溃疡性结肠炎
药理学
结肠炎
体内
炎症性肠病
活性氧
多酚
材料科学
自愈水凝胶
透明质酸
巨噬细胞极化
体外
下调和上调
去唾液酸糖蛋白受体
巨噬细胞
炎症
MMP9公司
和厚朴酚
肠粘膜
药物输送
癌症研究
细胞凋亡
促炎细胞因子
伤口愈合
化学
右旋糖酐
医学
控制释放
细胞外基质
作者
Lu Wang,Bingwen Zhou,jiale chen,Zhimin Fan,Lina Yin,Xiu Yu,Jinrong Zheng,Xueping Zheng
标识
DOI:10.1021/acsami.5c26043
摘要
polyphenols with boric acid-modified manganese dioxide nanosheets (MNS) into a hyaluronic acid-dopamine (HA-DA) matrix for targeted UC therapy. The designed hydrogel exhibited a three-dimensional porous architecture and mucoadhesive characteristics, facilitating the sustained release of therapeutic components in the colonic microenvironment. In vitro studies demonstrated synergistic therapeutic effects, including oxygen generation, reactive oxygen species (ROS) scavenging, and controlled polyphenols release. In vivo assessments using murine colitis models revealed that the hydrogel significantly mitigated disease progression, as evidenced by attenuated body weight loss, reduced disease activity index (DAI) scores, and suppression of colon shortening. Histopathological and immunofluorescence analyses further confirmed the restoration of the intestinal epithelial barrier through upregulation of tight junction proteins (Claudin-1 and ZO-1) and modulation of macrophage polarization (M1-to-M2 phenotype transition). This multifunctional hydrogel platform represents a promising strategy for the in situ delivery of natural polyphenols, offering a potent and targeted approach for UC intervention.
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