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Effect of varying functional monomers in experimental self-adhesive composites : polymerization kinetics, cell metabolism influence and sealing ability

datacite.subject.fosEngenharia e Tecnologia::Engenharia dos Materiais
datacite.subject.fosCiências Médicas::Outras Ciências Médicas
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorFerreira, Marta Nunes
dc.contributor.authorSantos, Marta Neves Dos
dc.contributor.authorFernandes, Inês
dc.contributor.authorMarto, Carlos Miguel
dc.contributor.authorLaranjo, Mafalda
dc.contributor.authorSilva, Diana
dc.contributor.authorSerro, Ana Paula
dc.contributor.authorCarrilho, Eunice
dc.contributor.authorBotelho, Maria Filomena
dc.contributor.authorAzul, Ana Mano
dc.contributor.authorDelgado, António H. S.
dc.date.accessioned2026-02-20T11:49:46Z
dc.date.available2026-02-20T11:49:46Z
dc.date.issued2023-10
dc.description.abstractThe aim was to evaluate the effects of adding different functional monomers to experimental self-adhesive composites (SACs) on polymerization kinetics, cell metabolic activity, and sealing ability. SACs were formulated using urethane dimethacrylate as the base monomer and triethylene glycol dimethacrylate. Additionally, 10 wt.% of distinct functional monomers were added - 10-methacryloyloxydecyl dihydrogen phosphate, glycerol phosphate dimethacrylate (GPDM), 2-hydroxyethyl methacrylate (HEMA) or hydroxyethyl acrylamide (HEAA). ATR-FTIR was used to determine real-time polymerization kinetics (20 min, n = 3). The final extrapolated conversion and polymerization rates were determined (DC,max;Rp,max). The DC,max values were employed to calculate volumetric shrinkage. The MTT assay was performed on MDPC-23 cells using disc extracts at different concentrations (n = 8). Class V cavities were prepared in 60 sound human molars, assigned to six groups (n = 10), depending on the composite used and aging type (T0 or TC, if thermocycled for 10 000 cycles). One-way ANOVA, two-way, and Kruskal–Wallis tests were employed to treat the data (ɑ = 0.05). Varying the functional monomers had a large impact on DC,max, as confirmed by one-way ANOVA (p<0.001). The highest was obtained for HEMA (64 ± 3%). The HEMA and HEAA formulations were found to be significantly more toxic at concentrations below 100%. For microleakage, having a functional monomer or not did not show any improvement, irrespective of margin or aging period (Mann–Whitney U, p > 0.05). Larger functional monomers MDP and GPDM affected polymerization properties. Conversely, their acidity did not seem to be detrimental to cell metabolic activity. Regarding sealing ability, it seems that the functional monomers did not bring an advantage to the composites. Varying the functional monomer in SACs had a clear impact on the polymerization kinetics as well as on their cytotoxic potential. However, it did not confer better microleakage and sealing. Claiming self-adhesiveness based only on functional monomers seems dubious.eng
dc.identifier.citationFerreira, M. N., Neves Dos Santos, M., Fernandes, I., Marto, C. M., Laranjo, M., Silva, D., Serro, A. P., Carrilho, E., Botelho, M. F., Azul, A. M., & Delgado, A. H. (2023). Effect of varying functional monomers in experimental self-adhesive composites: polymerization kinetics, cell metabolism influence and sealing ability. Biomedical materials (Bristol, England), 18(6), 10.1088/1748-605X/acfc8d. https://doi.org/10.1088/1748-605X/acfc8d
dc.identifier.doi10.1088/1748-605X/acfc8d
dc.identifier.issn1748-605X
dc.identifier.urihttp://hdl.handle.net/10400.26/61785
dc.language.isoeng
dc.peerreviewedyes
dc.publisherIOP Publishing
dc.relation.hasversionhttps://doi.org/10.1088/1748-605X/acfc8d
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectmonomers
dc.subjectcomposites
dc.subjectself-adhesive
dc.subjectkinetics
dc.subjectpolymerization
dc.titleEffect of varying functional monomers in experimental self-adhesive composites : polymerization kinetics, cell metabolism influence and sealing abilityeng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.issue6
oaire.citation.startPage065014
oaire.citation.titleBiomedical Materials
oaire.citation.volume18
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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