生物利用度
化学
没食子酸
抗氧化剂
没食子酸表没食子酸酯
食品科学
多酚
茶氨酸
环糊精
体内
生物化学
药理学
绿茶
核化学
生物
生物技术
作者
Baogui Liu,Zhiyin Chen,Yangling Zhang,Enshuo Liu,Shuming Han,Zhihua Gong,Wenjun Xiao
标识
DOI:10.1016/j.jff.2022.104998
摘要
Epigallocatechin-3-gallate (EGCG) and L-theanine (LTA), which are active ingredients in green tea, can inhibit fat accumulation; however, EGCG bioavailability is <5%. Here, we aimed to improve EGCG bioavailability and efficacy by preparing EGCG + LTA/β-cyclodextrin (βCD) inclusion complexes by freeze-drying EGCG + LTA at their mass ratio (5:1) in green tea. Physicochemical characterisation revealed that the supramolecular EGCG + LTA/βCD inclusion complexes had distinct crystal structures formed via intermolecular hydrogen bonding. The inclusion complexes prevented simulated EGCG digestion in vitro while increasing its bioaccessibility and antioxidant activity (p < 0.05). In rats fed a high-fat diet, EGCG + LTA/βCD inclusion complexes significantly increased gut microflora diversity and the abundance of lipid metabolism-related genera but decreased the abundance of EGCG catabolism-related genera. Furthermore, the inclusion complexes significantly enhanced the lipid-lowering and weight loss effects of EGCG in vivo (p < 0.05), likely by improving gut microflora and EGCG bioavailability.
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