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Combination therapy with BMP-2 and BMSCs enhances bone healing efficacy of PCL scaffold fabricated using the 3D plotting system in a large segmental defect model

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dc.contributor.authorKang, Sun-Woong-
dc.contributor.authorBae, Ji-Hoon-
dc.contributor.authorPark, Su-A-
dc.contributor.authorKim, Wan-Doo-
dc.contributor.authorPark, Mi-Su-
dc.contributor.authorKo, You-Jin-
dc.contributor.authorJang, Hyon-Seok-
dc.contributor.authorPark, Jung-Ho-
dc.date.accessioned2021-09-06T18:12:59Z-
dc.date.available2021-09-06T18:12:59Z-
dc.date.created2021-06-18-
dc.date.issued2012-07-
dc.identifier.issn0141-5492-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/108074-
dc.description.abstractThe three-dimensional (3D) plotting system is a rapidly-developing scaffold fabrication method for bone tissue engineering. It yields a highly porous and inter-connective structure without the use of cytotoxic solvents. However, the therapeutic effects of a scaffold fabricated using the 3D plotting system in a large segmental defect model have not yet been demonstrated. We have tested two hypotheses: whether the bone healing efficacy of scaffold fabricated using the 3D plotting system would be enhanced by bone marrow-derived mesenchymal stem cell (BMSC) transplantation; and whether the combination of bone morphogenetic protein-2 (BMP-2) administration and BMSC transplantation onto the scaffold would act synergistically to enhance bone regeneration in a large segmental defect model. The use of the combined therapy did increase bone regeneration further as compared to that with monotherapy in large segmental bone defects.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectCELLS-
dc.subjectDEPOSITION-
dc.subjectSPONGES-
dc.subjectGROWTH-
dc.titleCombination therapy with BMP-2 and BMSCs enhances bone healing efficacy of PCL scaffold fabricated using the 3D plotting system in a large segmental defect model-
dc.typeArticle-
dc.contributor.affiliatedAuthorBae, Ji-Hoon-
dc.contributor.affiliatedAuthorJang, Hyon-Seok-
dc.contributor.affiliatedAuthorPark, Jung-Ho-
dc.identifier.doi10.1007/s10529-012-0900-0-
dc.identifier.scopusid2-s2.0-84862814802-
dc.identifier.wosid000305210900027-
dc.identifier.bibliographicCitationBIOTECHNOLOGY LETTERS, v.34, no.7, pp.1375 - 1384-
dc.relation.isPartOfBIOTECHNOLOGY LETTERS-
dc.citation.titleBIOTECHNOLOGY LETTERS-
dc.citation.volume34-
dc.citation.number7-
dc.citation.startPage1375-
dc.citation.endPage1384-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusDEPOSITION-
dc.subject.keywordPlusSPONGES-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorBone marrow-derived mesenchymal stem cells-
dc.subject.keywordAuthorBone morphogenetic protein-2-
dc.subject.keywordAuthorBone tissue engineering-
dc.subject.keywordAuthorPolycaprolactone scaffold-
dc.subject.keywordAuthor3D plotting system-
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