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Fabrication of a BMP-2-immobilized porous microsphere modified by heparin for bone tissue engineering

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dc.contributor.authorKim, Sung Eun-
dc.contributor.authorYun, Young-Pil-
dc.contributor.authorShim, Kyu-Sik-
dc.contributor.authorPark, Kyeongsoon-
dc.contributor.authorChoi, Sung-Wook-
dc.contributor.authorShin, Dong Hyup-
dc.contributor.authorSuh, Dong Hun-
dc.date.accessioned2021-09-04T11:47:34Z-
dc.date.available2021-09-04T11:47:34Z-
dc.date.created2021-06-10-
dc.date.issued2015-10-01-
dc.identifier.issn0927-7765-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/92228-
dc.description.abstractThe purpose of this study was to fabricate BMP-2-immobilized porous poly(lactide-co-glycolide) (PLGA) microspheres (PMS) modified with heparin for bone regeneration. A fluidic device was used to fabricate PMS and the fabricated PMS was modified with heparin-dopamine (Hep-DOPA). Bone morphogenic protein-2 (BMP-2) was immobilized on the heparinized PMS (Hep-PMS) via electrostatic interactions. Both PMS and modified PMS were characterized using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). MG-63 cell activity on PMS and modified PMS were assessed via alkaline phosphatase (ALP) activity, calcium deposition, and osteocalcin and osteopontin mRNA expression. Immobilized Hep-DOPA and BMP-2 on PMS were demonstrated by XPS analysis. BMP-2-immobilized Hep-PMS provided significantly higher ALP activity, calcium deposition, and osteocalcin and osteopontin mRNA expression compared to PMS alone. These results suggest that BMP-2-immobilized Hep-PMS effectively improves MG-63 cell activity. In conclusion, BMP-2-immobilized Hep-PMS can be used to effectively regenerate bone defects. (C) 2015 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectMESENCHYMAL STEM-CELLS-
dc.subjectMORPHOGENIC PROTEIN-2-
dc.subjectIN-VITRO-
dc.subjectPOLY(LACTIC-CO-GLYCOLIC ACID)-
dc.subjectOSTEOGENIC DIFFERENTIATION-
dc.subjectCONTROLLED-RELEASE-
dc.subjectPLGA MICROSPHERES-
dc.subjectIMMOBILIZATION-
dc.subjectSCAFFOLDS-
dc.subjectTITANIUM-
dc.titleFabrication of a BMP-2-immobilized porous microsphere modified by heparin for bone tissue engineering-
dc.typeArticle-
dc.contributor.affiliatedAuthorSuh, Dong Hun-
dc.identifier.doi10.1016/j.colsurfb.2015.05.003-
dc.identifier.scopusid2-s2.0-84938071385-
dc.identifier.wosid000362142000057-
dc.identifier.bibliographicCitationCOLLOIDS AND SURFACES B-BIOINTERFACES, v.134, pp.453 - 460-
dc.relation.isPartOfCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.citation.titleCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.citation.volume134-
dc.citation.startPage453-
dc.citation.endPage460-
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.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusMORPHOGENIC PROTEIN-2-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusPOLY(LACTIC-CO-GLYCOLIC ACID)-
dc.subject.keywordPlusOSTEOGENIC DIFFERENTIATION-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusPLGA MICROSPHERES-
dc.subject.keywordPlusIMMOBILIZATION-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusTITANIUM-
dc.subject.keywordAuthorBone morphogenic protein-2 (BMP-2)-
dc.subject.keywordAuthorPorous microspheres-
dc.subject.keywordAuthorFluidic device-
dc.subject.keywordAuthorHeparin-
dc.subject.keywordAuthorBone tissue engineering-
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