Target gene delivery from targeting ligand conjugated chitosan-PEI copolymer for cancer therapy

被引:73
作者
Nam, Joung-Pyo [1 ]
Nah, Jae-Woon [1 ]
机构
[1] Sunchon Natl Univ, Dept Polymer Sci & Engn, Sunchon, Jeollanam Do, South Korea
基金
新加坡国家研究基金会;
关键词
siRNA; Gene delivery carrier; Polysaccharide; Gene therapy; LOW-MOLECULAR-WEIGHT; CARBOXYMETHYL-CHITOSAN; IN-VITRO; BRANCHED POLYETHYLENIMINE; TRANSFECTION EFFICIENCY; DNA TRANSFECTION; DRUG-DELIVERY; BREAST-CANCER; EXPRESSION; VIVO;
D O I
10.1016/j.carbpol.2015.08.053
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this study, we designed a novel carrier which was having low cytotoxicity, site-specific target function, and high transfection efficiency using low molecular weight water soluble O-carboxymethyl chitosan (OCMCh), branched low molecular weight poly(ethyleneimine) (bPEI), and targeting ligand (epitope type, HER-2/neu). OCMCh/bPEI/targeting ligand, HPOCP copolymer, and targeting ligand-modified polyamphoteric polymer, and were prepared by chemical reaction and characterized by H-1 NMR and FT-IR. The binding affinity, protecting efficiency, and releasing ability of gene/HPOCP polyplex were confirmed by gel retardation assay. The pDNA(pEGFP)/HPOCP polyplexes showed high gene transfection efficiency in HCT 119 cell. In addition, siRNA/HPOCP polyplexes formed spherical shape and have particle sizes from 100 to 300 nm. The siRNA/HPOCP polyplexes have lower cytotoxicity than PEI in the all of siRNA concentrations ranging from 0 to 2 mu g/mu L in HEK 293 cells. The cell viability of siRNA/HPOCP polyplexes was performed in SK-Br3 cells with VEGF siRNA or BCL2 siRNA. In addition, confocal laser-scanning microscopy and flow cytometry assay were performed for cellular localization and cellular uptake efficiency of siRNA/HPOCP polyplexes. The results of the present study demonstrate that HPOCP copolymer is a good candidate as gene delivery carriers for gene delivery system or gene therapy. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:153 / 161
页数:9
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