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Bio-inspired catechol conjugation converts water-insoluble chitosan into a highly water-soluble, adhesive chitosan derivative for hydrogels and LbL assembly

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dc.contributor.authorKim, Kyuri-
dc.contributor.authorRyu, Ji Hyun-
dc.contributor.authorLee, Dong Yun-
dc.contributor.authorLee, Haeshin-
dc.date.accessioned2022-07-16T09:08:33Z-
dc.date.available2022-07-16T09:08:33Z-
dc.date.created2021-05-12-
dc.date.issued2013-07-
dc.identifier.issn2047-4830-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/162370-
dc.description.abstractThis report describes a simple method to prepare water-soluble chitosan derivative by conjugation of an enediol group, catechol. Chitosan functionalized with a catechol-containing compound, 3,4-dihydroxy-hydrocinnamic acid, by a carbodiimide coupling method resulted in chitosan-catechol conjugates. This one-step chemical modification of high-molecular-weight chitosan (approximately 100 kDa) dramatically increased the water solubility of the chitosan derivative to 60 mg mL(-1) at pH 7.0. The degree of catechol conjugation was found critical in determining the solubility. The chitosan-catechol conjugates are not only water-soluble but are adhesive, due to the intrinsic adhesive properties of catechol. Also, the water-soluble chitosan derivative allows one to directly form chitosan hydrogel in neutral buffer solutions. The utility of both the water solubility and the adhesive property of the chitosan-catechol was demonstrated by the effective layer-by-layer assembly on substrates. The water-soluble chitosan-catechol is expected to be useful in many areas of surface functionalization, drug delivery, tissue engineering, and tissue adhesives.-
dc.language영어-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleBio-inspired catechol conjugation converts water-insoluble chitosan into a highly water-soluble, adhesive chitosan derivative for hydrogels and LbL assembly-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Dong Yun-
dc.identifier.doi10.1039/c3bm00004d-
dc.identifier.scopusid2-s2.0-84883230992-
dc.identifier.wosid000330136100011-
dc.identifier.bibliographicCitationBIOMATERIALS SCIENCE, v.1, no.7, pp.783 - 790-
dc.relation.isPartOfBIOMATERIALS SCIENCE-
dc.citation.titleBIOMATERIALS SCIENCE-
dc.citation.volume1-
dc.citation.number7-
dc.citation.startPage783-
dc.citation.endPage790-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusPOLY(ETHYLENE GLYCOL)-
dc.subject.keywordPlusMOLECULAR-WEIGHT-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusBIODISTRIBUTION-
dc.subject.keywordPlusTOXICITY-
dc.subject.keywordPlusIMPROVES-
dc.subject.keywordPlusDOPA-
dc.subject.keywordPlusPH-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2013/BM/c3bm00004d-
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