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Improvement of Osteoblast Functions by Sustained Release of Bone Morphogenetic Protein-2 (BMP-2) from Heparin-coated Chitosan Scaffold

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dc.contributor.authorYun, Young-Pil-
dc.contributor.authorLee, Su-Young-
dc.contributor.authorKim, Hak-Jun-
dc.contributor.authorSong, Jae-Jun-
dc.contributor.authorKim, Sung Eun-
dc.date.accessioned2021-09-05T23:26:56Z-
dc.date.available2021-09-05T23:26:56Z-
dc.date.created2021-06-14-
dc.date.issued2013-08-
dc.identifier.issn1738-2696-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102641-
dc.description.abstractThe aim of this study was to investigate the improvement in osteoblast functions by using bone morphogenetic protein-2 (BMP-2) immobilized heparin-coated chitosan scaffolds and comparing it with that using chitosan scaffold or BMP-2/chitosan scaffold in vitro. BMP-2 was released from the heparin-coated chitosan scaffold in a sustained manner compared to that released from the chitosan scaffold. The osteoblast functions of MG-63 cells grown on the chitosan scaffold, the BMP-2/chitosan scaffold, the BMP-2/Hep/chitosan scaffold were investigated by assessing cell proliferation, alkaline phosphatase (ALP) activity, calcium deposition, and gene expression. The results of the in vitro studies demonstrated that MG-63 cells grown on the BMP-2/Hep/chitosan scaffold showed a significant increment in ALP activity, and calcium deposition as compared to those grown on the chitosan scaffold by sustained release of BMP-2 due to the influence of heparin. Therefore, BMP-2 immobilized heparin-coated chitosan scaffolds are promising materials for improving osteoblast functions through sustained release of BMP-2.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN TISSUE ENGINEERING REGENERATIVE MEDICINE SOC-
dc.subjectSTEM-CELLS-
dc.subjectDELIVERY-
dc.subjectENHANCEMENT-
dc.subjectTITANIUM-
dc.subjectFUNCTIONALIZATION-
dc.subjectTRANSPLANTATION-
dc.subjectIMMOBILIZATION-
dc.subjectMICROSPHERES-
dc.subjectINDUCTION-
dc.subjectHYDROGEL-
dc.titleImprovement of Osteoblast Functions by Sustained Release of Bone Morphogenetic Protein-2 (BMP-2) from Heparin-coated Chitosan Scaffold-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hak-Jun-
dc.contributor.affiliatedAuthorKim, Sung Eun-
dc.identifier.doi10.1007/s13770-013-0389-1-
dc.identifier.scopusid2-s2.0-84896723879-
dc.identifier.wosid000323082700005-
dc.identifier.bibliographicCitationTISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.10, no.4, pp.183 - 191-
dc.relation.isPartOfTISSUE ENGINEERING AND REGENERATIVE MEDICINE-
dc.citation.titleTISSUE ENGINEERING AND REGENERATIVE MEDICINE-
dc.citation.volume10-
dc.citation.number4-
dc.citation.startPage183-
dc.citation.endPage191-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001791137-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.description.journalRegisteredClassother-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryCell & Tissue Engineering-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusENHANCEMENT-
dc.subject.keywordPlusTITANIUM-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusTRANSPLANTATION-
dc.subject.keywordPlusIMMOBILIZATION-
dc.subject.keywordPlusMICROSPHERES-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusHYDROGEL-
dc.subject.keywordAuthorbone morphogenetic protein-2 (BMP-2)-
dc.subject.keywordAuthorheparin-
dc.subject.keywordAuthorosteoblast function-
dc.subject.keywordAuthorsustained release-
dc.subject.keywordAuthorchitosan scaffold-
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