新出现的脂质体治疗糖尿病视网膜病变:新的靶向方法和视网膜健康结果的进展综述。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2025-12-01 Epub Date: 2025-05-29 DOI:10.1080/10717544.2025.2509973
Ravi Parashar, Preeti K Suresh
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引用次数: 0

摘要

糖尿病性视网膜病变(DR)是导致永久性视力丧失的主要原因,影响着全球数百万人。目前的治疗方法,包括玻璃体内抗血管内皮生长因子(VEGF)药物和激光光凝,都受到频繁给药和副作用的限制。脂质体具有包裹亲水和疏水药物的能力,可提供量身定制的给药、延长释放时间和低全身毒性。本研究着眼于解决DR多因素病因的脂质体制剂的进展,包括抗血管生成、抗炎和抗氧化过程。我们评估新的制备方法(如超临界CO2,微流体)和临床考虑,包括稳定性和成本效益。为了解决DR的异质性,未来的努力将优先考虑组合药物和定制治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging liposomal therapies for diabetic retinopathy: a review of novel targeting approaches and advances in retinal health outcomes.

Diabetic retinopathy (DR), which affects over millions of individuals globally, is the leading cause of permanent visual loss. Current therapies, including as intravitreal anti-vascular endothelial growth factor (VEGF) medications and laser photocoagulation, are limited by frequent dosing and side effects. Liposomes, with their ability to encapsulate hydrophilic and hydrophobic medications, offer tailored delivery, prolonged release, and low systemic toxicity. This study looks at advances in liposomal formulations that address DR's multifactorial etiology, including as anti-angiogenic, anti-inflammatory, and antioxidant processes. We assess new preparation methods (e.g. supercritical CO2, microfluidics) and clinical considerations, including stability and cost-effectiveness. To address the heterogeneity of DR, future endeavors will prioritize combinatorial medications and customized therapy.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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