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Bone formation of middle ear cavity using biphasic calcium phosphate lyophilized with Escherichia coli-derived recombinant human bone morphogenetic protein 2 using animal model

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dc.contributor.authorKim, Sung Eun-
dc.contributor.authorYun, Young-Pil-
dc.contributor.authorSong, Hae-Ryong-
dc.contributor.authorChoi, Kyung-Hee-
dc.contributor.authorKim, Bo Hae-
dc.contributor.authorLee, Eun Kyeung-
dc.contributor.authorSong, Jae-Jun-
dc.date.accessioned2021-09-05T22:02:25Z-
dc.date.available2021-09-05T22:02:25Z-
dc.date.created2021-06-14-
dc.date.issued2013-09-
dc.identifier.issn0165-5876-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102242-
dc.description.abstractObjective: The aim of the study was to analyze the value of Escherichia coli-derived recombinant human bone morphogenetic protein-2 (ErhBMP-2) coated biphasic calcium phosphate (BCP) for the obliteration of middle ear bone defect after mastoid surgery. Methods: Twenty-four specific pathogen-free Sprague-Dawley rats were randomly assigned to the BCP group (n = 12) and BCP-ErhBMP-2 group (n = 12; in which BCP scaffold of the granular type was coated with ErhBMP-2). In both groups, BCP scaffold was used to surgically fill the middle ear bulla. New bone formation was evaluated by measuring bone density (%) after 4 and 8 weeks in all rats in both groups. Results: At 4 weeks, new bone was visible at the periphery and center of the middle ear cavity in both groups. In the BCP group, a moderate amount of fibrous tissue had infiltrated into the interspace of the scaffolds. New bone almost totally filled the interspace in the BCP-ErhBMP-2 group. At 8 weeks, copious new bone formation had occurred. Histometric measurements showed that bone density in the BCP group was smaller than in the BCP-ErhBMP-2 group at 4 weeks (25.10% and 38.43%, respectively; p < 0.05) and 8 weeks (25.54% and 34.18%, respectively; p < 0.05). Conclusions: New bone formation was greater in the presence of BCP-ErhBMP-2 scaffolds. ErhBMP-2 coated BCP scaffolds is a potentially useful material for middle ear obliteration after mastoidectomy. (C) 2013 Elsevier Ireland Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectMASTOID OBLITERATION-
dc.subjectHYDROXYAPATITE CEMENT-
dc.subjectCANAL WALL-
dc.subjectRECONSTRUCTION-
dc.subjectDELIVERY-
dc.subjectRHBMP-2-
dc.subjectFLAP-
dc.titleBone formation of middle ear cavity using biphasic calcium phosphate lyophilized with Escherichia coli-derived recombinant human bone morphogenetic protein 2 using animal model-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Sung Eun-
dc.contributor.affiliatedAuthorSong, Hae-Ryong-
dc.identifier.doi10.1016/j.ijporl.2013.05.035-
dc.identifier.scopusid2-s2.0-84882620081-
dc.identifier.wosid000324363400009-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, v.77, no.9, pp.1430 - 1433-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY-
dc.citation.titleINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY-
dc.citation.volume77-
dc.citation.number9-
dc.citation.startPage1430-
dc.citation.endPage1433-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOtorhinolaryngology-
dc.relation.journalResearchAreaPediatrics-
dc.relation.journalWebOfScienceCategoryOtorhinolaryngology-
dc.relation.journalWebOfScienceCategoryPediatrics-
dc.subject.keywordPlusMASTOID OBLITERATION-
dc.subject.keywordPlusHYDROXYAPATITE CEMENT-
dc.subject.keywordPlusCANAL WALL-
dc.subject.keywordPlusRECONSTRUCTION-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusRHBMP-2-
dc.subject.keywordPlusFLAP-
dc.subject.keywordAuthorOtitis media-
dc.subject.keywordAuthorMastoid obliteration-
dc.subject.keywordAuthorScaffold-
dc.subject.keywordAuthorBone morphogenetic protein-
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