炎症性肠病
失调
活性氧
化学
肠道菌群
微生物学
炎症
益生菌
药理学
溃疡性结肠炎
促炎细胞因子
细胞生物学
败血症
生物化学
三氧化钨
作者
Y S Yang,Liucan Wang,Guoqing Chen,Y Zhang,Jiarui Shi,Wenzhe Fan,Min Yu,Jixi Zhang,H P Yang
摘要
ABSTRACT Integrating probiotics with functional nanomaterials to disrupt the cycle of gut microbiota dysbiosis and reactive oxygen species (ROS) overload is an emerging therapeutic strategy for inflammatory bowel disease (IBD). However, simplistic combinations of therapeutics often result in spatiotemporal mismatch within the gastrointestinal tract, preventing precise intervention at target inflammatory sites. To address this, a composite probiotic system, BSCS@WO 3 @PDA is developed, centered around programmed ROS‐mediated cascade regulation for intelligent synergistic therapeutic intervention. The system is constructed by electrostatic assembly of polydopamine (PDA)‐coated tungsten trioxide nanoparticles onto chitosan‐encapsulated Bacillus subtilis (BS), thereby significantly enhancing gastrointestinal stability and promoting prolonged retention in the inflamed colon. At the inflammatory site, the ROS‐responsive PDA shell enabled on‐demand ROS scavenging while undergoing degradation, leading to the sustained release of tungsten ions. These ions specifically inhibited molybdenum cofactor‐dependent nitrate reductase activity in Enterobacteriaceae metabolism, thereby creating a favorable ecological niche for probiotics. Consequently, the retained BS promoted beneficial microbes and metabolites, reversing colitis‐associated metabolic disorders and synergistically enhancing intestinal barrier repair. This study proposes a novel paradigm of precise cascade metabolic regulation by integrating ROS scavenging and pathogen inhibition. The BSCS@WO 3 @PDA system offers a powerful new strategy for restoring gut microecological homeostasis and treating inflammatory diseases.
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