Feng Wanshan, Qin Chaolong, Cipolla Elena, Lee Jong Bong, Zgair Atheer, Chu Yenju, Ortori Catherine A, Stocks Michael J, Constantinescu Cris S, Barrett David A, Fischer Peter M, Gershkovich Pavel
School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, UK.
School of Pharmacy, Universita di Roma Tor Vergata, 00173 Rome, Italy.
Pharmaceutics. 2021 Aug 27;13(9):1349. doi: 10.3390/pharmaceutics13091349.
Oral sesame oil-based formulation facilitates the delivery of poorly water-soluble drug cannabidiol (CBD) to the lymphatic system and blood circulation. However, this natural oil-based formulation also leads to considerable variability in absorption of CBD. In this work, the performance of lipid-based formulations with the addition of medium-chain triglyceride (MCT) or surfactants to the sesame oil vehicle has been tested in vitro and in vivo using CBD as a model drug. The in vitro lipolysis has shown that addition of the MCT leads to a higher distribution of CBD into the micellar phase. Further addition of surfactants to MCT-containing formulations did not improve distribution of the drug into the micellar phase. In vivo, formulations containing MCT led to lower or similar concentrations of CBD in serum, lymph and MLNs, but with reduced variability. MCT improves the emulsification and micellar solubilization of CBD, but surfactants did not facilitate further the rate and extent of lipolysis. Even though addition of MCT reduces the variability, the in vivo performance for the extent of both lymphatic transport and systemic bioavailability remains superior with a pure natural oil vehicle.
基于芝麻油的口服制剂有助于将水溶性差的药物大麻二酚(CBD)输送至淋巴系统和血液循环。然而,这种基于天然油的制剂也导致CBD吸收存在相当大的变异性。在这项研究中,以CBD作为模型药物,在体外和体内测试了在芝麻油载体中添加中链甘油三酯(MCT)或表面活性剂的脂质制剂的性能。体外脂解表明,添加MCT会使CBD在胶束相中的分布更高。在含MCT的制剂中进一步添加表面活性剂并不能改善药物在胶束相中的分布。在体内,含MCT的制剂导致血清、淋巴和肠系膜淋巴结中CBD浓度较低或相似,但变异性降低。MCT改善了CBD的乳化和胶束增溶作用,但表面活性剂并未进一步促进脂解速率和程度。尽管添加MCT降低了变异性,但对于淋巴转运程度和全身生物利用度而言,纯天然油载体的体内性能仍然更优。