Improvements in the analytical methodology for the residue determination of the herbicide glyphosate in soils by liquid chromatography coupled to mass spectrometry

被引:67
作者
Botero-Coy, A. M. [1 ]
Ibanez, M. [1 ]
Sancho, J. V. [1 ]
Hernandez, F. [1 ]
机构
[1] Univ Jaume 1, Res Inst Pesticides & Water, Castellon de La Plana 12071, Spain
关键词
Glyphosate; AMPA; Latin-American soils; UHPLC-MS/MS; Clean-up; FMOC derivatization; Matrix effects; QTOF MS; Confirmation; AMINOMETHYLPHOSPHONIC ACID; RAPID-DETERMINATION; PRECOLUMN DERIVATIZATION; MICROBIAL ACTIVITY; SCREENING METHOD; ORGANIC-MATTER; WATER; GLUFOSINATE; AMPA; SAMPLES;
D O I
10.1016/j.chroma.2012.12.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The determination of glyphosate (GLY) in soils is of great interest due to the widespread use of this herbicide and the need of assessing its impact on the soil/water environment. However, its residue determination is very problematic especially in soils with high organic matter content, where strong interferences are normally observed, and because of the particular physico-chemical characteristics of this polar/ionic herbicide. In the present work, we have improved previous LC MS/MS analytical methodology reported for GLY and its main metabolite AMPA in order to be applied to "difficult" soils, like those commonly found in South-America, where this herbicide is extensively used in large areas devoted to soya or maize, among other crops. The method is based on derivatization with FMOC followed by LC MS/MS analysis, using triple quadrupole. After extraction with potassium hydroxide, a combination of extract dilution, adjustment to appropriate pH, and solid phase extraction (SPE) clean-up was applied to minimize the strong interferences observed. Despite the clean-up performed, the use of isotope labelled glyphosate as internal standard (ILIS) was necessary for the correction of matrix effects and to compensate for any error occurring during sample processing. The analytical methodology was satisfactorily validated in four soils from Colombia and Argentina fortified at 0.5 and 5 mg/kg. In contrast to most LC MS/MS methods, where the acquisition of two transitions is recommended, monitoring all available transitions was required for confirmation of positive samples, as some of them were interfered by unknown soil components. This was observed not only for GLY and AMPA but also for the ILLS. Analysis by QTOF MS was useful to confirm the presence of interferent compounds that shared the same nominal mass of analytes as well as some of their main product ions. Therefore, the selection of specific transitions was crucial to avoid interferences. The methodology developed was applied to the analysis of 26 soils from different areas of Colombia and Argentina, and the method robustness was demonstrated by analysis of quality control samples along 4 months. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 141
页数:10
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