Wang Ce, Dong Chao, Lu Yingcong, Freeman Kalev, Wang Cuina, Guo Mingruo
Department of Food Science, College of Food Science and Engineering, Jilin University, Changchun 130062, China; National Engineering Research Center of Seafood, School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, China.
Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Colloids Surf B Biointerfaces. 2023 Mar;223:113154. doi: 10.1016/j.colsurfb.2023.113154. Epub 2023 Jan 18.
An emulsion delivery system may be affected significantly by oil phase composition in terms of digestion behavior and bioavailability of the delivered substance. In this study, emulsions loaded with cannabidiol (CBD) were prepared with medium chain triglyceride (MCT), long chain triglyceride (LCT) or MCT/LCT(1:1) as carrier oil and whey protein-maltodextrin conjugate as emulsifier, and the digestion behavior of emulsion and bioavailability of CBD were assessed in vitro and in vivo. The particle size of emulsions throughout the in vitro digestion process was in the order of MCT < MCT/LCT < LCT, and three emulsions showed consistent particle size changes: stable in oral phase, sharply increased in gastric phase, and decreased in small intestine. After intestinal digestion, about 90% of free fatty acids (FFA) was released in MCT emulsion, followed by MCT/LCT (76%) and then LCT (45%). CBD was degraded during gastrointestinal digestion and the transformation stability of CBD in oil phase was in the order of LCT > MCT/LCT > MCT. Although CBD had higher bioaccessibility in MCT and MCT/LCT emulsions, the bioavailability of CBD in LCT was the highest (43%), followed by MCT/LCT (39%), MCT (33%). In vivo pharmacokinetic study showed that MCT/LCT and LCT were more favorable for CBD transport and absorption. The results may provide useful information for the construction of delivery systems, protecting CBD molecules, and improving their bioavailability.
乳液递送系统在递送物质的消化行为和生物利用度方面可能会受到油相组成的显著影响。在本研究中,以中链甘油三酯(MCT)、长链甘油三酯(LCT)或MCT/LCT(1:1)为载体油,乳清蛋白-麦芽糊精共轭物为乳化剂,制备了负载大麻二酚(CBD)的乳液,并在体外和体内评估了乳液的消化行为和CBD的生物利用度。在整个体外消化过程中,乳液的粒径大小顺序为MCT < MCT/LCT < LCT,三种乳液表现出一致的粒径变化:在口腔阶段稳定,在胃阶段急剧增加,在小肠中减小。肠道消化后,MCT乳液中约90%的游离脂肪酸(FFA)被释放,其次是MCT/LCT(76%),然后是LCT(45%)。CBD在胃肠道消化过程中会降解,且CBD在油相中的转化稳定性顺序为LCT > MCT/LCT > MCT。虽然CBD在MCT和MCT/LCT乳液中的生物可及性较高,但CBD在LCT中的生物利用度最高(43%),其次是MCT/LCT(39%)、MCT(33%)。体内药代动力学研究表明,MCT/LCT和LCT更有利于CBD的转运和吸收。这些结果可能为构建递送系统、保护CBD分子并提高其生物利用度提供有用信息。