The acute and chronic pharmacokinetic oral fluid profile of oral cannabidiol (CBD) with and without low doses of delta-9-tetrahydrocannabinol (Δ9-THC) in healthy human volunteers

Δ9-tetrahydrocannabinol (Δ9-THC)-dominant cannabis use can cause impairment and risks to workplace safety, which makes the detection of Δ9-THC in oral fluid (OF) important for workplace drug testing. However, cannabidiol (CBD)-dominant cannabis sold as legal hemp products (≤0.3% Δ9-THC) often contain some Δ9-THC. In the present study, participants self-administered 1.5 mL medium-chain triglyceride (MCT) oil containing 100 mg CBD and either 0, 0.5, 1.0, 2.0, 2.8 or 3.7 mg Δ9-THC twice daily for 14 days (n = 10/Δ9-THC dose condition), followed by a 7-day washout period. OF CBD, 7-hydroxy-cannabidiol (7-OH-CBD), 7-carboxy-cannabidiol (7-COOH-CBD), Δ9-THC, 11-hydroxy-Δ9-tetrahydrocannabinol (11-OH-Δ9-THC), and 11-nor-9-carboxy-Δ9-tetrahydrocannabinol (Δ9-THC-COOH) were measured by LC-MS/MS (cutoff 0.025 ng/mL). Median CBD peaked at 2,198 ng/mL 0.5 h after dosing, which likely reflects a high amount of direct oral cavity deposition, followed by a rapid decline. CBD pharmacokinetics were unaffected by the co-administration of Δ9-THC. CBD and Δ9-THC metabolite concentrations were low (<2 ng/mL), with some accumulation observed for 7-COOH-CBD with twice-daily exposure. After dosing with 100 mg CBD + 0.5 mg Δ9-THC, 1/10 participants had a positive OF test (≥2 ng/mL Δ9-THC) 1.5-6 h after a single acute dose. The rate of positive test results increased as Δ9-THC doses increased to 8/10 participants testing positive after acute doses of 100 mg CBD + 2.8 or 3.7 mg Δ9-THC. A consumer of hemp products might be unaware of the risk of a positive drug test as many products do not specify that they contain Δ9-THC. One positive sample was obtained at baseline, possibly due to direct oral cavity deposition of environmental contamination. Five samples in the CBD alone group, collected 0.5 h after dosing, were positive, likely due to minimal (0.02-0.15%) conversion of CBD to Δ9-THC during analysis. Laboratories are advised to take action to identify specimens where OF Δ9-THC results could be influenced by these factors.

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Publication Details

Journal
Journal of Analytical Toxicology
Published
2025-11-14
DOI
https://doi.org/10.1093/jat/bkaf102
Primary Topic
Cannabis and Cannabinoid Research
Type
article
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article

The acute and chronic pharmacokinetic oral fluid profile of oral cannabidiol (CBD) with and without low doses of delta-9-tetrahydrocannabinol (Δ9-THC) in healthy human volunteers

Ryan G. Vandrey, C. Austin Zamarripa, Svante Vikingsson, Ronald Flegel et al.
Journal of Analytical Toxicology
Cannabis and Cannabinoid Research
article

The acute and chronic pharmacokinetic oral fluid profile of oral cannabidiol (CBD) with and without low doses of delta-9-tetrahydrocannabinol (Δ9-THC) in healthy human volunteers

Ryan G. Vandrey, C. Austin Zamarripa, Svante Vikingsson, Ronald Flegel, Tory R. Spindle, E. J. Cone, David Isaac Wolinsky, Mitchell Klausner, Eugene D Hayes, Ruth E. Winecker, Lisa S Davis, D Kuntz
article en

Abstract

Δ9-tetrahydrocannabinol (Δ9-THC)-dominant cannabis use can cause impairment and risks to workplace safety, which makes the detection of Δ9-THC in oral fluid (OF) important for workplace drug testing. However, cannabidiol (CBD)-dominant cannabis sold as legal hemp products (≤0.3% Δ9-THC) often contain some Δ9-THC. In the present study, participants self-administered 1.5 mL medium-chain triglyceride (MCT) oil containing 100 mg CBD and either 0, 0.5, 1.0, 2.0, 2.8 or 3.7 mg Δ9-THC twice daily for 14 days (n = 10/Δ9-THC dose condition), followed by a 7-day washout period. OF CBD, 7-hydroxy-cannabidiol (7-OH-CBD), 7-carboxy-cannabidiol (7-COOH-CBD), Δ9-THC, 11-hydroxy-Δ9-tetrahydrocannabinol (11-OH-Δ9-THC), and 11-nor-9-carboxy-Δ9-tetrahydrocannabinol (Δ9-THC-COOH) were measured by LC-MS/MS (cutoff 0.025 ng/mL). Median CBD peaked at 2,198 ng/mL 0.5 h after dosing, which likely reflects a high amount of direct oral cavity deposition, followed by a rapid decline. CBD pharmacokinetics were unaffected by the co-administration of Δ9-THC. CBD and Δ9-THC metabolite concentrations were low (<2 ng/mL), with some accumulation observed for 7-COOH-CBD with twice-daily exposure. After dosing with 100 mg CBD + 0.5 mg Δ9-THC, 1/10 participants had a positive OF test (≥2 ng/mL Δ9-THC) 1.5-6 h after a single acute dose. The rate of positive test results increased as Δ9-THC doses increased to 8/10 participants testing positive after acute doses of 100 mg CBD + 2.8 or 3.7 mg Δ9-THC. A consumer of hemp products might be unaware of the risk of a positive drug test as many products do not specify that they contain Δ9-THC. One positive sample was obtained at baseline, possibly due to direct oral cavity deposition of environmental contamination. Five samples in the CBD alone group, collected 0.5 h after dosing, were positive, likely due to minimal (0.02-0.15%) conversion of CBD to Δ9-THC during analysis. Laboratories are advised to take action to identify specimens where OF Δ9-THC results could be influenced by these factors.

Journal of Analytical Toxicology
Substance Abuse and Mental Health Services Administration (US), Johns Hopkins University (US), RTI International (US), Behavioral Pharma (United States) (US), Laboratoire National de Référence (MA), American College of Clinical Pharmacy (US)
Openalex Percentile: Top 61%
Cannabis and Cannabinoid Research
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