File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Ultrastructural identification of cells involved in the healing of intramembranous bone grafts in both the presence and absence of demineralised intramembranous bone matrix.

TitleUltrastructural identification of cells involved in the healing of intramembranous bone grafts in both the presence and absence of demineralised intramembranous bone matrix.
Authors
Issue Date2000
Citation
Australian Orthodontic Journal, 2000, v. 16 n. 2, p. 88-97 How to Cite?
AbstractAlveolar bone defects are conditions that impede the progress of orthodontic treatment. This study compared the mechanics of the healing of autogenous intramembranous (IM) bone grafts and grafts comprising a mixture of IM and demineralised bone matrix of autogenous intramembranous origin (DBMIM), in an attempt to determine the reliability of each material. Thirty-two New Zealand white rabbits had a single defect created in their skull. Sixteen were grafted with IM bone alone (Group I: autogenous IM), and the other 16 had a combined graft of composite IM sandwiched between two layers of DBMIM (Group II: composite IM-DBMIM). A third group (Group III) of eight rabbits each had two defects created in their skull; one defect was left empty (A: passive control) and the other filled with rabbit-skin collagen (B: active control). In Groups I and II, inflammatory cells were found to be present on Days 1 and 2 of tissue retrieval. The appearance of the mesenchymal cells and preosteoblasts, osteoblasts and osteocytes was earlier (Day 3) in Group II than in Group I (Day 5). In both groups, preosteoblasts, osteoblasts and osteocytes were observed with no cartilage at the intermediate stage. In conclusion, autogenous IM bone grafts and IM bone grafts in the presence of DBMIM healed through an osteogenic ossification route.
Persistent Identifierhttp://hdl.handle.net/10722/154109
ISSN
2018 Impact Factor: 0.269

 

DC FieldValueLanguage
dc.contributor.authorChay, SHen_HK
dc.contributor.authorRabie, ABen_HK
dc.contributor.authorItthagarun, Aen_HK
dc.date.accessioned2012-08-08T08:23:18Z-
dc.date.available2012-08-08T08:23:18Z-
dc.date.issued2000en_HK
dc.identifier.citationAustralian Orthodontic Journal, 2000, v. 16 n. 2, p. 88-97en_HK
dc.identifier.issn0587-3908en_HK
dc.identifier.urihttp://hdl.handle.net/10722/154109-
dc.description.abstractAlveolar bone defects are conditions that impede the progress of orthodontic treatment. This study compared the mechanics of the healing of autogenous intramembranous (IM) bone grafts and grafts comprising a mixture of IM and demineralised bone matrix of autogenous intramembranous origin (DBMIM), in an attempt to determine the reliability of each material. Thirty-two New Zealand white rabbits had a single defect created in their skull. Sixteen were grafted with IM bone alone (Group I: autogenous IM), and the other 16 had a combined graft of composite IM sandwiched between two layers of DBMIM (Group II: composite IM-DBMIM). A third group (Group III) of eight rabbits each had two defects created in their skull; one defect was left empty (A: passive control) and the other filled with rabbit-skin collagen (B: active control). In Groups I and II, inflammatory cells were found to be present on Days 1 and 2 of tissue retrieval. The appearance of the mesenchymal cells and preosteoblasts, osteoblasts and osteocytes was earlier (Day 3) in Group II than in Group I (Day 5). In both groups, preosteoblasts, osteoblasts and osteocytes were observed with no cartilage at the intermediate stage. In conclusion, autogenous IM bone grafts and IM bone grafts in the presence of DBMIM healed through an osteogenic ossification route.en_HK
dc.languageengen_US
dc.relation.ispartofAustralian orthodontic journalen_HK
dc.subject.meshAnimalsen_US
dc.subject.meshBone Matrix - Pathology - Transplantationen_US
dc.subject.meshBone Substitutes - Therapeutic Useen_US
dc.subject.meshBone Transplantation - Pathologyen_US
dc.subject.meshCollagen - Therapeutic Useen_US
dc.subject.meshConnective Tissue - Ultrastructureen_US
dc.subject.meshDecalcification Techniqueen_US
dc.subject.meshMacrophages - Ultrastructureen_US
dc.subject.meshMesoderm - Ultrastructureen_US
dc.subject.meshNeutrophils - Ultrastructureen_US
dc.subject.meshOsteoblasts - Ultrastructureen_US
dc.subject.meshOsteocytes - Ultrastructureen_US
dc.subject.meshOsteogenesis - Physiologyen_US
dc.subject.meshParietal Bone - Surgeryen_US
dc.subject.meshRabbitsen_US
dc.subject.meshTransplantation, Autologousen_US
dc.subject.meshTransplantation, Homologousen_US
dc.subject.meshWound Healingen_US
dc.titleUltrastructural identification of cells involved in the healing of intramembranous bone grafts in both the presence and absence of demineralised intramembranous bone matrix.en_HK
dc.typeArticleen_HK
dc.identifier.emailRabie, AB: rabie@hku.hken_HK
dc.identifier.authorityRabie, AB=rp00029en_HK
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.pmid11201969en_HK
dc.identifier.scopuseid_2-s2.0-0034231807en_HK
dc.identifier.hkuros106599-
dc.identifier.volume16en_HK
dc.identifier.issue2en_HK
dc.identifier.spage88en_HK
dc.identifier.epage97en_HK
dc.publisher.placeAustraliaen_HK
dc.identifier.scopusauthoridChay, SH=7003856668en_HK
dc.identifier.scopusauthoridRabie, AB=7007172734en_HK
dc.identifier.scopusauthoridItthagarun, A=6701591745en_HK
dc.identifier.issnl0587-3908-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats