The development of a rapid method for the isolation of four azaspiracids for use as reference materials for quantitative LC-MS-MS methods

被引:3
|
作者
Canas, Isa Ruppen [2 ]
O'Callaghan, Keith [1 ,2 ]
Moroney, Cian [2 ]
Hamilton, Brett [2 ]
James, Kevin J. [2 ,3 ]
Furey, Ambrose [1 ,2 ]
机构
[1] Cork Inst Technol, Dept Chem, Team Elucidate, Cork, Ireland
[2] Cork Inst Technol, Dept Chem, Proteobio Mass Spectrometry Ctr, Cork, Ireland
[3] Univ Coll Cork, Environm Res Inst, Cork, Ireland
关键词
Marine toxins; Azaspiracids; Azaspiracid shellfish poisoning; AZP; Mass spectrometry; Quadrupole ion-trap MS; LC-MS-MS; QTOF MS; TANDEM MASS-SPECTROMETRY; MUSSELS MYTILUS-EDULIS; LIQUID-CHROMATOGRAPHY; FRAGMENTATION PATHWAYS; MARINE TOXIN; PART; SHELLFISH; IDENTIFICATION; CONFIRMATION; ANALOGS;
D O I
10.1007/s00216-010-4007-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The azaspiracids are a family of lipophilic polyether marine biotoxins that have caused a number of human intoxication incidents in Europe since 1995 after consumption of contaminated shellfish (Mytilus edulis). Levels of azaspiracids in shellfish for human consumption are monitored in accordance with EU guidelines: only shellfish with less than 160 mu gkg(-1) are deemed safe. The limited availability of commercially available standards for azaspiracids is a serious problem, because validated LC-MS methods are required for routine analysis of these toxins in shellfish tissues. The procedure described herein has been used for the separation and the isolation of four azaspiracid (AZA) toxins from shellfish, for use as LC-MS-MS reference materials. Five separation steps have been used to isolate azaspiracids 1, 2, 3, and 6. The purity of the toxins obtained has been confirmed by multiple mass spectrometric methods using authentic azaspiracid standards. The same techniques have been used for quantification of the toxins extracted. The isolation procedure involves several chromatographic purification techniques: solid-phase extraction (diol sorbent, 90% mass reduction, and 95 +/- 1% toxin recovery); Sephadex size-exclusion chromatography (87% mass reduction and up to 95 +/- 2% toxin recovery), Toyopearl HW size-exclusion chromatography (90% mass reduction and up to 92.5 +/- 2.5% toxin recovery), and semi-preparative LC (78 +/- 3% toxin recovery). The procedure effectively separates the toxins from the sample matrix and furnishes azaspiracid toxins (AZA1, AZA2, AZA3 and AZA6) of sufficient purity with an average yield of 65% (n=5). Triple-quadrupole mass spectrometry was used for qualitative and quantitative monitoring of the isolation efficiency after each stage of the process. High-resolution mass spectrometric evaluation of the toxic isolated material in both positive and negative modes suggests high purity.
引用
收藏
页码:1477 / 1491
页数:15
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