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多酶样纳米酶包裹的眼部微针用于角膜炎治疗。

Multienzyme-Like Nanozyme Encapsulated Ocular Microneedles for Keratitis Treatment.

机构信息

College of Materials Science and Engineering, Qingdao University of Science and Technology, 53 Zhengzhou Road, Qingdao, Shandong, 266042, China.

College of Chemical Engineering, Qingdao University of Science and Technology, 53 Zhengzhou Road, Qingdao, Shandong, 266042, China.

出版信息

Small. 2024 May;20(21):e2308403. doi: 10.1002/smll.202308403. Epub 2023 Dec 15.

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/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.

摘要

角膜炎是由细菌或真菌感染引起的角膜炎症,是导致严重视力障碍和失明的主要原因之一。角膜炎的治疗需要预防感染和减轻炎症。然而,由于其治疗功能有限,除了眼部屏障外,现有的常规药物的疗效差、生物利用度低,需要高剂量或频繁的局部治疗,这给患者带来了负担,并增加了副作用的风险。在这项研究中,开发了氧化锰纳米簇修饰的石墨炔纳米片(MnO/GDY)作为多酶样纳米酶,用于治疗感染性角膜炎,并将其装载到透明质酸和聚甲基丙烯酸甲酯基眼部微针(MGMN)中。MGMN 不仅由于其具有氧化酶、过氧化物酶、过氧化氢酶和超氧化物歧化酶模拟物等多酶样活性而具有抗菌和抗炎作用,而且还可以通过微针系统穿过眼部屏障并增加生物利用度。此外,在体外、离体和体内实验中,MGMN 被证明可以消除病原体、防止生物膜形成、减轻炎症、缓解眼部缺氧并促进角膜上皮损伤的修复,从而提供比商业眼科伏立康唑更好的治疗效果,且没有明显的微生物耐药性或细胞毒性。

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