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Receptor-mediated gene delivery using chemically modified chitosan

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dc.contributor.authorKim, T. H.-
dc.contributor.authorJiang, H. L.-
dc.contributor.authorNah, J. W.-
dc.contributor.authorCho, M. H.-
dc.contributor.authorAkaike, T.-
dc.contributor.authorCho, C. S.-
dc.date.accessioned2021-01-31T08:40:45Z-
dc.date.available2021-01-31T08:40:45Z-
dc.date.created2018-04-11-
dc.date.issued2007-09-
dc.identifier.citationBiomedical Materials (Bristol), Vol.2 No.3, pp.S95-S100-
dc.identifier.issn1748-6041-
dc.identifier.other30998-
dc.identifier.urihttps://hdl.handle.net/10371/172347-
dc.description.abstractChitosan has been investigated as a non-viral vector because it has several advantages such as biocompatibility, biodegradability and low toxicity with high cationic potential. However, the low specificity and low transfection efficiency of chitosan need to be solved prior to clinical application. In this paper, we focused on the galactose or mannose ligand modification of chitosan for enhancement of cell specificity and transfection efficiency via receptor-mediated endocytosis in vitro and in vivo.-
dc.language영어-
dc.publisherInstitute of Physics Publishing-
dc.titleReceptor-mediated gene delivery using chemically modified chitosan-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.identifier.doi10.1088/1748-6041/2/3/S02-
dc.citation.journaltitleBiomedical Materials (Bristol)-
dc.identifier.wosid000249597800003-
dc.identifier.scopusid2-s2.0-34548424564-
dc.citation.endpageS100-
dc.citation.number3-
dc.citation.startpageS95-
dc.citation.volume2-
dc.identifier.sci000249597800003-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorCho, M. H.-
dc.contributor.affiliatedAuthorCho, C. S.-
dc.type.docTypeArticle; Proceedings Paper-
dc.description.journalClass1-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusTRANSFECTION-
dc.subject.keywordPlusHEPATOCYTES-
dc.subject.keywordPlusMACROPHAGES-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusVACCINES-
dc.subject.keywordPlusIMMUNITY-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

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