Suppr超能文献

药物滥用的毛发分析。十五。3,4-亚甲基二氧基甲基苯丙胺(摇头丸)及其相关化合物在大鼠毛发中的分布以及在摇头丸滥用毛发分析中的应用。

Hair analysis for drug abuse. XV. Disposition of 3, 4-methylenedioxymethamphetamine (MDMA) and its related compounds into rat hair and application to hair analysis for MDMA abuse.

作者信息

Kikura R, Nakahara Y, Mieczkowski T, Tagliaro F

机构信息

National Institute of Health Sciences, Tokyo, Japan.

出版信息

Forensic Sci Int. 1997 Jan 17;84(1-3):165-77. doi: 10.1016/s0379-0738(96)02060-9.

Abstract

In order to clarify the mechanism of drug incorporation into hair, disposition of 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethamphetamine (MDMA), 3,4-methylenedioxyethylamphetamine (MDEA), 3-methoxy-4,5-methylenedioxyamphetamine (MMDA) and metabolites of MDMA, 4-hydroxy-3-methoxyamphetamine (HMAP) and 4-hydroxy-3-methoxymethamphetamine (HMMA), into hair was investigated with an animal model. After the intraperitoneal administration of those six drugs to pigmented hairy rats (5 mg/kg/day, 10 days, n = 3), the parent compounds and their metabolites in the rat plasma (5, 15, 30, 60, 120, 360 min after administration) and in the newly grown rat hair for 4 weeks were determined by GC/MS-SIM. When the ratio of hair concentration to area under the concentration versus time curves (AUCs) in plasma was represented as an index of incorporation rate (ICR) of drugs into hair, the order of ICRs was HMAP < MDA < HMMA < MDMA < MDEA < MMDA. In the comparison between MDA, MDMA and MDEA, their ICRs increased according to the length of carbon branches from proton to ethyl at the N position. From the point of view that the ICRs of MMDA was 2.3 times as much as that of MDA, the methoxy group on the benzene ring seemed to serve as a positive factor for the ICR. However, the ICRs of 4-hydroxy-3-methoxy compounds, HMAP and HMMA, were lower in comparison with those of MDA and MDMA, respectively. On the other hand, the ICRs of MDA, MDMA and MDEA were 5.5-6.1 times larger than those of amphetamine, methamphetamine and ethylamphetamine, suggesting that the methylenedioxy group on the benzene ring raises their ICRs very positively. Moreover, in order to apply the results from the animal experiments to human cases, the scalp hair samples of seven MDMA abusers were analyzed. MDMA and its metabolites, MDA; were simultaneously detected in all the samples by GC/MS. In the two samples, MDEA was found in addition to MDMA and MDA. It was shown that a hair sample is a good specimen for the confirmation of retrospective use of methylenedioxyamphetamines.

摘要

为阐明药物掺入毛发的机制,采用动物模型研究了3,4-亚甲基二氧基苯丙胺(MDA)、3,4-亚甲基二氧基甲基苯丙胺(摇头丸)、3,4-亚甲基二氧基乙基苯丙胺(MDEA)、3-甲氧基-4,5-亚甲基二氧基苯丙胺(MMDA)以及摇头丸的代谢产物4-羟基-3-甲氧基苯丙胺(HMAP)和4-羟基-3-甲氧基甲基苯丙胺(HMMA)在毛发中的分布情况。给有色多毛大鼠腹腔注射这六种药物(5mg/kg/天,共10天,n = 3)后,通过气相色谱/质谱-选择离子监测法测定大鼠血浆(给药后5、15、30、60、120、360分钟)和新生长4周的大鼠毛发中的母体化合物及其代谢产物。当将毛发浓度与血浆中浓度-时间曲线下面积(AUC)的比值作为药物掺入毛发的掺入率(ICR)指标时,ICR的顺序为HMAP<MDA<HMMA<摇头丸<MDEA<MMDA。在比较MDA、摇头丸和MDEA时,它们的ICR随着N位从质子到乙基的碳支链长度增加而升高。从MMDA的ICR是MDA的2.3倍这一点来看,苯环上的甲氧基似乎是ICR的一个正向因素。然而,4-羟基-3-甲氧基化合物HMAP和HMMA的ICR分别低于MDA和摇头丸。另一方面,MDA、摇头丸和MDEA的ICR比苯丙胺、甲基苯丙胺和乙基苯丙胺的ICR大5.5 - 6.1倍,这表明苯环上的亚甲二氧基非常显著地提高了它们的ICR。此外,为了将动物实验结果应用于人类病例,对7名摇头丸滥用者的头皮毛发样本进行了分析。通过气相色谱/质谱法在所有样本中同时检测到了摇头丸及其代谢产物MDA;在两个样本中,除了摇头丸和MDA外还发现了MDEA。结果表明,毛发样本是确认回顾性使用亚甲二氧基苯丙胺的良好标本。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验