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建立和验证用于肝脏中抗凝血杀鼠剂的超高效液相色谱-串联质谱定量分析方法

Development and Validation of Quantitative Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry Assay for Anticoagulant Rodenticides in Liver.

机构信息

University of Kentucky Veterinary Diagnostic Laboratory, Toxicology Laboratory, University of Kentucky , Lexington, Kentucky 40511, United States.

California Animal Health and Food Safety Laboratory System, Toxicology Laboratory, University of California , Davis, California 95616, United States.

出版信息

J Agric Food Chem. 2017 Aug 9;65(31):6682-6691. doi: 10.1021/acs.jafc.7b02280. Epub 2017 Jul 27.

DOI:10.1021/acs.jafc.7b02280
PMID:28699743
Abstract

Anticoagulant rodenticides (ARs) are used to control rodent populations; however, exposure to nontarget animals occurs. A sensitive and rugged quantitative method was developed, optimized, and validated for eight ARs in liver. Target analytes comprised two chemical classes: hydroxycoumarins (warfarin, coumachlor, dicoumarol, bromadiolone, brodifacoum, and difethialone) and indanediones (diphacinone and chlorophacinone). In this method, liver extracts were cleaned using dispersive solid phase extraction (d-SPE) to remove matrix interferences and analyzed by reverse phase ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Electrospray ionization in negative ion mode combined with multiple reaction monitoring (MRM) using a triple quadrupole mass spectrometer provided simultaneous confirmation and quantitation. Detection limits spanned 0.75-25 ng/g, and lower quantitation limits were established as 50 ng/g. Interassay method accuracy ranged from 92 to 110% across the analytical range (50-2500 ng/g) using matrix-matched calibrants with good repeatability (relative standard deviations 2-16%). Successful method transfer to another laboratory utilizing an Orbitrap mass analyzer, providing high mass accuracy, was assessed by good method reproducibility during blinded study analyses (6-29%; Horwitz ratios (HORRAT) ≤ 1.5).

摘要

抗凝血灭鼠剂(ARs)用于控制鼠类种群;然而,非靶标动物也会接触到这些药剂。本研究开发、优化并验证了一种用于肝脏中 8 种 ARs 的灵敏且稳健的定量方法。目标分析物包括两类化学物质:羟基香豆素(华法林、杀鼠氯、敌鼠、溴敌隆、溴鼠灵和大隆)和茚满二酮(敌鼠酮和氯鼠酮)。在该方法中,采用分散固相萃取(d-SPE)对肝脏提取物进行净化,以去除基质干扰,然后采用反相超高效液相色谱-串联质谱法(UPLC-MS/MS)进行分析。负离子模式下的电喷雾电离与三重四极杆质谱联用的多反应监测(MRM)提供了同时确证和定量的功能。检测限为 0.75-25ng/g,定量下限为 50ng/g。使用基质匹配校准物,在整个分析范围内(50-2500ng/g),方法的准确度在 92%-110%之间,具有良好的重复性(相对标准偏差为 2-16%)。通过在盲法研究分析中评估在另一个使用轨道阱质谱仪的实验室中的良好方法重现性(6-29%;HORRAT 值≤1.5),成功地实现了方法转移。

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