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Osteoblast activity of MG-63 cells is enhanced by growth on a lactoferrin-immobilized titanium substrate

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dc.contributor.authorKim, Sung Eun-
dc.contributor.authorYun, Young-Pil-
dc.contributor.authorLee, Jae Yong-
dc.contributor.authorPark, Kyeongsoon-
dc.contributor.authorSuh, Dong Hun-
dc.date.accessioned2021-09-05T03:07:14Z-
dc.date.available2021-09-05T03:07:14Z-
dc.date.created2021-06-15-
dc.date.issued2014-11-01-
dc.identifier.issn0927-7765-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/96809-
dc.description.abstractThe aim of this study was to develop a lactoferrin (LF)-immobilized titanium (Ti) substrate to enhance the osteoblast activity of MG-63 cells. Ti substrates were first modified through heparin-dopamine (Hep-DOPA) anchorage. Then, LF was immobilized on the Hep-Ti substrates via electrostatic interactions. Hep-Ti substrates, with or without LF, were evaluated by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and contact angle measurements. Sustained release of LF on the Ti substrates was observed over a 28-day period. In vitro studies of osteoblast activity showed increased alkaline phosphatase activity and calcium deposition by MG-63 cells cultured on LF-immobilized Ti substrates as compared to those cultured on pristine Ti substrates, indicating that LF-immobilized Ti substrates were effective at enhancing osteoblast activity. (C) 2014 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.subjectBONE MORPHOGENETIC PROTEIN-2-
dc.subjectOSTEOGENIC DIFFERENTIATION-
dc.subjectSURFACE FUNCTIONALIZATION-
dc.subjectDELIVERY-SYSTEMS-
dc.subjectIN-VITRO-
dc.subjectIMPLANT-
dc.subjectREGENERATION-
dc.subjectHYDROGEL-
dc.subjectHEPARIN-
dc.subjectHYDROXYAPATITE-
dc.titleOsteoblast activity of MG-63 cells is enhanced by growth on a lactoferrin-immobilized titanium substrate-
dc.typeArticle-
dc.contributor.affiliatedAuthorSuh, Dong Hun-
dc.identifier.doi10.1016/j.colsurfb.2014.09.014-
dc.identifier.scopusid2-s2.0-84915752700-
dc.identifier.wosid000347580500025-
dc.identifier.bibliographicCitationCOLLOIDS AND SURFACES B-BIOINTERFACES, v.123, pp.191 - 198-
dc.relation.isPartOfCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.citation.titleCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.citation.volume123-
dc.citation.startPage191-
dc.citation.endPage198-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusBONE MORPHOGENETIC PROTEIN-2-
dc.subject.keywordPlusOSTEOGENIC DIFFERENTIATION-
dc.subject.keywordPlusSURFACE FUNCTIONALIZATION-
dc.subject.keywordPlusDELIVERY-SYSTEMS-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusIMPLANT-
dc.subject.keywordPlusREGENERATION-
dc.subject.keywordPlusHYDROGEL-
dc.subject.keywordPlusHEPARIN-
dc.subject.keywordPlusHYDROXYAPATITE-
dc.subject.keywordAuthorTitanium-
dc.subject.keywordAuthorLactoferrin-
dc.subject.keywordAuthorHeparin-dopamine-
dc.subject.keywordAuthorOsteoblast-
dc.subject.keywordAuthorOsteogenic differentiation-
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