首页 | 本学科首页   官方微博 | 高级检索  
     检索      

超高效液相色谱-串联质联用法筛查猪肉中66种药物残留
引用本文:吴宁鹏.超高效液相色谱-串联质联用法筛查猪肉中66种药物残留[J].中国兽药杂志,2014,48(6):40-51.
作者姓名:吴宁鹏
作者单位:河南省兽药监察所
基金项目:河南省重点科技攻关计划项目(132102110078)
摘    要:建立了猪肉中磺胺类、氟喹诺酮类、四环素类、大环内酯类、林可胺类、硝基咪唑类、氯霉素类、解热镇痛类、抗病毒类、镇定剂类和头孢类等11类66种药物液相色谱-串联质谱(UPLC—MS/MS)检测方法。样品经乙腈-甲醇(V/V,95:5)和乙腈-水(V/V,15:2)溶液分别提取后,Agela Cleanert@PEP-2固相萃取柱净化后采用UPLC—MS/MS测定,外标法定量。结果表明,猪肉中66药物检测限为O.2~5μg/kg,定量限为0.5-20μg/kg。在2~100μg/kg添加浓度范围内药物回收率在35%~140%之间,批内相对标准偏差均小于20%。本方法可实现对多种兽药的同时检测,为动物源性食品中药物残留监控提供快速、灵敏的分析手段,具有很重要的现实意义。

关 键 词:猪肉  残留  测定  超高效液相色谱-串联质谱
收稿时间:2014/5/13 0:00:00
修稿时间:2014/5/28 0:00:00

Simultaneous Determination of 66 Kindsof Veterinary Drugs in Porcine Muscle Using Ultra Performance Liquid Chromatography coupled with tandem Mass Spectrometry Simultaneous Determination of 66 Kindsof Veterinary Drugs in Porcine Muscle Using Ultra Performance Liquid Chromatography coupled with tandem Mass Spectrometry
BAN Fu-guo,HU Xing-juan,WU Ning-peng,PENG Li,MENG Lei,ZHOU Hong-xia,MAO Jian-hui.Simultaneous Determination of 66 Kindsof Veterinary Drugs in Porcine Muscle Using Ultra Performance Liquid Chromatography coupled with tandem Mass Spectrometry Simultaneous Determination of 66 Kindsof Veterinary Drugs in Porcine Muscle Using Ultra Performance Liquid Chromatography coupled with tandem Mass Spectrometry[J].Chinese Journal of Veterinary Drug,2014,48(6):40-51.
Authors:BAN Fu-guo  HU Xing-juan  WU Ning-peng  PENG Li  MENG Lei  ZHOU Hong-xia  MAO Jian-hui
Institution:1.Henan Institute of Veterinary Drug Control, Zhengzhou 450008, China ; 2. Zhengzhou University, Zhengzhou 450008, China ; 3.Branch of Xuchang, Center for Animal Products Quality and Safety Monitoring and Testing, Henan, Xuchang 461000, China)
Abstract:A method based on ultra performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) was developed for simultaneous determination of 66 kinds veterinary drugs of sulfonamides, fluoroquinolones, tetracyclines, macrolides, lincosamides, nitroimidazoles, chloramphenicols, antipyretic analgesics, antiviral agents, tranquilizers, cephalosporin etc. from 11 classes in porcine muscle. The analyte was extracted with acetonitrile-methanol (V/V,95 : 5) and acetonitrile-water( V/V, 15 : 2),and was cleaned up by the Agela Cleanert~ PEP-2cartridge. Quantification of the analyte was achieved by UPLC-MS/MS with multiple reaction monitoring (MRM) using external standard method. The results indicated that the detection limits and quantification limits of the method were 0.2 - 5 μg/kg and 0.5- 20 μg/kg. The average recoveries of the drugs ranged from 35% to 140% at spiked levels of 2- 100 μg/kg with RSD less than 20%. The method can achieve the simultaneous analysis of different compound groups, and wasreliable and sensitive for monitoring drug residues in animal derived food, which has a very important practical significance.
Keywords:porcine muscle  residues  simultaneous determination  UPLC-MS/MS
本文献已被 维普 等数据库收录!
点击此处可从《中国兽药杂志》浏览原始摘要信息
点击此处可从《中国兽药杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号