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光激活抗血管联合疗法治疗脉络膜新生血管。

Light-Activated Anti-Vascular Combination Therapy against Choroidal Neovascularization.

机构信息

State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, 999077, China.

Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, 999077, China.

出版信息

Adv Sci (Weinh). 2024 Oct;11(40):e2404218. doi: 10.1002/advs.202404218. Epub 2024 Aug 29.

DOI:10.1002/advs.202404218
PMID:39206706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11516295/
Abstract

Choroidal neovascularization (CNV) underlies the crux of many angiogenic eye disorders. Although medications that target vascular endothelial growth factor (VEGF) are approved for treating CNV, their effectiveness in destroying new blood vessels is limited, and invasive intravitreal administration is required. Additionally, other drugs that destroy established neovessels, such as combretastatin A-4, may have systemic side effects that limit their therapeutic benefits. To overcome these shortcomings, a two-pronged anti-vascular approach is presented for CNV treatment using a photoactivatable nanoparticle system that can release a VEGF receptor inhibitor and a vascular disrupting agent when irradiated with 690 nm light. The nanoparticles can be injected intravenously to enable anti-angiogenic and vascular disrupting combination therapy for CNV through light irradiation to the eyes. This approach can potentiate therapeutic effects while maintaining a favorable biosafety profile for choroidal vascular diseases.

摘要

脉络膜新生血管(CNV)是许多血管生成性眼病的关键所在。虽然针对血管内皮生长因子(VEGF)的药物已被批准用于治疗 CNV,但它们在破坏新血管方面的效果有限,且需要进行侵入性的玻璃体内给药。此外,其他破坏已建立的新生血管的药物,如 combretastatin A-4,可能具有全身性副作用,限制了它们的治疗益处。为了克服这些缺点,提出了一种双管齐下的抗血管方法,用于 CNV 治疗,使用光活化纳米颗粒系统,当用 690nm 光照射时,可以释放 VEGF 受体抑制剂和血管破坏剂。这些纳米颗粒可以通过静脉注射,通过对眼睛进行光照射,实现抗血管生成和血管破坏联合治疗 CNV。这种方法可以增强治疗效果,同时保持对脉络膜血管疾病有利的生物安全性特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/a48f0c7ef86c/ADVS-11-2404218-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/89570f37aae5/ADVS-11-2404218-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/515cb926f1d2/ADVS-11-2404218-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/c40ca733fb39/ADVS-11-2404218-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/b1983c7026f6/ADVS-11-2404218-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/a48f0c7ef86c/ADVS-11-2404218-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/89570f37aae5/ADVS-11-2404218-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/515cb926f1d2/ADVS-11-2404218-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/c40ca733fb39/ADVS-11-2404218-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/b1983c7026f6/ADVS-11-2404218-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf3/11516295/a48f0c7ef86c/ADVS-11-2404218-g005.jpg

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