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A simple and rapid assay based on hot water extraction and liquid chromatography-tandem mass spectrometry for monitoring quinolone residues in bovine milk

机译:基于热水萃取和液相色谱-串联质谱的简单,快速检测牛乳中喹诺酮残留的方法

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摘要

A rapid, specific and sensitive procedure for determining residues of eight widespread used quinolone antimicrobials in bovine milk is presented. The method is based on the matrix solid-phase dispersion technique with hot water as extractant followed by LC/MS/MS. The entire sample treatment did not take more than 40 min. Hot water appeared to be an efficient extracting medium, since absolute recoveries of the analytes in milk were 77-90%. The method proved to be robust as matrix effects did not affect significantly the accuracy of the method, as evidenced by analyzing six different batches of milk. Using norfloxacin as surrogate analyte, the accuracy of the method at three different spike levels of the analytes in milk was 93-110% with RSDs not larger than 10%. On the basis of a S/N of 10, estimated LOQs of this method range from 0.3 to 1.5 ng/ml, well below the tolerance levels of quinolones in milk set by the European Union.
机译:提出了一种快速,特异性和灵敏的方法,用于测定牛乳中八种广泛使用的喹诺酮类抗生素的残留量。该方法基于基质固相分散技术,先以热水为萃取剂,再进行LC / MS / MS。整个样品处理时间不超过40分钟。热水似乎是一种有效的提取介质,因为牛奶中分析物的绝对回收率为77-90%。通过分析六批不同的牛奶,证明了该方法的鲁棒性,因为基质效应不会显着影响该方法的准确性。使用诺氟沙星作为替代分析物,在牛奶中分析物的三个不同加标水平下,该方法的准确度为93-110%,RSD不大于10%。以10的信噪比(S / N)为基础,此方法的估计LOQ范围为0.3到1.5 ng / ml,远低于欧盟设定的牛奶中喹诺酮类药物的耐受水平。

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