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超高效液相色谱质谱法测定水中除草剂的残留量
引用本文:丛梅梅,刘思洁. 超高效液相色谱质谱法测定水中除草剂的残留量[J]. 国外医学:卫生学分册, 2013, 0(2): 129-131,135
作者姓名:丛梅梅  刘思洁
作者单位:吉林省通化市疾病预防控制中心;吉林省疾病预防控制中心
摘    要:目的建立超高效液相色谱串联质谱法同时测定水中多种除草剂残留量的检测方法。方法水样经Oasis HLB柱净化浓缩,用乙睛洗脱,采用1.7μm的C18色谱柱,用乙腈和甲酸(0.1%)水为流动相,进行线性梯度洗脱,并在色谱质谱条件下进行检测。结果该方法检测30种除草剂,加标回收率为76.2%~101.3%%,相对标准偏差(RSD)为3.2%~9.3%之间(n=6),最低检测限(LOQ)在0.1~1.0μg/L间,线性范围在0.0~200μg/L之间。结论该方法操作简便,快速准确,提高了样品检出灵敏度,能同时检测30种除草剂的残留量。

关 键 词:超高效液相色谱串联质谱    除草剂残留

Determination of Residual Content of Herbicides by the Method of Ultra-high Performance Liquid Chromatography-mass Spectrometry
Cong Meimei,Liu Sijie. Determination of Residual Content of Herbicides by the Method of Ultra-high Performance Liquid Chromatography-mass Spectrometry[J]. Foreign Medical Sciences(Section of Hygiene), 2013, 0(2): 129-131,135
Authors:Cong Meimei  Liu Sijie
Abstract:Objectives To establish a method for detecting the residual content of several kinds of herbicides in water using ultra-high performance liquid chromatography-mass spectrometry.Methods Water sample was purified and concentrated by Oasis HLB column and then eluted by acetonitrile.The determination by chromatography-mass spectrometry was performed on 1.7 μm C18 column,using acetonitrile,formic acid(0.1%) and water as mobile phase in linear gradient elution.Results The method can detect 30 kinds of herbicides.The spiked recovery rate varied in the range from 76.2% to 101.3%,with relative standard deviation in the range of 3.2% to 9.3%(n=6).The limit of operation was 0.1~1.0 μg/L with the linear range varying in the range of 0.0 to 200 μg/L.Conclusions The method is sensitive,specific and simple in operation.It can detect the residual content of 30 kinds of herbicides at the same time.
Keywords:herbicide residue  water  UPLC-MS/MS
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