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231225s2022 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202108360
|2 doi
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|a pubmed24n1108.xml
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|a (NLM)34726299
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Zhao, Xinxin
|e verfasserin
|4 aut
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|a Antiangiogenic Nanomicelles for the Topical Delivery of Aflibercept to Treat Retinal Neovascular Disease
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 24.06.2022
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|a Date Revised 24.06.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2021 Wiley-VCH GmbH.
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|a 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
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|a Journal Article
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|a angiogenesis inhibitors
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|a drug carriers
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|a drug delivery systems
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|a micelles
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|a ophthalmic solutions
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|a retinal diseases
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|a Angiogenesis Inhibitors
|2 NLM
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|a Recombinant Fusion Proteins
|2 NLM
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|a Vascular Endothelial Growth Factor A
|2 NLM
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|a aflibercept
|2 NLM
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|a 15C2VL427D
|2 NLM
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|a Receptors, Vascular Endothelial Growth Factor
|2 NLM
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|a EC 2.7.10.1
|2 NLM
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|a Seah, Ivan
|e verfasserin
|4 aut
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|a Xue, Kun
|e verfasserin
|4 aut
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|a Wong, Wendy
|e verfasserin
|4 aut
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|a Tan, Queenie Shu Woon
|e verfasserin
|4 aut
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|a Ma, Xiaoxiao
|e verfasserin
|4 aut
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|a Lin, Qianyu
|e verfasserin
|4 aut
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|a Lim, Jason Y C
|e verfasserin
|4 aut
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|a Liu, Zengping
|e verfasserin
|4 aut
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|a Parikh, Bhav Harshad
|e verfasserin
|4 aut
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|a Mehta, Karishma N
|e verfasserin
|4 aut
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|a Lai, Joel Weijia
|e verfasserin
|4 aut
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|a Yang, Binxia
|e verfasserin
|4 aut
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|a Tran, Kim Chi
|e verfasserin
|4 aut
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|a Barathi, Veluchamy Amutha
|e verfasserin
|4 aut
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|a Cheong, Kang Hao
|e verfasserin
|4 aut
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|a Hunziker, Walter
|e verfasserin
|4 aut
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|a Su, Xinyi
|e verfasserin
|4 aut
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|a Loh, Xian Jun
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 34(2022), 25 vom: 02. Juni, Seite e2108360
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
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|g volume:34
|g year:2022
|g number:25
|g day:02
|g month:06
|g pages:e2108360
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|u http://dx.doi.org/10.1002/adma.202108360
|3 Volltext
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