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海洛因过量中毒时吗啡及吗啡葡萄糖醛酸苷的死后分布模式

Postmortem distribution pattern of morphine and morphine glucuronides in heroin overdose.

作者信息

Skopp G, Lutz R, Ganssmann B, Mattern R, Aderjan R

机构信息

Institut für Rechtsmedizin, Ruprecht-Karls-Universität, Heidelberg, Germany.

出版信息

Int J Legal Med. 1996;109(3):118-24. doi: 10.1007/BF01369670.

Abstract

The postmortem distribution of morphine and its metabolites was investigated in four cases of heroin overdose to evaluate some of the factors that influence intravasal blood concentrations. Variables included were the chemical stability of morphine conjugates, hemoconcentration, incomplete distribution of the drug and diffusion processes. Blood samples from different sampling sites including the aorta, the infra- and suprarenal portion of the inferior vena cava, the superior vena cava, the femoral and subclavian veins, and the right and left ventricles were examined for morphine, morphine-3-glucuronide and morphine-6-glucuronide, hematocrit and water content. Drug concentrations were determined by HPLC based on the native fluorescence of the analytes. Morphine glucuronides proved to be stable for a time period of 72 h. The water content ranged from 65 to 83% and hematocrit values from 25 to 75%, and were seen as contributory factors to the dramatic differences observed for drug concentrations from different sampling sites. The differences could neither be attributed to incomplete distribution during life-time nor to a diffusion process following the different distribution volumes of morphine and its conjugates. A definite relationship between the ratio of the molar concentrations of morphine and its glucuronides, as assessed in pharmacokinetical studies after morphine dosing, could not be established. For a better understanding more cases and changes over time and tissue concentrations should be analysed.

摘要

对4例海洛因过量致死病例的尸体进行了吗啡及其代谢产物分布的研究,以评估影响血管内血药浓度的一些因素。所涉及的变量包括吗啡结合物的化学稳定性、血液浓缩、药物分布不完全以及扩散过程。采集了来自不同采样部位的血样,包括主动脉、下腔静脉的肾上腺下和肾上腺上部分、上腔静脉、股静脉和锁骨下静脉以及左右心室,检测其中吗啡、吗啡-3-葡萄糖醛酸苷和吗啡-6-葡萄糖醛酸苷、血细胞比容和含水量。基于分析物的天然荧光,采用高效液相色谱法测定药物浓度。结果表明,吗啡葡萄糖醛酸苷在72小时内保持稳定。含水量在65%至83%之间,血细胞比容值在25%至75%之间,这些被视为导致不同采样部位药物浓度出现显著差异的因素。这些差异既不能归因于生前分布不完全,也不能归因于吗啡及其结合物不同分布容积后的扩散过程。在吗啡给药后的药代动力学研究中,无法确定吗啡及其葡萄糖醛酸苷摩尔浓度比之间的明确关系。为了更好地理解,应分析更多病例以及随时间的变化和组织浓度。

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