Digestion behavior, in vitro and in vivo bioavailability of cannabidiol in emulsions stabilized by whey protein-maltodextrin conjugate: Impact of carrier oil

被引:15
作者
Wang, Ce [1 ,2 ]
Dong, Chao [3 ]
Lu, Yingcong [1 ]
Freeman, Kalev [4 ]
Wang, Cuina [1 ,6 ]
Guo, Mingruo [5 ,7 ]
机构
[1] Jilin Univ, Coll Food Sci & Engn, Dept Food Sci, Changchun 130062, Peoples R China
[2] Dalian Polytech Univ, Natl Engn Res Ctr Seafood, Sch Food Sci & Technol, Dalian 116034, Peoples R China
[3] Jilin Univ, Key Lab Pathobiol, Minist Educ, Changchun 130021, Peoples R China
[4] Univ Vermont, Larner Coll Med, Dept Pharmacol, Burlington, VT 05405 USA
[5] Univ Vermont, Coll Agr & Life Sci, Dept Nutr & Food Sci, Burlington, VT 05405 USA
[6] Jilin Univ, 5333 Xian Rd, Changchun 130062, Peoples R China
[7] Univ Vermont, 109 Carrigan Dr,351 Marsh Life Sci, Burlington, VT 05405 USA
关键词
Oil composition; MCT; LCT; Emulsion; Cannabidiol; Bioavailability; MEDIUM-CHAIN TRIGLYCERIDES; DELIVERY-SYSTEMS; BETA-CAROTENE; NUTRACEUTICAL BIOAVAILABILITY; PANCREATIC LIPASE; LIPID-COMPOSITION; LONG-CHAIN; VITAMIN-E; BIOACCESSIBILITY; NANOEMULSION;
D O I
10.1016/j.colsurfb.2023.113154
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
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页数:10
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