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口服右旋苯丙胺后12小时内人体尿液中苯丙胺和甲基苯丙胺的气相色谱-质谱测定:缺乏支持既定甲基苯丙胺确证法医指南的证据。

GC-MS determination of amphetamine and methamphetamine in human urine for 12 hours following oral administration of dextro-methamphetamine: lack of evidence supporting the established forensic guidelines for methamphetamine confirmation.

作者信息

Valentine J L, Kearns G L, Sparks C, Letzig L G, Valentine C R, Shappell S A, Neri D F, DeJohn C A

机构信息

Department of Pediatrics, University of Arkansas for Medical Sciences and Toxicology, Arkansas Children's Hospital, Little Rock 72202-3591, USA.

出版信息

J Anal Toxicol. 1995 Nov-Dec;19(7):581-90. doi: 10.1093/jat/19.7.581.

Abstract

Ten human volunteers, naive to amphetamines and divided into two groups of five each, were given an oral dose of 30 mg/70 kg D-methamphetamine in one of two different paradigms: the initial dose at 0930 h or the initial dose at 2130 h. One week later, each subject was crossed over with regard to time but given the same dose. A total of 214 urine specimens were collected either prior to dosing or at each micturition for a 12-h period post dose. Specimens were analyzed on a blind basis for methamphetamine and one of its metabolites, amphetamine, by gas chromatography-mass spectrometry (GC-MS) using coinjection of extracted sample and pentafluoropropionic anhydride and selected-ion monitoring. Approximately 20% of the D-methamphetamine was recovered unchanged from the urine specimens, and 2% was recovered as amphetamine. The mean urine methamphetamine concentration in both groups reached a maximum within 4-6 h and declined thereafter. A residual amount of methamphetamine was found in some predose specimens at the crossover evaluation, reflecting that methamphetamine may be detected in urine for up to 7 days. The amphetamine concentration reached a plateau by 4-6 h. This observation coupled with the finding that all subjects excreted approximately 2% of the methamphetamine dose as amphetamine suggested a saturable process for its biotransformation. Concentrations of both methamphetamine and amphetamine tended to be higher, but were not significantly different, for night administration. Methamphetamine concentrations were consistently greater than the 500-ng/mL cutoff in most post-dosing specimens, whereas amphetamine concentrations generally did not achieve the 200-ng/mL cutoff specified by the Substance Abuse and Mental Health Services Administration (SAMHSA) guidelines for GC-MS confirmation of methamphetamine. Some specimens containing methamphetamine had no amphetamine metabolite. The current guidelines would have resulted in 90.2% of the specimens containing methamphetamine being ruled negative by confirmation following either night or day administration, whereas one subject following the initial day administration and another following night crossover administration would have been judged positive at most time intervals. These findings suggest that the current SAMHSA guidelines select for individual metabolic variations and that GC-MS confirmation of methamphetamine will result in most occasional users being ruled negative following an oral dose of methamphetamine while some will be ruled positive.

摘要

10名未曾使用过苯丙胺类药物的人类志愿者被分为两组,每组5人,在两种不同的给药模式下口服30mg/70kg的D-甲基苯丙胺:初始剂量在0930时或初始剂量在2130时。一周后,每位受试者在给药时间上进行交叉,但给予相同剂量。在给药前或给药后12小时内每次排尿时共收集了214份尿液标本。标本通过气相色谱-质谱联用仪(GC-MS),采用提取样品与五氟丙酸酐共注入及选择离子监测的方法,在盲态下分析甲基苯丙胺及其一种代谢产物苯丙胺。约20%的D-甲基苯丙胺从尿液标本中以原形回收,2%以苯丙胺形式回收。两组的尿甲基苯丙胺平均浓度在4-6小时内达到峰值,此后下降。在交叉评估时,一些给药前标本中发现有残留的甲基苯丙胺,这表明甲基苯丙胺在尿液中可能长达7天均可被检测到。苯丙胺浓度在4-6小时达到平台期。这一观察结果,再加上所有受试者均将约2%的甲基苯丙胺剂量以苯丙胺形式排泄这一发现,提示其生物转化过程存在饱和现象。夜间给药时,甲基苯丙胺和苯丙胺的浓度往往较高,但无显著差异。大多数给药后标本中甲基苯丙胺浓度持续高于500ng/mL的临界值,而苯丙胺浓度通常未达到物质滥用和精神健康服务管理局(SAMHSA)关于GC-MS确认甲基苯丙胺的指南规定的200ng/mL临界值。一些含有甲基苯丙胺的标本没有苯丙胺代谢产物。按照现行指南,无论夜间还是日间给药,90.2%含有甲基苯丙胺的标本经确认后将被判为阴性,而在初始日间给药后的一名受试者以及夜间交叉给药后的另一名受试者在大多数时间间隔内将被判为阳性。这些发现表明,现行的SAMHSA指南会筛选出个体代谢差异,并且GC-MS确认甲基苯丙胺会导致大多数偶尔使用者在口服甲基苯丙胺后被判为阴性,而一些人则被判为阳性。

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