Department of Pharmacology and Toxicology, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
J Chromatogr A. 2013 May 31;1292:96-103. doi: 10.1016/j.chroma.2012.09.006. Epub 2012 Sep 6.
This paper presents a sensitive and confirmatory multi-residue method for the analysis of 23 veterinary drugs and metabolites belonging to three classes (nitroimidazoles, benzimidazoles, and chloramphenicols) in porcine muscle, liver, and kidney. After extracted with ethyl acetate and basic ethyl acetate sequentially, the crude extracts were defatted with hexane and further purified using Oasis MCX solid-phase extraction cartridges. Rapid determination was carried out by ultra-high performance liquid chromatography-electrospray ionization tandem mass spectrometry. Data acquisition was performed under positive and negative mode simultaneously. Recoveries based on matrix-matched calibrations for meat, liver, and kidney ranged from 50.6 to 108.1%. The method quantification limits were in the range of 3-100ng/kg.
本文建立了一种灵敏确证的多残留分析方法,用于检测猪肉、猪肝和猪肾中 23 种兽药及代谢物(包括硝咪唑类、苯并咪唑类和氯霉素类)。经乙酸乙酯和碱性乙酸乙酯提取后,先用正己烷脱脂,再用 Oasis MCX 固相萃取小柱净化。采用超高效液相色谱-电喷雾串联质谱法进行快速检测,正、负离子同时采集数据。基于基质匹配校准,该方法在肉、肝和肾中的回收率为 50.6%至 108.1%。方法定量限为 3-100ng/kg。