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人体口服大麻素后血浆中的Δ⁹-四氢大麻酚、11-羟基-Δ⁹-四氢大麻酚和11-去甲-9-羧基-Δ⁹-四氢大麻酚

Delta(9)-tetrahydrocannabinol, 11-hydroxy-delta(9)-tetrahydrocannabinol and 11-nor-9-carboxy-delta(9)-tetrahydrocannabinol in human plasma after controlled oral administration of cannabinoids.

作者信息

Goodwin Robert S, Gustafson Richard A, Barnes Allan, Nebro Wesenyalsh, Moolchan Eric T, Huestis Marilyn A

机构信息

Chemistry and Drug Metabolism Section, IRP, NIDA, NIH, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA.

出版信息

Ther Drug Monit. 2006 Aug;28(4):545-51. doi: 10.1097/00007691-200608000-00010.

Abstract

A clinical study to investigate the pharmacokinetics and pharmacodynamics of oral tetrahydrocannabinol was performed. This randomized, double-blind, placebo-controlled, within-subject, inpatient study compared the effects of THC-containing hemp oils in liquid and capsule form to dronabinol (synthetic THC) in doses used for appetite stimulation. The National Institute on Drug Abuse Institutional Review Board approved the protocol and each participant provided informed consent. Detection times and concentrations of THC, 11-hydroxy-Delta-tetrahydrocannabinol (11-OH-THC), and 11-nor-9-carboxy-Delta-tetrahydrocannabinol (THCCOOH) in plasma were determined by gas chromatography-mass spectrometry [limits of quantification (LOQ)=0.5, 0.5, and 1.0 ng/mL, respectively] after oral THC administration. Six volunteers ingested liquid hemp oil (0.39 and 14.8 mg THC/d), hemp oil in capsules (0.47 mg THC/d), dronabinol capsules (7.5 mg THC/d), and placebo. Plasma specimens were collected during and after each dosing condition. THC and 11-OH-THC concentrations were low and never exceeded 6.1 ng/mL. Analytes were detectable 1.5 hour after initiating dosing with the 7.5 mg THC/d regimen and 4.5 hour after starting the 14.8 mg THC/d sessions. THCCOOH was detected 1.5 hour after the first dose, except for the 0.47 mg THC/d session, which required 4.5 hour for concentrations to reach the LOQ. THCCOOH concentrations peaked at 3.1 ng/mL during dosing with the low-dose hemp oils. Plasma THC and 11-OH-THC concentrations were negative for all participants at all doses within 15.5 hours after the last THC dose. Plasma THCCOOH persisted for at least 39.5 hours after the end of dosing and at much higher concentrations (up to 43.0 ng/mL). This study demonstrated that subjects who used high THC content hemp oil (347 mug/mL) as a dietary supplement had THC and metabolites in plasma in quantities comparable to those of patients using dronabinol for appetite stimulation. There was a significant correlation between body mass index and Cmax and body mass index and number of specimens positive for THC and 11-OH-THC.

摘要

开展了一项临床研究,以调查口服四氢大麻酚的药代动力学和药效学。这项随机、双盲、安慰剂对照、受试者自身的住院研究,比较了液体和胶囊形式的含四氢大麻酚(THC)大麻油与用于刺激食欲剂量的屈大麻酚(合成THC)的效果。美国国立药物滥用研究所机构审查委员会批准了该方案,每位参与者均提供了知情同意书。口服THC后,通过气相色谱 - 质谱法[定量限(LOQ)分别为0.5、0.5和1.0 ng/mL]测定血浆中THC、11 - 羟基 - Δ - 四氢大麻酚(11 - OH - THC)和11 - 去甲 - 9 - 羧基 - Δ - 四氢大麻酚(THCCOOH)的检测时间和浓度。6名志愿者分别摄入液体大麻油(0.39和14.8 mg THC/天)、胶囊形式的大麻油(0.47 mg THC/天)、屈大麻酚胶囊(7.5 mg THC/天)和安慰剂。在每种给药条件期间及之后采集血浆样本。THC和11 - OH - THC浓度较低,从未超过6.1 ng/mL。在开始7.5 mg THC/天给药方案后1.5小时以及开始14.8 mg THC/天给药后4.5小时可检测到分析物。除了0.47 mg THC/天的给药情况,其浓度达到LOQ需要4.5小时外,首次给药后1.5小时可检测到THCCOOH。在低剂量大麻油给药期间,THCCOOH浓度峰值为3.1 ng/mL。在最后一次THC给药后15.5小时内,所有剂量下所有参与者的血浆THC和11 - OH - THC浓度均为阴性。给药结束后,血浆THCCOOH持续至少39.5小时,且浓度高得多(高达43.0 ng/mL)。这项研究表明,将高THC含量(347 μg/mL)的大麻油用作膳食补充剂的受试者,其血浆中THC及其代谢物的量与使用屈大麻酚刺激食欲的患者相当。体重指数与Cmax之间以及体重指数与THC和11 - OH - THC阳性样本数量之间存在显著相关性。

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