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用超高效液相色谱-串联质谱法测定水体中32种药物
引用本文:赵健,许秀琴,吕燕,吴银良,杨挺.用超高效液相色谱-串联质谱法测定水体中32种药物[J].江西农业学报,2014(7):104-107.
作者姓名:赵健  许秀琴  吕燕  吴银良  杨挺
作者单位:浙江省宁波市农业科学研究院,浙江宁波315101
基金项目:浙江省宁波市农业科研攻关项目(2011C10005).
摘    要:建立了采用超高效液相色谱-串联质谱法同时测定水中32种药物的方法,即:水样经稀硫酸酸化至pH 2.0,上样体积为500 mL,经HLB固相萃取小柱富集净化,超高效液相色谱-串联质谱仪测定,ESI正负离子同时扫描,以多反应监测(MRM)方式采集数据,外标法定量。各药物的平均加标回收率为61.4%~116.0%,RSD为0.7%~17.3%,检出限为0.4~2.9 ng/L。

关 键 词:超高效液相色谱-串联质谱  药物  水体  检测

Simultaneous Determination of 32 Drugs in Water Body by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry
ZHAO Jian,XU Xiu-qin,LV Yan,WU Yin-liang,YANG Ting.Simultaneous Determination of 32 Drugs in Water Body by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry[J].Acta Agriculturae Jiangxi,2014(7):104-107.
Authors:ZHAO Jian  XU Xiu-qin  LV Yan  WU Yin-liang  YANG Ting
Institution:(Ningbo Academy of Agricultural Sciences in Zhejiang Province, Ningbo 315101, China)
Abstract:An ultra-high performance liquid chromatography -electrospray ionization tandem mass spectrometry ( UPLC-ESI-MS/MS) method was developed for the simultaneous determination of 32 drugs in water body .Firstly, the water sample was a-cidized to pH 2.0 by dilute sulphuric acid, and its volume was 500 mL;then the sample was richened and purified through solid -phase extraction with an Oasis HLB column;finally it was detected by using UPLC -ESI-MS/MS method.The ESI-MS/MS de-tection was achieved through the simultaneous scanning of ESI positive and negative ions , multiple reaction monitoring ( MRM) for data collection , and external standard method for quantitative analysis .The average standard -adding recovery of various drugs was 61.4%~116.0%, the RSD varied from 0.7%to 17.3%, and their detection limit was 0.4~2.9 ng/L.
Keywords:Ultra-high performance liquid chromatography -tandem mass spectrometry  Drug  Water body  Determination
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