首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >New method for the analysis of lipophilic marine biotoxins in fresh and canned bivalves by liquid chromatography coupled to high resolution mass spectrometry: A quick, easy, cheap, efficient, rugged, safe approach
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New method for the analysis of lipophilic marine biotoxins in fresh and canned bivalves by liquid chromatography coupled to high resolution mass spectrometry: A quick, easy, cheap, efficient, rugged, safe approach

机译:液相色谱与高分辨率质谱联用分析新鲜和罐装双壳类动物中亲脂性海洋生物毒素的新方法:一种快速,简便,廉价,高效,坚固,安全的方法

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A new method for the analysis of lipophilic marine biotoxins (okadaic acid, dinophysistoxins, azaspiracids, pectenotoxins, yessotoxins, spirolids) in fresh and canned bivalves has been developed. A QuEChERS methodology is applied; i.e. the analytes are extracted with acetonitrile and clean-up of the extracts is performed by dispersive solid phase extraction with C-18. The extracts are analyzed by ultra-high performance liquid chromatography coupled to a hybrid quadrupole-Orbitrap mass spectrometer, operating in tandem mass spectrometry mode, with resolution set at 70,000 (m/z 200, FWHM). Separation of the analytes, which takes about 10min, is carried out in gradient elution mode with a BEH C-18 column and mobile phases based on 6.7 mM ammonia aqueous solution and acetonitrile mixtures. For each analyte the molecular ion and 1 or 2 product ions are acquired, with a mass accuracy better than 5 ppm. The quantification is performed using surrogate matrix matched standards, with eprinomectin as internal standard. The high-throughput method, which has been successfully validated, fulfills the requirements of European Union legislation, and has been implemented as a routine method in a public health laboratory. (c) 2015 Elsevier B.V. All rights reserved.
机译:已开发出一种用于分析新鲜和罐装双壳类动物中亲脂性海洋生物毒素(冈田酸,双歧杆菌毒素,氮杂螺菌酸,果胶毒素,叶蜡毒素,螺旋藻)的新方法。采用QuEChERS方法;即用乙腈萃取分析物,并用C-18分散固相萃取进行萃取物的净化。萃取物通过与串联四极杆-Orbitrap质谱仪混合的超高效液相色谱仪进行分析,串联质谱仪以串联质谱模式运行,分辨率设置为70,000(m / z 200,FWHM)。使用BEH C-18色谱柱和基于6.7 mM氨水溶液和乙腈混合物的流动相,以梯度洗脱模式进行分析物的分离,大约需要10分钟。对于每种分析物,均获得了质量离子优于5 ppm的分子离子和1或2个产物离子。使用替代基质匹配标准品,以依普连菌素作为内标物进行定量。高通量方法已成功验证,符合欧盟法规的要求,并已在公共卫生实验室作为常规方法实施。 (c)2015 Elsevier B.V.保留所有权利。

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