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Effects of the immobilization of heparin and rhPDGF-BB to titanium surfaces for the enhancement of osteoblastic functions and anti-inflammation

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dc.contributor.authorHuh, Jung-Bo-
dc.contributor.authorLee, Jeong-Yol-
dc.contributor.authorLee, Kyung-Lae-
dc.contributor.authorKim, Sung-Eun-
dc.contributor.authorYun, Mi-Jung-
dc.contributor.authorShim, Ji-Suk-
dc.contributor.authorShim, June-Sung-
dc.contributor.authorShin, Sang-Wan-
dc.date.accessioned2021-09-07T21:34:46Z-
dc.date.available2021-09-07T21:34:46Z-
dc.date.created2021-06-14-
dc.date.issued2011-
dc.identifier.issn2005-7806-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/114971-
dc.description.abstractPURPOSE. This study was to investigate the effects of recombinant human platelet-derived growth factor (rhPDGF-BB) and heparin to titanium surfaces for enhancement of osteoblastic functions and inhibition of inflammation activity. MATERIALS AND METHODS. The anodized titanium discs, not coated with any material, were used as a control group. In heparinized- Ti group, dopamine was anchored to the surface of Ti substrates, and coated with heparin. In PDGF-Ti group, rhPDGF-BB was immobilized onto heparinized Ti surface. The surface morphologies were investigated by the scanning electron microscope in each group. The release kinetics of rhPDGF-BB were analyzed, and cytotoxicity tests for each group were conducted. The biocompatibilities were characterized by measuring cell proliferation, alkaline phosphatase activity, and calcium deposition using MG-63 cells. Statistical comparisons were carried out by one-way ANOVA tests. Differences were considered statistically significant at *P<.05 and **P<.001. RESULTS. The combination of rhPDGF-BB and heparin stimulated alkaline phosphatase activity and OCN mRNA expression in osteoblastic cells (*P<.05 and **P<.001). MG-63 cells grown on PDGF-Ti had significantly higher amounts of calcium deposition than those grown on anodized Ti (**P<.001). Heparinized Ti was more anti-inflammatory compared to anodized Ti, when exposed to lipopolysaccharide using the transcript levels of TNF-alpha and IL-6 of proinflammatory cytokine (*P<.05 and **P<.001) CONCLUSION. The result of this study demonstrated that the incorporation of rhPDGF-BB and heparin onto Ti surface enhanced osteoblastic functions and inhibited inflammation. [J Adv Prosthodont 2011;3:152-60]-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN ACAD PROSTHODONTICS-
dc.subjectGROWTH-FACTOR-
dc.subjectPERIODONTAL REGENERATION-
dc.subjectCONTROLLED-RELEASE-
dc.subjectIMPLANT INTERFACE-
dc.subjectBONE-
dc.subjectPEPTIDE-
dc.subjectCOMBINATION-
dc.subjectEXPRESSION-
dc.subjectPROTEIN-2-
dc.subjectCOATINGS-
dc.titleEffects of the immobilization of heparin and rhPDGF-BB to titanium surfaces for the enhancement of osteoblastic functions and anti-inflammation-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Jeong-Yol-
dc.contributor.affiliatedAuthorKim, Sung-Eun-
dc.contributor.affiliatedAuthorShin, Sang-Wan-
dc.identifier.doi10.4047/jap.2011.3.3.152-
dc.identifier.scopusid2-s2.0-84883165789-
dc.identifier.wosid000309321900008-
dc.identifier.bibliographicCitationJOURNAL OF ADVANCED PROSTHODONTICS, v.3, no.3, pp.152 - 160-
dc.relation.isPartOfJOURNAL OF ADVANCED PROSTHODONTICS-
dc.citation.titleJOURNAL OF ADVANCED PROSTHODONTICS-
dc.citation.volume3-
dc.citation.number3-
dc.citation.startPage152-
dc.citation.endPage160-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001587230-
dc.description.journalClass1-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaDentistry, Oral Surgery & Medicine-
dc.relation.journalWebOfScienceCategoryDentistry, Oral Surgery & Medicine-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusPERIODONTAL REGENERATION-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusIMPLANT INTERFACE-
dc.subject.keywordPlusBONE-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROTEIN-2-
dc.subject.keywordPlusCOATINGS-
dc.subject.keywordAuthorTitanium-
dc.subject.keywordAuthorHeparin-
dc.subject.keywordAuthorrhPDGF-BB-
dc.subject.keywordAuthorAnti-inflammation-
dc.subject.keywordAuthorOsteoblastic function-
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