Stajić M, Caplan Y H, Backer R C
J Forensic Sci. 1979 Oct;24(4):732-44.
Liver tends to concentrate drugs in quantities generally higher than those found in blood or other body compartments. This fact as well as the general availability of liver in postmortem cases makes it an important specimen for comprehensive toxicologic investigation. A scheme for the analysis of liver for drugs with tissue hydrolysis, XAD-2 resin extraction, and TLC has been developed and the parameters affecting recovery have been studied. The hydrolysis of liver specimens at various pH conditions resulted in an improved recovery for morphine by using pH 2 (2N hydrochloric acid). Recoveries of barbiturates, codeine, and meperidine were essentially the same at pH 2 and pH 3. A considerable loss (22 to 55%) was observed for four drugs (pentobarbital, morphine, codeine, and meperidine) as a result of drug binding to the tissue pellets during the process of centrifuging the liver homogenates. This method is recommended as a comprehensive screening procedure for drugs in liver tissue. For quantitative purposes, however, it is necessary to determine a correction factor for all the losses occurring at the various steps of the procedure. This procedure compared favorably with other procedures for liver analysis reported in literature.
肝脏往往会浓缩药物,其含量通常高于血液或其他身体腔室中的含量。这一事实以及肝脏在尸检病例中的普遍可得性,使其成为全面毒理学调查的重要标本。已开发出一种通过组织水解、XAD - 2树脂萃取和薄层色谱法分析肝脏中药物的方案,并研究了影响回收率的参数。在不同pH条件下对肝脏标本进行水解,使用pH 2(2N盐酸)时吗啡的回收率有所提高。巴比妥类药物、可待因和哌替啶在pH 2和pH 3时的回收率基本相同。在离心肝脏匀浆的过程中,观察到四种药物(戊巴比妥、吗啡、可待因和哌替啶)由于与组织沉淀结合而有相当大的损失(22%至55%)。该方法被推荐为肝脏组织中药物的综合筛查程序。然而,为了进行定量,有必要确定该程序各个步骤中发生的所有损失的校正因子。该程序与文献中报道的其他肝脏分析程序相比具有优势。