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液相色谱-串联质谱法测定植物基质中草甘膦、草铵膦及其代谢物残留分析方法的优化与验证

Optimization and Validation of a Residue Analysis Method for Glyphosate, Glufosinate, and Their Metabolites in Plant Matrixes by Liquid Chromatography with Tandem Mass Spectrometry.

作者信息

Oulkar Dasharath P, Hingmire Sandip, Goon Arnab, Jadhav Manjusha, Ugare Bharat, Thekkumpurath Ahammed Shabeer, Banerjee Kaushik

机构信息

Indian Council of Agricultural Research, National Research Centre for Grapes, National Referral Laboratory, PO Manjri Farm, Pune 412 307, India.

出版信息

J AOAC Int. 2017 May 1;100(3):631-639. doi: 10.5740/jaoacint.17-0046. Epub 2017 Mar 23.

DOI:10.5740/jaoacint.17-0046
PMID:28300023
Abstract

A sensitive and accurate LC with tandem MS (MS/MS)-based method was developed and validated for the analysis of the herbicide glyphosate, its metabolite aminomethylphosphonic acid (AMPA), and glufosinate after derivatization with 9-fluorenylmethyl chloroformate (FMOC-Cl) in various plant matrixes. The method also covers direct analysis of the glufosinate metabolites 3-methylphosphinicopropionic acid (3-MPPA) and N-acetyl-glufosinate (NAG). The homogenized samples were extracted with 0.1% formic acid in water-dichloromethane (50 + 50). The aqueous layer was derivatized with FMOC-Cl, cleaned through an HLB SPE cartridge, and determined by LC-MS/MS. The sample size, extraction solvent, sample-to-solvent ratio, derivatization conditions, and cleanup procedure were thoroughly optimized, the LOQs of glyphosate, glufosinate, and AMPA were 0.5 ng/g in grape, corn (leaf and seed), and cotton (leaf, seed, and oil) and 2 ng/g in soybean and tea. The LOQs of NAG and 3-MPPA were 50 ng/g in all the test matrixes, except tea and soybean, for which the LOQ was 100 ng/g. In all cases, average recoveries were >80%. The method successfully performed the estimation of glyphosate in incurred corn and cotton leaf samples collected from supervised field trials.

摘要

开发并验证了一种基于液相色谱-串联质谱(MS/MS)的灵敏且准确的方法,用于分析在各种植物基质中经9-芴甲基氯甲酸酯(FMOC-Cl)衍生化后的除草剂草甘膦、其代谢物氨甲基膦酸(AMPA)和草铵膦。该方法还涵盖了草铵膦代谢物3-甲基膦酰基丙酸(3-MPPA)和N-乙酰基草铵膦(NAG)的直接分析。将匀浆后的样品用0.1%甲酸的水-二氯甲烷(50 + 50)混合溶液萃取。水相用FMOC-Cl进行衍生化,通过HLB固相萃取柱净化,然后用液相色谱-串联质谱测定。对样品量、萃取溶剂、样品与溶剂的比例、衍生化条件和净化程序进行了全面优化,草甘膦、草铵膦和AMPA在葡萄、玉米(叶和种子)以及棉花(叶、种子和油)中的定量限为0.5 ng/g,在大豆和茶叶中的定量限为2 ng/g。NAG和3-MPPA在所有测试基质中的定量限为50 ng/g,但在茶叶和大豆中定量限为100 ng/g。在所有情况下,平均回收率均>80%。该方法成功地对从监督田间试验中采集的玉米和棉花叶片实际样品中的草甘膦进行了测定。

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