Muta Thabata, Khetan Riya, Song Yunmei, Garg Sanjay
Centre for Pharmaceutical Innovation (CPI), Clinical & Health Science, University of South Australia, Adelaide, SA 5000, Australia.
Int J Mol Sci. 2025 Mar 14;26(6):2647. doi: 10.3390/ijms26062647.
Cannabidiol (CBD) has demonstrated therapeutic potential in treating epilepsy, multiple sclerosis, Alzheimer's, Parkinson's, and Crohn's diseases. Despite its promising effects and analgesic, anti-inflammatory, and anxiolytic properties, oral CBD's full potential is hindered by poor water solubility (0.7-10 μg/mL), low permeability, and chemical instability. This study aimed to enhance CBD's dissolution, stability, and gastrointestinal (GI) permeability by forming a CBD-phospholipid complex (CBD-PLC). We hypothesised that CBD-PLC would enhance CBD's hydrophilicity, thus improving GI barrier permeability. This study involved screening an optimal phospholipid (PL) using a Design of Experiments (DoE) approach to prepare CBD-PLC with nanosized droplets (194.3 nm). Dissolution studies revealed significantly enhanced release rates for CBD-PLC-44.7% at 2 h and 67.1% at 3 h-compared to 0% for pure CBD and 7.2% for a physical mixture (PM). Cellular uptake studies showed that at 30 µM, CBD-PLC exhibited 32.7% higher apparent permeability coefficients (P), nearly doubling at 40 µM compared to pure CBD. Cytotoxicity tests confirmed safety over 24 h, while 12-month stability tests demonstrated consistent performance under varied conditions. The results indicate that CBD-PLC improves CBD's solubility, permeability, and stability, offering a promising strategy to address the limitations of oral CBD delivery systems.
大麻二酚(CBD)已在治疗癫痫、多发性硬化症、阿尔茨海默病、帕金森病和克罗恩病方面展现出治疗潜力。尽管其具有良好的效果以及镇痛、抗炎和抗焦虑特性,但口服CBD的全部潜力因水溶性差(0.7 - 10μg/mL)、渗透性低和化学不稳定性而受到阻碍。本研究旨在通过形成CBD - 磷脂复合物(CBD - PLC)来提高CBD的溶解性、稳定性和胃肠道(GI)渗透性。我们假设CBD - PLC会增强CBD的亲水性,从而改善胃肠道屏障的渗透性。本研究采用实验设计(DoE)方法筛选最佳磷脂(PL),以制备具有纳米级液滴(194.3nm)的CBD - PLC。溶出度研究表明,与纯CBD在2小时时0%和物理混合物(PM)在2小时时7.2%的释放率相比,CBD - PLC在2小时时释放率显著提高至44.7%,在3小时时达到67.1%。细胞摄取研究表明,在30μM时,CBD - PLC的表观渗透系数(P)比纯CBD高32.7%,在40μM时几乎翻倍。细胞毒性测试证实了24小时内的安全性,而12个月的稳定性测试表明在不同条件下性能一致。结果表明,CBD - PLC提高了CBD的溶解度、渗透性和稳定性,为解决口服CBD递送系统的局限性提供了一种有前景的策略。