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

被引:163
作者
Koo, Heebeom [1 ]
Moon, Hyungwon [2 ]
Han, Hyounkoo [2 ]
Na, Jin Hee [1 ]
Huh, Myung Sook [1 ]
Park, Jae Hyung [3 ]
Wood, Se Joon [4 ]
Park, Kyu Hyung [4 ]
Kwon, Ick Chan [1 ]
Kim, Kwangmeyung [1 ]
Kim, Hyuncheol [2 ]
机构
[1] Korea Inst Sci & Technol, Ctr Theragnosis, Biomed Res Inst, Seoul 136791, South Korea
[2] Sogang Univ, Seoul 121742, South Korea
[3] Sungkyunkwan Univ, Dept Polymer Sci & Engn, Suwon 440746, South Korea
[4] Seoul Natl Univ, Bundang Hosp, Coll Med, Dept Ophthalmol, Seongnarn 463707, South Korea
基金
新加坡国家研究基金会;
关键词
Ocular; Intravitreal; Nanoparticle; Drug delivery; Vitreous; Retina; GROWTH-FACTOR THERAPY; DRUG-DELIVERY; MACULAR DEGENERATION; TARGETED DELIVERY; GENE DELIVERY; ORGANIZATION; CHITOSAN; SYSTEM; SIRNA;
D O I
10.1016/j.biomaterials.2012.01.030
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页码:3485 / 3493
页数:9
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