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- Publisher Website: 10.1111/j.1600-0501.2010.02039.x
- Scopus: eid_2-s2.0-79953711414
- PMID: 21121956
- WOS: WOS:000289253200008
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Article: Bone regeneration in the presence of a synthetic hydroxyapatite/silica oxide-based and a xenogenic hydroxyapatite-based bone substitute material
Title | Bone regeneration in the presence of a synthetic hydroxyapatite/silica oxide-based and a xenogenic hydroxyapatite-based bone substitute material |
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Authors | |
Keywords | Bone regeneration Bone substitute material Nano-crystalline hydroxyapatite |
Issue Date | 2011 |
Publisher | Wiley-Blackwell Publishing, Inc.. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CLR |
Citation | Clinical Oral Implants Research, 2011, v. 22 n. 5, p. 506-511 How to Cite? |
Abstract | OBJECTIVES: A comparison of synthetic hydroxyapatite/silica oxide, xenogenic hydroxyapatite-based bone substitute materials with empty control sites in terms of bone regeneration enhancement in a rabbit calvarial four non-critical-sized defect model. METHODS: In each of six rabbits, four bicortical calvarial bone defects were generated. The following four treatment modalities were randomly allocated: (1) empty control site, (2) synthetic hydroxyapatite/silica oxide-based (HA/SiO) test granules, (3) xenogenic hydroxyapatite -based granules, (4) synthetic hydroxyapatite/silica oxide -based (HA/SiO) test two granules. The results of the latter granules have not been reported due to their size being three times bigger than the other two granule types. After 4 weeks, the animals were sacrificed and un-decalcified sections were obtained for histological analyses. For statistical analysis, the Kruskal-Wallis test was applied (P<0.05). RESULTS: Histomorphometric analysis showed an average area fraction of newly formed bone of 12.32+/-10.36% for the empty control, 17.47+/-6.42% for the xenogenic hydroxyapatite -based granules group, and 21.2+/-5.32% for the group treated with synthetic hydroxyapatite/silica oxide -based granules. Based on the middle section, newly formed bone bridged the defect to 38.33+/-37.55% in the empty control group, 54.33+/-22.12% in the xenogenic hydroxyapatite -based granules group, and to 79+/-13.31% in the synthetic hydroxyapatite/silica oxide -based granules group. The bone-to-bone substitute contact was 46.38+/-18.98% for the xenogenic and 59.86+/-14.92% for the synthetic hydroxyapatite/silica oxide-based granules group. No significant difference in terms of bone formation and defect bridging could be detected between the two bone substitute materials or the empty defect. CONCLUSION: There is evidence that the synthetic hydroxyapatite/silica oxide granules provide comparable results with a standard xenogenic bovine mineral in terms of bone formation and defect bridging in non-critical size defects. |
Persistent Identifier | http://hdl.handle.net/10722/138877 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.865 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Kruse, A | en_HK |
dc.contributor.author | Jung, RE | en_HK |
dc.contributor.author | Nicholls, F | en_HK |
dc.contributor.author | Zwahlen, RA | en_HK |
dc.contributor.author | Haemmerle, CHF | en_HK |
dc.contributor.author | Weber, FE | en_HK |
dc.date.accessioned | 2011-09-23T05:41:35Z | - |
dc.date.available | 2011-09-23T05:41:35Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Clinical Oral Implants Research, 2011, v. 22 n. 5, p. 506-511 | en_HK |
dc.identifier.issn | 0905-7161 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/138877 | - |
dc.description.abstract | OBJECTIVES: A comparison of synthetic hydroxyapatite/silica oxide, xenogenic hydroxyapatite-based bone substitute materials with empty control sites in terms of bone regeneration enhancement in a rabbit calvarial four non-critical-sized defect model. METHODS: In each of six rabbits, four bicortical calvarial bone defects were generated. The following four treatment modalities were randomly allocated: (1) empty control site, (2) synthetic hydroxyapatite/silica oxide-based (HA/SiO) test granules, (3) xenogenic hydroxyapatite -based granules, (4) synthetic hydroxyapatite/silica oxide -based (HA/SiO) test two granules. The results of the latter granules have not been reported due to their size being three times bigger than the other two granule types. After 4 weeks, the animals were sacrificed and un-decalcified sections were obtained for histological analyses. For statistical analysis, the Kruskal-Wallis test was applied (P<0.05). RESULTS: Histomorphometric analysis showed an average area fraction of newly formed bone of 12.32+/-10.36% for the empty control, 17.47+/-6.42% for the xenogenic hydroxyapatite -based granules group, and 21.2+/-5.32% for the group treated with synthetic hydroxyapatite/silica oxide -based granules. Based on the middle section, newly formed bone bridged the defect to 38.33+/-37.55% in the empty control group, 54.33+/-22.12% in the xenogenic hydroxyapatite -based granules group, and to 79+/-13.31% in the synthetic hydroxyapatite/silica oxide -based granules group. The bone-to-bone substitute contact was 46.38+/-18.98% for the xenogenic and 59.86+/-14.92% for the synthetic hydroxyapatite/silica oxide-based granules group. No significant difference in terms of bone formation and defect bridging could be detected between the two bone substitute materials or the empty defect. CONCLUSION: There is evidence that the synthetic hydroxyapatite/silica oxide granules provide comparable results with a standard xenogenic bovine mineral in terms of bone formation and defect bridging in non-critical size defects. | en_HK |
dc.language | eng | en_US |
dc.publisher | Wiley-Blackwell Publishing, Inc.. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CLR | en_HK |
dc.relation.ispartof | Clinical Oral Implants Research | en_HK |
dc.rights | The definitive version is available at www3.interscience.wiley.com | - |
dc.subject | Bone regeneration | - |
dc.subject | Bone substitute material | - |
dc.subject | Nano-crystalline hydroxyapatite | - |
dc.subject.mesh | Bone Matrix - transplantation | en_HK |
dc.subject.mesh | Bone Regeneration - physiology | en_HK |
dc.subject.mesh | Bone Substitutes - therapeutic use | en_HK |
dc.subject.mesh | Durapatite - therapeutic use | en_HK |
dc.subject.mesh | Minerals - therapeutic use | en_HK |
dc.title | Bone regeneration in the presence of a synthetic hydroxyapatite/silica oxide-based and a xenogenic hydroxyapatite-based bone substitute material | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Zwahlen, RA: zwahlen@hku.hk | en_HK |
dc.identifier.email | Weber, FE: franz.weber@zzmk.uzh.ch | - |
dc.identifier.authority | Zwahlen, RA=rp00055 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1600-0501.2010.02039.x | en_HK |
dc.identifier.pmid | 21121956 | - |
dc.identifier.scopus | eid_2-s2.0-79953711414 | en_HK |
dc.identifier.hkuros | 193660 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79953711414&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 22 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 506 | en_HK |
dc.identifier.epage | 511 | en_HK |
dc.identifier.isi | WOS:000289253200008 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Weber, FE=7201702808 | en_HK |
dc.identifier.scopusauthorid | Hämmerle, CHF=7005331848 | en_HK |
dc.identifier.scopusauthorid | Zwahlen, RA=7004217269 | en_HK |
dc.identifier.scopusauthorid | Nicholls, F=36244274900 | en_HK |
dc.identifier.scopusauthorid | Jung, RE=7201892502 | en_HK |
dc.identifier.scopusauthorid | Kruse, A=26967781900 | en_HK |
dc.identifier.citeulike | 9130199 | - |
dc.identifier.issnl | 0905-7161 | - |