化学
姜黄素
跨细胞
抗氧化剂
外体
体内
内质网
生物化学
纳米载体
细胞生物学
生物物理学
微泡
生物
药物输送
内吞作用
生物技术
小RNA
有机化学
基因
细胞
作者
Dan Li,Gaoyang Yi,Guifang Cao,Adam C. Midgley,Yongli Yang,Dan Yang,Wenguang Liu,Yujuan He,Pan Zhang,Guoliang Li
出处
期刊:Small
[Wiley]
日期:2025-03-13
标识
DOI:10.1002/smll.202410124
摘要
Abstract The utilization of plant‐derived exosome‐like nanovesicles (ELNs) as nanocarriers for oral delivery of bioactives has garnered significant attention. However, their distinctive lipid membrane composition may result in elevated membrane permeability within the gastrointestinal environment, leading to the leakage of carried bioactives. Inspired by the concept of projectile design, Tartary buckwheat‐derived ELNs (TB‐ELNs) based dual‐carriers are fabricated by loading chlorogenic acid (CGA) into the cores and bonding selenium nanoparticles (SeNPs) to the lipid membrane. The results indicate that SeNPs bond markedly augments the membrane rigidity, and therefore enhances the stability of TB‐ELNs and the retention rate of the loaded CGA during gastrointestinal digestion. In vitro and in vivo studies indicates that the TB‐ELNs based dual‐carriers are internalized by epithelial cells and transcytosis via the endoplasmic reticulum, and show the synergistic regulatory effect on high‐fat diet‐induced hyperglycemia in the intestine‐liver axis. These results may be attributed to the fact that SeNPs combination reduces the gastrointestinal degradation of the carried bioactives. Moreover, SeNPs with antioxidant property can protect ELNs and their carried bioactives from oxidative damage, thereby enhancing their biological activities. Collectively, this study offers a new strategy to develop highly efficient oral delivery systems for bioactives to alleviate hyperglycemia and diabetes.
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