食品安全导刊2024,Issue(31) :97-99.

超高效液相色谱-质谱联用法测定猪肉中4种喹诺酮类药物残留

Determination of Four Quinolone Residues in Pork by Ultra-High Performance Liquid Chromatography-Mass Spectrometry

陈美娜
食品安全导刊2024,Issue(31) :97-99.

超高效液相色谱-质谱联用法测定猪肉中4种喹诺酮类药物残留

Determination of Four Quinolone Residues in Pork by Ultra-High Performance Liquid Chromatography-Mass Spectrometry

陈美娜1
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作者信息

  • 1. 深圳市计量质量检测研究院,广东 深圳 518000
  • 折叠

摘要

建立超高效液相色谱-质谱联用法测定猪肉中恩诺沙星、环丙沙星、氧氟沙星、沙拉沙星 4 种喹诺酮类药物残留的分析方法.试样经EDTA-Mcllvaine缓冲溶液提取,用HLB固相萃取柱净化,氮吹浓缩后用 1 mL甲酸水溶液(0.1%)复溶,上机测定.结果表明,4 种喹诺酮类药物残留组分在2.5~100.0 μg·L-1 线性关系良好,方法检出限为 1.0~2.5 μg·kg-1,定量限为 3.0~8.0 μg·kg-1,加标回收率在 90.0%~109.2%,相对标准偏差(Relative Standard Deviation,RSD)为 1.01%~5.74%,适用于猪肉中4 种喹诺酮类药物残留的检测.

Abstract

Establish an analytical method for the determination of residues of four quinolone drugs,including enrofloxacin,ciprofloxacin,ofloxacin,and sarafloxacin,in pork using ultra-high performance liquid chromatography-mass spectrometry.The sample was extracted with EDTA Mcllvaine buffer solution,purified with HLB solid-phase extraction column,concentrated with nitrogen blowing,and then dissolved in 1 mL formic acid aqueous solution(0.1%)for measurement on the machine.The results showed that there was a good linear relationship between the residual components of the four quinolone drugs in the range of 2.5~100.0 μg·L-1.The detection limit of the method was 1.0~2.5 μg·kg-1,and the quantification limit was 3.0~8.0 μg·kg-1.The recovery rate was in the range of 90.0%~109.2%,and the relative standard deviation(RSD)was 1.01%~5.74%.It is suitable for the detection of four quinolone drug residues in pork.

关键词

超高效液相色谱-质谱联用法/猪肉/喹诺酮

Key words

ultra high performance liquid chromatography-mass spectrometry/pork/quinolone

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出版年

2024
食品安全导刊
商业科技质量中心 北京肉类食品协会

食品安全导刊

影响因子:0.065
ISSN:1674-0270
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