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抗血管生成纳米胶束经皮递送达比非尼治疗视网膜新生血管疾病

Antiangiogenic Nanomicelles for the Topical Delivery of Aflibercept to Treat Retinal Neovascular Disease.

机构信息

Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), 61 Biopolis Drive, Singapore, 138 673, Singapore.

Department of Ophthalmology, National University Hospital, 1E Kent Ridge Road, NUHS Tower Block Level 7, Singapore, 119 228, Singapore.

出版信息

Adv Mater. 2022 Jun;34(25):e2108360. doi: 10.1002/adma.202108360. Epub 2021 Dec 2.

Abstract

The traditional intravitreal injection delivery of antivascular endothelial growth factor (anti-VEGF) to the posterior segment of the eye for treatment of retinal diseases is invasive and associated with sight-threatening complications. To avoid such complications, there has been significant interest in developing polymers for topical drug delivery to the retina. This study reports a nanomicelle drug delivery system made of a copolymer EPC (nEPCs), which is capable of delivering aflibercept to the posterior segment topically through corneal-scleral routes. EPC is composed of poly(ethylene glycol) (PEG), poly(propylene glycol) (PPG), and polycaprolactone (PCL) segments. In this study, aflibercept-loaded nEPCs (nEPCs + A) are capable of penetrating the cornea in ex vivo porcine eye models and deliver a clinically significant amount of aflibercept to the retina in laser-induced choroidal neovascularization (CNV) murine models, causing CNV regression. nEPCs + A also demonstrate biocompatibility in vitro and in vivo. Interestingly, this study also suggests that nEPCs have intrinsic antiangiogenic properties. The ability to deliver anti-VEGF drugs and the intrinsic antiangiogenic properties of nEPCs may result in synergistic effects, which can be harnessed for effective therapeutics. nEPCs may be a promising topical anti-VEGF delivery platform for the treatment of retinal diseases.

摘要

传统的将抗血管内皮生长因子(anti-VEGF)通过玻璃体内注射递送至眼底以治疗视网膜疾病的方法具有侵袭性,并且与威胁视力的并发症相关。为了避免此类并发症,人们对开发用于将药物递送至视网膜的聚合物类局部给药系统产生了浓厚兴趣。本研究报告了一种由共聚物 EPC(nEPCs)制成的纳米胶束药物递送系统,该系统能够通过角膜巩膜途径将阿柏西普递送至眼底局部。EPC 由聚乙二醇(PEG)、聚丙二醇(PPG)和聚己内酯(PCL)段组成。在本研究中,载阿柏西普的 nEPCs(nEPCs+A)能够穿透离体猪眼模型中的角膜,并将临床上有意义量的阿柏西普递送至激光诱导脉络膜新生血管(CNV)小鼠模型的视网膜中,从而导致 CNV 消退。nEPCs+A 在体外和体内也表现出良好的生物相容性。有趣的是,本研究还表明 nEPCs 具有内在的抗血管生成特性。递送抗 VEGF 药物的能力和 nEPCs 的内在抗血管生成特性可能会产生协同作用,从而可用于有效的治疗。nEPCs 可能成为一种有前途的用于治疗视网膜疾病的局部抗 VEGF 递送平台。

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