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[超高效液相色谱-三重四极杆质谱联用快速同时测定牛奶中53种β-内酰胺类抗生素及其代谢物]

[Rapid simultaneous determination of 53 beta-lactam antibiotics and their metabolites in milk by ultra-performance liquid chromatography coupled with triple quadrupole mass spectrometry].

作者信息

Zhang Xiuyao, Cai Xinxin

出版信息

Se Pu. 2014 Jul;32(7):693-701. doi: 10.3724/sp.j.1123.2014.03019.

DOI:10.3724/sp.j.1123.2014.03019
PMID:25255560
Abstract

A rapid method for the determination of 53 beta-lactams and their metabolites residues in milk was developed by ultra-performance liquid chromatography-triple quadrupole mass spectrometry (UPLC-MS/MS). The method was based on protein precipitation by adding equal quantity of acetonitrile, followed by the ultra filtration of the extracts. The analysis of the residues was achieved on an ACQUITY BEH C18 column with gradient elution using mobile phases of 0.1% formic acid in water and acetonitrile. The analytes were detected by positive electrospray ionization tandem mass spectrometry in the multiple reaction monitoring (MRM) mode, and quantified by matrix-matched internal standard calibration. The cycle time of each analysis was 10 min. Under the optimum operation conditions, excellent linear dynamic range was observed from the quantification limits to 200 microg/kg with the correlation coefficients better than 0.991 1 for all the compounds. The average recoveries for all the beta-lactams and their metabolites ranged from 71% to 121% with the relative standard deviations of 1.7%-19% (n = 6). This method enabled the screening for more than 50 samples per day by one person and also showed good performance for quantitation, and allowed the determination of the beta-lactams and their metabolites residues in milk below the maximum residue levels (MRLs) according to the Bulletin No. 235 (2002) of Ministry of Agriculture, P. R. China and EU Regulation 2377/90/EC (2008 Revised).

摘要

建立了一种超高效液相色谱 - 三重四极杆质谱法(UPLC-MS/MS)快速测定牛奶中53种β-内酰胺类及其代谢物残留量的方法。该方法基于加入等量乙腈进行蛋白质沉淀,随后对提取物进行超滤。在ACQUITY BEH C18柱上,采用0.1%甲酸水溶液和乙腈作为流动相进行梯度洗脱,对残留量进行分析。采用正电喷雾电离串联质谱在多反应监测(MRM)模式下检测分析物,并通过基质匹配内标校准进行定量。每次分析的循环时间为10分钟。在最佳操作条件下,从定量限到200μg/kg观察到了良好的线性动态范围,所有化合物的相关系数均优于0.991 1。所有β-内酰胺类及其代谢物的平均回收率在71%至121%之间,相对标准偏差为1.7% - 19%(n = 6)。该方法单人每天能够筛选50多个样品,并且在定量方面表现良好,能够测定牛奶中低于中国农业部第235号公告(2002年)和欧盟法规2377/90/EC(2008年修订)规定的最大残留限量(MRLs)的β-内酰胺类及其代谢物残留量。

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