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高效液相色谱-串联质谱法分析蔬菜中残留的麦草畏
引用本文:马有宁,陈铭学,曹赵云,牟仁祥,朱国念.高效液相色谱-串联质谱法分析蔬菜中残留的麦草畏[J].农药学学报,2012,14(3):349-352.
作者姓名:马有宁  陈铭学  曹赵云  牟仁祥  朱国念
作者单位:1.浙江大学 农药与环境毒理研究所, 杭州 310029
基金项目:中央级公益性科研院所基本科研业务费专项资金(2009RG006-1).
摘    要:采用高效液相色谱-串联质谱仪(HPLC-MS/MS)建立了蔬菜中麦草畏的残留分析方法,其中蔬菜基质包括白菜、黄瓜、番茄、豇豆、萝卜、芹菜和葱。样品经 V (乙腈) : V (甲酸) : V (水)=49.5 :0.2 :0.3的混合溶剂提取,并用氯化钠盐析,旋转蒸发浓缩后直接用HPLC-MS/MS测定。采用C18色谱柱,以5 mmol/L的甲酸铵-甲醇为流动相,梯度法洗脱,以电喷雾负离子化模式在多反应监测模式下测定。结果表明,麦草畏在0.005~0.5 mg/L范围内线性关系良好,相关系数( r )为0.999 7。对空白蔬菜样品进行的3个水平(0.01、0.05、0.1mg/kg)的添加回收实验结果表明,麦草畏的平均回收率和相对标准偏差( RSD )分别为80%~120%和0.58%~18.23%,方法检出限为2.0 μg/kg。该方法快速、灵敏,适用于蔬菜中麦草畏的残留分析。

关 键 词:高效液相色谱-串联质谱    麦草畏    蔬菜    残留
收稿时间:2/6/2012 12:00:00 AM
修稿时间:2012/3/12 0:00:00

Determination of dicamba residue in vegetables using high performance liquid chromatography-tandem mass spectrometry
MA Youning,CHEN Mingxue,CAO Zhaoyun,MOU Renxiang and ZHU Guonian.Determination of dicamba residue in vegetables using high performance liquid chromatography-tandem mass spectrometry[J].Chinese Journal of Pesticide Science,2012,14(3):349-352.
Authors:MA Youning  CHEN Mingxue  CAO Zhaoyun  MOU Renxiang and ZHU Guonian
Institution:1.Institute of Pesticide and Environmental Toxicology, Zhejiang University, Hangzhou 310029, China2.Rice Product Quality Inspection and Supervision Center, Ministry of Agriculture, China National Rice Research Institute, Hangzhou 310006, China
Abstract:An analytical method using high performance liquid chromatography tandem mass spectrometry(HPLC-MS/MS) was developed for analysis of dicamba residue in Chinese cabbage,cucumber,tomato,cowpea,white radish,celery and shallot.The sample was extracted with V(acetonitrile) ∶V(formic acid)∶V(water)=49.5∶0.2∶0.3 and salted-out by sodium chloride.After that,the sample was concentrated by rotary evaporator.Seperation was performed on a C18 column with gradient elution by mobile phase of methanol and 5 mmol/L ammonium formate,and finally detected with negative-ion electrospray ionization-mass spectrometry(ESI-MS) under multiple reaction monitoring(MRM) mode.The results showed that the linearity of method for dicamba was in the concentration range of 0.005 to 0.5 mg/L with the correlation coefficients of 0.999 7.The mean spiked recoveries of dicamba at 3 spiked levels(0.01,0.05,0.1 mg/kg) ranged from 80% to 120% with relative standard deviations(RSD,n=3) of 0.58%-18%.The limit of detection was 2.0 μg/kg for dicamba.The method is rapid,sensitive and suitable for determination of dicamba in vegetables.
Keywords:high performance liquid chromatography-tandem mass spectrometry  dicamba  vegetables  residue
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