稳定同位素内标-超高压液相色谱-串联质谱法同时测定动物源性食品中8种抗生素残留
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(安徽省疾病预防控制中心,安徽 合肥 230601)

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刘柏林 男 检验师 研究方向为食品安全理化检验E-mail:liubolin087@163.com

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Simultaneous determination of eight antibiotics residues in animal food by ultra pressure liquid chromatography-tandem mass spectrometry with stable isotope-labelled internal standards
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(Anhui Provincial Center for Disease Control and Prevention,Anhui Hefei 230601,China)

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    摘要:

    建立超高压液相色谱-串联质谱法(UPLC-MS/MS)测定动物源性食品中8种抗生素药物残留的方法。方法 待测物经乙酸乙酯提取,采用电喷雾电离,正负离子扫描,多反应监测模式(MRM),基质匹配内标标准曲线法定量。结果 在最佳试验条件下,8种抗生素残留物在0.05~50.0 μg/kg的浓度范围内线性良好,相关系数r2均大于0.995,检出限范围为0.05~0.1 μg/kg,平均回收率为56.8%~108.2%,相对标准偏差(RSD)小于15.4%。结论 本方法的样品前处理过程简单,净化效果好,灵敏度高,有效解决了基质效应问题,适用于大批量食品中抗生素残留的快速定量分析。

    Abstract:

    A method for the determination of eight antibiotic residues in animal food by the ultra pressure liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established.Methods The analytes were extracted by ethyl acetate, and the identification was achieved by electrospray ionization in positive and negative mode (ESI+/ESI-) using multiple reaction monitoring (MRM). The quantifications were performed by the matrix matched internal standards. Results Under the optimum experimental conditions, the calibration curves of the eight analytes showed a good linearity in the concentrations of 0.05-50.0 μg/kg with r2 above 0.995. Recoveries were between 56.8% and 108.2% with RSD less than 15.4%. The limits of detection were 0.05-0.1 μg/kg.Conclusion The method had the advantages of simple pretreatment, high sensitivity, and lower matrix effects, which was suitable for rapid, high-throughput quantitative food analysis.

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刘柏林,谢继安,赵紫微,韦莹,单晓梅.稳定同位素内标-超高压液相色谱-串联质谱法同时测定动物源性食品中8种抗生素残留[J].中国食品卫生杂志,2016,28(4):461-467.

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  • 收稿日期:2015-11-27
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  • 在线发布日期: 2016-08-18
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