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在通过气相色谱-串联质谱法(GC/MS/MS)和气相色谱-电子捕获检测器/氮磷检测器(GC/ECD/NPD)对土壤中多残留农药进行分析时,QuEChERS改进方法对回收率和基质效应的影响

Influence of QuEChERS modifications on recovery and matrix effect during the multi-residue pesticide analysis in soil by GC/MS/MS and GC/ECD/NPD.

作者信息

Łozowicka Bożena, Rutkowska Ewa, Jankowska Magdalena

机构信息

Plant Protection Institute - National Research Institute, Laboratory of Pesticide Residues, Chelmonskiego 22, Postal code: 15-195, Bialystok, Poland.

出版信息

Environ Sci Pollut Res Int. 2017 Mar;24(8):7124-7138. doi: 10.1007/s11356-016-8334-1. Epub 2017 Jan 16.

Abstract

A QuEChERS extraction followed by GC/MS/MS and GC-μECD/NPD for 216 pesticide and metabolites determination in soil simultaneously were developed and compared. Volume of water, volume and polarity of solvent, and cleanup sorbents (C18, GCB, PSA) were optimized. The QuEChERS with and without purification step were applied to estimate effectiveness of the method. The recovery and matrix effect (ME) were critical parameters within each tested procedure. The optimal method without cleanup was validated. Accuracy (expressed as recovery), precision (expressed as RSD), linearity, LOQ, and uncertainty were determined. The recoveries at the three spiking levels using matrix-matched standards ranged between 65 and 116% with RSD ≤17 and 60-112% with RSD ≤18% for MS/MS and μEC/NP, respectively. The LOQ ranged from 0.005-0.01 mg/kg for MS/MS to 0.05 mg/kg for μEC/NP. The ME for most of pesticides resulted in enhancement of the signal and depended on the analyte and detection system: MS/MS showed ME from -25 to 74%, while μEC/NP from -45 to 96%. A principal component analysis was performed to explain the relationships between physicochemical parameters and ME of 216 pesticides. The QuEChERS protocol without the cleanup step is a promising option to make the method less expensive and faster. This methodology was applied in routine analysis of 263 soil samples in which p,p' DDT was the most frequently detected (23.5% of samples) and pendimethalin with the highest concentration (1.63 mg/kg).

摘要

开发并比较了一种采用QuEChERS萃取法,随后结合气相色谱-串联质谱(GC/MS/MS)和气相色谱-微池电子捕获检测器/氮磷检测器(GC-μECD/NPD)同时测定土壤中216种农药及其代谢物的方法。对水的体积、溶剂的体积和极性以及净化吸附剂(C18、GCB、PSA)进行了优化。应用有无净化步骤的QuEChERS方法来评估该方法的有效性。回收率和基质效应(ME)是每个测试程序中的关键参数。对无需净化的最佳方法进行了验证。测定了准确度(以回收率表示)、精密度(以相对标准偏差RSD表示)、线性、定量限(LOQ)和不确定度。使用基质匹配标准品在三个加标水平下的回收率,对于MS/MS分别为65%至116%,RSD≤17%;对于μEC/NP分别为60%至112%,RSD≤18%。定量限范围从MS/MS的0.005 - 0.01 mg/kg到μEC/NP的0.05 mg/kg。大多数农药的基质效应导致信号增强,并且取决于分析物和检测系统:MS/MS的基质效应为-25%至74%,而μEC/NP的基质效应为-45%至96%。进行了主成分分析以解释216种农药的物理化学参数与基质效应之间的关系。无需净化步骤的QuEChERS方案是使该方法成本更低且速度更快的一个有前景的选择。该方法应用于263个土壤样品的常规分析,其中p,p'滴滴涕是最常检测到的(占样品的23.5%),二甲戊灵的浓度最高(1.63 mg/kg)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea9/5383684/5f9cfc6517ba/11356_2016_8334_Fig1_HTML.jpg

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