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首页> 外文期刊>Food Control >Determination of avermectin and milbemycin residues in bovine muscle by liquid chromatography-tandem mass spectrometry and fluorescence detection using solvent extraction and low temperature cleanup.
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Determination of avermectin and milbemycin residues in bovine muscle by liquid chromatography-tandem mass spectrometry and fluorescence detection using solvent extraction and low temperature cleanup.

机译:液相色谱-串联质谱法和溶剂萃取和低温净化荧光检测法测定牛肌肉中阿维菌素和米尔贝霉素的残留量。

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摘要

A simple and inexpensive sample preparation method based on solvent extraction, followed by low temperature cleanup, was demonstrated to be applicable for the determination of avermectin and milbemycin residues in bovine muscle by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and liquid chromatography with fluorescence (LC-FL) detection. The analytical methodology was validated according to the Commission Decision 2002/657/EC, using LC-MS/MS for confirmatory and LC-FL for quantitative purposes. Mean recovery was between 88.9 and 100.7% in three distinct concentrations. The coefficient of variation for repeatability and within-laboratory reproducibility ranged from 0.78 to 5.1% and from 0.28 to 9.0%, respectively. Method precision led to satisfactory values of decision limits (CC alpha) and detection capabilities (CC beta). The proposed method has been applied in the Brazilian National Residue Control Plan since 2010 for the determination of avermectins and milbemycin residues in bovine muscle samples. A total of 760 samples were analyzed and none of them presented residues at concentrations above the permitted levels established by the more recently applied directives. All rights reserved, Elsevier.
机译:液相色谱-串联质谱法(LC-MS / MS)和液相色谱法证明了一种基于溶剂萃取然后低温净化的简单且廉价的样品制备方法可用于测定牛肌肉中的阿维菌素和米尔倍霉素残留荧光(LC-FL)检测色谱。根据委员会决定2002/657 / EC对分析方法进行了验证,使用LC-MS / MS进行确认,使用LC-FL进行定量。在三个不同的浓度下,平均回收率在88.9至100.7%之间。重复性和实验室内重复性的变异系数分别为0.78至5.1%和0.28至9.0%。方法的精确度带来了令人满意的决策极限(CC alpha)和检测能力(CC beta)值。自2010年以来,该提议的方法已应用于巴西国家残留控制计划中,用于测定牛肌肉样品中的阿维菌素和米尔贝霉素残留。总共对760个样品进行了分析,没有一个样品的残留浓度高于最近采用的指令所确定的允许水平。保留所有权利,Elsevier。

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