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比较四种不同的多类、多残留样品前处理方法在鱼类和其他食品基质中兽药分析的应用。

Comparison of four different multiclass, multiresidue sample preparation methods in the analysis of veterinary drugs in fish and other food matrices.

机构信息

U.S. Department of Agriculture, Agricultural Research Service, Eastern Regional Research Center, 600 East Mermaid Lane, Wyndmoor, PA, 19038, USA.

出版信息

Anal Bioanal Chem. 2021 May;413(12):3223-3241. doi: 10.1007/s00216-021-03259-x. Epub 2021 Mar 13.

Abstract

In 2018, AOAC International issued Standard Method Performance Requirements (SPMR) 2018.010 - Screening and Identification Method for Regulated Veterinary Drug Residues in Food. In response, we compared 4 different multiresidue methods of sample preparation using the same analytical method entailing ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Tilapia was chosen for testing, and the analytes and monitoring levels were from SPMR 2018.010. The methods consist of efficient procedures with published validation results from the US Department of Agriculture (USDA), Food and Drug Administration (FDA), and Canadian Food Inspection Agency (CFIA), and an enhanced-matrix removal (EMR)-Lipid protocol from China. Each method was used to prepare 102 final extracts of tilapia spiked or not at different levels with the 78 targeted analytes plus metabolites. The same FDA/USDA rules of mass spectral identification were employed in all analyses to assess rates of false positives and negatives. Quantitative accuracy of the methods was also compared in terms of recoveries and reproducibility of spiked tilapia, incurred catfish, and spiked and certified reference material of bovine muscle. Each method yielded generally acceptable results for the targeted veterinary drugs, but the USDA "extract & inject" method was the fastest, simplest, and cheapest to achieve equally or more acceptable results for the widest scope of analytes for the tested food matrices.

摘要

2018 年,AOAC 国际发布了标准方法性能要求(SPMR)2018.010-食品中受监管的兽药残留的筛选和鉴定方法。对此,我们比较了 4 种不同的多残留样品制备方法,使用相同的分析方法,涉及超高效液相色谱-串联质谱(UHPLC-MS/MS)。我们选择罗非鱼进行测试,分析物和监测水平来自 SPMR 2018.010。这些方法包括经过验证的高效程序,这些程序已经得到美国农业部(USDA)、美国食品和药物管理局(FDA)和加拿大食品检验局(CFIA)的公布验证结果,以及来自中国的增强基质去除(EMR)-脂质协议。每种方法都用于制备 102 份最终的罗非鱼提取物,这些提取物要么未添加,要么在不同水平下添加了 78 种目标分析物加代谢物。在所有分析中,都采用了相同的 FDA/USDA 质谱鉴定规则来评估假阳性和假阴性的比率。还根据添加罗非鱼、鲶鱼和添加及认证的牛肌肉参考物质的回收率和重现性来比较方法的定量准确性。每种方法通常都能得到目标兽药的可接受结果,但 USDA 的“提取并注射”方法最快、最简单、最便宜,能够获得更广泛的测试食品基质的分析物的可接受结果。

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