化学
炎症
角膜病
活性氧
角膜
促炎细胞因子
细胞因子
氧化损伤
医学
一氧化碳
角膜疾病
生物物理学
眼科
角膜上皮
发病机制
巨噬细胞极化
氧气
病理
角膜炎症
疾病
氧化磷酸化
药理学
眼病
角膜炎
氧化应激
癌症研究
兔形目
炎症反应
生物医学工程
作者
Hongjin Li,Bei Wang,C P Chen,柯浪,Jinfa Ye,Shundong Cai,Yun Han,Peiyu Wang,Gang Liu,Chengchao Chu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-07-13
卷期号:26 (28): 9151-9162
被引量:1
标识
DOI:10.1021/acs.nanolett.6c01749
摘要
Dry eye disease (DED) is a multifactorial ocular disorder driven by a reinforcing cycle of oxidative stress, inflammation, and epithelial damage, rendering single-target therapies ineffective. Here, we establish carbon monoxide (CO) gas therapy as a therapeutic modality for DED using a visible-light-activated nanoplatform, TiZr-MOF/CO@F127 (MCF), which simultaneously provides anti-inflammatory, antioxidant, and epithelial-reparative effects. A photosensitive TiZr-MOF loaded with a CO donor [BrMn(CO) 5 ] enables controlled CO release under visible light, while the thermosensitive F127 hydrogel prolongs corneal retention. In a murine DED model, topical administration of MCF for 5 days achieved 84% corneal epithelial recovery and alleviated corneal inflammation and tissue injury. Mechanistically, CO scavenged reactive oxygen species, suppressed MMP-9 expression, promoted macrophage polarization from M1 to M2 phenotype, reduced inflammatory cytokine production, and enhanced corneal epithelial proliferation. This study establishes a light-activated CO gas therapy strategy for DED and highlights the potential of responsive nanoplatforms for ocular surface disease treatment.
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