Nanoemulsion improves bioaccessibility of cannabidiol and reduces inflammation in macrophages, indicating new therapeutic potential.
Oral delivery of cannabidiol (CBD) is challenging because of its poor water solubility and low bioavailability, which restrict its therapeutic potential. In this study, we used a CBD-loaded oil-in-water nanoemulsion prepared from octenyl succinate anhydride (OSA)-modified starch to address these challenges. The CBD-encapsulated nanoemulsion (CBD-NE) exhibited a uniform particle size of 39.18 ± 0.15 nm, high encapsulation efficiency of 99.80 ± 0.13%, and maintained colloidal stability during storage for 28 days. Simulated gastrointestinal digestion demonstrated that the bioaccessibility of CBD in CBD-NE was higher than that in unformulated CBD. Furthermore, in vitro experiments using RAW264.7 macrophages showed that CBD-NE significantly (p < 0.05) suppressed lipopolysaccharide-induced secretion of the pro-inflammatory cytokines interleukin-6 and tumor necrosis factor-α. Collectively, the improved bioaccessibility and potent anti-inflammatory efficacy of CBD-NE highlight its potential for therapeutic and nutraceutical applications.
No takes yet. Share an insight, caveat, or question.
Lee et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: