H'/> Simultaneous determination of 16 macrolide antibiotics and 4 metabolites in milk by using Quick, Easy, Cheap, Effective, Rugged, and Safe extraction (QuEChERS) and high performance liquid chromatography tandem mass spectrometry
首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of 16 macrolide antibiotics and 4 metabolites in milk by using Quick, Easy, Cheap, Effective, Rugged, and Safe extraction (QuEChERS) and high performance liquid chromatography tandem mass spectrometry
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Simultaneous determination of 16 macrolide antibiotics and 4 metabolites in milk by using Quick, Easy, Cheap, Effective, Rugged, and Safe extraction (QuEChERS) and high performance liquid chromatography tandem mass spectrometry

机译:通过使用快速,容易,便宜,有效,粗糙,安全提取(Quechers)和高效液相色谱串联质谱法同时测定牛奶中16种大氯化物抗生素和4代谢物的测定

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Highlights ? HPLC- ESI–MS/MS for determination of macrolide antibiotics and their metabolites. ? Multiresidue analysis method to monitor 21 macrolides and their metabolites simultaneous in food. ? The modified QuEChERS extraction method with a cost-effective, time-efficient and easy-to-use clean-up step. Abstract A novel analytical method was developed and validated for simultaneous analysis of 16 macrolide antibiotics and 4 metabolites in milk. A modified quick, easy, cheap, effective, rugged, and safe extraction method (QuEChERS) optimized by response surface methodology (RSM) was used for sample preparation. All the drugs were subsequently separated and detected by high performance liquid chromatography tandem mass spectrometry (HPLC–MS/MS), using roxithromycin as internal standards for maximum accuracy and precision. The method was validated following the guidelines specified in Commission Decision 2002/657/EC. The recoveries of all the analytes were in the range of 62.27%-115.28%. Most macrolide antibiotics and metabolites could be detected in the concentration of 1–100ng/mL with good correlation coefficient (r 2 0.998). The LODs and LOQs of all analytes were in the range of 0.30-0.85μg/kg and 1.1-4.0μg/kg, respectively. The intra-day and inter-day precision were lower than 10% and 15%, respectively. The developed method has been successfully applied to screen these compounds in different milk products. ]]>
机译:<![cdata [ 突出显示 HPLC-esi-MS / MS,用于测定大环内酯抗生素及其代谢物。 监测21大啰啉和代谢物的多迹分析方法同时在食物中。 修改的Quechers提取方法,具有成本效益,时间效率且易于使用的清理步骤。 Abstract 开发了一种新的分析方法,并验证了16种大啰啉抗生素和4个代谢物在牛奶中的同时分析。通过响应表面方法(RSM)优化的改进的快速,简单,便宜,有效,粗糙,安全的提取方法(Quechers)用于样品制备。随后通过高效液相色谱串联质谱(HPLC-MS / MS)分离并检测所有药物,使用罗西霉素作为内部标准,以获得最大精度和精度。根据委员会决定2002/657 / EC指定的指导方针验证了该方法。所有分析物的回收率在62.27%-115.28%的范围内。大多数大环族抗生素和代谢物可以在浓度为1-100 ng / ml,具有良好的相关系数( r 2> 2 0.998)。所有分析物的LOD和LOQ分别为0.30-0.85 μg/ kg和1.1-4.0 μg/ kg。日期内和日间精度分别低于10%和15%。已成功应用于筛选这些化合物在不同的乳制品中。 ]]>

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