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超快速液相色谱-串联质谱联用固相萃取法测定当归中135种农药及其代谢物

[Determination of 135 pesticides and their metabolites in Angelica sinensis by ultra-fast liquid chromatography-tandem mass spectrometry coupled with solid-phase extraction].

作者信息

Liu Jie, Tong Ling, Meng Wenting, Zhao Yunli, Yu Zhiguo

出版信息

Se Pu. 2015 Dec;33(12):1257-68. doi: 10.3724/sp.j.1123.2015.09014.

Abstract

A method using solid-phase extraction (SPE) followed by ultra-fast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) has been established for simultaneously quantitative determination of 135 pesticides and their metabolites (organophosphorus pesticides, pyrethroid pesticides and carbamate pesticides, etc.) in Angelica sinensis. The pesticide residues were extracted from the samples by acetonitrile, cleaned-up with a primary secondary amine (PSA) column and then analyzed using UFLC-MS/MS in multiple reaction monitoring (MRM) mode with positive electrospray ionization. The pesticide residues were quantified by matrix matched standard solution-internal standard method. All of the pesticides had good linear responses with r > 0.99. The average recoveries of the pesticides at the spiked levels of 10, 50, 100 μg/kg ranged from 71.3% - 119.7% with the RSDs of 1.0% - 19.9%, except for clethodim (62.0% - 68.2%). The limits of quantification of the 135 pesticides and their metabolites were 1.0-10.0 μg/kg. The results demonstrated that the method is simple, fast, sensitive and can be used for the analysis of the multiclass of pesticide residues in Angelica sinensis.

摘要

建立了一种采用固相萃取(SPE)结合超快速液相色谱-串联质谱(UFLC-MS/MS)同时定量测定当归中135种农药及其代谢物(有机磷农药、拟除虫菊酯类农药和氨基甲酸酯类农药等)的方法。用乙腈从样品中提取农药残留,通过伯仲胺(PSA)柱净化,然后采用正电喷雾电离的多反应监测(MRM)模式用UFLC-MS/MS进行分析。农药残留采用基质匹配标准溶液-内标法进行定量。所有农药均具有良好的线性响应,r>0.99。除烯禾啶(62.0%-68.2%)外,加标水平为10、50、100μg/kg时农药的平均回收率为71.3%-119.7%,相对标准偏差为1.0%-19.9%。135种农药及其代谢物的定量限为1.0-10.0μg/kg。结果表明,该方法简便、快速、灵敏,可用于当归中多类农药残留的分析。

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