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Review
. 2024 Apr 1;16(4):484.
doi: 10.3390/pharmaceutics16040484.

CBD and THC in Special Populations: Pharmacokinetics and Drug-Drug Interactions

Affiliations
Review

CBD and THC in Special Populations: Pharmacokinetics and Drug-Drug Interactions

Lixuan Qian et al. Pharmaceutics. .

Abstract

Cannabinoid use has surged in the past decade, with a growing interest in expanding cannabidiol (CBD) and delta-9-tetrahydrocannabinol (THC) applications into special populations. Consequently, the increased use of CBD and THC raises the risk of drug-drug interactions (DDIs). Nevertheless, DDIs for cannabinoids, especially in special populations, remain inadequately investigated. While some clinical trials have explored DDIs between therapeutic drugs like antiepileptic drugs and CBD/THC, more potential interactions remain to be examined. This review summarizes the published studies on CBD and THC-drug interactions, outlines the mechanisms involved, discusses the physiological considerations in pharmacokinetics (PK) and DDI studies in special populations (including pregnant and lactating women, pediatrics, older adults, patients with hepatic or renal impairments, and others), and presents modeling approaches that can describe the DDIs associated with CBD and THC in special populations. The PK of CBD and THC in special populations remain poorly characterized, with limited studies investigating DDIs involving CBD/THC in these populations. Therefore, it is critical to evaluate potential DDIs between CBD/THC and medications that are commonly used in special populations. Modeling approaches can aid in understanding these interactions.

Keywords: cannabidiol; delta-9-tetrahydrocannabinol; drug–drug interaction; special population.

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Conflict of interest statement

The authors declare no conflicts of interest.

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References

    1. Cox E.J., Maharao N., Patilea-Vrana G., Unadkat J.D., Rettie A.E., McCune J.S., Paine M.F. A Marijuana-Drug Interaction Primer: Precipitants, Pharmacology, and Pharmacokinetics. Pharmacol. Ther. 2019;201:25–38. doi: 10.1016/j.pharmthera.2019.05.001. - DOI - PMC - PubMed
    1. Lafaye G., Karila L., Blecha L., Benyamina A. Cannabis, Cannabinoids, and Health. Dialogues Clin. Neurosci. 2017;19:309–316. doi: 10.31887/DCNS.2017.19.3/glafaye. - DOI - PMC - PubMed
    1. Zhou Z., Paine M.F., Spindle T.R., Huang S., Zhang L. Cannabis for Medical Use: Clinical Pharmacology Perspectives on Scientific and Regulatory Challenges. Clin. Pharmacol. Ther. 2022;111:732–735. doi: 10.1002/cpt.2470. - DOI - PMC - PubMed
    1. Lucas C.J., Galettis P., Schneider J. The Pharmacokinetics and the Pharmacodynamics of Cannabinoids. Br. J. Clin. Pharmacol. 2018;84:2477–2482. doi: 10.1111/bcp.13710. - DOI - PMC - PubMed
    1. Kesner A.J., Lovinger D.M. Cannabis Use, Abuse, and Withdrawal: Cannabinergic Mechanisms, Clinical, and Preclinical Findings. J. Neurochem. 2021;157:1674–1696. doi: 10.1111/jnc.15369. - DOI - PMC - PubMed

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