Answers are grounded in this paper and cite their sources.
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.
No takes yet. Share an insight, caveat, or question.
Li et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: