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植物油和黄油脂肪中拟除虫菊酯类杀虫剂的快速预浓缩方法及气相色谱-电子捕获检测和气相色谱-质谱联用同时测定法

Rapid preconcentration method for the determination of pyrethroid insecticides in vegetable oils and butter fat and simultaneous determination by gas chromatography-electron capture detection and gas chromatography-mass spectrometry.

作者信息

Ramesh A, Balasubramanian M

机构信息

Department of Pesticide Chemistry, Fredrick Institute of Plant Protection and Toxicology, Chennai, Tamil Nadu, India.

出版信息

Analyst. 1998 Sep;123(9):1799-802. doi: 10.1039/a803097i.

Abstract

A simple and rapid solid-phase extraction (SPE)-GC method for the preconcentration and quantification of pyrethroids at low nanogram levels in oils and high fat content samples is presented. The method was studied using seven highly persistent pyrethroid insecticides, viz., cypermethrin, deltamethrin, fenvalerate, cyfluthrin, allethrin, cyhalothrin and permethrin. Preconcentration was achieved by treating the oil samples with methyltrioctylammonium chloride and subsequent elution of the pyrethroid molecules from a graphitized carbon black SPE cartridge using 5 ml of acetonitrile. Pyrethroid quantification was achieved by GC with electron capture detection. Recoveries of the pyrethroids at fortification levels of 0.05-0.5 ppm were 94-105%. Storage on graphitized carbon black for 30 d lowered the recovery of the pyrethroids by only 3-6%. The method compared well with results obtained by a GC-MS method. The relative standard deviation at a concentration level of 0.05-0.2 microgram ml-1 ranged from 1.31 to 5.16%. The limit of detection achieved was 0.002 microgram ml-1 without any additional clean-up and with little interference from lipids during analysis.

摘要

本文介绍了一种简单快速的固相萃取(SPE)-气相色谱(GC)方法,用于在油类和高脂肪含量样品中对低纳克水平的拟除虫菊酯进行预浓缩和定量分析。该方法使用了七种高持久性拟除虫菊酯杀虫剂,即氯氰菊酯、溴氰菊酯、氰戊菊酯、氟氯氰菊酯、丙烯菊酯、氯氟氰菊酯和氯菊酯。通过用甲基三辛基氯化铵处理油样并随后使用5毫升乙腈从石墨化炭黑SPE柱上洗脱拟除虫菊酯分子来实现预浓缩。通过带有电子捕获检测的气相色谱法实现拟除虫菊酯的定量分析。在0.05 - 0.5 ppm的强化水平下,拟除虫菊酯的回收率为94 - 105%。在石墨化炭黑上储存30天仅使拟除虫菊酯的回收率降低了3 - 6%。该方法与气相色谱 - 质谱法获得的结果相比良好。在0.05 - 0.2微克毫升-1的浓度水平下,相对标准偏差范围为1.31%至5.16%。在无需任何额外净化且分析过程中脂质干扰极小的情况下,实现的检测限为0.002微克毫升-1。

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