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近期大麻使用的鉴定:受控吸食大麻后全血和血浆游离型及结合型大麻素药代动力学。

Identification of recent cannabis use: whole-blood and plasma free and glucuronidated cannabinoid pharmacokinetics following controlled smoked cannabis administration.

机构信息

Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, NIH, Biomedical Research Center, Baltimore, MD 21224, USA.

出版信息

Clin Chem. 2011 Oct;57(10):1406-14. doi: 10.1373/clinchem.2011.171777. Epub 2011 Aug 11.

Abstract

BACKGROUND

Δ⁹-Tetrahydrocannabinol (THC) is the most frequently observed illicit drug in investigations of accidents and driving under the influence of drugs. THC-glucuronide has been suggested as a marker of recent cannabis use, but there are no blood data following controlled THC administration to test this hypothesis. Furthermore, there are no studies directly examining whole-blood cannabinoid pharmacokinetics, although this matrix is often the only available specimen.

METHODS

Participants (9 men, 1 woman) resided on a closed research unit and smoked one 6.8% THC cannabis cigarette ad libitum. We quantified THC, 11-hydroxy-THC (11-OH-THC), 11-nor-9-carboxy-THC (THCCOOH), cannabidiol (CBD), cannabinol (CBN), THC-glucuronide and THCCOOH-glucuronide directly in whole blood and plasma by liquid chromatography/tandem mass spectrometry within 24 h of collection to obviate stability issues.

RESULTS

Median whole blood (plasma) observed maximum concentrations (C(max)) were 50 (76), 6.4 (10), 41 (67), 1.3 (2.0), 2.4 (3.6), 89 (190), and 0.7 (1.4) μg/L 0.25 h after starting smoking for THC, 11-OH- THC, THCCOOH, CBD, CBN, and THCCOOH-glucuronide, respectively, and 0.5 h for THC-glucuronide. At observed C(max), whole-blood (plasma) detection rates were 60% (80%), 80% (90%), and 50% (80%) for CBD, CBN, and THC-glucuronide, respectively. CBD and CBN were not detectable after 1 h in either matrix (LOQ 1.0 μg/L).

CONCLUSIONS

Human whole-blood cannabinoid data following cannabis smoking will assist whole blood and plasma cannabinoid interpretation, while furthering identification of recent cannabis intake.

摘要

背景

在对事故和药物影响下的驾驶进行的调查中,Δ⁹-四氢大麻酚(THC)是最常被观察到的非法药物。THC-葡糖苷酸已被提议作为最近大麻使用的标志物,但在受控 THC 给药后,没有血液数据来检验这一假设。此外,尽管全血通常是唯一可用的标本,但目前还没有直接研究全血中大麻素药代动力学的研究。

方法

参与者(9 名男性,1 名女性)居住在一个封闭的研究单位,并随意吸食一支 6.8%THC 的大麻香烟。我们通过液相色谱/串联质谱法直接在全血和血浆中定量检测 THC、11-羟基-THC(11-OH-THC)、11-去甲-9-羧酸-THC(THCCOOH)、大麻二酚(CBD)、大麻酚(CBN)、THC-葡糖苷酸和 THCCOOH-葡糖苷酸,在采集后 24 小时内进行,以避免稳定性问题。

结果

吸烟后 0.25 小时,观察到 50(76)、6.4(10)、41(67)、1.3(2.0)、2.4(3.6)、89(190)和 0.7(1.4)μg/L 的中位全血(血浆)最大浓度(C(max)),分别为 THC、11-OH-THC、THCCOOH、CBD、CBN 和 THCCOOH-葡糖苷酸,THC-葡糖苷酸为 0.5 小时。在观察到的 C(max)时,CBD、CBN 和 THC-葡糖苷酸在全血(血浆)中的检测率分别为 60%(80%)、80%(90%)和 50%(80%)。在这两种基质中,CBD 和 CBN 在 1 小时后均无法检测到(LOQ 1.0μg/L)。

结论

吸食大麻后,人体全血大麻素数据将有助于全血和血浆大麻素的解释,同时进一步确定最近的大麻摄入量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9307/3717336/7a22de93ca68/nihms487023f1.jpg

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