Departments of Anesthesiology and.
Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus.
Ther Drug Monit. 2024 Oct 1;46(5):672-680. doi: 10.1097/FTD.0000000000001224. Epub 2024 May 23.
Unusually high variability in blood Δ9-tetrahydrocannabinol (THC) concentrations have been observed in subjects inhaling similar cannabis products over similar time periods when consumption is ad libitum. This makes simple gravimetric dose estimation a poor predictor of THC exposure. Population pharmacokinetic analyses of blood THC concentration versus time data are routinely used to estimate pharmacokinetic parameters. The aim of this study was to estimate the inhaled dose of THC in occasional and daily users of high potency market cannabis.
Blood THC concentrations were measured for 135 minutes from 29 participants who either smoked high concentration flower or inhaled concentrates ad libitum during a 15-minute session. Frequent blood samples were obtained over the following 135 minutes.
The estimated central and rapidly equilibrating volumes of distribution of a 3-compartment model were 19.9 ± 1.2 and 51.6 ± 4.7 L whereas the intercompartmental clearances were 1.65 ± 0.14 and 1.75 ± 0.10 L/min, respectively. Covariate-adjusted analysis revealed that the estimated inhaled THC dose was considerably less among occasional users compared with daily users.
Three-compartment pharmacokinetics of THC did not differ among the 3 user groups, and the early phase (first 135 minutes postinception of inhalation) kinetics were similar to those previously described after smoking low potency cannabis products. Therefore, inhaled THC dose can be estimated from pharmacokinetic data and covariate-driven adjustments can be used to estimate THC doses, based on the participant cannabis usage pattern (occasional versus daily), improving the accuracy of THC exposure estimates compared with those derived from weighed THC content alone.
在自由摄入相似的大麻产品且时间相似的情况下,吸入者的血液中 Δ9-四氢大麻酚(THC)浓度存在异常高的变异性。这使得简单的称重剂量估计无法准确预测 THC 的暴露情况。通常使用血液 THC 浓度与时间数据的群体药代动力学分析来估计药代动力学参数。本研究的目的是估计偶尔和经常使用高浓度大麻的人群中吸入 THC 的剂量。
29 名参与者在 15 分钟的时间内自由吸食高浓度大麻花或吸食浓缩物,在接下来的 135 分钟内每隔一段时间测量一次血液 THC 浓度。
3 分量室模型的中央和快速平衡分布体积分别为 19.9 ± 1.2 和 51.6 ± 4.7 L,而隔室间清除率分别为 1.65 ± 0.14 和 1.75 ± 0.10 L/min。协变量调整分析显示,与每日使用者相比,偶尔使用者的估计吸入 THC 剂量要低得多。
3 种使用者群体的 THC 三分量室药代动力学没有差异,早期(吸入开始后 135 分钟内)动力学与之前描述的吸食低浓度大麻产品后的动力学相似。因此,可以根据药代动力学数据估计吸入的 THC 剂量,并根据参与者的大麻使用模式(偶尔使用与每日使用)进行协变量调整,以估计 THC 剂量,与仅基于称重 THC 含量的估计相比,可提高 THC 暴露量的准确性。