A facile method to prepare heparin-functionalized nanoparticles for controlled release of growth factors

被引:100
作者
Chung, YI
Tae, G
Yuk, SH
机构
[1] Gwangju Inst Sci & Technol, Dept Mat Sci & Engn, Kwangju 500712, South Korea
[2] Hannam Univ, Dept Polymer Sci & Engn, Taejon 306791, South Korea
关键词
heparin; pluronic; PLGA; nanoparticle; controlled release; growth factor;
D O I
10.1016/j.biomaterials.2005.11.043
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A new, facile method to prepare the heparin-functionalized PLGA nanoparticle (HEP-PLGA NP) for the controlled release of growth factors is developed. This system is composed of PLGA as a hydrophobic core, Pluronic F-127 as a hydrophilic surface layer, and heparin as the functional moiety. HEP-PLGA NPs were prepared by a solvent-diffusion method without chemical modification of the components. The entrapment of heparin molecules was confirmed by a negatively increased zeta potential value and the specific binding affinity to antithrombin III. The average diameter and the surface charge of the nanoparticles were ranged from 139 +/- 2 to 188 +/- 4 nm and from -26.0 +/- 1.1 to -44.1 +/- 1.3 mV by increasing the amount of heparin during the nanoparticle preparation. Accordingly, the amount of heparin on the nanoparticle increased from 0% to 4.7%. As a model in vitro release experiment, lysozyme was loaded into HEP-PLGA NPs. and a sustained release profile over 2 weeks was obtained with maintaining its bioactivity. The release of rhVEGF, one of the heparin-binding growth factors, showed a more sustained and prolonged profile than that of lysozyme over one month. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2621 / 2626
页数:6
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