Chitosan-graft-polyethylenimine as a gene carrier

被引:271
作者
Jiang, Hu-Lin
Kim, You-Kyoung
Arote, Rohidas
Nah, Jae-Woon
Cho, Myung-Haing
Choi, Yun-Jaie
Akaike, Toshihiro
Cho, Chong-Su [1 ]
机构
[1] Seoul Natl Univ, Sch Agr Biotechnol, Seoul 151921, South Korea
[2] Dept Polymer Sci & Engn, Sunchon 540742, South Korea
[3] Seoul Natl Univ, Coll Vet Med, Toxicol Lab, Seoul 151742, South Korea
[4] Tokyo Inst Technol, Dept Biomol Engn, Yokohama, Kanagawa 2268501, Japan
关键词
non-viral gene delivery; chitosan; polyethylenimine; chitosan-graft-PEI; cytotoxicity; transfection efficiency; gene therapy;
D O I
10.1016/j.jconrel.2006.10.025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chitosans have been proposed as biocompatible alternative cationic polymers that are suitable for non-viral delivery. However, the transfection efficiency of chitosan-DNA nanoparticles is still very low. To improve transfection efficiency, we prepared chitosan-graft-polyethylenimine (CHI-g-PEI) copolymer by an imine reaction between periodate-oxidized chitosan and polyethylenimine (PEI). The molecular weight and composition of the CHI-g-PEI copolymer were characterized, using multi-angle laser scattering (GPC-MALS) and H-1 nuclear magnetic resonance (H-1 NMR), respectively. The copolymer was complexed with plasmid DNA (pDNA) in various copolymer/DNA (N/P) charge ratios, and the complex was characterized. CHI-g-PEI showed good DNA binding ability and high protection of DNA from nuclease attack. Also, with an increase in charge ratio, the sizes of the CHI-g-PEI/DNA complex showed a tendency to decrease, whereas the zeta potential of the complex showed an increase. The CHI-g-PEI copolymer had low cytotoxicity, compared to PEI 25K from cytotoxicity assays. At high N/P ratios, the CHI-g-PEI/DNA complex showed higher transfection efficiency than PEI 25K in HeLa, 293T and HepG2 cell lines. Our results indicate that the CHI-g-PEI copolymer has potential as a gene carrier in vitro. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:273 / 280
页数:8
相关论文
共 30 条
[1]  
Anderson WF, 1998, NATURE, V392, P25
[2]   INHIBITION OF PROTEIN-KINASE-C BY CATIONIC AMPHIPHILES [J].
BOTTEGA, R ;
EPAND, RM .
BIOCHEMISTRY, 1992, 31 (37) :9025-9030
[3]   Gene delivery with synthetic (non viral) carriers [J].
Brown, MD ;
Schätzlein, AG ;
Uchegbu, IF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 229 (1-2) :1-21
[4]   Chitosan-based vector/DNA complexes for gene delivery: Biophysical characteristics and transfection ability [J].
Erbacher, P ;
Zou, SM ;
Bettinger, T ;
Steffan, AM ;
Remy, JS .
PHARMACEUTICAL RESEARCH, 1998, 15 (09) :1332-1339
[5]   A novel non-viral vector for DNA delivery based on low molecular weight, branched polyethylenimine:: Effect of molecular weight on transfection efficiency and cytotoxicity [J].
Fischer, D ;
Bieber, T ;
Li, YX ;
Elsässer, HP ;
Kissel, T .
PHARMACEUTICAL RESEARCH, 1999, 16 (08) :1273-1279
[6]   Poly(ethylenimine) and its role in gene delivery [J].
Godbey, WT ;
Wu, KK ;
Mikos, AG .
JOURNAL OF CONTROLLED RELEASE, 1999, 60 (2-3) :149-160
[7]   In vitro and in vivo gene delivery mediated by a synthetic polycationic amino polymer [J].
Goldman, CK ;
Soroceanu, L ;
Smith, N ;
Gillespie, GY ;
Shaw, W ;
Burgess, S ;
Bilbao, G ;
Curiel, DT .
NATURE BIOTECHNOLOGY, 1997, 15 (05) :462-466
[8]  
HUANG L, 1999, NONVIRAL VECTORS GEN, P3
[9]   Polyethylenimine-mediated gene delivery: a mechanistic study [J].
Kichler, A ;
Leborgne, C ;
Coeytaux, E ;
Danos, O .
JOURNAL OF GENE MEDICINE, 2001, 3 (02) :135-144
[10]   Synergistic effect of poly(ethylenimine) on the transfection efficiency of galactosylated chitosan/DNA complexes [J].
Kim, TH ;
Kim, SI ;
Akaike, T ;
Cho, CS .
JOURNAL OF CONTROLLED RELEASE, 2005, 105 (03) :354-366