ArticleDrug delivery and translational research2026
Sunitinib-eluting thin films for Inhibition of corneal neovascularization.
Article in Drug delivery and translational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Emerging ophthalmic drug delivery.Drug delivery and translational research · 2026Article
Corrections and comments
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Authors and funding
13 authors.
Funding
Abstract
Corneal disease is a leading cause of blindness globally, and is commonly associated with corneal neovascularization, which results in the loss of optical clarity and visual impairment. A wide variety of factors contribute to abnormal growth of new blood vessels into the cornea, including contact lens wear, infectious keratitis, corneal graft rejection, inflammatory disorders and trauma. In each case, proangiogenic factors such as vascular endothelial, platelet-derived, and fibroblast growth factors fuel new blood vessel growth and proliferation. Topical corticosteroids are a front-line treatment for corneal neovascularization, but require patient compliance and long-term use, which can limit efficacy and lead to increased intraocular pressure or cataract development, respectively. There is a need for a simple, effective treatment for corneal neovascularization that improves access and alleviates compliance issues. Here, biodegradable, sunitinib-loaded, nano- and micro-structured thin films were manufactured via electrospinning and applied topically in a rat model of corneal neovascularization. Thin films were characterized for morphology, mechanical and physicochemical properties, and drug release prior to in vivo assessment of biocompatibility and efficacy. Nano-structured thin films demonstrated sustained in vitro release of sunitinib for 30 days, provided sufficient strength for extended topical application, and were biocompatible on rat eyes. Importantly, sunitinib-loaded thin films inhibited corneal neovascularization more significantly than 3x daily sunitinib eye drops, as evidenced by greater reductions in vessel area, length, and vascular endothelial growth factor expression. This sustained drug-delivery platform has potential to provide a safe and effective treatment for ocular surface and corneal disorders.
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