Development of an ultra-performance liquid chromatography-mass spectrometry method for the detection of lipophilic marine toxins

被引:89
|
作者
Fux, Elie [1 ]
McMillan, Daniel
Bire, Ronel
Hess, Philipp
机构
[1] Inst Marine, Biotoxins Chem, Galway, Ireland
[2] Dublin Inst Technol, Sch Chem & Pharmaceut Sci, Dublin 8, Ireland
[3] Waters Corp, Manchester M22 5PP, Lancs, England
关键词
lipophilic shellfish toxins; UPLC; matrix effects; okadaic acid; azaspiracids;
D O I
10.1016/j.chroma.2007.05.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid method for the detection of marine toxins was developed using an ultra-performance liquid chromatography (UPLC) system coupled to a latest generation mass spectrometry (MS) system. The analysis of 21 lipophilic marine toxins was achieved on an Acquity C18 column using a water-acetonitrile gradient with a cycle time of 6.6 min, reducing analysis time by more than a factor two compared to HPLC while maintaining peak resolution. Linear ranges, limits of detection and limits of quantification were established for okadaic acid (OA), pectenotoxin-2, azaspiracid-1 (AZAI), yessotoxin, gymnoclimine and 13-desmethylspirolide C. The method was found to be accurate when using a triplicate methanolic extraction. Matrix effects were assessed by standard addition of OA and AZA I in extracts of raw and heat-treated flesh of mussels and oysters. For the analysis of AZAI, the UPLC-MS method was always prone to signal suppression, while for OA analysis signal suppression was observed in extracts of raw shellfish flesh and signal enhancement in extracts of heat-treated flesh. Matrix effects occurring in the method presented are diminished compared to previous studies. (c) 2007 Elsevier B.V. All fights reserved.
引用
收藏
页码:273 / 280
页数:8
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