Extended Intraocular Drug-Delivery Platforms for the Treatment of Retinal and Choroidal Diseases.

IF 0.5 Q4 OPHTHALMOLOGY Journal of VitreoRetinal Diseases Pub Date : 2024-08-22 eCollection Date: 2024-09-01 DOI:10.1177/24741264241267065
Charles C Wykoff, Baruch D Kuppermann, Carl D Regillo, Margaret Chang, Seenu M Hariprasad, Jay S Duker, Syed Altaf, Saïd Saïm
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Abstract

Purpose: To review sustained-release intraocular platforms used to treat diseases of the retina and choroid. Methods: A literature review of the current applications of biomaterials for sustained-release therapy in retinal and choroidal diseases was performed. Results: Retinal and choroidal diseases, such as neovascular age-related macular degeneration (nAMD), diabetic retinopathy (DR), diabetic macular edema (DME), and uveitis, are commonly treated using intravitreal (IVT) therapies that require frequent IVT injections. Multiple sustained-release options for IVT therapy have been approved by the US Food and Drug Administration for the treatment of inflammatory eye diseases, including noninfectious uveitis, infectious diseases, and exudative retinal diseases (eg, retinal venous occlusive disease and DME) using drugs such as fluocinolone acetonide, ganciclovir, and dexamethasone. The platforms for these drugs are biodegradable or nonbiodegradable. They use biomaterials such as polymers and hydrogels and are typically implanted surgically or injected into the vitreous, where they release the drug gradually over months or years. Building on these technologies, novel platforms are being studied that are intended to treat conditions including nAMD, DR, DME, and uveitis. These platforms are being tested for their safety, efficacy, and ability to reduce the injection and visit burden. Conclusions: Multiple sustained-release ocular drug-delivery platforms are currently commercially available, and many new sustained-release IVT platforms are being investigated. The hope is that meaningfully reducing the injection burden by extending intervals between treatments while maintaining optimal efficacy will improve long-term outcomes.

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用于治疗视网膜和脉络膜疾病的扩展眼内给药平台。
目的:回顾用于治疗视网膜和脉络膜疾病的缓释眼内平台。方法:对目前用于视网膜和脉络膜疾病持续释放疗法的生物材料的应用进行文献综述。结果:视网膜和脉络膜疾病,如新生血管性老年性黄斑变性(nAMD)、糖尿病视网膜病变(DR)、糖尿病黄斑水肿(DME)和葡萄膜炎,通常采用需要频繁静脉注射的玻璃体内(IVT)疗法进行治疗。美国食品和药物管理局已经批准了多种静脉注射疗法的缓释方案,用于治疗炎症性眼病,包括非感染性葡萄膜炎、感染性疾病和渗出性视网膜疾病(如视网膜静脉闭塞症和 DME),使用的药物有氟西萘酮缩丙酮、更昔洛韦和地塞米松。这些药物的平台可生物降解或不可生物降解。它们使用聚合物和水凝胶等生物材料,通常通过手术植入或注射到玻璃体内,在数月或数年内逐渐释放药物。在这些技术的基础上,目前正在研究新型平台,旨在治疗包括nAMD、DR、DME和葡萄膜炎在内的疾病。目前正在测试这些平台的安全性、有效性以及减少注射和就诊负担的能力。结论目前市场上有多种缓释眼部给药平台,许多新的缓释静脉注射平台也在研究之中。希望通过延长治疗间隔时间,在保持最佳疗效的同时切实减轻注射负担,从而改善长期疗效。
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CiteScore
1.20
自引率
16.70%
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0
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From the Editor-in-Chief. Update on Retinal Drug Safety: Proceedings of the ASRS ReST Committee Webinar Part 1. Extended Intraocular Drug-Delivery Platforms for the Treatment of Retinal and Choroidal Diseases. Successful Treatment of Central Retinal Artery Occlusion With Tissue Plasminogen Activator Followed by Recurrent Retinal Ischemia 2024 Distinguished Contributor Awards.
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