RESUMO
This study evaluated the three-year lifespan of the bond to dentin of experimental self-etch adhesives containing benzodioxole derivatives - 1,3-benzodioxole (BDO) and piperonyl alcohol (PA) - as co-initiator alternative to amines. Adhesive resins were formulated using Bis-GMA, TEGDMA, HEMA, camphorquinone and different co-initiators: BDO, PA or ethyl 4-dimethylamino benzoate (EDAB - amine). An experimental self-etch primer was used to complete the two-step, self-etch adhesive system. Clearfil SE Bond (CSE) was used as commercial reference. Bond strength to human dentin was assessed by microtensile bond strength (µTBS) test, and failure mode was classified. Morphology of the dentin bonding interface was assessed via scanning electron microscopy (SEM). Irrespective of the dental adhesives evaluated, µTBS was higher after 24 hours compared with that after 1.5 and 3 years (p ≤ 0.001). However, adhesives with BDO and PA as co-initiators showed significantly higher bond strength than the bonding resin with EDAB (p ≤ 0.002), independent of the time evaluated. The commercial adhesive CSE showed similar bond strength compared with the other groups (p ≥ 0.05). Mixed failures were mainly observed after 24 hours, while adhesive failures were more frequently observed after 1.5 and 3 years. No notable differences in homogeneity and continuity along the bonded interfaces were detected among the materials in the SEM analysis. In conclusion, benzodioxole derivatives are feasible alternative co-initiators to tertiary amine in camphorquinone-based self-etching dental adhesive formulations.
Assuntos
Benzodioxóis/química , Álcoois Benzílicos/química , Adesivos Dentinários/química , Dentina/efeitos dos fármacos , Dioxóis/química , Cimentos de Resina/química , para-Aminobenzoatos/química , Bis-Fenol A-Glicidil Metacrilato/química , Cânfora/análogos & derivados , Cânfora/química , Colagem Dentária/métodos , Dentina/química , Humanos , Teste de Materiais , Metacrilatos/química , Microscopia Eletrônica de Varredura , Polietilenoglicóis/química , Ácidos Polimetacrílicos/química , Reprodutibilidade dos Testes , Propriedades de Superfície , Resistência à Tração , Fatores de TempoRESUMO
PURPOSE: A systematic review was conducted to determine whether there were composition strategies available to reduce and control polymerization shrinkage stress development in resin-based restorative dental materials. DATA SOURCES: This report was reported in accordance with the PRISMA Statement. Two reviewers performed a literature search up to December 2016, without restriction of the year of publication, in seven databases: PubMed, Web of Science, Scopus, SciELO, LILACS, IBECS, and BBO. STUDY SELECTION: Only laboratory studies that evaluated polymerization shrinkage stress by direct testing were included. Pilot studies, reviews and in vitro studies that evaluated polymerization shrinkage stress by indirect methods (e.g., microleakage or cuspal deflection measurements), finite elemental analysis, or theoretical and mathematical models were excluded. Of the 6113 eligible articles, 62 studies were included in the qualitative analysis, and the meta-analysis was performed with 58 studies. The composition strategy was subdivided according to the modified part of the material: filler phase, coupling agent, or resin matrix. A global comparison was performed with random-effects models (αâ¯=â¯0.05). The only subgroup that did not show a statistical difference between the alternative strategy and the control was 'the use of alternative photo-initiators' (pâ¯=â¯0.29). CONCLUSION: Modification of the resin matrix made the largest contribution to minimizing stress development. The technology used for decreasing stress in the formulation of low-shrinkage and bulk-fill materials was shown to be a promising application for reducing and controlling stress development.
Assuntos
Polimerização , Resinas Sintéticas/química , Estresse Mecânico , Análise de Elementos Finitos , Teste de MateriaisRESUMO
This study evaluated the shear bond strength (SBS) of self-adhesive resin cements (SARCs) to dentin and their physical-chemical properties. Five commercial SARCs were evaluated [SmartCem®2 - DENTSPLY (SC2); BisCem® - Bisco (BC); SeT PP® - SDI (SeT); Relyx U100® - 3M ESPE (U100) and YCEM® SA - Yller (YCEM)]. The SARCs were evaluated for SBS to dentin (n = 10) after 24 h, 6 months, and 12 months. The dentin demineralization caused by acidic monomers was observed by SEM, and pH-neutralization of eluate was observed for 24 h. Degree of conversion (DC), rate of polymerization (Rp), flexural strength (FS), and elastic modulus (E) were evaluated. Immediate SBS of SC2, SET, U100, and YCEM were statistically higher than that of BC (p < 0.001). After 12 months, all SARCs showed reduced SBS values and U100 showed values similar to those of SET and YCEM, and higher than those of BC and SC2 (p = 0.001). Demineralization pattern of SARCs was similar. At 24h, all SARCs showed no differences in the pH-value, except BC and U100 (p < 0.001). YCEM showed the highest Rp. U100, YCEM, and SC2 showed statistically higher FS (p<0.001) and E (p < 0.001) when compared with SET and BC. U100 and YCEM showed the best long-term bonding irrespective of the storage period. A significant reduction in SBS was found for all groups after 12 months. SBS was not shown to be correlated with physical-chemical properties, and appeared to be material-dependent. The polymerization profile suggested that an increased time of light activation, longer than that recommended by manufacturers, would be necessary to optimize DC of SARCs.
Assuntos
Resinas Compostas/química , Dentina/efeitos dos fármacos , Cura Luminosa de Adesivos Dentários/métodos , Cimentos de Resina/química , Análise de Variância , Dentina/química , Módulo de Elasticidade , Teste de Materiais , Microscopia Eletrônica de Varredura , Transição de Fase/efeitos dos fármacos , Maleabilidade , Polimerização , Valores de Referência , Reprodutibilidade dos Testes , Resistência ao Cisalhamento , Propriedades de Superfície/efeitos dos fármacos , Fatores de TempoRESUMO
PURPOSE: A systematic review was conducted to determine whether there were any alternative technique or additional step strategies available to reduce and control polymerization shrinkage stress development in dental resin-based restorative materials. DATA SOURCES: This report followed the PRISMA Statement. A total of 36 studies were included in this review. Two reviewers performed a literature search up to December 2016, without restriction of the year of publication, in seven databases: PubMed, Web of Science, Scopus, SciELO, LILACS, IBECS, and BBO. STUDY SELECTION: Only in vitro studies that evaluated polymerization shrinkage stress by direct testing were included. Pilot studies, reviews and in vitro studies that evaluated polymerization shrinkage stress by indirect methods (e.g., microleakage or cuspal deflection measurements), finite elemental analysis or mathematical models were excluded. Of the 6.113 eligible articles, 36 studies were included in the qualitative analysis, and the meta-analysis was performed with 25 studies. A global comparison was performed with random-effects models (αâ¯=â¯0.05). The strategies were subdivided as follows: the use of an alternative technique protocol of placing the material inside the tooth cavity; the modification of the irradiation intensity or total energy delivered to the material; the use of an alternative light-curing source; or the use of an alternative photo-activation mode. All alternative strategies showed statistically significant differences when compared with their respective controls (pâ¯<â¯0.05). CONCLUSION: The use of alternative light-curing sources contributed more to minimizing stress development than placing the material by means of an alternative technique protocol or by modifying the irradiant intensity or total energy delivered to the material during photo-activation. Moreover, the use of an alternative photo-activation mode (intermittent light, exponential, soft-start or pulse delay modes) was shown to be an effective strategy for reducing and controlling stress development in resin-based dental materials.
Assuntos
Processos Fotoquímicos , Polimerização , Resinas Sintéticas/química , Estresse Mecânico , Análise de Elementos FinitosRESUMO
Abstract This study evaluated the shear bond strength (SBS) of self-adhesive resin cements (SARCs) to dentin and their physical-chemical properties. Five commercial SARCs were evaluated [SmartCem®2 - DENTSPLY (SC2); BisCem® - Bisco (BC); SeT PP® − SDI (SeT); Relyx U100® - 3M ESPE (U100) and YCEM® SA - Yller (YCEM)]. The SARCs were evaluated for SBS to dentin (n = 10) after 24 h, 6 months, and 12 months. The dentin demineralization caused by acidic monomers was observed by SEM, and pH-neutralization of eluate was observed for 24 h. Degree of conversion (DC), rate of polymerization (Rp), flexural strength (FS), and elastic modulus (E) were evaluated. Immediate SBS of SC2, SET, U100, and YCEM were statistically higher than that of BC (p < 0.001). After 12 months, all SARCs showed reduced SBS values and U100 showed values similar to those of SET and YCEM, and higher than those of BC and SC2 (p = 0.001). Demineralization pattern of SARCs was similar. At 24h, all SARCs showed no differences in the pH-value, except BC and U100 (p < 0.001). YCEM showed the highest Rp. U100, YCEM, and SC2 showed statistically higher FS (p<0.001) and E (p < 0.001) when compared with SET and BC. U100 and YCEM showed the best long-term bonding irrespective of the storage period. A significant reduction in SBS was found for all groups after 12 months. SBS was not shown to be correlated with physical-chemical properties, and appeared to be material-dependent. The polymerization profile suggested that an increased time of light activation, longer than that recommended by manufacturers, would be necessary to optimize DC of SARCs.
Assuntos
Resinas Compostas/química , Cimentos de Resina/química , Dentina/efeitos dos fármacos , Cura Luminosa de Adesivos Dentários/métodos , Valores de Referência , Propriedades de Superfície/efeitos dos fármacos , Fatores de Tempo , Teste de Materiais , Microscopia Eletrônica de Varredura , Reprodutibilidade dos Testes , Análise de Variância , Maleabilidade , Resistência ao Cisalhamento , Dentina/química , Transição de Fase/efeitos dos fármacos , Módulo de Elasticidade , PolimerizaçãoRESUMO
Aim: The aim of this study was to evaluate a new method for measuring the retention values of different denture adhesives. Methods: The adhesive strength values of three different commercial denture adhesives (Corega powder, Corega adhesive tape and Ultra Corega cream) were evaluated using three different moisturizing agents (distilled water, artificial saliva and natural saliva). The adhesive test was performed on a universal testing machine, after applying the adhesive products to acrylic resin specimens, under two different test conditions (wetting or dipping). Tensile bond strength values in MPa were obtained for each denture adhesive presentation and test condition. Viscosity of the denture adhesives mixed with the different moisturizing agents was determined using a rotary rheometer. Maximum viscosity values were analyzed using the one-way ANOVA test. Tensile bond strength data was analyzed using Kruskal-Wallis and the Tukey's test. Pooled data of each denture adhesive presentations for all test conditions was also carried out. Correlation between viscosity and pooled tensile strength values was analyzed through linear regression analysis. A significance level of α=0.05 was set for all analyses. Results: Results showed that statistically higher adhesion strength was obtained with tape and cream adhesives when using natural saliva as moisturizing agents (p<0.05). The adhesive strength values obtained with the dipping method were similar to those obtained with the conventional wetting method. The denture retention strength was influenced by both the denture adhesive type and moisturizing agent used. Conclusion: The dipping method showed to be a reliable test capable to simulate the oral conditions and should be better explored in further studies
Assuntos
Resistência à Tração , Retenção de Dentadura , Bases de DentaduraRESUMO
Abstract This study evaluated the three-year lifespan of the bond to dentin of experimental self-etch adhesives containing benzodioxole derivatives - 1,3-benzodioxole (BDO) and piperonyl alcohol (PA) - as co-initiator alternative to amines. Adhesive resins were formulated using Bis-GMA, TEGDMA, HEMA, camphorquinone and different co-initiators: BDO, PA or ethyl 4-dimethylamino benzoate (EDAB - amine). An experimental self-etch primer was used to complete the two-step, self-etch adhesive system. Clearfil SE Bond (CSE) was used as commercial reference. Bond strength to human dentin was assessed by microtensile bond strength (µTBS) test, and failure mode was classified. Morphology of the dentin bonding interface was assessed via scanning electron microscopy (SEM). Irrespective of the dental adhesives evaluated, µTBS was higher after 24 hours compared with that after 1.5 and 3 years (p ≤ 0.001). However, adhesives with BDO and PA as co-initiators showed significantly higher bond strength than the bonding resin with EDAB (p ≤ 0.002), independent of the time evaluated. The commercial adhesive CSE showed similar bond strength compared with the other groups (p ≥ 0.05). Mixed failures were mainly observed after 24 hours, while adhesive failures were more frequently observed after 1.5 and 3 years. No notable differences in homogeneity and continuity along the bonded interfaces were detected among the materials in the SEM analysis. In conclusion, benzodioxole derivatives are feasible alternative co-initiators to tertiary amine in camphorquinone-based self-etching dental adhesive formulations.
Assuntos
Humanos , Álcoois Benzílicos/química , Adesivos Dentinários/química , Cimentos de Resina/química , Dentina/efeitos dos fármacos , Dioxóis/química , Benzodioxóis/química , para-Aminobenzoatos/química , Polietilenoglicóis/química , Ácidos Polimetacrílicos/química , Propriedades de Superfície , Resistência à Tração , Fatores de Tempo , Teste de Materiais , Cânfora/análogos & derivados , Cânfora/química , Microscopia Eletrônica de Varredura , Reprodutibilidade dos Testes , Colagem Dentária/métodos , Bis-Fenol A-Glicidil Metacrilato/química , Dentina/química , Metacrilatos/químicaRESUMO
INTRODUCTION: In this study, we evaluated the caries inhibition and shear bond strength achieved with the addition of the antibacterial monomer [2-(Methacryloyloxy)ethyl] trimethylammonium chloride (MADQUAT) to an adhesive used to bond orthodontic brackets. METHODS: Experimental adhesives were formulated with addition of 0% (control), 5%, or 10% MADQUAT followed by measurement of the degree of conversion. These adhesives were used to lute brackets to the enamel of premolars (n = 30). Biofilm from a microcosm model was cultivated in half of the specimens under cariogenic challenge for 5 days. The brackets were subjected to a shear bond strength test followed by measurement of the internal hardness of the enamel around the brackets to calculate the integrated mineral loss. RESULTS: The addition of MADQUAT slightly increased the degree of conversion. Adhesive containing 10% MADQUAT significantly reduced the integrated mineral loss around the bracket but also resulted in the lowest values of bond strength. No effects on bond strength and integrated mineral loss were observed with the addition of 5% MADQUAT to the adhesive. The cariogenic challenge did not affect the bond strength and the failure mode. CONCLUSIONS: MADQUAT was effective to reduce the integrated mineral loss only when added to the adhesive at a concentration of 10% despite the reduction of bond strength.
Assuntos
Colagem Dentária/métodos , Cárie Dentária/prevenção & controle , Cimentos Dentários/uso terapêutico , Metacrilatos/uso terapêutico , Braquetes Ortodônticos , Antibacterianos/uso terapêutico , Biofilmes/crescimento & desenvolvimento , Colagem Dentária/efeitos adversos , Análise do Estresse Dentário , Humanos , Técnicas In Vitro , Braquetes Ortodônticos/efeitos adversosRESUMO
AIM: This study evaluated the in vitro effect of 35% hydrogen peroxide (HP) on surface enamel change when activated with different light curing units (LCUs). MATERIALS AND METHODS: Enamel blocks (4 × 4 × 2 mm) were obtained from bovine incisors. The initial microhardness of the enamel was determined for each specimen. After this enamel blocks were randomly divided into four groups (n = 10) and treated as follows: Control, no bleaching procedure performed; HP - LCU, application of 35% HP gel without light activation; HP + QTH, application of 35% HP gel and light activation with a Quartz Tungsten-Halogen (QTH); and HP + Light Emitting Diode, application of 35% HP gel and light-activation with a LED. New microhardness measurements were obtained, immediately, 7 and 14 days after treatment. The percentage of surface mineral change was calculated according to the baseline and post-treatment microhardness values. Additionally, six samples from each group were randomly selected and prepared for scanning electron microscopy (SEM) characterization. The data were analyzed using an analysis of variance (ANOVA) to detect differences between the three time periods, and an ANOVA and Tukey's test with a confidence level of 95%. RESULTS: There was no significant difference between the initial hardness values and hardness values after treatment in any of the groups or time periods (p > 0.05). No major surface alterations were detected with SEM when comparing control groups to those undergoing bleaching treatments. CONCLUSION: The use of 35% HP in combination to QTH or LED light curing units LCU does not have detrimental effect on the enamel surface topography or in the mineral content, when compared with unbleached enamel or enamel submitted to 35% HP treatment alone.