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In vivo preservation of the hybrid layer by chlorhexidine

dc.contributor.authorCarrilho, M. R. O.
dc.contributor.authorGeraldeli, S.
dc.contributor.authorTay, F.
dc.contributor.authorGoes, M. F. de
dc.contributor.authorCarvalho, R. M.
dc.contributor.authorTjäderhane, L.
dc.contributor.authorReis, A. F.
dc.contributor.authorHebling, J.
dc.contributor.authorMazzoni, A.
dc.contributor.authorBreschi, L.
dc.contributor.authorPashley, D.
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionMedical College of Georgia
dc.contributor.institutionUniversity of Iowa
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversity of Helsinki
dc.contributor.institutionUniversidade de Guarulhos (UnG)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Bologna
dc.contributor.institutionUniversity of Trieste
dc.date.accessioned2014-05-27T11:22:29Z
dc.date.available2014-05-27T11:22:29Z
dc.date.issued2007-06-01
dc.description.abstractHost-derived proteases have been reported to degrade the collagen matrix of incompletely-resin-infiltrated dentin. This study tested the hypothesis that interfacial degradation of resin-dentin bonds may be prevented or delayed by the application of chlorhexidine (CHX), a matrix metalloproteinase inhibitor, to dentin after phosphoric acid-etching. Contralateral pairs of resin-bonded Class I restorations in non-carious third molars were kept under intra-oral function for 14 months. Preservation of resin-dentin bonds was assessed by microtensile bond strength tests and TEM examination. In vivo bond strength remained stable in the CHX-treated specimens, while bond strength decreased significantly in control teeth. Resin-infiltrated dentin in CHX-treated specimens exhibited normal structural integrity of the collagen network. Conversely, progressive disintegration of the fibrillar network was identified in control specimens. Auto-degradation of collagen matrices can occur in resin-infiltrated dentin, but may be prevented by the application of a synthetic protease inhibitor, such as chlorhexidine.en
dc.description.affiliationDepartment of Restorative Dentistry Piracicaba School of Dentistry University of Campinas, Dental Materials Area, Piracicaba/SP
dc.description.affiliationDepartment of Oral Biology and Maxillofacial Pathology
dc.description.affiliationDepartment of Endodontics School of Dentistry Medical College of Georgia, Augusta, GA 30912-1129
dc.description.affiliationDepartment of Operative Dentistry School of Dentistry University of Iowa, Iowa City, IA
dc.description.affiliationDepartment of Prosthodontics University of São Paulo Bauru School of Dentistry, Bauru/SP
dc.description.affiliationDepartment of Oral and Maxillofacial Diseases University of Helsinki Helsinki University Central Hospital (HUCU), Helsinki
dc.description.affiliationDepartment of Operative Dentistry University of Guarulhos School of Dentistry, Guarulhos/SP
dc.description.affiliationDepartment of Orthodontics and Pwdiatric Dentistry University of São Paulo State Araraquara Dental School, Araraquara/SP
dc.description.affiliationDepartment of SAU and FAL University of Bologna, Bologna
dc.description.affiliationDivision of Dental Sciences and Biomaterials Department of Biomedicine University of Trieste, Trieste
dc.format.extent529-533
dc.identifierhttp://dx.doi.org/10.1177/154405910708600608
dc.identifier.citationJournal of Dental Research, v. 86, n. 6, p. 529-533, 2007.
dc.identifier.doi10.1177/154405910708600608
dc.identifier.issn0022-0345
dc.identifier.scopus2-s2.0-34347228117
dc.identifier.urihttp://hdl.handle.net/11449/69683
dc.language.isoeng
dc.relation.ispartofJournal of Dental Research
dc.relation.ispartofjcr5.380
dc.relation.ispartofsjr2,302
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectChlorhexidine
dc.subjectDegradation
dc.subjectEtch-and-rinse adhesive
dc.subjectHybrid layer
dc.subjectIn vivo
dc.subjectMMP
dc.subjectbisphenol A bis(2 hydroxypropyl) ether dimethacrylate
dc.subjectchlorhexidine
dc.subjectdentin bonding agent
dc.subjectfibrillar collagen
dc.subjectmatrix metalloproteinase
dc.subjectphosphoric acid
dc.subjectproteinase inhibitor
dc.subjectresin
dc.subjectsingle bond
dc.subjectunclassified drug
dc.subjectchemistry
dc.subjectdental acid etching
dc.subjectdental bonding
dc.subjectdental surgery
dc.subjectdentin
dc.subjectdrug antagonism
dc.subjecthuman
dc.subjectmaterials testing
dc.subjectmechanical stress
dc.subjectmethodology
dc.subjectsurface property
dc.subjecttensile strength
dc.subjecttime
dc.subjecttransmission electron microscopy
dc.subjectultrastructure
dc.subjectAcid Etching, Dental
dc.subjectBisphenol A-Glycidyl Methacrylate
dc.subjectComposite Resins
dc.subjectDental Bonding
dc.subjectDental Restoration, Permanent
dc.subjectDentin
dc.subjectDentin-Bonding Agents
dc.subjectFibrillar Collagens
dc.subjectHumans
dc.subjectMaterials Testing
dc.subjectMatrix Metalloproteinases
dc.subjectMicroscopy, Electron, Transmission
dc.subjectPhosphoric Acids
dc.subjectProtease Inhibitors
dc.subjectStress, Mechanical
dc.subjectSurface Properties
dc.subjectTensile Strength
dc.subjectTime Factors
dc.titleIn vivo preservation of the hybrid layer by chlorhexidineen
dc.typeArtigo
dcterms.licensehttp://www.sagepub.com/authors/journal/permissions.sp#7
dspace.entity.typePublication

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