High-efficiency antioxidant ROS-responsive thermosensitive hydrogel encapsulated Fenofibrate for the treatment of corneal neovascularization

非诺贝特 角膜新生血管 化学 新生血管 抗氧化剂 PEG比率 药理学 血管生成 生物化学 医学 癌症研究 业务 财务
作者
Kai Fan,Dejun Yang,Xinyi Zhu,Lan Zheng,Yi Han,Jingwei Lin,Zixun Xiang,Yafei Guo,Keyu Tao,Juntong Li,Jia Qu,Yun‐Long Wu,Huaqiong Li,Cheng Li
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:382: 113650-113650 被引量:11
标识
DOI:10.1016/j.jconrel.2025.113650
摘要

Corneal neovascularization (CNV) has become one of the common blinding ocular diseases recognized worldwide, affecting millions of people every year. Numerous studies have shown that oxidative stress and inflammation are important factors for the occurrence and development of CNV. In the present study, we established an antioxidant and reactive oxygen species (ROS) responsive thermosensitive hydrogel for long-acting drug delivery, combining with the loaded anti-angiogenic drug to the therapy for CNV. Se-PEG-PPG (SePEP) could in-situ gelling on the ocular surface temperature and cover the ocular surface. The hydrophobic interaction between the selenium ether segment and ocular mucin will further increase its adhesion on the ocular surface, which is conducive to drug Fenofibrate (Feno) retention and sustained release on the ocular surface. SePEP also played a role in reducing intracellular oxidative stress and oxidative responsive sustained release drug due to its selenium ether groups that scavenge ROS. Finally, the combined anti-oxidation, anti-inflammation, and anti-angiogenesis therapeutic effect of Feno@Se-PEG-PPG (SePEP-Feno) eye drops were demonstrated in a corneal neovascularization animal model. In conclusion, the multifunctional delivery system provided a promising method for the treatment of CNV and various ROS-related ocular diseases.
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