Yuan Minghao, Wan Yan, Wang Yulu, Li Sihui, Tang Jiamei, Liang Xue, Tan Xin, Yi Sirui, Wei Xiaohang, Li Xiaohong, Guo Li, Guo Yiping
State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, Sichuan, China; School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, Sichuan, China.
State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, Sichuan, China; School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, Sichuan, China.
Food Chem. 2025 Apr 1;470:142708. doi: 10.1016/j.foodchem.2024.142708. Epub 2024 Dec 29.
Oleanolic acid (OA) is a food-derived bioactive component with antidiabetic activity, but its water solubility and oral bioavailability are notably restricted. In this study, to overcome these limitations, ursodeoxycholic acid-modified chitosan oligosaccharide (UCOS) was synthesized to encapsulate OA in self-assembled nanomicelles (UCOS-OA). The encapsulation efficiency and drug loading of UCOS-OA were 86 % and 11 %, respectively. UCOS-OA exhibited enhanced gastrointestinal stability and prolonged intestinal retention time when compared with free OA, resulting in a 10.6-fold increase in oral bioavailability. The enhanced antidiabetic activity of UCOS-OA was confirmed in the type 2 diabetes mellitus mice model, as it significantly improved glycolipid metabolism disorders and mitigated liver injury. Furthermore, UCOS-OA ameliorated the dysbiosis of gut microbiota and fecal metabolites. In conclusion, UCOS serves as an effective polymeric carrier for encapsulating OA, thereby improving its bioavailability and antidiabetic activity. This work provides valuable insights for the advancement of oral delivery systems for bioactive compounds.
齐墩果酸(OA)是一种具有抗糖尿病活性的食物来源生物活性成分,但其水溶性和口服生物利用度受到显著限制。在本研究中,为克服这些局限性,合成了熊去氧胆酸修饰的壳寡糖(UCOS),以将OA包裹在自组装纳米胶束(UCOS-OA)中。UCOS-OA的包封率和载药量分别为86%和11%。与游离OA相比,UCOS-OA表现出增强的胃肠道稳定性和延长的肠道滞留时间,导致口服生物利用度提高了10.6倍。在2型糖尿病小鼠模型中证实了UCOS-OA增强的抗糖尿病活性,因为它显著改善了糖脂代谢紊乱并减轻了肝损伤。此外,UCOS-OA改善了肠道微生物群和粪便代谢物的失调。总之,UCOS作为一种有效的聚合物载体用于包裹OA,从而提高其生物利用度和抗糖尿病活性。这项工作为生物活性化合物口服给药系统的发展提供了有价值的见解。