The movement of self-assembled amphiphilic polymeric nanoparticles in the vitreous and retina after intravitreal injection

Authors
Koo, HeebeomMoon, HyungwonHan, HyounkooNa, Jin HeeHuh, Myung SookPark, Jae HyungWood, Se JoonPark, Kyu HyungKwon, Ick ChanKim, KwangmeyungKim, Hyuncheol
Issue Date
2012-04
Publisher
ELSEVIER SCI LTD
Citation
BIOMATERIALS, v.33, no.12, pp.3485 - 3493
Abstract
The purpose of this study is to determine the correlation between the distribution of nanoparticles in the vitreous and retina and their surface properties after intravitreal injection. For this purpose, we synthesized seven kinds of nanoparticles through self-assembly of amphiphilic polymer conjugates in aqueous condition. They showed similar size but different surface properties. They were labeled with fluorescent dyes for efficient tracking. After intravitreal injection of these nanoparticles into a rodent eye, their time-dependent distribution in the vitreous and retina was determined in stacking tissue images by confocal microscopy. The results demonstrated that the surface property of nanoparticles is a key factor in determining their distribution in the vitreous and retina after intravitreal injection. In addition, immunohistochemistry and TEM images of retina tissues suggested the important mechanism related with Muffler cells for intravitreally administered nanoparticles to overcome the physical barrier of inner limiting membrane and to penetrate into the deeper retinal structures. Therefore, we expect that this study can provide valuable information for biomedical researchers to develop optimized nanoparticles as drug or gene carriers for retinal and optic nerve disorders such as glaucoma, age-related macular degeneration, and diabetic retinopathy. (C) 2012 Elsevier Ltd. All rights reserved.
Keywords
GROWTH-FACTOR THERAPY; DRUG-DELIVERY; MACULAR DEGENERATION; TARGETED DELIVERY; GENE DELIVERY; ORGANIZATION; CHITOSAN; SYSTEM; SIRNA; GROWTH-FACTOR THERAPY; DRUG-DELIVERY; MACULAR DEGENERATION; TARGETED DELIVERY; GENE DELIVERY; ORGANIZATION; CHITOSAN; SYSTEM; SIRNA; Ocular; Intravitreal; Nanoparticle; Drug delivery; Vitreous; Retina
ISSN
0142-9612
URI
https://pubs.kist.re.kr/handle/201004/129407
DOI
10.1016/j.biomaterials.2012.01.030
Appears in Collections:
KIST Article > 2012
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