Evaluation of Bond Strength, Nanoleakage, and Marginal Adaptation of Bulk-fill Composites Submitted to Thermomechanical Aging.

PURPOSE: To evaluate the bond strength (BS), nanoleakage, and marginal adaptation (MA) of three bulk-fill and one conventional composite, submitted or not to mechanical and thermal cycling. MATERIALS AND METHODS: Ninety-six molars were selected and 4-mm-deep class I cavities were prepared and restored. Half of the teeth were submitted to mechanical and thermal cycling (MTC). Teeth were divided into 8 groups (n = 12), according to the composite used - Filtek Z350 XT (Z350), Tetric N-Ceram Bulk Fill (TET), Filtek Bulk Fill Posterior Restorative (FBF) and SonicFill (SF) - and aging, submitted or not to MTC. Fifty-six teeth (n = 7) were used for bond-strength testing, which was performed on stick-shaped specimens obtained from the restored area. Two sticks per tooth were selected to assess nanoleakage. For MA analysis, 40 teeth (n = 5) were sectioned parallel and perpendicular to the occlusal surface and resin-based replicas from the obtained surfaces were prepared. Fracture pattern, nanoleakage, and MA were evaluated using SEM. Quantitative analysis of nanoleakage and MA were performed with ImageJ software. Data obtained were submitted to two-way ANOVA and Tukey's test (ɑ = 0.05). RESULTS: TET presented good MA and higher values of BS when compared to SF. Z350 and FBF presented poorer MA and lower BS, which was statically similar to the other groups. SF obtained the best MA values. Regarding nanoleakage, the highest values were obtained for TET, which differed significantly from the other groups, which presented similar results among themselves. Aging by MTC solely affected MA. CONCLUSION: Bulk-fill composites presented similar performance to the conventional nanocomposite and remained stable when aged.

Physical and photoelastic properties of bulk-fill and conventional composites.

PURPOSE: This study evaluated the influence of thickness increment on degree of conversion (DC), Knoop microhardness (KHN), and polymerization-shrinkage stress (PSS) by photoelasticity of three dental composites. METHODS: For DC and KHN, 45 samples were prepared and divided into nine groups (n=5), according to composite (microhybrid [Filtek Z250 - Z250], bulk-fill flowable [SureFil SDR Flow - SDR], and nanohybrid composite [N'Durance - NDU]) and increment thickness (1, 1.5, and 3 mm). PSS was measured by photoelastic analysis. Composites were placed into a photo-elastic model cavity and light-cured. DC and KHN data were subjected to two-way ANOVA and Bonferroni post hoc test. PSS results were qualitatively evaluated through Kruskal-Wallis test. RESULTS: SDR showed the highest DC values. At top and bottom surfaces, the highest KHN was obtained by Z250. Z250 showed higher PSS than SDR in 1.5 mm increments. NDU showed higher PSS than SDR in 3 mm increments. CONCLUSION: The bulk-fill composite demonstrated better DC and similar KHN and PSS in deeper layers compared to conventional composites. Bulk-fill composites may perform as well as conventional nanohybrid and microhybrid composites.

Influence of a hydrophobic monomer on the physical and mechanical properties of experimental surface sealants.

This study evaluated the effect of adding the hydrophobic monomer 1,12 dodecanediol dimethacrylate (DDDMA) to experimental sealants with and without thermocycling on degree of conversion (DC), water sorption (WS), water solubility (WSB), color stability (ΔE), and micro-shear bond strength (µSBS). Five experimental and one commercially available sealant (Bisco - BIS) were tested. The experimental sealants were formulated by mixing different percentages of DDDMA monomers and urethane dimethacrylate (UDMA). The photoinitiator system was composed by camphorquinone (CQ) and tertiary amine 4-ethyl benzoate dimetilamiono (EDBA). Ethanol was used as a solvent. The experimental groups were named sequentially according to the monomeric content (DDDMA/UDMA): S40/40 (40/40), S50/30 (50/30), S60/20 (60/20), S70/10 (70/10) and S80/0 (80/0). Data were analyzed separately by one-way ANOVA, followed by Tukey's test (p<0.05). The values of DC ranged from 94.59% (S40/40) to 54.02% (S80/10). BIS showed the highest WS value (p<0.05) and S40/40, S50/30, S60/20 and S80/0 showed the lowest WS values of all tested sealants. WSB values ranged from 7.88 µg/mm3 (BIS) to 13.27 µg/mm3 (S70/10). The highest ΔE value was 11.05±2.88 for BIS and the highest µSBS value was found for S60/20. No significant difference was observed in bond strength between sealants and bovine enamel after thermocycling. Adding DDDMA to the composition of surface sealants can improve its performance, once the monomer increased the degree of conversion and the color stability.

Effect of different concentrations of nanohydroxyapatite on tooth bleaching effectiveness and enamel bond strength / Efeito de diferentes concentrações de nanohidroxiapatita na efetividade clareadora e força de adesão ao esmalte

Objective: To evaluate the effect of 35% hydrogen peroxide (35% HP) combined to different concentrations of nanohydroxyapatite (nHA) on the effectiveness of dental bleaching (superficial enamel and deep dentin) and enamel bond strength. Material and Methods: Fifty bovine dental specimens (5x5x2mm) were divided into 5 groups, according to the treatments (n = 10): no bleaching (negative control); 35% HP (positive control); 35% HP+ 5% nHA; 35% HP + 10% nHa; and 35% HP + 15% nHA. Three in-office bleaching sessions were made. The color analysis was performed on the enamel surface and the opposite dentin, using a spectrophotometer. The results were expressed in the CIE L*a*b* system. After this, the adhesive system was applied to the tooth structure, and the dental specimens received a composite restoration. The microshear bond strength test was performed 24 h after the restoration. Data were submitted to ANOVA and Tukey's test (α=0.05). Results: For the enamel color analysis, all bleached groups differed statistically from the unbleached group, with increasing L* values and decreasing b* values. The addition of different concentrations of nHA did not interfere with the bleaching effectiveness for the enamel and opposite dentin. For microshear bond strength, no statistically significant differences were presented between groups. The adhesive failure rate of the 35% HP + 10% nHA group was lower than the 35% HP group and similar to the negative control. Conclusion: The addition of different concentrations of nHA in 35% of hydrogen peroxide did not interfere with the bleaching efficacy of enamel and deep dentin and did not affect the enamel bond strength after bleaching.(AU)

Objetivo: avaliar o efeito do peróxido de hidrogênio a 35% (HP 35%) associado a diferentes concentrações de nanohidroxiapatita (nHA) sobre a efetividade clareadora do esmalte superficial, dentina profunda e da força de adesão ao esmalte. Material e Métodos: Cinquenta espécimes bovinos (5x5x2mm) foram divididos 5 grupos (n = 10): sem clareamento (controle negativo); HP 35% (controle positivo); HP 35% + nHA 5%; HP 35% + nHA 10%; e HP 35% + nHA 15%. Três sessões de clareamento de consultório foram realizadas. A análise de cor foi realizada na superfície do esmalte e na dentina oposta e os resultados expressos no sistema CIE L*a*b*. Depois disso, os sistemas adesivos foram aplicados no esmalte, e os blocos receberam uma restauração em resina composta. O teste microcisalhamento foi realizado 24 h após a restauração. Os dados foram submetidos à ANOVA e ao teste de Tukey (α = 0,05). Resultados: Para a análise de cor do esmalte, todos os grupos clareados diferiram estatisticamente do grupo não clareado. A adição de diferentes concentrações de nHA não interferiu com a eficácia clareadora para o esmalte e dentina. Para o microcisalhamento, não houve diferença entre os grupos. A taxa de falha adesiva do grupo HP 35% + nHA 10% foi menor do que o grupo HP 35% e similar ao controle negativo. Conclusão: a adição de diferentes concentrações de nHA em PH 35% não interferiu na eficácia clareadora do esmalte e da dentina e não afetou a força de adesão do esmalte após o clareamento (AU)

Influence of a hydrophobic monomer on the physical and mechanical properties of experimental surface sealants

Abstract This study evaluated the effect of adding the hydrophobic monomer 1,12 dodecanediol dimethacrylate (DDDMA) to experimental sealants with and without thermocycling on degree of conversion (DC), water sorption (WS), water solubility (WSB), color stability (ΔE), and micro-shear bond strength (μSBS). Five experimental and one commercially available sealant (Bisco - BIS) were tested. The experimental sealants were formulated by mixing different percentages of DDDMA monomers and urethane dimethacrylate (UDMA). The photoinitiator system was composed by camphorquinone (CQ) and tertiary amine 4-ethyl benzoate dimetilamiono (EDBA). Ethanol was used as a solvent. The experimental groups were named sequentially according to the monomeric content (DDDMA/UDMA): S40/40 (40/40), S50/30 (50/30), S60/20 (60/20), S70/10 (70/10) and S80/0 (80/0). Data were analyzed separately by one-way ANOVA, followed by Tukey's test (p<0.05). The values of DC ranged from 94.59% (S40/40) to 54.02% (S80/10). BIS showed the highest WS value (p<0.05) and S40/40, S50/30, S60/20 and S80/0 showed the lowest WS values of all tested sealants. WSB values ranged from 7.88 µg/mm3 (BIS) to 13.27 µg/mm3 (S70/10). The highest ΔE value was 11.05±2.88 for BIS and the highest μSBS value was found for S60/20. No significant difference was observed in bond strength between sealants and bovine enamel after thermocycling. Adding DDDMA to the composition of surface sealants can improve its performance, once the monomer increased the degree of conversion and the color stability.

Influence of Water Storage and Bonding Material on Bond Strength of Metallic Brackets to Ceramic.

This study investigated the influence of water storage (24 h and 6 months), and Transbond XT and Fuji Ortho LC bonding materials on the bond strength of metallic brackets bonded to feldspathic ceramic. Four cylinders of feldspathic ceramic were etched with 10% hydrofluoric acid for 60 s. Each cylinder received two layers of silane. Metallic brackets were bonded to the cylinders using Transbond XT or Fuji Ortho LC. Light-activation was carried out with 40 s total exposure time using Bluephase G2. Half the specimens for each bonding materials (n=20) were stored in distilled water at 37 °C for 24 h and the other half for 6 months. Shear bond strength testing was performed after storage times at a crosshead speed of 1 mm/min. The adhesive remnant index (ARI) was used to evaluate the amount of adhesive remaining on the ceramic surface at ×8 magnification. Data were subjected to two-way ANOVA and Tukey's test (p<0.05). Transbond XT showed significantly higher bond strength (p<0.05) than Fuji Ortho LC. Significant differences in bond strength (p<0.05) were found when 24 h and 6 months storage times were compared between materials. ARI showed a predominance of score 0 for all groups, and higher scores at 1, 2 and 3 for 24 h storage time. In conclusion, storage time and bonding materials showed significant influence on the bond strength of brackets to ceramic.

Influence of Water Storage and Bonding Material on Bond Strength of Metallic Brackets to Ceramic

Abstract: This study investigated the influence of water storage (24 h and 6 months), and Transbond XT and Fuji Ortho LC bonding materials on the bond strength of metallic brackets bonded to feldspathic ceramic. Four cylinders of feldspathic ceramic were etched with 10% hydrofluoric acid for 60 s. Each cylinder received two layers of silane. Metallic brackets were bonded to the cylinders using Transbond XT or Fuji Ortho LC. Light-activation was carried out with 40 s total exposure time using Bluephase G2. Half the specimens for each bonding materials (n=20) were stored in distilled water at 37 °C for 24 h and the other half for 6 months. Shear bond strength testing was performed after storage times at a crosshead speed of 1 mm/min. The adhesive remnant index (ARI) was used to evaluate the amount of adhesive remaining on the ceramic surface at ×8 magnification. Data were subjected to two-way ANOVA and Tukey's test (p<0.05). Transbond XT showed significantly higher bond strength (p<0.05) than Fuji Ortho LC. Significant differences in bond strength (p<0.05) were found when 24 h and 6 months storage times were compared between materials. ARI showed a predominance of score 0 for all groups, and higher scores at 1, 2 and 3 for 24 h storage time. In conclusion, storage time and bonding materials showed significant influence on the bond strength of brackets to ceramic.

Resumo: Este estudo investigou a influência da armazenagem em água (24 h e 6 meses) e dos materiais para colagem Transbond XT e Fuji Ortho LCO na resistência da união de bráquetes metálicos fixados a cerâmica feldspática. Quatro cilindros de cerâmica foram condicionados com ácido fluorídrico a 10% por 60 s. Todos os cilindros receberam duas camadas de silano. Bráquetes metálicos foram fixados aos cilindros utilizando os materiais Transbond XT ou Fuji Ortho LC. A fotoativação foi realizada com tempo de exposição total de 40 s utilizando Bluephase G2. Metade das amostras de cada material de colagem (n=20) foi armazenada em água destilada a 37 °C por 24 h e outra metade por 6 meses. O ensaio de resistência da união ao cisalhamento foi realizado após os períodos de armazenagem à velocidade de 1 mm/minuto. O Índice de Remanescente Adesivo (IRA) foi utilizado para avaliar a quantidade de adesivo residual na superfície da cerâmica, em lupa estereoscópica com aumento de 8x. Os dados foram submetidos à Análise de Variância de dois fatores e teste de Tukey (p<0,05). Transbond XT apresentou resistência de união significativamente maior do que Fuji Ortho LC. Diferença significante (p<0,05) na resistência da união foi encontrada entre os períodos de armazenagem, qualquer que fosse o material para colagem. O IRA mostrou predominância de escore 0 para todos os grupos, com aumento de escores 1, 2 e 3 para o período de armazenagem de 24 h. Em conclusão, o período de armazenagem e os materiais de colagem influenciaram significativamente a resistência da união de bráquetes à cerâmica.

Influence of successive light-activation on degree of conversion and Knoop hardness of the first layered composite increment.

PURPOSE: To evaluate the influence of light-activation of second, third and fourth increments on degree of conversion (DC) and microhardness (KHN) of the top (T) and bottom (B) surface of the first increment. MATERIALS AND METHODS: Forty samples (n = 5) were prepared. In groups 1-4, after each increment light-activation (multiple irradiation), T and B of the first increment were measured in DC and KHN. In groups 5-8, only the first increment was made (single irradiation) and measurements of DC and KHN were taken at 15 min intervals. The light-activation modes were (XL) 500 mW/cm(2) × 38 s (G1/G5); (S) 1000 mW/cm(2) × 19 s (G2/G6), (HP) 1400 mW/cm(2) × 14 s (G3/G7); (PE) 3200 mW/cm(2) × 6 s (G4/G8). Data for DC and KHN were analyzed separately by using PROC MIXED for repeated measures and Tukey-Kramer test (α = 0.05). RESULTS: For KHN, B showed lower values than T. PE resulted in lower values of KHN in B surface. For single and multiple irradiations, T and B of first measurement showed the lowest KHN and the fourth measurement showed the highest, with significant difference between them. For single irradiation, first and second increments presented similar KHN, different from the third and fourth increment, which did not differ between them. For multiple irradiations, the second light-activation resulted in KHN similar to first, third and fourth increments. For DC, except QTH, T presented higher DC than B. CONCLUSION: The light-activation of successive increments was not able to influence the KHN and DC of the first increment.

Adhesive Restorations as An Esthetic Solution in Dentinogenesis Imperfecta.

Loss of tooth structure is the main sequela of dentinogenesis imperfecta (DI). Due to severe enamel attrition, patients with DI often present with esthetic, occlusal, endodontic, and speech complications. Therefore, an interdisciplinary approach, divided into separate clinical steps, should be developed to provide comprehensive dental rehabilitation. The purpose of this case report is to discuss the use of composite resin restorations as a transitional treatment step for the anterior teeth of an eight-year-old boy with DI until his bone and dental development permit orthodontic and orthognatic surgery.

In vitro evaluation of the effect of different polishing techniques on the surface roughness of composite resins submitted to at-home and in-office bleaching procedures.

OBJECTIVE: Bleaching agents may affect the properties of dental materials. The aim of this study was to evaluate the effect of different polishing techniques on the surface roughness of composite resins submitted to the at-home and in-office bleaching treatment. MATERIALS AND METHODS: Disc-shaped specimens were carried out of nanofilled and microhybrid composites (n = 10). Finishing step was performed after light curing (L1) and polishing after 24 h with two systems (L2). Then, specimens were submitted to the home or in-office bleaching procedures, and roughness was re-evaluated (L3). The surface roughness (Ra) readings were measured at L1, L2, and L3 times using a profilometer. Data were statistically analyzed by multiple-way analysis of variance and Tukey test (α = 0.05). RESULTS: The polishing procedures decreased Ra for both composites compared to baseline values (L1). The roughness of specimens polished with jiffy did not present significant difference after polishing step (L2) and bleaching treatment (L3). However, the groups polished with Sof-Lex discs had increase on the Ra values after bleaching. CONCLUSION: The polishing is an important procedure to reduce the roughness of dental restorations and composite surface polished with jiffy system improved the degradation resistance to the bleaching agents compared to Sof-Lex discs.

Influence of softening test and light-activation protocols on resin composite polymer structure.

OBJECTIVE: This study analyzed the influences of the light-activation protocol and softening test on the degree of conversion (DC) and Knoop Hardness (KHN) of a microhybrid resin composite. MATERIALS AND METHODS: Filtek Z250 (3M ESPE) was light-activated with a third-generation light-emitting diode (Valo Ultradent) by three protocols - standard, high power, and plasma emulation - or with a quartz-tungsten halogen XL 3000 (3M ESPE) in conventional mode. All modes were set to deliver 19 J/cm(2). The DC (N = 20) was determined by Fourier transform infrared spectrometry on the top (T) and bottom (B) surfaces. For the KHN test, samples were subdivided in four groups (n = 5 each) according to the storage media: absolute ethanol, 75% ethanol, distilled water, and air (control group). The KHN values were evaluated on T and B before and 24 h after immersion in the storage media. Data were analyzed by split-plot analysis of variance (ANOVA; for DC) or repeated-measures split-plot ANOVA (for KHN), followed by Tukey's test (α = 0.05). RESULTS: For the DC, the light-activation protocol did not influence the results and there was no difference between T and B. For the KHN test, the light-activation protocol did not influence the results and T showed higher microhardness values than B for all experimental conditions. There were significant differences in KHN depending on the storage media. Samples immersed in absolute ethanol generally presented lower KHN values, with no differences compared to samples in 75% ethanol. CONCLUSION: The storage media affected the outcomes of the softening test.

Effect of different monomer-based composites and acid etching pre-treatment of enamel on the microleakage using self-etch adhesives systems.

OBJECTIVE: To evaluate quantitatively the marginal microleakage of restorations carried out with self-etching adhesives with or without prior phosphoric enamel acid etching of silorane or methacrylate resin-based composite restorations subjected to thermal cycling. MATERIALS AND METHODS: Forty cavities were prepared at the proximal surface of bovine incisors and randomly divided according to the etching of the enamel and restorative system used. The groups were restored with methacrylate [Adper SE Plus adhesive (3M ESPE) + Filtek Z250 (3M ESPE)] or silorane [Filtek LS adhesive (3M ESPE) + Filtek LS composite (3M ESPE)] restorative systems, light-cured using a LED unit (Bluephase 16i, Vivadent). After restorative procedure and thermocycling (1000 cycles), the specimens were immersed in methylene blue for 2 h. The specimens were triturated and the powder was used for analysis in an absorbance spectrophotometer. Data were statistically analyzed by 2-way ANOVA (alpha = 0.05). RESULTS: No statistical difference between the restorative materials tested with or without previous acid etching of enamel in Class II marginal microleakage was observed (p > 0.05). CONCLUSIONS: The use of acid etching prior to self-etching adhesives did not interfere on the microleakage of methacrylate- or silorane-based restorations.

Influência do selamento de superfície na rugosidade e microdureza de compósitos dentais antes e após o clareamento dental / Influence of the surface sealing on the roughness and microhardness of dental composites before and after dental bleaching

O objetivo deste estudo foi avaliar a rugosidade de superfície e microdureza Knoop de compósitos microhíbrido e nanoparticulado, selados ou não, antes e após o clareamento dental. Vinte amostras foram confeccionadas (5 mm x 2 mm) e fotopolimerizadas usando um LED, com irradiância de 1390 mW/cm2. As amostras foram divididas em 4 grupos (n = 5) de acordo com o tipo de compósito e selamento ou não da superfície. Após a polimerização foi realizado o polimento das amostras com discos de óxido de alumínio, em seguida, aplicado o selante de superfície de acordo com os grupos experimentais. A rugosidade de superfície média (Ra) foi avaliada com um perfilômetro e a microdureza utilizando um indentador Knoop com carga de 10 g durante 10 s. Foram realizadas duas leituras (L1 e L2); a leitura L1 foi feita 24 h após a confecção das amostras e L2 após a aplicação do agente clareador. Os resultados obtidos foram submetidos a ANOVA e teste de Tukey (a = 0,05). O clareamento não afetou a microdureza Knoop e rugosidade de superfície, e a aplicação do selante reduziu apenas a microdureza. A manutenção dos menores valores de dureza para os grupos selados após o tratamento clareador indica a manutenção deste material

Does an additional UV LED improve the degree of conversion and Knoop Hardness of light-shade composite resins?

OBJECTIVE: The purpose of this study was to evaluate the degree of conversion (DC) using FT-Raman spectroscopy and the Knoop hardness (KHN) of composites cured by second and third-generation LED light curing-units (LCU), Radii Cal and Ultralume 5. METHODS: Three composites (Filtek Supreme XT, Filtek Z350, and Esthet X) were selected for this study. KHN testing (n=10) was performed with 10 indentations for the top (T) and bottom (B) surfaces. For DC (n=10), both the T and B surfaces were analyzed. RESULTS: For KHN, the three composites differed in hardens. There was a "LCU-surface" interaction, in which Radii Cal showed significantly greater hardens in the B surface. For DC, there was a "composite-surface-LCU" interaction. For the "composite" factor, there was no significant difference between the groups, except for Supreme XT-Radii Cal (T or B surfaces). For the "LCU" factor there was a significant difference for Supreme XT T surface, Ultralume 5 obtained a higher DC. For the Z350 T surface, a significant difference in the DC in which Radii Cal obtained better results. For the "surface" factor, all groups presented T surfaces with a higher DC than the B surfaces, the sole exceptions involved Esthet X-Radii Cal and Z350-Ultralume 5. CONCLUSION: Knowledge regarding composite composition and the characteristics of LCUs are important for effective polymerization.

Avaliação de dureza knoop de resina composta ativada por diferentes fontes de luz / Knoop hardness of composites polymerized by differents light curing units

O objetivo deste estudo foi avaliar a influência das fontes fotoativadoras LED pulsante (LD13 - GGDent) ou halógena(Optilux 501 - Demetron) na microdureza Knoop da resina composta Z250 (3MESPE) na cor A3, em três profundidades distintas. Para tanto, foram confeccionadas 20 cavidades classe I em terceiros molares humanos, separados em 2 grupos (n=10). As cavidades foram preparadas utilizando-se broca 245 (KG Sorensen) nas dimensões de 3 x 4 x 3mm e as restaurações foram confeccionadas em três incrementos oblíquos, sendo a fotoativação de cada incremento realizada com 20s em modo contínuo para fonte halógena ou 60s para fonte LED (10s em modo pulsante e 50s em modo contínuo). Em seguida, as amostras foram armazenadas por sete dias em 100% umidade relativa na temperatura de 37°C + 1. Apóso período de armazenagem, as coroas foram seccionadas no sentido mésio-distal em cortadeira metalográfica. As raízes foram seccionadas logo abaixo da junção cemento-esmalte e perpendicularmente ao longo eixo do dente, sendo então descartadas. As hemicoroas foram incluídas em resina de poliestireno e a superfície que continha a restauração recebeuacabamento com lixas de óxido de alumínio nas granulações de 600, 1200 e 2000 e polimento com discos de feltro e pastas diamantadas com granulações de 6, 3 e 1 μm. O ensaio de microdureza Knoop foi realizado com carga de 25gdurante 20s. Foram realizadas 15 penetrações em cada hemicoroa, sendo 5 em cada profundidade estudada. Os dados foram transformados em número de dureza Knoop (KHN), submetidos à Análise de Variância e comparados pelo teste de Variação Múltipla de Tukey (5%). Os resultados obtidos revelaram que não houve diferença estatística significativa entre as profundidades estudadas. A maior média de dureza obtida foi com a fonte LED (82,98), apresentando diferença estatística significativa com a fonte halógena (61,27). Pode-se concluir que a densidade de energia dos aparelhosinfluenciou nos resultados de dureza obtidos.