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The efficacy of BMP-2 preloaded on bone substitute or hydrogel for bone regeneration at peri-implant defects in dogs.

Identifieur interne : 000041 ( PubMed/Checkpoint ); précédent : 000040; suivant : 000042

The efficacy of BMP-2 preloaded on bone substitute or hydrogel for bone regeneration at peri-implant defects in dogs.

Auteurs : Ui-Won Jung [Corée du Sud] ; In-Kyeong Lee [Corée du Sud] ; Jin-Young Park [Corée du Sud] ; Daniel S. Thoma [Suisse] ; Christoph H F. H Mmerle [Suisse] ; Ronald E. Jung [Suisse]

Source :

RBID : pubmed:25263966

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English descriptors

Abstract

The objective of this experiment was to test whether or not a synthetic bone substitute (SBS) was more effective than a polyethylene glycol hydrogel as a carrier material for bone morphogenetic protein-2 (BMP-2) when attempting to regenerate bone.

DOI: 10.1111/clr.12491
PubMed: 25263966


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pubmed:25263966

Le document en format XML

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<term>Dental Implantation, Endosseous (methods)</term>
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<term>Animaux</term>
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<term>Implants dentaires</term>
<term>Lâchage de suture (imagerie diagnostique)</term>
<term>Lâchage de suture (traitement médicamenteux)</term>
<term>Mandibule ()</term>
<term>Mandibule (imagerie diagnostique)</term>
<term>Microtomographie aux rayons X</term>
<term>Mâle</term>
<term>Polyéthylène glycols (pharmacologie)</term>
<term>Pose d'implant dentaire endo-osseux ()</term>
<term>Protéine morphogénétique osseuse de type 2 (pharmacologie)</term>
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<term>Surgical Wound Dehiscence</term>
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<term>Lâchage de suture</term>
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<term>Dental Implantation, Endosseous</term>
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<term>Polyéthylène glycols</term>
<term>Protéine morphogénétique osseuse de type 2</term>
<term>Substituts osseux</term>
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<term>Dental Implants</term>
<term>Dogs</term>
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<term>Chiens</term>
<term>Implants dentaires</term>
<term>Mandibule</term>
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<div type="abstract" xml:lang="en">The objective of this experiment was to test whether or not a synthetic bone substitute (SBS) was more effective than a polyethylene glycol hydrogel as a carrier material for bone morphogenetic protein-2 (BMP-2) when attempting to regenerate bone.</div>
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<Year>2017</Year>
<Month>05</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>11</Month>
<Day>16</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1600-0501</ISSN>
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<Volume>26</Volume>
<Issue>12</Issue>
<PubDate>
<Year>2015</Year>
<Month>Dec</Month>
</PubDate>
</JournalIssue>
<Title>Clinical oral implants research</Title>
<ISOAbbreviation>Clin Oral Implants Res</ISOAbbreviation>
</Journal>
<ArticleTitle>The efficacy of BMP-2 preloaded on bone substitute or hydrogel for bone regeneration at peri-implant defects in dogs.</ArticleTitle>
<Pagination>
<MedlinePgn>1456-65</MedlinePgn>
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<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">The objective of this experiment was to test whether or not a synthetic bone substitute (SBS) was more effective than a polyethylene glycol hydrogel as a carrier material for bone morphogenetic protein-2 (BMP-2) when attempting to regenerate bone.</AbstractText>
<AbstractText Label="MATERIAL AND METHODS" NlmCategory="METHODS">Two identical, box-type dehiscence defects (4 × 4 mm buccolingually and apicocoronally, and 8 mm mesiodistally) were surgically prepared on buccal sides of the left and right edentulous ridge in five beagle dogs. Following implant placement, the defects either received (i) no graft, (ii) SBS+hydrogel, (iii) SBS+BMP-2 loaded hydrogel, and (iv) BMP-2-loaded SBS+hydrogel. The animals were euthanized at 8 weeks postsurgery. Radiographic and histomorphometric analyses were performed.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The hydrogel alone was not able to stabilize the grafted bone particles at 8 weeks, and SBS+hydrogel group did not significantly differ from the control group in all volumetric measurements. On the other hand, extensively regenerated new bone was connected with most of the remaining SBS particles in the BMP-2 groups. The BMP-2 groups exhibited significantly greater new bone formation (10.65 mm(3) and 1.47 mm(2) in the SBS+BMP-2-loaded hydrogel group; 14.17 mm(3) and 0.93 mm(2) in the BMP-2-loaded SBS+hydrogel) than non-BMP-2 groups (1.27 mm(3) and 0.00 mm(2) in the control group; 2.01 mm(3) and 0.19 mm(2) in the SBS+hydrogel group) in volumetric and histomorphometric analyses (P < 0.001). However, there were no significant differences between both BMP-2 groups.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">BMP-2 could yield enhanced bone regeneration in the critical-size peri-implant defects regardless of whether SBS or hydrogel is used for preloading, although the outcomes seem to be more reproducible with BMP-2 preloaded on SBS.</AbstractText>
<CopyrightInformation>© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation>
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<LastName>Jung</LastName>
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<Affiliation>Department of Periodontology, Research Institute for Periodontal Regeneration, College of Dentistry, Yonsei University, Seoul, South Korea.</Affiliation>
</AffiliationInfo>
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<LastName>Jung</LastName>
<ForeName>Ronald E</ForeName>
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<Affiliation>Department of Fixed and Removable Prosthodontics and Dental Material Science, Dental School, University of Zurich, Zurich, Switzerland.</Affiliation>
</AffiliationInfo>
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<Country>Denmark</Country>
<MedlineTA>Clin Oral Implants Res</MedlineTA>
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<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C525718">BMP2 protein, human</NameOfSubstance>
</Chemical>
<Chemical>
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<NameOfSubstance UI="D055396">Bone Morphogenetic Protein 2</NameOfSubstance>
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<NameOfSubstance UI="D018786">Bone Substitutes</NameOfSubstance>
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<RegistryNumber>25852-47-5</RegistryNumber>
<NameOfSubstance UI="D020136">Hydrogel, Polyethylene Glycol Dimethacrylate</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>30IQX730WE</RegistryNumber>
<NameOfSubstance UI="D011092">Polyethylene Glycols</NameOfSubstance>
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<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
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<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
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<DescriptorName UI="D013529" MajorTopicYN="N">Surgical Wound Dehiscence</DescriptorName>
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<Keyword MajorTopicYN="N">drug delivery system</Keyword>
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