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Simple and Fast Extraction-Coupled UPLC-MS/MS Method for the Determination of Mequindox and Its Major Metabolites in Food Animal Tissues

机译:简单快速的萃取-耦合UPLC-MS / MS法测定食用动物组织中甲喹诺酮及其主要代谢物

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摘要

This research described a sensitive and rapid UPLC-MS/MS method for the determination of mequindox and its six major metabolites in chicken muscle, chicken liver, swine muscle, and swine liver. Among the metabolites, carbonyl reduction-1,4-bisdesoxy-mequindox is novel. Target analytes could be extracted by ethyl acetate without any acidolysis or enzymolysis steps. After purification by a Bond Elut C,8 cartridge, analysis was carried out by UPLC-MS/MS using positive ion multiple reaction monitoring (MRM) mode. Validation was performed in spiked samples, and mean recoveries ranged from 64.3 to 114.4%, with intraday and interday variations of less than 14.7 and 19.2%, respectively. The limit of detection (LOD) was <1.0 mu g kg(-1), whereas the limit of quantification (LOQ) was <4.0 mu g kg(-1). This procedure will help monitor mequindox residues in animal-derived food, and it will also facilitate further pharmacokinetics of mequindox.
机译:这项研究描述了一种灵敏,快速的UPLC-MS / MS方法,用于测定鸡肌肉,鸡肝,猪肌肉和猪肝中的甲喹酮及其六种主要代谢物。在代谢产物中,羰基还原-1,4-双脱氧-甲基喹喔啉是新颖的。无需任何酸解或酶解步骤,即可用乙酸乙酯萃取目标分析物。通过Bond Elut C,8柱纯化后,使用阳离子多反应监测(MRM)模式通过UPLC-MS / MS进行分析。在加标样品中进行验证,平均回收率在64.3%至114.4%之间,日内和日间差异分别小于14.7%和19.2%。检出限(LOD)<1.0μg kg(-1),而定量限(LOQ)<4.0μg kg(-1)。该程序将有助于监测动物源性食品中的甲喹酮残留量,也将促进甲喹酮的进一步药代动力学。

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