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首页> 外文期刊>European Journal of Chemistry >A quick method for surveillance of 59 pesticide residues in fruits and vegetables using rapid three-dimensional gas chromatography (GC/MSD/u-ECD/FPD) and LC/MS-MS
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A quick method for surveillance of 59 pesticide residues in fruits and vegetables using rapid three-dimensional gas chromatography (GC/MSD/u-ECD/FPD) and LC/MS-MS

机译:快速三维气相色谱(GC / MSD / u-ECD / FPD)和LC / MS-MS快速监测水果和蔬菜中59种农药残留的方法

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摘要

This article describes a simple, quick and inexpensive method for determination of pesticides in fruits and vegetables. The method, known as the quick, easy, cheap, effective, rugged and safe (QuEChERS) method for pesticide residues, involves the extraction and simultaneous liquid-liquid partitioning formed by adding anhydrous magnesium sulfate (MgSCU) plus sodium acetate (NaAc) followed by a simple cleanup step known as dispersive solid-phase extraction (dSPE). The extracts were analyzed by three-dimensional gas chromatography GC/MSD/u-ECD/FPD in trace ion mode and liquid chromatography/tandem mass spectrometry (LC/MS-MS). Method sensitivity, linearity, repeatability and reproducibility, accuracy, matrix effects, and overall uncertainties have been studied for method validation according to the international norm ISO/IEC: 17025:2005 for both techniques. Identification, quantification and reporting with Total and Extracted ion chromatograms, uECD and DFPD were facilitated to a great extent by Deconvolution Reporting Software (DRS) for GC and Mass hunter software for LC. For all compounds LODs were 0.001 to 0.01 mg/kg and LOQs were 0.005 to 0.020 mg/kg. Correlation coefficients of the calibration curves were >0.991. To validate the effects of matrices, repeatability, reproducibility, recovery and overall uncertainty were calculated for twenty-four matrices at 0.020, 0.050 and 0.500 mg/kg. Recovery ranged between 75-107 % with RSD <17 % for repeatability and intermediate precision and UM of ± 13-22 %.
机译:本文介绍了一种简单,快速且廉价的测定水果和蔬菜中农药的方法。该方法被称为农药残留的快速,简便,廉价,有效,坚固而安全的方法(QuEChERS),涉及萃取和同时液-液分配,方法是先加入无水硫酸镁(MgSCU)再加乙酸钠(NaAc)。通过称为分散固相萃取(dSPE)的简单净化步骤。通过三维气相色谱GC / MSD / u-ECD / FPD以痕量离子模式和液相色谱/串联质谱(LC / MS-MS)分析提取物。根据国际规范ISO / IEC:17025:2005,已针对这两种技术研究了方法的灵敏度,线性,重复性和重现性,准确性,基质效应和总体不确定性,以进行方法验证。用于GC的解卷积报告软件(DRS)和用于LC的Mass hunter软件在很大程度上促进了总离子色谱图和提取离子色谱图,uECD和DFPD的鉴定,定量和报告。对于所有化合物,LOD为0.001至0.01 mg / kg,LOQ为0.005至0.020 mg / kg。校正曲线的相关系数> 0.991。为了验证基质的效果,计算了二十四种基质在0.020、0.050和0.500 mg / kg的重复性,重现性,回收率和总体不确定度。重复性和中等精度的回收率介于75-107%之间,RSD <17%,UM为±13-22%。

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