Suppr超能文献

生物材料在抗 VEGF 持续释放中的应用治疗视网膜疾病。

Use of biomaterials for sustained delivery of anti-VEGF to treat retinal diseases.

机构信息

Department of Ophthalmology, National University Hospital Singapore, Singapore, Singapore.

Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

出版信息

Eye (Lond). 2020 Aug;34(8):1341-1356. doi: 10.1038/s41433-020-0770-y. Epub 2020 Jan 30.

Abstract

Anti-vascular endothelial growth factors (anti-VEGF) have become the most common treatment modality for many retinal diseases. These include neovascular age-related macular degeneration (n-AMD), proliferative diabetic retinopathy (PDR) and retinal vein occlusions (RVO). However, these drugs are administered via intravitreal injections that are associated with sight-threatening complications. The most feared of these complications is endophthalmitis, a severe infection of the eye with extremely poor visual outcomes. Patients with retinal diseases typically have to undergo multiple injections before achieving the desired therapeutic effect. Each injection incurs the risk of the sight-threatening complications. As such, there has been great interest in developing sustained delivery platforms for anti-VEGF agents to the posterior segment of the eye. In recent years, there have been various strategies that have been conceptualised. These include non-biodegradable implants, nano-formulations and hydrogels. In this review, the barriers of drug delivery to the posterior segment of the eye will be explained. The characteristics of an ideal sustained delivery platform will then be discussed. Finally, the current available strategies will be analysed with the above-mentioned characteristics in mind to determine the advantages and disadvantages of each sustained drug delivery modality. Through the above, this review attempts to provide an overview of the sustained delivery platforms in their various phases of development.

摘要

抗血管内皮生长因子(anti-VEGF)已成为许多视网膜疾病的最常见治疗方式。这些疾病包括新生血管性年龄相关性黄斑变性(n-AMD)、增生性糖尿病视网膜病变(PDR)和视网膜静脉阻塞(RVO)。然而,这些药物是通过玻璃体内注射给药的,这与威胁视力的并发症有关。这些并发症中最可怕的是眼内炎,这是一种严重的眼部感染,视力预后极差。患有视网膜疾病的患者通常需要多次注射才能达到理想的治疗效果。每次注射都有威胁视力的并发症的风险。因此,人们对开发用于眼部后段的抗 VEGF 药物的缓释递送平台产生了浓厚的兴趣。近年来,已经有了各种概念化的策略。这些策略包括不可生物降解的植入物、纳米制剂和水凝胶。在这篇综述中,将解释药物递送至眼部后段的障碍。然后将讨论理想的缓释递送平台的特征。最后,将根据上述特征分析当前可用的策略,以确定每种缓释药物递送方式的优缺点。通过以上内容,本综述试图概述各种开发阶段的缓释递送平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc7/7376230/f59b5e241b62/41433_2020_770_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验