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The Efficacy of Bone Morphogenetic Protein-2 Depends on Its Mode of Delivery

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dc.contributor.authorLa, Wan-Geun-
dc.contributor.authorKang, Sun-Woong-
dc.contributor.authorYang, Hee Seok-
dc.contributor.authorBhang, Suk Ho-
dc.contributor.authorLee, Sun Hwa-
dc.contributor.authorPark, Jung-Ho-
dc.contributor.authorKim, Byung-Soo-
dc.date.accessioned2024-06-13T02:18:29Z-
dc.date.available2024-06-13T02:18:29Z-
dc.date.created2018-06-19-
dc.date.created2018-06-19-
dc.date.issued2010-12-
dc.identifier.citationARTIFICIAL ORGANS, Vol.34 No.12, pp.1150-1153-
dc.identifier.issn0160-564X-
dc.identifier.urihttps://hdl.handle.net/10371/204351-
dc.description.abstractBone morphogenetic protein-2 (BMP-2) induces bone regeneration in a dose-dependent manner, with higher doses of BMP-2 inducing greater bone formation. Previously, we showed that long-term delivery of BMP-2 provides better ectopic bone formation than short-term delivery of an equivalent dose. In the present study, we investigated the efficacy of orthotopic bone formation over a range of BMP-2 doses, using different delivery modes. Heparin-conjugated poly(lactic-co-glycolic acid) nanospheres suspended in fibrin gel were used as a long-term delivery system, and fibrin gel was used as a short-term delivery system. Different doses of BMP-2 were delivered to mouse calvarial defects using either long-term or short-term delivery systems. Eight weeks after treatment, bone regeneration was evaluated by histomorphometry. For both delivery systems, bone regeneration increased as the BMP-2 dose increased up to 1 mu g and did not increase beyond this dose. Importantly, at BMP-2 doses higher than 1 mu g, long-term delivery resulted in much greater bone formation than short-term delivery. This study shows that long-term delivery of BMP-2 is more effective at enhancing orthotopic bone formation than short-term delivery over a range of doses.-
dc.language영어-
dc.publisherWILEY-BLACKWELL PUBLISHING, INC-
dc.titleThe Efficacy of Bone Morphogenetic Protein-2 Depends on Its Mode of Delivery-
dc.typeArticle-
dc.identifier.doi10.1111/j.1525-1594.2009.00988.x-
dc.citation.journaltitleARTIFICIAL ORGANS-
dc.identifier.wosid000285302600013-
dc.identifier.scopusid2-s2.0-78650038240-
dc.citation.endpage1153-
dc.citation.number12-
dc.citation.startpage1150-
dc.citation.volume34-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Byung-Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusSUSTAINED-RELEASE-
dc.subject.keywordPlusLONG-TERM-
dc.subject.keywordPlusREGENERATION-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusRHBMP-2-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorBMP-2 delivery-
dc.subject.keywordAuthorBone formation-
dc.subject.keywordAuthorFibrin gel-
dc.subject.keywordAuthorHeparin-conjugated poly(lactic-co-glycolic acid) nanosphere-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area biomaterials, nanomedicine, regenerative medicine

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