Preparation of monodisperse and size-controlled poly(ethylene glycol) hydrogel nanoparticles using liposome templates

被引:50
|
作者
An, Se Yong [1 ]
Bui, Minh-Phuong Ngoc [1 ]
Nam, Yun Jung [1 ]
Han, Kwi Nam [1 ]
Li, Cheng Ai [1 ]
Choo, Jaebum [1 ]
Lee, Eun Kyu [2 ]
Katoh, Shigeo [2 ]
Kumada, Yoichi [3 ]
Seong, Gi Hun [1 ]
机构
[1] Hanyang Univ, Dept Appl Chem, Ansan 426791, South Korea
[2] Hanyang Univ, Dept Chem Engn, Ansan 426791, South Korea
[3] Kyoto Inst Technol, Dept Chem & Mat Technol, Kyoto 6068585, Japan
关键词
Liposome; Hydrogel; Photopolymerization; Poly(ethylene glycol) (PEG); POLYMERIC NANOPARTICLES; UNILAMELLAR LIPOSOMES; MICROFLUIDIC SYSTEMS; DELIVERY; PHOTOPOLYMERIZATION; FABRICATION; PARTICLES; BIOCOMPATIBILITY; MICROPARTICLES; MICROSPHERES;
D O I
10.1016/j.jcis.2008.11.022
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Liposomes were used as templates to prepare size-controlled and monodisperse poly(ethylene glycol) (PEG) hydrogel nanoparticles. The procedure for the preparation of PEG nanoparticles using liposomes consists of encapsulation of photopolymerizable PEG hydrogel solution into the cavity of the liposomes, extrusion through a membrane with a specific pore size, and photopolymerization of the contents inside the liposomes by UV irradiation. The size distributions of the prepared particles were 1.32 +/- 0.16 mu m (12%), 450 +/- 62 nm (14%), and 94 +/- 12 nm (13%) after extrusion through membrane filters with pore sizes of I pm, 400 nm, and 100 nm, respectively. With this approach, it is also possible to modify the surface of the hydrogel nanoparticles with various functional groups in a one-step procedure. To functionalize the surface of a PEG nanoparticle, methoxy poly(ethylene glycol)-aldehyde was added as copolymer to the hydrogel-forming components and aldehyde-functionalized PEG nanoparticles could be obtained easily by UV-induced photopolymerization, following conjugation with poly-L-lysine-FITC through amine-aldehyde coupling. The prepared PEG particles showed strong fluorescence from FITC on the edge of the particles using confocal Microscopy. The immobilization of biomaterials such as enzymes in hydrogel particles could be performed with loading beta-galactosidases during the hydration step for liposome preparation without additional procedures. The resorufin produced by applying resorufin beta-D-galactopyranoside as the substrate showed the fluorescence under the confocal Microscopy. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 103
页数:6
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