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采用 UPLC-MS/MS 法同时测定尿液中新型烟碱类、氨基甲酸酯/硫代氨基甲酸酯类、三唑类、有机磷和拟除虫菊酯类农药及其代谢物的方法优化。

Method optimization for a simultaneous determination of neonicotinoid, carbamate/thiocarbamate, triazole, organophosphate and pyrethroid pesticides and their metabolites in urine using UPLC-MS/MS.

机构信息

Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Barcelona, Catalonia, Spain; Faculty of Chemistry, Universitat de Barcelona (UB), Barcelona, Catalonia, Spain.

Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Barcelona, Catalonia, Spain.

出版信息

J Chromatogr A. 2024 Aug 16;1730:465054. doi: 10.1016/j.chroma.2024.465054. Epub 2024 Jun 19.

Abstract

An accurate and sensitive method for the determination of a total of 23 pesticides and their metabolites in human urine has been optimised. The methodology is based on a previously published method based on solid-phase extraction with methanol and acetone followed by ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) in the selected reaction mode (SRM) with both positive and negative electrospray ionization (ESI+/-). The detection settings of the previous method, which allowed to determine the metabolites from 6 organophosphate and 2 pyrethroid pesticides, were optimised in order to include further pesticide groups, such as 11 neonicotinoids, 3 carbamates/thiocarbamates and 2 triazoles. The 5-windows method enduring 22 min was optimized with acceptable results in relation to accuracy (recoveries >75 %), precision (coefficients of variation <26 %) and linearity (R> 0.9915). The limits of detection ranged between 0.012 ng/mL and 0.058 ng/mL. Samples from the German External Quality Assessment Scheme (G-EQUAS) encompassing 2 pyrethroids, 2 organophosphate and one neonicotinoid (6-chloronicotinic acid, a common metabolite of imidacloprid and acetamiprid) were analysed, and the latter, included in this newest optimization, provided good reference results. The method is optimal as a human biomonitoring tool for health risk assessment in large population surveys.

摘要

已经优化了一种用于准确灵敏地测定人尿中总共 23 种农药及其代谢物的方法。该方法基于先前发表的方法,该方法基于固相萃取,用甲醇和丙酮提取,然后采用超高效液相色谱-串联质谱(UPLC-MS/MS)在正、负离子模式(ESI+/-)下进行选择反应监测(SRM)。先前的方法的检测设置允许测定 6 种有机磷和 2 种拟除虫菊酯农药的代谢物,现在对其进行了优化,以包括其他农药类别,如 11 种新烟碱类、3 种氨基甲酸酯/硫代氨基甲酸酯和 2 种三唑类。持续 22 分钟的 5 窗法经过优化,在准确性(回收率>75%)、精密度(变异系数<26%)和线性(R>0.9915)方面取得了可接受的结果。检测限范围在 0.012 至 0.058ng/mL 之间。分析了来自德国外部质量评估计划(G-EQUAS)的样本,其中包括 2 种拟除虫菊酯、2 种有机磷和 1 种新烟碱类(6-氯烟酸,是吡虫啉和噻虫胺的常见代谢物),此次优化中包括了后者,其提供了良好的参考结果。该方法是一种用于健康风险评估的大型人群调查中的人体生物监测工具,是最佳选择。

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