纳米医学
免疫系统
炎症性肠病
肠道菌群
肿瘤坏死因子α
结肠炎
医学
免疫学
疾病
纳米技术
材料科学
内科学
纳米颗粒
作者
Huan He,Qiaozhen Qin,Fang Xu,Yitong Chen,Shuquan Rao,Chao Wang,Xiaoxia Jiang,Xiong Lu,Chaoming Xie
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-05-26
卷期号:9 (21)
被引量:50
标识
DOI:10.1126/sciadv.adf3887
摘要
Developing oral nanomedicines that suppress intestinal inflammation while modulating gut microbiota and brain interactions is essential for effectively treating inflammatory bowel disease. Here, we report an oral polyphenol-armored nanomedicine based on tumor necrosis factor-α (TNF-α)-small interfering RNA and gallic acid-mediated graphene quantum dot (GAGQD)-encapsulated bovine serum albumin nanoparticle, with a chitosan and tannin acid (CHI/TA) multilayer. Referred to "armor," the CHI/TA multilayer resists the harsh environment of the gastrointestinal tract and adheres to inflamed colon sites in a targeted manner. TA provides antioxidative stress and prebiotic activities that modulate the diverse gut microbiota. Moreover, GAGQD protected TNF-α-siRNA delivery. Unexpectedly, the armored nanomedicine suppressed hyperactive immune responses and modulated bacterial gut microbiota homeostasis in a mouse model of acute colitis. Notably, the armored nanomedicine alleviated anxiety- and depression-like behaviors and cognitive impairment in mice with colitis. This armor strategy sheds light on the effect of oral nanomedicines on bacterial gut microbiome-brain interactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI