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Methacrylated epigallocatechin gallate functionalized dental adhesives: Antiproteolytic activity and dentin bonding studies

dc.contributor.authorDuque, Cristiane [UNESP]
dc.contributor.authorChrisostomo, Daniela Alvim
dc.contributor.authorScaffa, Polliana Mendes Candia
dc.contributor.authorGouveia, Zach
dc.contributor.authorNascimento, Fabio Dupart
dc.contributor.authorPlotnikov, Sergey V
dc.contributor.authorPrakki, Anuradha
dc.date.accessioned2026-04-14T20:18:14Z
dc.date.issued2025-06-03
dc.description.abstractOBJECTIVES: To assess the antiproteolytic effect of EGCG-methacrylate monomers and its inhibitory effect on gelatinolytic activity in the hybrid layer. Also, to investigate the effect of an adhesive material functionalized with EGCG-methacrylate monomers on immediate and long-term dentin-resin bond strength. METHODS: Neat EGCG (E0) was reacted with three different ratios of methacryloyl ester and dissolved in ethyl acetate to obtain EGCG-methacrylates with hydroxyl functionalization at 33 % (M-E33), 67 % (M-E67) and 100 % (M-E100) levels. Resin composite blocks were built on human dentin surfaces using self-etching adhesive containing E0, M-E33, M-E67, and M-E100 at 1 wt%. Demineralized human dentin disks were immersed in deionized water (DW) or lactic acid (LA) and subsequently treated with DW, acetone (as controls), E0, M-E33, M-E67 and M-E100 diluted in acetone. Concentrations of solubilized type I collagen C-terminal (CTX and ICTP) and N-terminal (NTX) telopeptides were determined from 7-day extracts of dentin matrix specimens by ELISA assays. In situ zymography of adhesive-dentin interface slices from restored teeth was performed by confocal microscope after 24 h dentin treatment. Microtensile bond strength (µTBS) and failure pattern were evaluated after 24 h and 6 months. Data were analyzed using two-way ANOVA and Tukey post hoc test (p < 0.05). RESULTS: All experimental groups statistically reduced the release of solubilized telopeptides from dentin samples in DW and LA. E0 and M-E100 incorporated into the adhesive system reduced the gelatinolytic activity within the hybrid layer. The lowest µTBS values for restored teeth were observed for E0 and M-E100 groups, after 24 h and 6 months, respectively. The most prevalent failure observed was classified as type 4, except for M-E100. SIGNIFICANCE: EGCG-methacrylate monomers effectively protected collagen from degradation. When incorporated into adhesive systems, EGCG-methacrylates reduced gelatinolytic activity within the hybrid layer, and did not affect immediate and long-term bond strength values of restorations.
dc.description.affiliationDepartment of Preventive and Restorative Dentistry, School of Dentistry, São Paulo State University, Araçatuba, SP, Brazil; Faculty of Dental Medicine, Centre for Interdisciplinary Research in Health (CIIS), Universidade Católica Portuguesa, Viseu, Portugal; Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.
dc.description.affiliationDental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.
dc.description.affiliationDivision of Biomaterials and Biomechanics, Department of Restorative Dentistry, Oregon Health & Science University, OHSU, Portland, OR, USA.
dc.description.affiliationDental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada; Department of Biochemistry, Molecular Biology Division, Federal University of Sao Paulo, Sao Paulo, SP, Brazil.
dc.description.affiliationDepartment of Cell and Systems Biology, Faculty of Arts and Science, University of Toronto, Toronto, ON, Canada.
dc.description.affiliationDental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada. Electronic address: a.prakki@dentistry.utoronto.ca.
dc.description.affiliationUnespDepartment of Preventive and Restorative Dentistry, School of Dentistry, São Paulo State University, Araçatuba, SP, Brazil; Faculty of Dental Medicine, Centre for Interdisciplinary Research in Health (CIIS), Universidade Católica Portuguesa, Viseu, Portugal; Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1189355067
dc.identifier.dimensionspub.1189355067
dc.identifier.doi10.1016/j.dental.2025.05.006
dc.identifier.issn0109-5641
dc.identifier.issn1879-0097
dc.identifier.orcid0000-0002-2575-279X
dc.identifier.orcid0000-0003-0622-8236
dc.identifier.orcid0000-0001-9702-3935
dc.identifier.orcid0000-0001-6672-3373
dc.identifier.orcid0000-0002-5561-8890
dc.identifier.orcid0000-0002-8969-9043
dc.identifier.pmid40467428
dc.identifier.urihttps://hdl.handle.net/11449/321819
dc.publisherElsevier
dc.relation.ispartofDental Materials; n. 7; v. 41; p. 892-900
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightshybrid
dc.sourceDimensions
dc.titleMethacrylated epigallocatechin gallate functionalized dental adhesives: Antiproteolytic activity and dentin bonding studies
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt

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