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抗精神病药物的时间依赖性死后再分布。

The time-dependant post-mortem redistribution of antipsychotic drugs.

机构信息

Department of Forensic Medicine, Monash University, Southbank 3006, Victoria, Australia.

出版信息

Forensic Sci Int. 2012 Oct 10;222(1-3):223-7. doi: 10.1016/j.forsciint.2012.05.028. Epub 2012 Jun 27.

Abstract

The post mortem redistribution of ten commonly prescribed antipsychotic drugs (APs) was investigated. Femoral blood was collected from 273 cases at admission to mortuary (AD) and at post-mortem (PM). The PM samples were collected at various times up to nine days after admission and the sample pairs analysed using LC-MS/MS. The drugs included in this study were 9OH-risperidone (paliperidone), amisulpride, chlorpromazine, clozapine, haloperidol, olanzapine, promethazine, quetiapine, risperidone, and zuclopenthixol. Haloperidol, quetiapine and risperidone showed minimal changes between AD and PM specimens, whereas the majority of drugs showed significant changes between the sample pairs collected at different time points post mortem (p<0.01) in addition to an average concentration change greater than the uncertainty of measurement of the applied method. Average increases in blood concentrations after admission to the mortuary ranged up to 112% (chlorpromazine and olanzapine) but also decreases up to -43% (9OH-risperidone) were seen. There were large standard deviations between sample pairs and substantial day-to-day unpredictable changes that highlight the difficulty in the interpretation of drug concentrations post-mortem. Based on the presented data, we recommend that specimens for toxicological analysis should to be taken as soon as possible after admission of a deceased person to the mortuary in order to minimise the effects of the PM interval on the drug concentration in blood.

摘要

本研究调查了十种常用抗精神病药物(APs)死后再分布的情况。从 273 例入殓时(AD)和死后(PM)的股骨血中采集了血液。PM 样本在入殓后不同时间采集,最多可达 9 天,并使用 LC-MS/MS 对样本对进行分析。本研究包括的药物有 9OH-risperidone(paliperidone)、amisulpride、chlorpromazine、clozapine、haloperidol、olanzapine、promethazine、quetiapine、risperidone 和 zuclopenthixol。Haloperidol、quetiapine 和 risperidone 在 AD 和 PM 标本之间变化最小,而大多数药物在死后不同时间点采集的样本对之间显示出显著变化(p<0.01),除了应用方法的测量不确定度大于平均浓度变化。死后入殓后血液浓度的平均增加幅度高达 112%(chlorpromazine 和 olanzapine),但也有高达-43%的下降(9OH-risperidone)。样本对之间存在较大的标准差和不可预测的日常变化,这突出了死后药物浓度解释的困难。基于所提供的数据,我们建议在死后尽快采集用于毒理学分析的标本,以最大程度地减少 PM 间隔对血液中药物浓度的影响。

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