic acids; carboxylic acids; toxins; okadaic acid; octanoic acid;
D O I
10.1016/S0021-9673(98)00069-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Application of a method for the "in situ" generation of 9-anthryldiazomethane (ADAM) to the derivatization of the carboxyl function in diarrhetic shellfish poisoning (DSP) toxins revealed the formation of artifact products. Using liquid chromatography-mass spectrometry, it was determined that these artifacts were due to base-catalyzed reactions between the solvent, ethyl acetate, and the hydroxyl groups of the analyte to produce O-acetylated ADAM derivatives. Using a new formulation, with tetrahydrofuran as solvent, it was possible to eliminate these artifact reactions. Various reaction parameters have also been re-optimized to ensure quantitative derivatizations. An assessment method was developed that was useful not only for optimizing reaction parameters, but also for evaluating the reagent potency before use on important samples. Finally, application of the method to the determination of DSP toxins in plankton and mussel tissue was demonstrated. Published by Elsevier Science B.V.
引用
收藏
页码:229 / 239
页数:11
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