Pharmacokinetics and pharmacodynamics of five distinct commercially available hemp-derived topical cannabidiol products

Author:

Zamarripa C Austin1ORCID,Tilton Hayleigh E1,Lin Spencer1,Cone Edward J1,Winecker Ruth E2,Flegel Ronald R3,Kuntz David4,Beals Melissa4,Jacques Martin4,Clark Michael4,Welsh Eric R5,Wagner Lynn5,Bonn-Miller Marcel O6,Vandrey Ryan1,Spindle Tory R1

Affiliation:

1. Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine , 5510 Nathan Shock Dr., Baltimore, MD 21224, USA

2. RTI International, Research Triangle Park , 3040 East Cornwallis Rd., Durham, NC 27709, USA

3. Substance Abuse and Mental Health Services Administration (SAMHSA), Division of Workplace Programs (DWP) , 5600 Fishers Lane, Rockville, MD 20857, USA

4. Clinical Reference Laboratory , 8433 Quivira Rd, Lenexa, KS 66214, USA

5. Department of Defense (DoD), Office of Drug Demand Reduction Program (ODDR) , 4100 Defense Pentagon, Room 5D636, Washington, DC 20301, USA

6. Charlotte’s Web , 700 Tech Ct, Louisville, CO 80027, USA

Abstract

Abstract Products containing cannabidiol (CBD) have proliferated after the 2018 Farm Bill legalized hemp (cannabis with ≤0.3% delta-9-tetrahydrocannabinol (Δ9-THC)). CBD-containing topical products have surged in popularity, but controlled clinical studies on them are limited. This study characterized the effects of five commercially available hemp-derived high CBD/low Δ9-THC topical products. Healthy adults (N = 46) received one of six study drugs: a CBD-containing cream (N = 8), lotion (N = 8), patch (N = 7), balm (N = 8), gel (N = 6) or placebo (N = 9; matched to an active formulation). The protocol included three phases conducted over 17 days: (i) an acute drug application laboratory session, (ii) a 9-day outpatient phase with twice daily product application (visits occurred on Days 2, 3, 7 and 10) (iii) a 1-week washout phase. In each phase, whole blood, oral fluid and urine specimens were collected and analyzed via liquid chromatography with tandem mass spectrometry (LC–MS-MS) for CBD, Δ9-THC and primary metabolites of each and pharmacodynamic outcomes (subjective, cognitive/psychomotor and physiological effects) were assessed. Transdermal absorption of CBD was observed for three active products. On average, CBD/metabolite concentrations peaked after 7–10 days of product use and were highest for the lotion, which contained the most CBD and a permeation enhancer (vitamin E). Δ9-THC/metabolites were below the limit of detection in blood for all products, and no urine samples tested “positive” for cannabis using current US federal workplace drug testing criteria (immunoassay cut-off of 50 ng/mL and confirmatory LC–MS-MS cut-off of 15 ng/mL). Unexpectedly, nine participants (seven lotions, one patch and one gel) exhibited Δ9-THC oral fluid concentrations ≥2 ng/mL (current US federal workplace threshold for a “positive” test). Products did not produce discernable pharmacodynamic effects and were well-tolerated. This study provides important initial data on the acute/chronic effects of hemp-derived topical CBD products, but more research is needed given the diversity of products in this market.

Funder

Department of Defense

Substance Abuse and Mental Health Services Administration

Publisher

Oxford University Press (OUP)

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