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Chitosan-graft-polyethylenimine as a gene carrier

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dc.contributor.authorJiang, Hu-Lin-
dc.contributor.authorKim, You-Kyoung-
dc.contributor.authorArote, Rohidas-
dc.contributor.authorNah, Jae-Woon-
dc.contributor.authorCho, Myung-Haing-
dc.contributor.authorChoi, Yun-Jaie-
dc.contributor.authorAkaike, Toshihiro-
dc.contributor.authorCho, Chong-Su-
dc.date.accessioned2009-08-07T02:44:34Z-
dc.date.available2009-08-07T02:44:34Z-
dc.date.created2018-04-11-
dc.date.issued2007-02-
dc.identifier.citationJournal of Controlled Release, Vol.117 No.2, pp.273-280-
dc.identifier.issn0168-3659-
dc.identifier.other31184-
dc.identifier.urihttps://hdl.handle.net/10371/6467-
dc.description.abstractChitosans 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.-
dc.language영어-
dc.language.isoenen
dc.publisherElsevier BV-
dc.titleChitosan-graft-polyethylenimine as a gene carrier-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.identifier.doi10.1016/j.jconrel.2006.10.025-
dc.citation.journaltitleJournal of Controlled Release-
dc.identifier.wosid000244624100016-
dc.identifier.scopusid2-s2.0-33846471958-
dc.citation.endpage280-
dc.citation.number2-
dc.citation.startpage273-
dc.citation.volume117-
dc.identifier.sci000244624100016-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorCho, Myung-Haing-
dc.contributor.affiliatedAuthorChoi, Yun-Jaie-
dc.contributor.affiliatedAuthorCho, Chong-Su-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusLOW-MOLECULAR-WEIGHT-
dc.subject.keywordPlusTRANSFECTION EFFICIENCY-
dc.subject.keywordPlusGLYCOL) COPOLYMERS-
dc.subject.keywordPlusNONVIRAL VECTOR-
dc.subject.keywordPlusDNA DELIVERY-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusPOLY(ETHYLENIMINE)-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusACID-
dc.subject.keywordAuthornon-viral gene delivery-
dc.subject.keywordAuthorchitosan-
dc.subject.keywordAuthorpolyethylenimine-
dc.subject.keywordAuthorchitosan-graft-PEI-
dc.subject.keywordAuthorcytotoxicity-
dc.subject.keywordAuthortransfection efficiency-
dc.subject.keywordAuthorgene therapy-
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  • Department of Veterinary Medicine
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