PEGylated nanoparticles for biological and pharmaceutical applications

被引:1177
作者
Otsuka, H
Nagasaki, Y
Kataoka, K
机构
[1] Univ Tokyo, Dept Mat Sci & Engn, Grad Sch Engn, Tokyo 1138656, Japan
[2] Natl Inst Mat Sci, Ctr Biomat, Tsukuba, Ibaraki 3050044, Japan
[3] Tokyo Univ Sci, Dept Mat Sci, Noda, Chiba 2788510, Japan
关键词
poly(ethylene glycol); block copolymers; biological and biomedical applications;
D O I
10.1016/S0169-409X(02)00226-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The utility of polymeric micelles formed through the multimolecular assembly of block copolymer was comprehensively described as novel core-shell typed colloidal carriers for drug and gene targeting. Particularly, novel approaches for the formation of functionalized poly(ethylene glycol) (PEG) layers as hydrophilic outer shell were focused to attain receptor-mediated drug and gene delivery through PEG-conjugated ligands with a minimal non-specific interaction with other proteins. Surface organization of block copolymer micelles with cross-linking core was also described from a standpoint of the preparation of a new functional surface-coating with a unique macromolecular architecture. The micelle-attached surface and the thin hydrogel layer made by layered micelles exhibited nonfouling properties and worked as the reservoir for hydrophobic reagents. Furthermore, the potential utility of multimolecular assembly derived from heterobifunctional PEGs and block copolymers were explored to systematically modify the properties of metal and semiconductor nanostructures by controlling their structure and their surface properties, making them extremely attractive for use in biological and biomedical applications. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:403 / 419
页数:17
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