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Pharmacokinetics and pharmacodynamics of five distinct commercially available hemp-derived topical cannabidiol products.
Zamarripa, C Austin; Tilton, Hayleigh E; Lin, Spencer; Cone, Edward J; Winecker, Ruth E; Flegel, Ronald R; Kuntz, David; Beals, Melissa; Jacques, Martin; Clark, Michael; Welsh, Eric R; Wagner, Lynn; Bonn-Miller, Marcel O; Vandrey, Ryan; Spindle, Tory R.
Afiliación
  • Zamarripa CA; Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Dr., Baltimore, MD 21224, USA.
  • Tilton HE; Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Dr., Baltimore, MD 21224, USA.
  • Lin S; Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Dr., Baltimore, MD 21224, USA.
  • Cone EJ; Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Dr., Baltimore, MD 21224, USA.
  • Winecker RE; RTI International, Research Triangle Park, 3040 East Cornwallis Rd., Durham, NC 27709, USA.
  • Flegel RR; Substance Abuse and Mental Health Services Administration (SAMHSA), Division of Workplace Programs (DWP), 5600 Fishers Lane, Rockville, MD 20857, USA.
  • Kuntz D; Clinical Reference Laboratory, 8433 Quivira Rd, Lenexa, KS 66214, USA.
  • Beals M; Clinical Reference Laboratory, 8433 Quivira Rd, Lenexa, KS 66214, USA.
  • Jacques M; Clinical Reference Laboratory, 8433 Quivira Rd, Lenexa, KS 66214, USA.
  • Clark M; Clinical Reference Laboratory, 8433 Quivira Rd, Lenexa, KS 66214, USA.
  • Welsh ER; Department of Defense (DoD), Office of Drug Demand Reduction Program (ODDR), 4100 Defense Pentagon, Room 5D636, Washington, DC 20301, USA.
  • Wagner L; Department of Defense (DoD), Office of Drug Demand Reduction Program (ODDR), 4100 Defense Pentagon, Room 5D636, Washington, DC 20301, USA.
  • Bonn-Miller MO; Charlotte's Web, 700 Tech Ct, Louisville, CO 80027, USA.
  • Vandrey R; Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Dr., Baltimore, MD 21224, USA.
  • Spindle TR; Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Dr., Baltimore, MD 21224, USA.
J Anal Toxicol ; 48(2): 81-98, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-38217086
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cannabidiol / Cannabis / Alucinógenos Tipo de estudio: Clinical_trials / Guideline Límite: Adult / Humans Idioma: En Revista: J Anal Toxicol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cannabidiol / Cannabis / Alucinógenos Tipo de estudio: Clinical_trials / Guideline Límite: Adult / Humans Idioma: En Revista: J Anal Toxicol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido