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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Combining the quick, easy, cheap, effective, rugged and safe approach and clean-up by immunoaffinity column for the analysis of 15 mycotoxins by isotope dilution liquid chromatography tandem mass spectrometry
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Combining the quick, easy, cheap, effective, rugged and safe approach and clean-up by immunoaffinity column for the analysis of 15 mycotoxins by isotope dilution liquid chromatography tandem mass spectrometry

机译:结合快速,简便,廉价,有效,坚固和安全的方法,并通过免疫亲和柱进行纯化,以通过同位素稀释液相色谱串联质谱法分析15种霉菌毒素

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摘要

Optimization and validation of a multi-mycotoxin method by LC-MS/MS is presented. The method covers the EU-regulated mycotoxins (aflatoxins, fumonisins, ochratoxin A, deoxynivalenol, zearalenone, T-2 and HT-2), as well as nivalenol and 3- and 15-acetyldeoxynivalenol for analysis of cereals, cocoa, oil, spices, infant formula, coffee and nuts. The proposed procedure combines two clean-up strategies: First, a generic preparation suitable for all mycotoxins based on the QuEChERS (for quick, easy, cheap, effective, rugged and safe) protocol. Second, a specific clean-up devoted to aflatoxins and ochratoxin A using immunoaffinity column (IAC) clean-up. Positive identification of mycotoxins in matrix was conducted according to the confirmation criteria defined in EU Commission Decision 2002/657/EC while quantification was performed by isotopic dilution using ~(13)C-labeled mycotoxins as internal standards. Limits of quantification were at or below the maximum levels set in the EC/1886/2006 document for all mycotoxin/matrix combinations under regulation. In particular, the inclusion of an IAC step allowed achieving LOQs as low as 0.05 and 0.25 μg/kg in cereals for aflatoxins and ochratoxin A, respectively. Other performance parameters like linearity [(r)~2 >0.99], recovery [71-118%], precision [(RSDr and RSD_(iR)) < 33%], and trueness [78-117%] were all compliant with the analytical requirements stipulated in the CEN/TR/16059 document. Method ruggedness was proved by a verification process conducted by another laboratory.
机译:提出了通过LC-MS / MS进行多真菌毒素方法的优化和验证。该方法涵盖了欧盟规定的霉菌毒素(黄曲霉毒素,伏马菌素,曲霉毒素A,脱氧雪茄烯醇,玉米赤霉烯酮,T-2和HT-2),以及用于分析谷物,可可,油,香料的雪茄烯酚和3-和15-乙酰基脱氧雪茄烯醇。 ,婴儿配方奶粉,咖啡和坚果。拟议的程序结合了两种清除策略:首先,基于QuEChERS(快速,简便,廉价,有效,坚固和安全)方案,适用于所有霉菌毒素的通用制剂。其次,使用免疫亲和柱(IAC)净化技术专门针对黄曲霉毒素和曲霉毒素A进行净化。根据EU Commission Decision 2002/657 / EC中定义的确认标准对基质中的霉菌毒素进行阳性鉴定,同时使用〜(13)C标记的霉菌毒素作为内标,通过同位素稀释进行定量。规定范围内所有真菌毒素/基质组合的定量限均在EC / 1886/2006文件中设定的最高水平或以下。特别是,通过包含IAC步骤,谷物中的黄曲霉毒素和曲霉毒素A的LOQ分别低至0.05和0.25μg/ kg。其他性能参数,如线性[[r]〜2> 0.99],恢复[71-118%],精度[(RSDr和RSD_(iR))<33%]和真实性[78-117%],均符合CEN / TR / 16059文件中规定的分析要求。通过其他实验室进行的验证过程证明了方法的坚固性。

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