脂质体
阳离子聚合
阳离子脂质体
清除
化学
DNA
遗传增强
生物化学
有机化学
抗氧化剂
基因
作者
Juan Wang,Jialuo Zhang,Shujing Liu,Jing Tang,Jiajun Liu,Ying Huang,Huazhang Zeng,Yang Hu,Boxuan Li
标识
DOI:10.1016/j.cej.2025.167638
摘要
The increasing prevalence of dry eye disease (DED) necessitates the development of effective therapeutic approaches. Elevated cell-free DNA (cfDNA) is closely associated with ocular inflammation and is a key factor that underpins the pathogenesis of DED. However, scavenging cfDNA to mitigate inflammation for DED management remains underexplored. Here, we report a cfDNA scavenging approach aimed to effectively treat DED by developing a cationic liposome (cL) with robust DNA binding affinity, enhanced pre-corneal retention, and superior trans-corneal permeability. As demonstrated in a DED mouse model, the use of this approach restored normal tear secretion, reinstated corneal barrier functions, increased the counts of conjunctival goblet cells, and attenuated immune cell infiltration. This non-invasive treatment highlights a viable direction in DED therapy by targeting cfDNA scavenging and suggests cL as a potential therapeutic agent. This approach may be applicable to treating other inflammatory disorders characterized by elevated cfDNA levels.
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