Simultaneous determination of triclabendazole and its metabolites in bovine and goat tissues by liquid chromatography-tandem mass spectrometry

被引:17
作者
Cai, Chengyuan [1 ]
Zhang, Lifang [1 ]
Xue, Feiqun [1 ]
Qiu, Minqi [1 ]
Zheng, Wenli [1 ]
机构
[1] Chinese Acad Agr Sci, Key Lab Vet Drug Safety Evaluat & Residues Res, Shanghai Vet Res Inst, Shanghai 200241, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2010年 / 878卷 / 30期
关键词
Triclabendazole; Metabolites; Residues; LC-MS/MS; MEASUREMENT UNCERTAINTY; FASCIOLA-HEPATICA; SHEEP; DISPOSITION; RESISTANCE; SULFOXIDE; CATTLE; MILK;
D O I
10.1016/j.jchromb.2010.09.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive liquid chromatography-tandem mass spectrometry method for the simultaneous determination of triclabendazole, its main metabolites (triclabendazole sulphone and triclabendazole sulphoxide) and a marker residue (ketotriclabendazole) in bovine and goat muscle, liver, and kidney samples is developed and validated. Analyte extraction from samples is effectively performed using liquid-liquid extraction by acetonitrile. Chromatographic separation is performed on a C-18 reversed-phase column with gradient elution. The analytes are detected by tandem quadrupole mass spectrometry after positive electrospray ionization by multiple reaction monitoring. The limits of detection for analytes are found to be 0.25-2.5 mu g/kg in muscle tissues and 1-10 mu g/kg in liver and kidney tissues, respectively. The recoveries of edible bovine and goat tissues range from 84.9% to 109.5% when spiked at different levels with analytes, with relative standard deviations generally below 12.8%. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:3106 / 3112
页数:7
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