溃疡性结肠炎
活性氧
氧化应激
体内
菊粉
药理学
炎症性肠病
脂质过氧化
癌症研究
发病机制
促炎细胞因子
结肠炎
炎症
化学
胃肠道
碳酸钙-2
KEAP1型
肠粘膜
肠上皮
医学
抗氧化剂
益生菌
药品
作者
Luolan Ouyang,Jia Ke,Shanshan Xiang,Jing Ding,Shufen Zhang,Zixu Wang,Si Chen,Tingting Meng,Hong Yuan,Fangying Yu,FUQIANG HU
标识
DOI:10.1021/acsami.5c21491
摘要
Ulcerative colitis (UC), a chronic inflammatory disorder of the colon, remains challenging to treat due to limited efficacy with current therapies. Ferroptosis, a newly identified form of programmed cell death, contributes significantly to UC pathogenesis and might offer promising therapeutic potential. Herein, we developed an oral synergistic regulation of ferroptosis using a solid lipid nanocomplex-embedded inulin gel (SLN/Que&OA@Gel) for colon-targeted UC therapy; solid lipid was utilized to encapsulate oleic acid (OA) and quercetin (Que) for better intestinal bioavailability, which was further embedded in an inulin gel to realize colon targeting. The system combines OA─which modulates lipid composition to reduce ferroptosis susceptibility─with Que, an antioxidant that scavenges reactive oxygen species (ROS) and suppresses oxidative stress to limit ferroptosis progression. Simultaneously, the incorporation of the inulin gel matrix ensures gastrointestinal tract protection, mucoadhesion, prolonged retention time at the lesion site, and sustained drug release, which promise a better curative effect. In vivo studies demonstrate that SLN/Que&OA@Gel effectively remodels the UC-associated pathological microenvironment by alleviating intestinal damage, restoring intestinal barrier integrity, and reducing inflammation. This strategy of synergistic regulation of ferroptosis and microenvironment remodeling presents a promising therapeutic avenue for UC management.
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