溃疡性结肠炎
炎症性肠病
肠道菌群
透明质酸
促炎细胞因子
免疫系统
炎症
结肠炎
氧化应激
化学
自愈水凝胶
巨噬细胞
肠粘膜
免疫学
医学
硫酸软骨素
癌症研究
平衡
肿瘤坏死因子α
碳酸钙-2
胃肠道
药理学
CD36
抗氧化剂
伤口愈合
紧密连接
作者
Xin Wang,Xin Liu,Guoliang Zhou,Yuhang Miao,Xiaomin Zhao,Yuqi Cao,Zhixiang Wang,Dawei Deng
标识
DOI:10.1002/adhm.202505873
摘要
Ulcerative colitis (UC) is a refractory inflammatory bowel disease marked by mucosal barrier damage, immune dysregulation, and microbial imbalance. Current treatments are limited by systemic toxicity and inadequate targeting. Drawing inspiration from the "watermelon seed and watermelon" concept, this study employs microfluidic technology to encapsulate chondroitin sulfate (CSU) based nanoparticles (NPs) loaded with the antioxidant quercetin (Qu@CSCP) within hyaluronic acid/calcium alginate (HACM) hydrogel microspheres. This process yields a "watermelon-like" micro/nano hierarchical hydrogel microsphere system (QC@HACM) specifically designed for targeted combination therapy of UC. The HACM shell protects Qu@CSCP from the harsh gastrointestinal (GI) environment and enables targeted accumulation in inflamed colon tissue. Owing to its colon-adhesive properties, QC@HACM enhances the expression of tight junction proteins and reshapes the gut microbiota, enriching beneficial probiotics. Upon localized release, Qu@CSCP NPs activate the Nrf2/HO-1 antioxidant pathway, induce M2 macrophage polarization, and modulate the Bax/Bcl-2 ratio to suppress epithelial apoptosis. This dual mechanism effectively relieves oxidative stress and promotes mucosal healing. The therapeutic efficacy of these microspheres was further validated in a murine model of UC, as evidenced by reduced levels of pro-inflammatory cytokines accompanied by restoration of gut microbiota homeostasis. Consequently, this oral delivery platform represents a promising stepwise therapeutic strategy for comprehensive UC management.
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