炎症性肠病
结肠炎
多酚
溃疡性结肠炎
医学
疾病
化学
微生物学
生物
免疫学
生物化学
内科学
抗氧化剂
作者
Qinglian Hu,Jingyu Li,Tong Wang,Xiangchi Xu,Yuxuan Duan,Yuanxiang Jin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-05-09
卷期号:18 (20): 12917-12932
被引量:88
标识
DOI:10.1021/acsnano.4c00830
摘要
Nissle 1917 layer by layer to construct the collaborative platform EcN@SA-pBDT-TA. The modified probiotics showed improved resistance to oxidative and inflammatory stress, which resulted in superior colon accumulation and retention in IBD model mice. Further, EcN@SA-pBDT-TA could alleviate dextran sulfate sodium (DSS)-induced colitis by controlling the inflammatory response, repairing intestinal barriers, and modulating gut microbiota. Importantly, EcN@SA-pBDT-TA-mediated IBD drug delivery could achieve an improved therapeutic effect in DSS model mice. Given the availability and functionality of polyphenol and prebiotics, we expected that nanostructured polyphenol-modified probiotics provided a solution to develop a collaborative platform for IBD treatment.
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