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通过分散固相萃取和超高效液相色谱-串联质谱法对烟草和土壤中三种酸性除草剂残留进行分离和定量分析。

Separation and quantitation of three acidic herbicide residues in tobacco and soil by dispersive solid-phase extraction and UPLC-MS/MS.

作者信息

Xiong Wei, Tao Xiaoqiu, Pang Su, Yang Xue, Tang GangLing, Bian Zhaoyang

机构信息

Sichuan Tobacco Quality Supervision and Testing Station, Chengdu, PR China.

Sichuan Tobacco Quality Supervision and Testing Station, Chengdu, PR China

出版信息

J Chromatogr Sci. 2014 Nov-Dec;52(10):1326-31. doi: 10.1093/chromsci/bmt172. Epub 2013 Dec 22.

DOI:10.1093/chromsci/bmt172
PMID:24366907
Abstract

A method for the determination of three acidic herbicides, dicamba, 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) in tobacco and soil has been developed based on the use of liquid-liquid extraction and dispersive solid-phase extraction (dispersive-SPE) followed by UPLC-MS/MS. Two percentage of (v/v) formic acid in acetonitrile as the extraction helped partitioning of analytes into the acetonitrile phase. The extract was then cleaned up by dispersive-SPE using primary secondary amine as selective sorbents. Quantitative analysis was done in the multiple-reaction monitoring mode using stable isotope-labeled internal standards for each compound. A separate internal standard for each analyte is required to minimize sample matrix effects on each analyte, which can lead to poor analyte recoveries and decreases in method accuracy and precision. The total analysis time was <4 min. The linear range of the method was from 1 to 100 ng mL(-1) with a limit of detection of each herbicide varied from 0.012 to 0.126 ng g(-1). The proposed method is faster, more sensitive and selective than the traditional methods and more accurate and robust than the published LC-MS/MS methods.

摘要

基于液液萃取和分散固相萃取(分散固相萃取),随后进行超高效液相色谱-串联质谱(UPLC-MS/MS),开发了一种测定烟草和土壤中三种酸性除草剂麦草畏、2,4-二氯苯氧乙酸(2,4-D)和2,4,5-三氯苯氧乙酸(2,4,5-T)的方法。乙腈中2%(v/v)的甲酸作为萃取剂有助于将分析物分配到乙腈相中。然后使用伯仲胺作为选择性吸附剂,通过分散固相萃取对提取物进行净化。使用每种化合物的稳定同位素标记内标,在多反应监测模式下进行定量分析。每种分析物都需要单独的内标,以尽量减少样品基质对每种分析物的影响,这可能导致分析物回收率低,并降低方法的准确性和精密度。总分析时间<4分钟。该方法的线性范围为1至100 ng mL(-1),每种除草剂的检测限在0.012至0.126 ng g(-1)之间变化。所提出的方法比传统方法更快、更灵敏、更具选择性,并且比已发表的LC-MS/MS方法更准确、更稳健。

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