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有记录的大麻使用者头发中的大麻素浓度。

Cannabinoid concentrations in hair from documented cannabis users.

作者信息

Huestis Marilyn A, Gustafson Richard A, Moolchan Eric T, Barnes Allan, Bourland James A, Sweeney Stacy A, Hayes Eugene F, Carpenter Patrick M, Smith Michael L

机构信息

Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, United States.

出版信息

Forensic Sci Int. 2007 Jul 4;169(2-3):129-36. doi: 10.1016/j.forsciint.2006.08.005. Epub 2006 Sep 11.

Abstract

Fifty-three head hair specimens were collected from 38 males with a history of cannabis use documented by questionnaire, urinalysis and controlled, double blind administration of delta9-tetrahydrocannabinol (THC) in an institutional review board approved protocol. The subjects completed a questionnaire indicating daily cannabis use (N=18) or non-daily use, i.e. one to five cannabis cigarettes per week (N=20). Drug use was also documented by a positive cannabinoid urinalysis, a hair specimen was collected from each subject and they were admitted to a closed research unit. Additional hair specimens were collected following smoking of two 2.7% THC cigarettes (N=13) or multiple oral doses totaling 116 mg THC (N=2). Cannabinoid concentrations in all hair specimens were determined by ELISA and GCMSMS. Pre- and post-dose detection rates did not differ statistically, therefore, all 53 specimens were considered as one group for further comparisons. Nineteen specimens (36%) had no detectable THC or 11-nor-9-carboxy-THC (THCCOOH) at the GCMSMS limits of quantification (LOQ) of 1.0 and 0.1 pg/mg hair, respectively. Two specimens (3.8%) had measurable THC only, 14 (26%) THCCOOH only, and 18 (34%) both cannabinoids. Detection rates were significantly different (p<0.05, Fishers' exact test) between daily cannabis users (85%) and non-daily users (52%). There was no difference in detection rates between African-American and Caucasian subjects (p>0.3, Fisher's exact test). For specimens with detectable cannabinoids, concentrations ranged from 3.4 to >100 pg THC/mg and 0.10 to 7.3 pg THCCOOH/mg hair. THC and THCCOOH concentrations were positively correlated (r=0.38, p<0.01, Pearson's product moment correlation). Using an immunoassay cutoff concentration of 5 pg THC equiv./mg hair, 83% of specimens that screened positive were confirmed by GCMSMS at a cutoff concentration of 0.1 pg THCCOOH/mg hair.

摘要

通过问卷调查、尿液分析以及在机构审查委员会批准的方案中对delta9-四氢大麻酚(THC)进行对照双盲给药,从38名有大麻使用史的男性中收集了53份头部毛发样本。受试者完成了一份问卷,表明每日使用大麻(N = 18)或非每日使用,即每周吸食一至五支大麻香烟(N = 20)。药物使用情况也通过大麻素尿液分析呈阳性记录,从每个受试者身上采集一份毛发样本,他们被收治到一个封闭的研究单元。在吸食两支含2.7% THC的香烟后(N = 13)或口服多剂总计116 mg THC后(N = 2),又采集了额外的毛发样本。所有毛发样本中的大麻素浓度通过酶联免疫吸附测定(ELISA)和气相色谱-串联质谱(GCMSMS)测定。给药前和给药后的检测率在统计学上没有差异,因此,将所有53个样本视为一组进行进一步比较。在GCMSMS分别为1.0和0.1 pg/mg毛发的定量限(LOQ)下,19个样本(36%)未检测到THC或11-去甲-9-羧基-THC(THCCOOH)。两个样本(3.8%)仅检测到可测量的THC,14个(26%)仅检测到THCCOOH,18个(34%)两种大麻素都检测到。每日大麻使用者(85%)和非每日使用者(52%)之间的检测率有显著差异(p<0.05,Fisher精确检验)。非裔美国人和白种人受试者之间的检测率没有差异(p>0.3,Fisher精确检验)。对于检测到大麻素的样本,浓度范围为3.4至>100 pg THC/mg毛发和0.10至7.3 pg THCCOOH/mg毛发。THC和THCCOOH浓度呈正相关(r = 0.38,p<0.01,Pearson积矩相关)。使用5 pg THC当量/mg毛发的免疫测定临界浓度,83%筛查呈阳性的样本在0.1 pg THCCOOH/mg毛发的临界浓度下通过GCMSMS得到确认。

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