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α-苄基-N-甲基苯乙胺(BNMPA),非法甲基苯丙胺合成的一种杂质:II. 代谢与尿排泄(人体)

alpha-Benzyl-N-methylphenethylamine (BNMPA), an impurity of illicit methamphetamine synthesis: II. Metabolism and urinary excretion (human).

作者信息

Moore K A, Poklis A

机构信息

Department of Pathology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0165, USA.

出版信息

J Anal Toxicol. 1995 Nov-Dec;19(7):549-53. doi: 10.1093/jat/19.7.549.

Abstract

Methamphetamine is a popular drug of abuse, which is readily synthesized in clandestine laboratories. Illicit synthesis results in the formation of various contaminants. Few impurities have been studied in vivo, and their metabolic fate is unknown. One such impurity is alpha-benzyl-N-methylphenethylamine (BNMPA). The detection of BNMPA or its metabolites in urine samples may provide a marker of use of illicitly synthesized methamphetamine. Benzphetamine is structurally similar to BNMPA. Based on metabolic studies of benzphetamine, we predicted the four major metabolites of BNMPA to be the N-demethyl compound, diphenyl-2-propanone (DP2P), p-hydroxy-N-demethyl BNMPA, and p-hydroxy-BNMPA. One male volunteer ingested 5 mg BNMPA. Seventeen urine specimens were collected over 50 h post ingestion. These specimens were analyzed for BNMPA and its four predicted major metabolites by gas chromatography-mass spectrometry following beta-glucuronidase hydrolysis or acid hydrolysis, liquid-liquid extraction, and derivatization with heptafluorobutyric anhydride. Specimens were also analyzed without hydrolysis to determine the abundance of nonconjugated ("free") metabolites. Only trace amounts of BNMPA and its N-demethyl metabolites were detected, and maximum excretion was from 2 to 4 h post ingestion. In the nonhydrolyzed samples, the phenyl-OH metabolites were also present in only trace amounts. Maximum excretion of DP2P was at 2 h. Following either hydrolysis procedure, phenyl-OH-BNMPA and phenyl-OH-N-demethyl BNMPA were the major metabolites detected. Maximum excretion of these two metabolites occurred at 4 h. With the exception of the parent compound and the N-demethyl metabolite, excretion of metabolites was greater than the limit of detection of this procedure (2.5 ng/mL) up to 21 h post ingestion. Metabolites were detectable in sufficient quantities to serve as an adequate marker of illicit methamphetamine consumption within the preceding 24 h.

摘要

甲基苯丙胺是一种常见的滥用药物,很容易在秘密实验室中合成。非法合成会产生各种污染物。很少有杂质在体内进行过研究,其代谢命运也未知。一种这样的杂质是α-苄基-N-甲基苯乙胺(BNMPA)。在尿液样本中检测到BNMPA或其代谢物可能提供非法合成甲基苯丙胺使用情况的标志物。苄非他明在结构上与BNMPA相似。基于苄非他明的代谢研究,我们预测BNMPA的四种主要代谢物为N-去甲基化合物、二苯基-2-丙酮(DP2P)、对羟基-N-去甲基BNMPA和对羟基-BNMPA。一名男性志愿者摄入了5毫克BNMPA。在摄入后50小时内收集了17份尿液样本。这些样本在经β-葡萄糖醛酸酶水解或酸水解、液-液萃取并用七氟丁酸酐衍生化后,通过气相色谱-质谱法分析其中的BNMPA及其四种预测的主要代谢物。样本也未经水解进行分析以确定非共轭(“游离”)代谢物的丰度。仅检测到痕量的BNMPA及其N-去甲基代谢物,最大排泄量出现在摄入后2至4小时。在未水解的样本中,苯基-OH代谢物也仅以痕量存在。DP2P的最大排泄量在2小时。经过任何一种水解程序后,苯基-OH-BNMPA和苯基-OH-N-去甲基BNMPA是检测到的主要代谢物。这两种代谢物的最大排泄量出现在4小时。除母体化合物和N-去甲基代谢物外,代谢物的排泄量在摄入后21小时内均大于该程序的检测限(2.5纳克/毫升)。代谢物能够被充分检测到,足以作为之前24小时内非法甲基苯丙胺消费的适当标志物。

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