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使用超高效液相色谱-电喷雾电离-四极杆轨道阱质谱法分析牛奶中兽药残留的多类方法的开发与验证

Development and Validation of a Multiclass Method for Analysis of Veterinary Drug Residues in Milk Using Ultrahigh Performance Liquid Chromatography Electrospray Ionization Quadrupole Orbitrap Mass Spectrometry.

作者信息

Wang Jian, Leung Daniel, Chow Willis, Chang James, Wong Jon W

机构信息

Canadian Food Inspection Agency , Calgary Laboratory, 3650-36th Street N.W., Calgary, Alberta T2L 2L1, Canada.

ThermoFisher Scientific , 355 River Oaks Parkway, San Jose, California 95134, United States.

出版信息

J Agric Food Chem. 2015 Oct 21;63(41):9175-87. doi: 10.1021/acs.jafc.5b04096. Epub 2015 Oct 9.

DOI:10.1021/acs.jafc.5b04096
PMID:26416602
Abstract

This paper presents the development and validation of a multiclass method for the analysis of veterinary drug residues in milk using ultrahigh performance liquid chromatography electrospray ionization quadrupole Orbitrap mass spectrometry (UHPLC/ESI Q-Orbitrap). The 12 classes of veterinary drugs (a total of 125) included in this study were endectocides, fluoroquinolones, ionophores, macrolides, nitroimidazole, NSAIDs, β-lactams, penicillins, phenicols, sulfonamides, tetracyclines, and aminoglycosides. Veterinary drug residues in milk were extracted using a modified salting-out supported liquid extraction (SOSLE) method, which entailed the precipitation of milk proteins using an extraction buffer (oxalic acid and EDTA, pH 3) and acetonitrile, a salting-out acetonitrile/water phase separation using ammonium sulfate, and solid-phase extraction (SPE) using polymeric reversed-phase sorbent cartridges. The final extracts were concentrated and reconstituted into a buffer solution and analyzed using UHPLC/ESI Q-Orbitrap mass spectrometry. The developed method was validated using a nested experimental design to evaluate the method performance characteristics, such as overall recovery, intermediate precision, and measurement uncertainty. The method was able to quantify or screen up to 105 veterinary drugs from 11 different classes, except aminoglycosides. The limits of quantification were as low as 1.0 μg/kg, with an analytical range from 1.0 to 100.0 μg/kg in milk.

摘要

本文介绍了一种使用超高效液相色谱-电喷雾电离四极杆轨道阱质谱法(UHPLC/ESI Q-Orbitrap)分析牛奶中兽药残留的多类别方法的开发与验证。本研究涵盖的12类兽药(共125种)包括体内外寄生虫驱避剂、氟喹诺酮类、离子载体类、大环内酯类、硝基咪唑类、非甾体抗炎药、β-内酰胺类、青霉素类、酚类、磺胺类、四环素类和氨基糖苷类。牛奶中的兽药残留采用改良的盐析支持液液萃取(SOSLE)方法进行提取,该方法包括使用提取缓冲液(草酸和乙二胺四乙酸,pH 3)和乙腈沉淀牛奶蛋白,使用硫酸铵进行盐析乙腈/水相分离,以及使用聚合物反相吸附剂小柱进行固相萃取(SPE)。最终提取物经浓缩并复溶至缓冲溶液中,然后使用UHPLC/ESI Q-Orbitrap质谱法进行分析。所开发的方法通过嵌套实验设计进行验证,以评估方法的性能特征,如总回收率、中间精密度和测量不确定度。该方法能够对11类不同兽药(氨基糖苷类除外)中的多达105种兽药进行定量或筛查。定量限低至1.0 μg/kg,在牛奶中的分析范围为1.0至100.0 μg/kg。

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