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一系列与可待因相关死亡案例中可待因、可待因 -6- 葡萄糖醛酸苷、去甲可待因、吗啡及吗啡葡萄糖醛酸苷的尸检水平和组织分布

Post-mortem levels and tissue distribution of codeine, codeine-6-glucuronide, norcodeine, morphine and morphine glucuronides in a series of codeine-related deaths.

作者信息

Frost Joachim, Løkken Trine Nordgård, Helland Arne, Nordrum Ivar Skjåk, Slørdal Lars

机构信息

Department of Laboratory Medicine, Children's and Womens's Health, Norwegian University of Science and Technology (NTNU), Trondheim, Norway; Department of Clinical Pharmacology, St. Olav University Hospital, Trondheim, Norway.

Department of Laboratory Medicine, Children's and Womens's Health, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.

出版信息

Forensic Sci Int. 2016 May;262:128-37. doi: 10.1016/j.forsciint.2016.02.051. Epub 2016 Mar 4.

Abstract

This article presents levels and tissue distribution of codeine, codeine-6-glucuronide (C6G), norcodeine, morphine and the morphine metabolites morphine-3-glucuronide (M3G) and morphine-6-glucuronide (M6G) in post-mortem blood (peripheral and heart blood), vitreous fluid, muscle, fat and brain tissue in a series of 23 codeine-related fatalities. CYP2D6 genotype is also determined and taken into account. Quantification of codeine, C6G, norcodeine, morphine, M3G and M6G was performed with a validated solid phase extraction LC-MS method. The series comprise 19 deaths (83%) attributed to mixed drug intoxication, 4 deaths (17%) attributed to other causes of death, and no cases of unambiguous monointoxication with codeine. The typical peripheral blood concentration pattern in individual cases was C6G≫codeine≫norcodeine>morphine, and M3G>M6G>morphine. In matrices other than blood, the concentration pattern was similar, although in a less systematic fashion. Measured concentrations were generally lower in matrices other than blood, especially in brain and fat, and in particular for the glucuronides (C6G, M3G and M6G) and, to some extent, morphine. In brain tissue, the presumed active moieties morphine and M6G were both below the LLOQ (0.0080mg/L and 0.058mg/L, respectively) in a majority of cases. In general, there was a large variability in both measured concentrations and calculated blood/tissue concentration ratios. There was also a large variability in calculated ratios of morphine to codeine, C6G to codeine and norcodeine to codeine in all matrices, and CYP2D6 genotype was not a reliable predictor of these ratios. The different blood/tissue concentration ratios showed no systematic relationship with the post-mortem interval. No coherent degradation or formation patterns for codeine, morphine, M3G and M6G were observed upon reanalysis in peripheral blood after storage.

摘要

本文呈现了23例与可待因相关的死亡案例中,死后血液(外周血和心脏血)、玻璃体液、肌肉、脂肪和脑组织中可待因、可待因-6-葡萄糖醛酸苷(C6G)、去甲可待因、吗啡以及吗啡代谢物吗啡-3-葡萄糖醛酸苷(M3G)和吗啡-6-葡萄糖醛酸苷(M6G)的含量水平及组织分布情况。同时还测定并考虑了CYP2D6基因型。采用经过验证的固相萃取液相色谱-质谱法对可待因、C6G、去甲可待因、吗啡、M3G和M6G进行定量分析。该系列案例包括19例(83%)因混合药物中毒导致的死亡,4例(17%)因其他死因导致的死亡,且无明确的可待因单一中毒案例。个体案例中外周血的典型浓度模式为C6G≫可待因≫去甲可待因>吗啡,且M3G>M6G>吗啡。在血液以外的基质中,浓度模式相似,不过不太有规律。除血液外,其他基质中的测量浓度通常较低,尤其是在脑和脂肪中,特别是对于葡萄糖醛酸苷(C6G、M3G和M6G)以及在一定程度上的吗啡。在大多数案例中,脑组织中推测的活性成分吗啡和M6G均低于定量下限(分别为0.0080mg/L和0.058mg/L)。总体而言,测量浓度和计算得到的血/组织浓度比均存在很大差异。在所有基质中,吗啡与可待因、C6G与可待因以及去甲可待因与可待因的计算比值也存在很大差异,且CYP2D6基因型并非这些比值的可靠预测指标。不同的血/组织浓度比与死后间隔时间没有系统的关联。储存后对外周血进行重新分析时,未观察到可待因、吗啡、M3G和M6G一致的降解或生成模式。

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