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Cited 10 time in webofscience Cited 11 time in scopus
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Visible light-induced photocurable (forming a film) low molecular weight chitosan derivatives for biomedical applications: Synthesis, characterization and in vitro biocompatibility

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dc.contributor.authorSeo, Si Yoong-
dc.contributor.authorPark, Shin Hye-
dc.contributor.authorLee, Hyung Jae-
dc.contributor.authorNa, Ha Na-
dc.contributor.authorKim, Kwang Il-
dc.contributor.authorHan, Dong Keun-
dc.contributor.authorLee, Jae Kwan-
dc.contributor.authorIto, Yoshihiro-
dc.contributor.authorSon, Tae Il-
dc.date.available2019-05-29T05:40:01Z-
dc.date.issued2012-07-
dc.identifier.issn1226-086X-
dc.identifier.issn1876-794X-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20182-
dc.description.abstractIn this work, visible light-induced photocurable low molecular weight chitosan derivatives (F-LMC: furfuryl-low molecular weight chitosan) were prepared by nitrous acid decomposition followed by modification with furfuryl glycidyl ether. The structure of the decomposition products (LMC: low molecular weight chitosan) was characterized by FT-IR analysis. The structure and molecular weight of F-LMC, prepared from the decomposition products by modification with furfuryl glycidyl ether, were characterized by H-1 NMR and GPC analysis, respectively. F-LMC was initially water-soluble, but after the exposure to visible light, it became water-insoluble, indicating that F-LMC undergoes visible light-induced inter- and intra-molecular cross-linking. The cross-linking was determined by concentration of F-LMC and time of exposure to visible light. The cytotoxicity test using fibroblast 3T3 showed no toxicity of F-LMC. Cross-linked F-LMC surface inhibited cell adherence. (c) 2012 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE INC-
dc.titleVisible light-induced photocurable (forming a film) low molecular weight chitosan derivatives for biomedical applications: Synthesis, characterization and in vitro biocompatibility-
dc.typeArticle-
dc.identifier.doi10.1016/j.jiec.2012.01.006-
dc.identifier.bibliographicCitationJOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, v.18, no.4, pp 1258 - 1262-
dc.identifier.kciidART001685396-
dc.description.isOpenAccessN-
dc.identifier.wosid000306164400011-
dc.identifier.scopusid2-s2.0-84862811640-
dc.citation.endPage1262-
dc.citation.number4-
dc.citation.startPage1258-
dc.citation.titleJOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY-
dc.citation.volume18-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorChitosan-
dc.subject.keywordAuthorLow molecular weight chitosan-
dc.subject.keywordAuthorFurfuryl glycidyl ether-
dc.subject.keywordAuthorPhotocurable polymers-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusCHITIN-
dc.subject.keywordPlusBTDA-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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