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Osteoconductive Properties of a Volume-Stable Collagen Matrix in Rat Calvaria Defects: A Pilot Study

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dc.contributor.author이중석-
dc.date.accessioned2021-09-29T01:58:05Z-
dc.date.available2021-09-29T01:58:05Z-
dc.date.issued2021-07-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/184640-
dc.description.abstractVolume-stable collagen matrices (VSCM) are conductive for the connective tissue upon soft tissue augmentation. Considering that collagen has osteoconductive properties, we have investigated the possibility that the VSCM also consolidates with the newly formed bone. To this end, we covered nine rat calvaria circular defects with a VSCM. After four weeks, histology, histomorphometry, quantitative backscattered electron imaging, and microcomputed tomography were performed. We report that the overall pattern of mineralization inside the VSCM was heterogeneous. Histology revealed, apart from the characteristic woven bone formation, areas of round-shaped hypertrophic chondrocyte-like cells surrounded by a mineralized extracellular matrix. Quantitative backscattered electron imaging confirmed the heterogenous mineralization occurring within the VSCM. Histomorphometry found new bone to be 0.7 mm2 (0.01 min; 2.4 max), similar to the chondrogenic mineralized extracellular matrix with 0.7 mm2 (0.0 min; 4.2 max). Microcomputed tomography showed the overall mineralized tissue in the defect to be 1.6 mm3 (min 0.0; max 13.3). These findings suggest that in a rat cranial defect, VSCM has a limited and heterogeneous capacity to support intramembranous bone formation but may allow the formation of bone via the endochondral route.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMDPI AG-
dc.relation.isPartOfBIOMEDICINES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleOsteoconductive Properties of a Volume-Stable Collagen Matrix in Rat Calvaria Defects: A Pilot Study-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Periodontics (치주과학교실)-
dc.contributor.googleauthorKarol Alí Apaza Alccayhuaman-
dc.contributor.googleauthorStefan Tangl-
dc.contributor.googleauthorStéphane Blouin-
dc.contributor.googleauthorMarkus A Hartmann-
dc.contributor.googleauthorPatrick Heimel-
dc.contributor.googleauthorUlrike Kuchler-
dc.contributor.googleauthorJung-Seok Lee-
dc.contributor.googleauthorReinhard Gruber-
dc.identifier.doi10.3390/biomedicines9070732-
dc.contributor.localIdA03185-
dc.relation.journalcodeJ03914-
dc.identifier.eissn2227-9059-
dc.identifier.pmid34202317-
dc.subject.keywordbone regeneration-
dc.subject.keywordcollagen matrix-
dc.subject.keywordhistology-
dc.subject.keywordqBEI-
dc.subject.keywordvolume-stable collagen matrix-
dc.contributor.alternativeNameLee, Jung Seok-
dc.contributor.affiliatedAuthor이중석-
dc.citation.volume9-
dc.citation.number7-
dc.citation.startPage732-
dc.identifier.bibliographicCitationBIOMEDICINES, Vol.9(7) : 732, 2021-07-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Periodontics (치주과학교실) > 1. Journal Papers

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