García-Repetto R, Giménez M P, Repetto M
Instituto Nacional de Toxicología, Departamento de Sevilla, Spain.
J AOAC Int. 2001 Mar-Apr;84(2):342-9.
An analytical method was developed for precise identification and quantitation of 10 pesticides in human blood. The pesticides studied, which have appeared frequently in actual cases, were endosulfan, lindane, parathion, ethyl-azinphos, diazinon, malathion, alachlor, tetradifon, fenthion and dicofol (o-p' and p-p' isomers). The current method replaces an earlier method which involved liquid-liquid extraction with a mixture of n-hexane-benzene (1 + 1). The extraction is performed by solid-phase extraction, with C18 cartridges and 2 internal standards, perthane and triphenylphosphate. Eluates were analyzed by gas chromatography (GC) with nitrogen-phosphorus and electrochemical detectors. Results were confirmed by GC-mass spectrometry in the electron impact mode. Blood blank samples spiked with 2 standard mixtures and an internal standard were used for quantitation. Mean recoveries ranged from 71.83 to 97.10%. Detection and quantitation limits are reported for each pesticide. Examples are provided to show the application of the present method to actual samples.
开发了一种分析方法,用于精确鉴定和定量人血液中的10种农药。所研究的农药在实际案例中经常出现,包括硫丹、林丹、对硫磷、乙基谷硫磷、二嗪农、马拉硫磷、甲草胺、三氯杀螨砜、倍硫磷和三氯杀螨醇(邻-对'和对-对'异构体)。当前方法取代了早期的方法,早期方法涉及用正己烷-苯(1 + 1)混合物进行液-液萃取。萃取通过固相萃取进行,使用C18柱和2种内标物,即全氯乙烷和磷酸三苯酯。洗脱液通过配备氮磷和电化学检测器的气相色谱(GC)进行分析。结果通过电子轰击模式下的GC-质谱法进行确证。用加有2种标准混合物和1种内标的血液空白样品进行定量。平均回收率在71.83%至97.10%之间。报告了每种农药的检测限和定量限。提供了实例以展示本方法在实际样品中的应用。