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Galactosylated chitosan-g-PEI/DNA complexes-loaded poly(organophosphazene) hydrogel as a hepatocyte targeting gene delivery system

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dc.contributor.authorJiang, Hu-Lin-
dc.contributor.authorKim, You-Kyoung-
dc.contributor.authorLee, Sun-Mi-
dc.contributor.authorPark, Mi-Ran-
dc.contributor.authorKim, Eun-Mi-
dc.contributor.authorJin, Yong-Mei-
dc.contributor.authorArote, Rohidas-
dc.contributor.authorJeong, Hwan-Jeong-
dc.contributor.authorSong, Soo-Chang-
dc.contributor.authorCho, Myung-Haing-
dc.contributor.authorCho, Chong-Su-
dc.date.accessioned2021-01-31T08:38:07Z-
dc.date.available2021-01-31T08:38:07Z-
dc.date.created2018-01-19-
dc.date.issued2010-04-
dc.identifier.citationArchives of Pharmacal Research, Vol.33 No.4, pp.551-556-
dc.identifier.issn0253-6269-
dc.identifier.other24534-
dc.identifier.urihttps://hdl.handle.net/10371/172304-
dc.description.abstractHydrogels are widely used in drug delivery systems because they can control the release and thereby enhance the efficiency of locally delivered bioactive molecules such as therapeutic drugs, proteins, or genes. For gene delivery, localized release of plasmid DNA or polymer/DNA complexes can transfect cells and produce sustained protein production. We tested the galactosylated chitosan-graft-polyethylenimine (GC-g-PEI)/DNA complexes-loaded poly(organophosphazene) thermosensitive biodegradable hydrogel as a hepatocyte targeting gene delivery system. The poly(organophosphazene) hydrogel loaded with GC-g-PEI/DNA complexes showed low cytotoxicity and higher transfection efficiency than PEI/DNA complexes, as well as good hepatocyte specificity in vitro and in vivo. Our results indicate that poly(organophosphazene) hydrogels loaded with GC-g-PEI/DNA complexes may be a safe and efficient hepatocyte targeting gene delivery system.-
dc.language영어-
dc.publisher대한약학회-
dc.titleGalactosylated chitosan-g-PEI/DNA complexes-loaded poly(organophosphazene) hydrogel as a hepatocyte targeting gene delivery system-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.identifier.doi10.1007/s12272-010-0409-9-
dc.citation.journaltitleArchives of Pharmacal Research-
dc.identifier.wosid000276970700010-
dc.identifier.scopusid2-s2.0-77954504897-
dc.citation.endpage556-
dc.citation.number4-
dc.citation.startpage551-
dc.citation.volume33-
dc.identifier.sci000276970700010-
dc.identifier.kciidART001438345-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorArote, Rohidas-
dc.contributor.affiliatedAuthorCho, Myung-Haing-
dc.contributor.affiliatedAuthorCho, Chong-Su-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusDNA DELIVERY-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusBIOMEDICAL APPLICATIONS-
dc.subject.keywordPlusGRAFT-POLYETHYLENIMINE-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusCARRIER-
dc.subject.keywordPlusPOLYPHOSPHAZENES-
dc.subject.keywordPlusMATRICES-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordAuthorGene therapy-
dc.subject.keywordAuthorGalactosylated chitosan-g-polyethylenimine-
dc.subject.keywordAuthorPoly(organophosphazene) hydrogel-
dc.subject.keywordAuthorHepatocyte targeting-
dc.subject.keywordAuthorCytotoxicity-
dc.subject.keywordAuthorTransfection efficiency-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

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