| Literature DB >> 34726299 |
Xinxin Zhao1, Ivan Seah2, Kun Xue3, Wendy Wong2, Queenie Shu Woon Tan1, Xiaoxiao Ma1, Qianyu Lin3, Jason Y C Lim3, Zengping Liu1,4, Bhav Harshad Parikh1,4, Karishma N Mehta1,5, Joel Weijia Lai6, Binxia Yang1, Kim Chi Tran4, Veluchamy Amutha Barathi7,8, Kang Hao Cheong6,9, Walter Hunziker1, Xinyi Su1,2,4,7, Xian Jun Loh3.
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.Entities:
Keywords: angiogenesis inhibitors; drug carriers; drug delivery systems; micelles; ophthalmic solutions; retinal diseases
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Year: 2021 PMID: 34726299 DOI: 10.1002/adma.202108360
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849