角膜炎
角膜
体内
隐形眼镜
离体
生物利用度
医学
微生物学
药理学
生物
皮肤病科
眼科
生物技术
作者
Shen Liu,Qiang Bai,Yujie Jiang,Yonghui Gao,Zhen Chen,Limin Shang,Siying Zhang,Linrong Yu,Dongqin Yang,Ning Sui,Zhiling Zhu
出处
期刊:Small
[Wiley]
日期:2023-12-15
卷期号:20 (21)
被引量:31
标识
DOI:10.1002/smll.202308403
摘要
Abstract Keratitis, an inflammation of the cornea caused by bacterial or fungal infections, is one of the leading causes of severe visual disability and blindness. Keratitis treatment requires both the prevention of infection and the reduction of inflammation. However, owing to their limited therapeutic functions, in addition to the ocular barrier, existing conventional medications are characterized by poor efficacy and low bioavailability, requiring high dosages or frequent topical treatment, which represents a burden on patients and increases the risk of side effects. In this study, manganese oxide nanocluster‐decorated graphdiyne nanosheets (MnO x /GDY) are developed as multienzyme‐like nanozymes for the treatment of infectious keratitis and loaded into hyaluronic acid and polymethyl methacrylate‐based ocular microneedles (MGMN). MGMN not only exhibits antimicrobial and anti‐inflammatory effects owing to its multienzyme‐like activities, including oxidase, peroxidase, catalase, and superoxide dismutase mimics but also crosses the ocular barrier and shows increased bioavailability via the microneedle system. Moreover, MGMN is demonstrated to eliminate pathogens, prevent biofilm formation, reduce inflammation, alleviate ocular hypoxia, and promote the repair of corneal epithelial damage in in vitro, ex vivo, and in vivo experiments, thus providing a better therapeutic effect than commercial ophthalmic voriconazole, with no obvious microbial resistance or cytotoxicity.
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