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Separation and Quantitation of Three Acidic Herbicide Residues in Tobacco and Soil by Dispersive Solid-Phase Extraction and UPLC–MS/MS
Author(s) -
Wei Xiong,
Xiaoqiu Tao,
Su Pang,
Xue Yang,
Gangling Tang,
Zhaoyang Bian
Publication year - 2013
Publication title -
journal of chromatographic science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.362
H-Index - 56
eISSN - 1945-239X
pISSN - 0021-9665
DOI - 10.1093/chromsci/bmt172
Subject(s) - chemistry , chromatography , solid phase extraction , analyte , extraction (chemistry) , formic acid , detection limit , acetonitrile , sample preparation , matrix (chemical analysis) , high performance liquid chromatography , dicamba , amine gas treating , organic chemistry , weed control , agronomy , biology
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.

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