Gene Delivery Efficacy of Polyethyleneimine-Introduced Chitosan Shell/Poly(methyl Methacrylate) Core Nanoparticles for Rat Mesenchymal Stem Cells

被引:33
|
作者
Pimpha, Nuttaporn [2 ]
Sunintaboon, Panya [3 ]
Inphonlek, Supharat [3 ]
Tabata, Yasuhiko [1 ]
机构
[1] Kyoto Univ, Dept Biomat, Inst Frontier Med Sci, Sakyo Ku, Kyoto 6068507, Japan
[2] Natl Nanotechnol Ctr, Pathum Thani 12120, Thailand
[3] Mahidol Univ, Fac Sci, Dept Chem, Bangkok 10400, Thailand
关键词
Nanoparticles; chitosan; polyethyleneimine; mesenchymal stem cells; non-viral carrier; IN-VITRO; DNA NANOPARTICLES; POLYMER STRUCTURE; BONE; DIFFERENTIATION; MICROSPHERES; CARTILAGE; CARRIERS; SCAFFOLD; SYSTEM;
D O I
10.1163/156856209X415503
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This work investigated polyethyleneimine (PEI)-introduced chitosan (CS) (CS/PEI) nanoparticles as non-viral carrier of plasmid DNA for rat mesenchymal stem cells (MSCs). The CS/PEI nanoparticles were prepared by the emulsifier-free emulsion polymerization of methyl methacrylate monomer induced by a small amount of t-butyl hydroperxide in the presence of different concentrations of PEI mixed with CS. The resulting nanoparticles were characterized by their surface properties and buffering capacity. In vitro gene transfection was also evaluated. The introduction of PEI affected the surface charge, dispersing stability and buffering capacity of the nanoparticles. The CS/PEI nanoparticles formed a complex upon mixing with a plasmid DNA of luciferase. The complex enhanced the level of gene transfection and prolonged the time period of expression for MSCs, compared with those of plasmid DNA-original CS and PEI nanoparticles. Cytotoxicity of CS/PEI complexes with plasmid DNA was significantly low, depending on the amount of PEI introduced. It is concluded that the CS/PEI nanoparticle was a promising carrier for gene delivery of MSCs. (C) Koninklijke Brill NV, Leiden, 2010
引用
收藏
页码:205 / 223
页数:19
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