Pharmacokinetics and oral bioavailability of cannabidiol in horses after intravenous and oral administration with oil and micellar formulations

Author:

Sánchez de Medina Antonia12,Serrano‐Rodríguez Juan Manuel3ORCID,Díez de Castro Elisa12ORCID,García‐Valverde María Teresa4,Saitua Aritz1,Becero Mireia1,Muñoz Ana25ORCID,Ferreiro‐Vera Carlos4,Sánchez de Medina Verónica4ORCID

Affiliation:

1. Veterinary Clinical Hospital, University of Cordoba Córdoba Spain

2. Department of Animal Medicine and Surgery, Veterinary Faculty University of Cordoba Córdoba Spain

3. Department of Nursing, Pharmacology and Physiotherapy, Veterinary Faculty University of Córdoba Córdoba Spain

4. Phytoplant Research S.L.U. Córdoba Spain

5. Equine Sport Medicine Center CEMEDE, Department of Animal Medicine and Surgery, Veterinary Faculty University of Córdoba Córdoba Spain

Abstract

AbstractBackgroundIntravenous pharmacokinetics and oral bioavailability of cannabidiol (CBD) with different formulations have not been investigated in horses and may represent a starting point for clinical studies.ObjectivesTo describe pharmacokinetics after intravenous and oral administrations with oil and micellar formulations and simulate different treatments.Study designSingle intravenous experiment and two‐way randomised oral experiments, Latin‐square design.MethodsEight healthy horses received intravenous CBD at 1.00 mg/kg dose, oral CBD in sesame oil and in micellar formulation, both at 10.00 mg/kg. Concentrations were measured using LC–MS/MS and fitted by nonlinear mixed effect modelling. Parameters obtained were used to simulate single and multiple treatments at steady state.ResultsIntravenous and oral concentrations were simultaneously fitted using a three‐compartment model. Final estimates indicate that CBD has a volume of distribution of 36 L/kg associated with a systemic clearance of 1.46 L/h/kg and half‐lives ranged between 24 and 34 h. Oral bioavailability was close to 14% for both oral administrations. Simulated dose regimen of CBD every 12 and 24 h predicted similar percentages to reach effective plasma concentration with both oral formulation at 10.00 mg/kg.Main limitationsA small horse population was used (8 horses per trial).Conclusions and clinical importanceOral bioavailability was low at the doses studied but fell within the range described for horse and other species. CBD had a high steady‐state volume of distribution, a high clearance and long half‐lives. No adverse reactions were detected at any dose or route. The micellar formulation showed a faster absorption and higher concentration peak, while the oil formulation presented lower levels, but more maintained over time. Simulations predicted that both could be useful in multiple oral dose treatments. These results indicated that CBD could be of interest, but further studies are needed to evaluate its clinical use in horses.

Funder

Hospital Del Mar Medical Research Institute

Publisher

Wiley

Subject

General Medicine

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