生物正交化学
青光眼
工厂(面向对象编程)
化学
纳米技术
组合化学
计算机科学
医学
材料科学
眼科
点击化学
程序设计语言
作者
Yuan Liang,Yi Tian,Jiamin Liu,Pengpeng Lei,Xinghuai Sun,Hongjie Zhang,Yuan Lei
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-03-18
标识
DOI:10.1021/acs.nanolett.5c00607
摘要
Glaucoma is characterized by high intraocular pressure (IOP), oxidative stress, and distinct optic nerve damage. Natural enzymes have unparalleled advantages in the treatment of glaucoma due to their high efficiency, specificity, and selectivity. However, their poor stability and recoverability have constrained their application. The selection of good immobilization carriers is an effective strategy to protect natural enzymes. Here, we employ a mild room-temperature aqueous-phase enzyme immobilization technique to immobilize superoxide dismutase and catalase. Then, l-arginine is added to the pores and further modified with DSPE-mPEG to construct a bioorthogonal catalytic factory (SC@COF-L-D) with excellent biocompatibility. This strategy greatly protects the natural enzyme from inactivation and improves the operational stability. SC@COF-L-D can scavenge a large amount of reactive oxygen species to reduce oxidative/nitrative damage and activate the soluble guanylate cyclase pathway, thereby lowering the IOP for effective treatment of glaucoma. This work provides a paradigm for the design of materials for glaucoma therapy.
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