| 注册
首页|期刊导航|中国药房|UPLC-MS法检测动物类药材中氯霉素类药物残留

UPLC-MS法检测动物类药材中氯霉素类药物残留

张治军 周文杰 李志芸

中国药房2017,Vol.28Issue(30):4271-4274,4.
中国药房2017,Vol.28Issue(30):4271-4274,4.DOI:10.6039/j.issn.1001-0408.2017.30.25

UPLC-MS法检测动物类药材中氯霉素类药物残留

Determination of Chloramphenicol Residue in Animal Medicinal Herbs by UPLC-MS

张治军 1周文杰 1李志芸2

作者信息

  • 1. 广西壮族自治区桂林食品药品检验所,广西桂林541001
  • 2. 桂林医学院药学院,广西桂林541004
  • 折叠

摘要

Abstract

OBJECTIVE:To establish the method for determination of chloramphenicol residue in animal medicinal herbs.METHODS:UPLC-MS method was adopted.The determination was performed on SB-C18 column with mobile phase consisted of acetonitrile-water (gradient elution) at the flow rate of 0.2 mL/min.The column temperature was 35 ℃,and sample size was 20 μL.The ion source was a jet stream ion focusing electrospray ion source.The temperature and flow of drying gas were 350 ℃ and 5 L/ min,and those of sheath gas were 250 ℃,11 L/min,and capillary voltage was 3 500 V.Negative ion scanning mode was conducted with multiple reaction monitoring (MRM) mode.RESULTS:The linear ranges of thiamphenicol,florfenicol and chloramphenicol were 0.5-15 ng/mL(r were 0.999 8,0.999 9,0.998 9,respectively).The limits of quantitation were 0.03,0.03,0.15 μg/kg,and the limits of detection were 0.01,0.01,0.05 μg/kg.RSDs of precision,stability and reproducibility tests were all lower than 3.0%.The recoveries were 84.00%-112.80% (RSD=10.15%,n=9),88.24%-109.80% (RSD=7.11%,n=9),88.24%-99.02% (RSD=3.91%,n=9). CONCLUSIONS:The method is simple,precise,stable and reproducible,and can be used for determination of chloramphenicol in animal medicinal herbs.

关键词

动物类药材/氯霉素类药物残留/超高效液相色谱-质谱法

Key words

Animal medicinal herbs/Chloramphenicol residue/UPLC-MS

分类

医药卫生

引用本文复制引用

张治军,周文杰,李志芸..UPLC-MS法检测动物类药材中氯霉素类药物残留[J].中国药房,2017,28(30):4271-4274,4.

基金项目

广西壮族自治区食品药品监督管理局科研项目(No.桂食药监科评函[2015]20号) (No.桂食药监科评函[2015]20号)

中国药房

OA北大核心CSTPCD

1001-0408

访问量0
|
下载量0
段落导航相关论文