CICS - Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Avenida Infante D. Henrique, 6201-001 Covilhã, Portugal.
Rapid Commun Mass Spectrom. 2010 Nov 15;24(21):3187-94. doi: 10.1002/rcm.4765.
A simple, rapid and sensitive method is described for the determination of omethoate, dimethoate, diazinon, chlorpyrifos, parathion-ethyl, chlorfenvinphos, quinalphos and azinphos-ethyl in postmortem whole blood samples. The analytes and internal standard (ethion) were isolated from the matrix by solid-phase extraction, and were analysed by gas chromatography/mass spectrometry in the selected ion monitoring mode. The method has shown to be selective after analysis of postmortem samples of 40 different origins. Calibration curves were established between 0.05 (0.1 for omethoate) and 25 µg/mL, and the values obtained for intra- and interday precision and accuracy were within the criteria usually accepted for bioanalytical method validation. Lower limits of quantitation were 50 ng/mL for all compounds, except for omethoate (100 ng/mL); the limits of identification of the method were 25 ng/mL for all analytes, except for omethoate, for which 50 ng/mL was obtained. Absolute recovery was determined at three concentration levels, and ranged from 31 to 108%. The proposed method is simple and fast, and can be routinely applied in the determination of these compounds in postmortem whole blood samples within the scope of forensic toxicology. In addition, mass spectrometry has demonstrated to be a powerful and indispensable tool for the unequivocal identification of the analytes, since the acceptance criteria were accomplished even at very low levels, thus allowing obtaining forensically valid and sound results.
本文描述了一种简单、快速和灵敏的方法,用于测定死后全血样本中的氧乐果、乐果、二嗪农、毒死蜱、对硫磷-乙基、氯蜱硫磷、喹硫磷和硫线磷。通过固相萃取从基质中分离分析物和内标(乙硫磷),并通过气相色谱/质谱在选择离子监测模式下进行分析。该方法在分析 40 种不同来源的死后样本后表现出选择性。在 0.05(氧乐果为 0.1)和 25µg/mL 之间建立了校准曲线,日内和日间精密度和准确度的测定值均在生物分析方法验证通常接受的标准范围内。除氧乐果(100ng/mL)外,所有化合物的定量下限均为 50ng/mL;除氧乐果外,所有分析物的鉴定下限均为 25ng/mL,氧乐果的鉴定下限为 50ng/mL。在三个浓度水平测定绝对回收率,范围为 31%至 108%。该方法简单快速,可常规应用于法医毒理学中死后全血样本中这些化合物的测定。此外,质谱对于分析物的明确识别是一种强大且不可或缺的工具,因为即使在非常低的水平下也能达到验收标准,从而可以获得有法律效力和可靠的结果。