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The use of chitosan as a condensing agent to enhance emulsion-mediated gene transfer

Authors
Lee, Mi-KyungChun, Soo-KyungChoi, Woo-JeongKim, Jin-KiChoi, Sung-HeeKim, AdeleOungbho, KwunchitPark, Jeong-SookAhn, Woong ShickKim, Chong-Kook
Issue Date
May-2005
Publisher
ELSEVIER SCI LTD
Keywords
gene therapy; non-viral vectors; chitosan; emulsion; precondensed DNA
Citation
BIOMATERIALS, v.26, no.14, pp.2147 - 2156
Indexed
SCIE
SCOPUS
Journal Title
BIOMATERIALS
Volume
26
Number
14
Start Page
2147
End Page
2156
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/45999
DOI
10.1016/j.biomaterials.2004.07.008
ISSN
0142-9612
Abstract
Previously we have formulated a new cationic emulsion, composed of 3beta [N-(N",N"-dimethylaminoethane) carbamoyl] cholsterol and dioleoylphosphatidyl ethanolamine, castor oil and Tween 80, and it efficiently delivered plasmid DNA into various cancer cells with low toxicity. Chitosan is a natural cationic polysaccharide and is able to form polyelectrolyte complexes with DNA, in which the DNA is condensed and protected against nuclease degradation. Based on these facts. chitosan was used as a condensing agent to enhance the transfection efficiency of cationic emulsion-mediated gene delivery vehicle. The particle size. zeta potential and transmission electron micrographs of DNA/emulsion complexes were observed before and after condensation by chitosan. In vitro transfection efficiency of naked or precondensed DNA/emulsion (pcDNA/E) complexes was investigated in human hepatoma cells (HepG2) using flow cytometer, confocal microscope and western blot. In addition. in vivo gene transfer was also evaluated as GFP mRNA expression by reverse transcriptase-polymerase chain reaction. The size of transfection complexes was reduced after the condensation of DNA by chitosan. Moreover. when the pcDNA/E complexes were administered into the mice. the GFP mRNA expression was prolonged in liver and lung until day 6. These results suggest that the use of chitosan enhance the in vitro transfection efficiency and extend in vivo gene transfer. (C) 2004 Elsevier Ltd. All rights reserved.
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