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采用微波辅助提取和 GC-FPD 分析技术,可直接测定生毛中 40 种有机磷农药。

Simple determination of 40 organophosphate pesticides in raw wool using microwave-assisted extraction and GC-FPD analysis.

机构信息

Farmacognosia y Productos Naturales, Facultad de Química, UdelaR , 11800 Montevideo, Uruguay.

出版信息

J Agric Food Chem. 2011 Jul 27;59(14):7601-8. doi: 10.1021/jf103983m. Epub 2011 Feb 22.

Abstract

A validated analytical method for the multiresidue analysis of 40 organophosphate pesticides (OPs) and conversion products in raw wool has been developed. The method is based on the selective microwave-assisted extraction (MAE) of raw wool with acetonitrile and analysis of extracts by gas chromatography-flame photometric detector. The optimum MAE conditions were 20 min duration at 80 °C with 30 mL of acetonitrile per gram of wool. A validation study was performed according to the European SANCO guidelines 10684/2009. Limits of detection and quantification for all pesticides tested were from 0.01 to 0.2 mg/kg and from 0.2 to 1.0 mg/kg, respectively. The average recoveries of pesticides spiked at different levels were in the range of 70-120% with relative standard deviations of ≤ 20%. The extraction performance was compared to the one obtained with a reference Soxhlet extraction. The method was also applied in the analysis of real wool (after field application) samples.

摘要

已经开发出一种用于分析生羊毛中 40 种有机磷农药(OPs)及其转化产物的多残留分析的验证分析方法。该方法基于用乙腈选择性微波辅助提取(MAE)生羊毛,并通过气相色谱-火焰光度检测器分析提取物。最佳 MAE 条件为 80°C 持续 20 分钟,每克羊毛用 30 毫升乙腈。根据欧洲 SANCO 指南 10684/2009 进行了验证研究。所有测试农药的检测限和定量限分别为 0.01 至 0.2 毫克/千克和 0.2 至 1.0 毫克/千克。在不同水平下添加农药的平均回收率在 70-120%之间,相对标准偏差≤20%。将提取性能与参考索氏提取获得的性能进行了比较。该方法还应用于分析实际羊毛(田间应用后)样品。

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