Methacrylated epigallocatechin gallate functionalized dental adhesives: Antiproteolytic activity and dentin bonding studies
| dc.contributor.author | Duque, Cristiane [UNESP] | |
| dc.contributor.author | Chrisostomo, Daniela Alvim | |
| dc.contributor.author | Scaffa, Polliana Mendes Candia | |
| dc.contributor.author | Gouveia, Zach | |
| dc.contributor.author | Nascimento, Fabio Dupart | |
| dc.contributor.author | Plotnikov, Sergey V | |
| dc.contributor.author | Prakki, Anuradha | |
| dc.date.accessioned | 2026-04-14T20:18:14Z | |
| dc.date.issued | 2025-06-03 | |
| dc.description.abstract | OBJECTIVES: 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.affiliation | Department 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.affiliation | Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada. | |
| dc.description.affiliation | Division of Biomaterials and Biomechanics, Department of Restorative Dentistry, Oregon Health & Science University, OHSU, Portland, OR, USA. | |
| dc.description.affiliation | Dental 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.affiliation | Department of Cell and Systems Biology, Faculty of Arts and Science, University of Toronto, Toronto, ON, Canada. | |
| dc.description.affiliation | Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada. Electronic address: a.prakki@dentistry.utoronto.ca. | |
| dc.description.affiliationUnesp | Department 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.identifier | https://app.dimensions.ai/details/publication/pub.1189355067 | |
| dc.identifier.dimensions | pub.1189355067 | |
| dc.identifier.doi | 10.1016/j.dental.2025.05.006 | |
| dc.identifier.issn | 0109-5641 | |
| dc.identifier.issn | 1879-0097 | |
| dc.identifier.orcid | 0000-0002-2575-279X | |
| dc.identifier.orcid | 0000-0003-0622-8236 | |
| dc.identifier.orcid | 0000-0001-9702-3935 | |
| dc.identifier.orcid | 0000-0001-6672-3373 | |
| dc.identifier.orcid | 0000-0002-5561-8890 | |
| dc.identifier.orcid | 0000-0002-8969-9043 | |
| dc.identifier.pmid | 40467428 | |
| dc.identifier.uri | https://hdl.handle.net/11449/321819 | |
| dc.publisher | Elsevier | |
| dc.relation.ispartof | Dental Materials; n. 7; v. 41; p. 892-900 | |
| dc.rights.accessRights | Acesso aberto | pt |
| dc.rights.sourceRights | oa_all | |
| dc.rights.sourceRights | hybrid | |
| dc.source | Dimensions | |
| dc.title | Methacrylated epigallocatechin gallate functionalized dental adhesives: Antiproteolytic activity and dentin bonding studies | |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isOrgUnitOfPublication | 8b3335a4-1163-438a-a0e2-921a46e0380d | |
| relation.isOrgUnitOfPublication.latestForDiscovery | 8b3335a4-1163-438a-a0e2-921a46e0380d | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatuba | pt |

