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分散液液微萃取结合液相色谱-串联质谱法测定土壤中的新一代农药

Dispersive liquid-liquid microextraction for the determination of new generation pesticides in soils by liquid chromatography and tandem mass spectrometry.

作者信息

Pastor-Belda Marta, Garrido Isabel, Campillo Natalia, Viñas Pilar, Hellín Pilar, Flores Pilar, Fenoll José

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, Regional Campus of International Excellence "Campus Mare Nostrum", University of Murcia, E-30100 Murcia, Spain.

Equipo de Calidad Alimentaria, Instituto Murciano de Investigación y Desarrollo Agrario y Alimentario (IMIDA), C/Mayor s/n, La Alberca, 30150 Murcia, Spain.

出版信息

J Chromatogr A. 2015 May 15;1394:1-8. doi: 10.1016/j.chroma.2015.03.032. Epub 2015 Mar 23.

Abstract

A sensitive method for the determination of five new generation pesticides (chlorantraniliprole, spirotetramat, spiromesifen, spirodiclofen and flubendiamide) in soil samples has been developed using liquid chromatography and tandem mass spectrometry (LC-MS(2)) with a triple-quadrupole in the multiple reaction monitoring mode. The target analytes are released from the solid matrix by single-phase extraction in acetonitrile (SLE), this organic phase being used as dispersant solvent in the dispersive liquid-liquid microextraction (DLLME) step. The different parameters affecting the extraction efficiency in DLLME were carefully studied, being 1.5mL of acetonitrile extract (disperser solvent), 125μL carbon tetrachloride (extraction solvent) and 10mL aqueous solution, the selected conditions. The enriched organic phase was evaporated, reconstituted with 50μL acetonitrile and injected into a liquid chromatograph with a mobile phase composed of acetonitrile and 0.1% (v/v) formic acid under gradient elution and a C8 stationary phase. Detection limits in the 0.0015-0.0090ngg(-1) range were obtained. Insecticide concentrations ranging from 0.03 to 197ngg(-1), depending on the compound, were found in the soil samples analysed. The recovery values obtained by SLE-DLLME-LC-ESI-MS(2) for three spiked soils at three concentration levels varied between 87 and 114%, with RSDs of between 5.5 and 14%.

摘要

已开发出一种灵敏的方法,用于测定土壤样品中的五种新一代农药(氯虫苯甲酰胺、螺虫乙酯、螺甲螨酯、乙螨唑和氟苯虫酰胺),该方法采用液相色谱-串联质谱联用仪(LC-MS(2)),配备三重四极杆,采用多反应监测模式。目标分析物通过乙腈中的单相萃取(SLE)从固体基质中释放出来,该有机相在分散液液微萃取(DLLME)步骤中用作分散溶剂。仔细研究了影响DLLME萃取效率的不同参数,选定的条件为1.5mL乙腈萃取液(分散溶剂)、125μL四氯化碳(萃取溶剂)和10mL水溶液。富集后的有机相经蒸发、用50μL乙腈复溶后,注入配备有由乙腈和0.1%(v/v)甲酸组成的流动相、采用梯度洗脱以及C8固定相的液相色谱仪中。获得了0.0015 - 0.0090ngg(-1)范围内的检测限。在所分析的土壤样品中,发现杀虫剂浓度在0.03至197ngg(-1)之间,具体取决于化合物。通过SLE-DLLME-LC-ESI-MS(2)对三种加标土壤在三个浓度水平下获得的回收率值在87%至114%之间,相对标准偏差在5.5%至14%之间。

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