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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Evaluation of two sample treatment methodologies for large-scale pesticide residue analysis in olive oil by fast liquid chromatography-electrospray mass spectrometry
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Evaluation of two sample treatment methodologies for large-scale pesticide residue analysis in olive oil by fast liquid chromatography-electrospray mass spectrometry

机译:快速液相色谱-电喷雾质谱法评估橄榄油中大量农药残留的两种样品处理方法

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摘要

In this study, a comprehensive evaluation of two simple sample treatment methodologies has been carried out for the development of large-scale multi-residue methods for pesticide testing in olive oil. The proposed methodologies are based on (a) liquid-liquid partitioning with acetonitrile followed by dispersive solid-phase extraction clean-up using graphitized carbon black, primary-secondary amine and C-18 sorbents; (b) liquid partitioning with acetonitrile saturated with petroleum ether followed by matrix solid-phase dispersion (MSPD) using aminopropyl as sorbent material and a Florisil cartridge for final clean-up in the elution step. To evaluate the proposed sample treatment methodologies, 105 representative multi-class pesticides were studied using fast liquid chromatography-electrospray time-of-flight mass spectrometry (LC-TOFMS). For validation purposes, recoveries studies were carried out at 10 and 100 mu g kg(-1) levels, yielding recovery rates in the range 70-130% for 72% of analytes using liquid-liquid procedure and for 57% analytes using MSPD procedure. The LC-MS method provided good linearity, precision and accuracy. The limits of detection obtained were lower than 10 mu g kg(-1) for more than 85% analytes using both sample treatment methodologies. In addition, minor matrix effects (i.e. signal suppression or enhancement <= 20%) were observed in ca. 70% of the studied compounds. Data obtained shows that both sample treatment methodologies proposed can be successfully applied for large-scale pesticide testing in olive oil samples, showing the ability to quickly detect trace amount of over one hundred target species with different physicochemical properties, without requiring expensive instrumentation for sample treatment step and involving relatively low amounts of solvent consumption and waste generation.
机译:在这项研究中,对两种简单的样品处理方法进行了综合评估,以开发用于橄榄油中农药检测的大规模多残留方法。所提出的方法基于(a)用乙腈进行液-液分配,然后使用石墨化的炭黑,伯-仲胺和C-18吸附剂进行分散固相萃取净化; (b)用石油醚饱和的乙腈进行液体分配,然后使用氨基丙基作为吸附剂材料和Florisil柱进行基质固相分散(MSPD),以在洗脱步骤中进行最终净化。为了评估建议的样品处理方法,使用快速液相色谱-电喷雾飞行时间质谱(LC-TOFMS)研究了105种代表性的多类农药。为了验证目的,在10和100μg kg(-1)的水平下进行了回收率研究,使用液-液法对72%的分析物和MSPD法对57%的分析物的回收率在70-130%的范围内。 LC-MS方法具有良好的线性,精度和准确性。使用两种样品处理方法,对于超过85%的分析物,检测限均低于10μg kg(-1)。另外,在大约1200nm处观察到较小的基质效应(即信号抑制或增强<= 20%)。 70%的研究化合物。所获得的数据表明,所提出的两种样品处理方法都可以成功地用于橄榄油样品中的大规模农药检测,显示出能够快速检测痕量的一百多种具有不同理化特性的目标物种的能力,而无需昂贵的仪器进行样品处理步骤,溶剂消耗和废料产生量相对较低。

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