A polymeric device for controlled transscleral multi-drug delivery to the posterior segment of the eye

被引:37
作者
Nagai, Nobuhiro [1 ]
Kaji, Hirokazu [2 ]
Onami, Hideyuki [1 ,3 ]
Ishikawa, Yumi [1 ]
Nishizawa, Matsuhiko [2 ]
Osumi, Noriko [4 ]
Nakazawa, Toru [3 ]
Abe, Toshiaki [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Div Clin Cell Therapy,United Ctr Adv Res & Transl, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Engn, Dept Bioengn & Robot, Aoba Ku, Sendai, Miyagi 9808579, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Ophthalmol, Aoba Ku, Sendai, Miyagi 9808574, Japan
[4] Tohoku Univ, Grad Sch Med, Div Dev Neurosci,United Ctr Adv Res & Translat Me, Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
Transscleral delivery; Multi-drug delivery; Retina; Poly(ethyleneglycol) dimethacrylate; DRUG-DELIVERY; MACULAR DEGENERATION; RELEASE; HYDROGEL; RETINA; SYSTEM; AGE; PERMEABILITY; EPITHELIUM; MOUSE;
D O I
10.1016/j.actbio.2013.11.004
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The design of drug delivery systems that can deliver multiple drugs to the posterior segment of the eye is a challenging task in retinal disease treatments. We report a polymeric device for multi-drug transscleral delivery at independently controlled release rates. The device comprises a microfabricated reservoir, controlled-release cover and three different fluorescent formulations, which were made of photopolymeized tri(ethyleneglycol)dimethacrylate (TEGDM) and poly(ethyleneglycol)dimethacrylate (PEGDM). The release rate of each fluorescent is controlled by varying the PEGDM/TEGDM ratio in its formulation and the cover. The release kinetics appeared to be related to the swelling ratio of the PEGDM/TEGDM polymers. When the devices were implanted onto rat sclerae, fluorescence was observable in the ocular tissues during 4 weeks' implantation and distributed locally around the implantation site. Our polymeric system, which can administer multiple compounds with distinct kinetics, provides prolonged action and less invasive transscleral administration, and is expected to provide new tools for the treatment of posterior eye diseases with new therapeutic modalities. (C) 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:680 / 687
页数:8
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