活性氧
溃疡性结肠炎
姜黄素
化学
普鲁士蓝
结肠炎
药理学
表型
药品
巨噬细胞
癌症研究
生物化学
体外
医学
免疫学
疾病
病理
基因
电化学
物理化学
电极
作者
Hang Yao,Feifei Wang,Hui Chong,Jingjing Wang,Jing Wang,Meng Du,Xiaohui Yuan,Xiaofei Yang,Ming Wu,Yuping Li,Huan Pang
标识
DOI:10.1002/advs.202300601
摘要
Abstract Overexpression of classically activated macrophages (M1) subtypes and assessed reactive oxygen species (ROS) levels are often observed in patients with ulcerative colitis. At present, the treatment system of these two problems has yet to be established. Here, the chemotherapy drug curcumin (CCM) is decorated with Prussian blue analogs in a straightforward and cost‐saving manner. Modified CCM can be released in inflammatory tissue (acidic environment), eventually causing M1 macrophages to transform into M2 macrophages and inhibiting pro‐inflammatory factors. Co(III) and Fe(II) have abundant valence variations, and the lower REDOX potential in CCM‐CoFe PBA enables ROS clearance through multi‐nanomase activity. In addition, CCM‐CoFe PBA effectively alleviated the symptoms of UC mice induced by DSS and inhibited the progression of the disease. Therefore, the present material may be used as a new therapeutic agent for UC.
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