Sex differences in the disposition of cannabidiol and its metabolites in mice

While cannabidiol (CBD) is widely used globally as a therapeutic agent, sex as a biological variable remains underexplored in determining its metabolism and overall pharmacokinetic patterns. The present study systematically evaluated sex differences in the pharmacokinetics of CBD and its major metabolites, 7-hydroxy-CBD (7-OH-CBD) and 7-carboxy-CBD (7-COOH-CBD), in a mouse model.

Male and female C57BL/6J mice received an intraperitoneal dose of CBD (120 mg/kg) and plasma concentrations of CBD and its metabolites were quantified by UPLC-MS/MS. Pharmacokinetic parameters were derived using non-compartmental analysis and compared between sexes.

Females exhibited significantly higher early exposure to CBD, with a ~ 1.5-fold higher [Formula: see text]than male mice (p = 0.03). The apparent clearance (CL/F) and ultimate total systemic exposure[Formula: see text] were comparable between sexes. In contrast, male mice demonstrated a markedly larger apparent volume of distribution (Vz/F; ~2.2-fold increase, p = 0.02) and consequently a longer terminal half-life (t_1/2; ~2.2-fold increase, p = 0.04), indicating greater tissue sequestration. Both metabolites were significantly higher in female vs. male mice (7-OH-CBD [Formula: see text]~1.6-fold, p = 0.03; 7-COOH-CBD [Formula: see text] ~1.7-fold, p = 0.03). The [Formula: see text] tended to be higher for 7-OH-CBD in female mice but was not significant (~ 1.4-fold, p = 0.11), whereas the 7-COOH-CBD [Formula: see text] was significantly greater in females (~ 1.8-fold, p = 0.04). Male mice displayed substantially longer terminal half-lives for both metabolites (7-OH-CBD ~2.4-fold, p = 0.0051; 7-COOH-CBD ~3.7-fold, p = 0.02).

These results demonstrate that sex is a critical determinant of CBD pharmacokinetics and highlight the need for sex-informed dosing considerations in both preclinical study design and potentially for future clinical applications of CBD.