黄斑变性
色素性视网膜炎
失明
视网膜
视力障碍
视网膜变性
医学
模式
重症监护医学
生物信息学
眼科
验光服务
生物
精神科
社会科学
社会学
作者
Matthew B. Appell,Jahnavi Pejavar,Ashwin Pasupathy,Sri Vishnu Kiran Rompicharla,Saed Abbasi,Kiersten Malmberg,Patricia Kolodziejski,Laura M. Ensign
标识
DOI:10.1016/j.jconrel.2024.01.063
摘要
Neurodegenerative diseases affecting the visual system encompass glaucoma, macular degeneration, retinopathies, and inherited genetic disorders such as retinitis pigmentosa. These ocular pathologies pose a serious burden of visual impairment and blindness worldwide. Current treatment modalities include small molecule drugs, biologics, or gene therapies, most of which are administered topically as eye drops or as injectables. However, the topical route of administration faces challenges in effectively reaching the posterior segment and achieving desired concentrations at the target site, while injections and implants risk severe complications, such as retinal detachment and endophthalmitis. This necessitates the development of innovative therapeutic strategies that can prolong drug release, deliver effective concentrations to the back of the eye with minimal systemic exposure, and improve patient compliance and safety. In this review, we introduce retinal degenerative diseases, followed by a discussion of the existing clinical standard of care. We then delve into detail about drug and gene delivery systems currently in preclinical and clinical development, including formulation and delivery advantages/drawbacks, with a special emphasis on potential for clinical translation.
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