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Plasma cannabinoid pharmacokinetics following the inhalation of vaporised cannabis with and without cannabidiol.

Daniel L. Hall, Edward Chesney, Claire Mokrysz, Anna Caldwell, John Halket, Kat Petrilli, Matthew B. Wall, H Val Curran, Tom P. Freeman, Will Lawn

Drug and Alcohol Dependence July 1, 2026 DOI: 10.1016/j.drugalcdep.2026.113160 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomised, double-blind, placebo-controlled, cross-over study Randomized Peer reviewed
Sample size 48
Population Adolescents aged 16-17 years and adults aged 26-29 years
Interventions THC+CBD placebo
Dose 8 mg THC/75 kg (THC-alone); 8 mg THC and 24 mg CBD/75 kg (THC+CBD)
Topics Cannabis CBD
Keywords Adolescent Cannabinoid Inhalation Pharmacokinetic Plasma
Key points The THC+CBD vaporised cannabis condition produced significantly greater plasma levels of THC, OH-THC, and COOH-THC than the THC-alone condition, measured by natural-log-transformed area-under-the-curve and peak concentration, except for OH-THC peak concentration. The authors report no strong evidence of age-related differences in cannabinoid pharmacokinetics between adolescents and adults.

Abstract

The presence of cannabidiol (CBD) in cannabis may alter cannabinoid pharmacokinetics, however previous research has produced mixed results. Furthermore, no prior research has explored how cannabinoid pharmacokinetics are moderated by age. Using vaporised and inhaled cannabis, we aimed to (1) examine the effect of CBD on the plasma concentration of delta-9-tetrahydrocannabinol (THC) and its metabolites, and (2) compare cannabinoid plasma pharmacokinetics in adolescents and adults. We conducted a randomised, double-blind, placebo-controlled, cross-over study. We compared the effects of three vaporized, weight-adjusted cannabis preparations: 'THC-alone' (8mg THC/75kg), 'THC+CBD' (8mg THC and 24mg CBD/75kg) and placebo, in 48 participants, aged 16-17-years and 26-29-years. Blood samples were taken prior to inhalation, then 20, 30, and 160min after inhalation began. Thirty-five participants had complete pharmacokinetic datasets, which were analysed. Plasma was analysed for concentrations of THC, 11-hydroxy-THC (OH-THC) and 11-Nor-9-carboxy-THC (COOH-THC), CBD, 7-hydroxy-cannabidiol (OH-CBD) and 7-carboxy-cannabidiol (COOH-CBD). The 'THC+CBD' condition produced significantly greater THC, OH-THC, and COOH-THC plasma levels than the 'THC-alone' condition, in terms of natural-log-transformed area-under-the-curve (AUC) and peak concentration (Cmax) values, with the exception of Cmax for OH-THC. Geometric mean ratios showed the 'THC+CBD' condition led to higher THC plasma levels. There was no strong evidence of age-related differences. The presence of CBD in vaporised cannabis increased circulating levels of THC and THC-metabolites. However, further research is needed to understand discrepancies across studies regarding the impact of CBD on THC pharmacokinetics.

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Cannabidiol inhibits THC-elicited paranoid symptoms and hippocampal-dependent memory impairment Healthy participants 2012 Randomized controlled trial n = 48
Distinct Effects of Δ9-Tetrahydrocannabinol and Cannabidiol on Neural Activation During Emotional Processing Healthy, English-native, right-handed men who had used cannabis 15 times or less in... 2009 Double-blind, randomized, placebo-controlled crossover trial n = 15
Inverted U-Shaped Dose-Response Curve of the Anxiolytic Effect of Cannabidiol during Public Speaking in Real Life Healthy subjects aged 18 to 35 years 2017 Randomized controlled trial n = 60
Acute Effects of a Single, Oral dose of d9-tetrahydrocannabinol (THC) and Cannabidiol (CBD) Administration in Healthy Volunteers Healthy male subjects 2012 Randomized controlled trial n = 16
Modulation of Mediotemporal and Ventrostriatal Function in Humans by Δ9-Tetrahydrocannabinol Healthy, native English-speaking, right-handed men of white race/ethnicity who had used... 2009 Randomized controlled trial n = 15

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