首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Multiresidue determination of fluoroquinolones in poultry muscle and kidney according to the regulation 2002/657/EC. A systematic comparison of two different approaches: Liquid chromatography coupled to high-resolution mass spectrometry or tandem mass spectrometry
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Multiresidue determination of fluoroquinolones in poultry muscle and kidney according to the regulation 2002/657/EC. A systematic comparison of two different approaches: Liquid chromatography coupled to high-resolution mass spectrometry or tandem mass spectrometry

机译:根据法规2002/657 / EC对家禽肌肉和肾脏中的氟喹诺酮类化合物进行多残留测定。两种不同方法的系统比较:液相色谱与高分辨率质谱或串联质谱联用

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This work involved the optimization and validation of two methods according to the Commission Decision 2002/657/EC directives for determining fluoroquinolones residues in samples of poultry muscle and kidney: ciprofloxacin, danofloxacin, difloxacin, enrofloxacin, flumequine, marbofloxacin, nalidixic acid, norfloxacin, ofloxacin, oxolinic acid, pipemidic acid and sarafloxacin. The extraction procedure was based on a QuEChERS approach, whose optimization employed a Box-Behnken 3(3) factorial design. A liquid chromatography-tandem mass spectrometry method (LC-MS/MS) was developed for determining the twelve analytes using the multiple reaction monitoring mode (MRM). Accuracy, evaluated by recovery studies, varied from 88.8 to 112.2% for the selected levels with RSD values lower than 12.3%. The second validated method employed high resolution mass spectrometry (HRMS) performed in the single ion monitoring mode (SIM), determining nine among twelve analytes. The validation parameters were evaluated as satisfactory, with recoveries from 82.5 to 114.4% and RSD lower than 8.7%. Decision limits and detection capabilities for both methods were reported. The two methods were statistically compared using the Student's t test, at 95% confidence level, resulting in no significant difference. (C) 2015 Published by Elsevier B.V.
机译:根据委员会决定2002/657 / EC指令,这项工作涉及两种方法的优化和验证,这些方法用于确定家禽肌肉和肾脏样品中的氟喹诺酮类药物残留:环丙沙星,达氟沙星,地氟沙星,恩诺沙星,氟喹喹,马波沙星,萘啶酸,诺氟沙星,氧氟沙星,草酸,哌啶酸和沙拉沙星。提取过程基于QuEChERS方法,其优化采用Box-Behnken 3(3)析因设计。开发了一种液相色谱-串联质谱法(LC-MS / MS),用于使用多反应监测模式(MRM)测定十二种分析物。通过回收率研究评估的准确性,所选水平的RDS值低于12.3%,从88.8%到112.2%。第二种经过验证的方法采用了以单离子监测模式(SIM)执行的高分辨率质谱(HRMS),可确定12种分析物中的9种。验证参数的评估结果令人满意,回收率从82.5%降至114.4%,RSD低于8.7%。报告了两种方法的决策极限和检测能力。使用Student's t检验对这两种方法进行了统计学比较,置信度为95%,无显着差异。 (C)2015由Elsevier B.V.发布

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