Characterization of whitening toothpastes and their effect on the physical properties of bulk-fill composites

Abstract Objective To characterize activated charcoal and 2% hydrogen peroxide-based toothpastes and investigate their effects on roughness, color change, and gloss of bulk-fill composite resin. Methodology Composite resin specimens (Aura Bulk Fill, SDI) were subjected to 5,000 brushing cycles with regular toothpaste (Colgate Total 12, [RT]), activated charcoal toothpaste (Bianco Dental Carbon, [AC]), or hydrogen peroxide-containing toothpaste (Colgate Luminous White Advanced, [HP]), with or without coffee exposure. The pH, particle characterization by scanning electron microscopy (SEM), and weight% of solid particles in the toothpaste were assessed. Roughness (Ra) was evaluated using a surface profile-measuring device, color change (∆Eab/∆E00) by reflectance spectrophotometer, and gloss unit (GU) by glossmeter. Kruskal-Wallis, Dunn, Friedman, and Nemenyi tests were used, and the correlation coefficient test was performed between Ra and GU (α=0.05). Results RT presented a higher Ra after brushing and did not change after staining with coffee; moreover, the ∆Eab/∆E00 values were higher for RT than HP. Regarding gloss, AC and HP obtained higher values compared to RT. A significant negative correlation between gloss and Ra was found for RT exposed to coffee. All toothpastes had a neutral pH; however, RT had the largest percentage of solids by weight. SEM images showed particles of many sizes: irregular shape (RT), more regular particles (AC), and spherical clusters (HP). Although surface roughness, color change, and gloss may compromise the longevity of restorations, the whitening toothpastes tested did not promote more morphology changes than regular toothpastes.

Influence of restorative materials on occlusal and internal adaptation of CAD-CAM inlays

Aim: To evaluate the occlusal and internal marginal adaptation of inlay restorations made of different materials, using CAD-CAM. Methods: Preparations were made for MOD inlays of one-third intercuspal width and 4 mm depth in 30 third human molars. The teeth were restored using CAD-CAM materials (n=10) of nanoceramic resin (Lava Ultimate), polymer-infiltrated ceramic network (VITA ENAMIC), or lithium disilicate glass-ceramic (IPS e.max CAD). The specimens were cemented with dual resin cement and sectioned at the center of the restoration, after which the two halves were evaluated, and photographed The occlusal and internal discrepancy (µm) was determined at five points: cavosurface angle of the occlusal-facial wall (CA-O); center of the facial wall (FW); faciopulpal angle (FPA); center of the pulpal wall (PW); and center of the lingual wall (LW). The data were submitted to the Kruskal-Wallis and the Dunn tests (α=0.05). Results: No difference was observed among the materials regarding the occlusal discrepancy at the CA-O, FPA, or PW internal points. The e.max CAD measurement at FW showed larger internal discrepancy than that of Lava (p=0.02). The internal discrepancy at LW was greater for e.max CAD than VITA ENAMIC (p=0.02). Conclusion: Lithium disilicate glass-ceramic presented greater internal discrepancy in relation to the surrounding walls of the inlay preparations

Effect of acid challenge and photoactivation distance on microhardness and roughness of flow bulk-fill composite resins / Efeito do desafio ácido e distância de fotoativação na microdureza e rugosidade de resinas compostas bulk-fill flow

Abstract Introduction composite resins are indicated to the reconstruction of proximal walls and the evaluation of properties of flow bulk-fill composite resins exposed to acid challenge is necessary. Objective to evaluate the microhardness and roughness at different depths of photoactivation of bulk-fill flow composites (Filtek Bulk Fill Flow; SureFil SDR Flow; Tetric N Ceram Bulk fill) and conventional composite resin (control, Filtek Z350 XT) subjected to acid challenge. Material and method forty composites brick shaped specimens (3x3x4 mm) were made using a polyacetal matrix. To simulate pH challenges, the samples were immersed in a demineralizing solution. Each sample had Knoop microhardness (KHN) and roughness (Ra) evaluated at three depths (superficial, medium, and cervical), considering the lateral surface of the sample. Data were submitted to Kruskal-Wallis, Friedman's and Dunn's tests with a significance level of 5%. Result comparing the composites among themselves, in superficial (p=0.693), medium (p=0.053) and cervical (p=0.176) regions, there was no difference in the KHN values. There were also no differences in roughness between the composites in superficial (p=0.356), medium (p=0.734) and cervical (p=0.207) regions. Only the Filtek Z350 XT (p=0.027) showed less difference in KHN in the middle region caused by acid challenge. Changes in roughness showed that the greatest difference was at the cervical region for Bulk Fill Flow SDR (p=0.014) and Tetric N-Ceram Bulk Fill (p = 0.003) with an increase after acid challenge. Conclusion after acid challenge, bulk-fill flow composites showed alterations similar to those presented by the conventional nanoparticulate resin composite.

Resumo Introdução as resinas compostas são indicadas para reconstrução de paredes proximais e a avaliação das propriedades das resinas compostas bulk-fill flow expostas ao desafio ácido mostra-se necessária. Objetivo avaliar a microdureza e rugosidade em diferentes profundidades de fotoativação de resinas compostas bulk-fill flow (Filtek Bulk Fill Flow; SureFil SDR Flow; Tetric N Ceram Bulk fill) e convencional (controle, Filtek Z350 XT) submetidas ao desafio ácido. Material e método quarenta amostras retangulares (3x3x4 mm) foram confeccionadas utilizando uma matriz de poliacetal. Para simular o desafio ácido, as amostras foram imersas em uma solução desmineralizante. Cada amostra teve a microdureza Knoop (KHN) e rugosidade (Ra) avaliadas em três profundidades (superficial, média e cervical), considerando a superfície lateral da amostra. Os dados foram submetidos aos testes de Kruskal-Wallis, Friedman e Dunn com nível de significância de 5%. Resultado comparando as resinas compostas entre si, nas regiões superficial (p=0,693), média (p=0,053) e cervical (p=0,176), não houve diferença nos valores de KHN. Também não houve diferenças na rugosidade entre os materiais nas regiões superficial (p=0,356), média (p=0,734) e cervical (p=0,207). Apenas o Filtek Z350 XT (p=0,027) apresentou menor diferença de KHN na região intermediária causada pelo desafio ácido. As mudanças na rugosidade mostraram que a maior diferença foi na região cervical para Bulk Fill Flow SDR (p=0,014) e Tetric N-Ceram Bulk Fill (p=0,003), com aumento após o desafio ácido. Conclusão após desafio ácido, as resinas compostas bulk-fill flow apresentaram alterações semelhantes às apresentadas pela resina composta convencional nanoparticulada.

TiO2 nanotube-containing glass ionomer cements display reduced aluminum release rates

Abstract Titanium dioxide nanotubes (TiO2-nts) were incorporated into a glass ionomer cement (GIC) with improved mechanical properties and antibacterial activity. The aims of the present in vitro study were to define the elemental characterization, aluminum (Al) release rate, and initial working time for GIC reinforced with TiO2-nts, in an experimental caries model. TiO2-nts were incorporated into GIC powder components at 5% by weight, and compared with unblended GIC. Experimental approaches used energy-dispersive spectrometry (EDS), atomic absorption spectrophotometry (AAS), and brightness loss to define surface element properties, Al release rates, and initial working time, respectively. Statistical analysis was performed by 2-way ANOVA, Tukey's test, generalized linear models, and Student's t test (a = 0.05). EDS data analysis revealed that TiO2-nts incorporated into GIC had no significant impact on the typical elemental composition of GICs in an in vitro caries model. Regarding the demineralizing solution, GIC with TiO2-nt significantly decreased the Al release rate, compared with the control group (p < 0.0001). Moreover, TiO2-nt incorporated into GIC did not alter the initial working time of the material (p > 0.05). These findings add information to our scientific body of knowledge concerning the potential impact of TiO2-nt on the performance of conventional GICs.

Effect of erosive challenge and cigarette smoke on dentin microhardness, surface morphology and bond strength / Efeito de desafios erosivos e fumaça de cigarro na microdureza, morfologia de superfície e resistência de união à dentina

Objective: This study aimed to evaluate the surface microhardness and morphology, as well as the microshear bond strength of a self-etching adhesive (Clearfil SE, Kuraray) to eroded dentin, exposed or not to cigarette smoke. Forty dental crowns were divided into 4 groups (n = 10): no treatment (control) (C); erosion (E); erosion + cigarette smoke exposure (ES); cigarette smoke exposure (S). Samples were prepared through third molars polishing until dentin exposure, followed by crown section. Erosive cycles were performed 5 times/day for 30 s at 60 min intervals. Cigarette smoke was produced with twenty cigarettes/day, during 5 days. Microhardness was evaluated initially and after the treatments. Microshear bond strength was tested after the treatments and dentin restoration with flow composite. Failure patterns and dentin morphology was evaluated by Scanning Electron Microscopy. Microshear bond strength data was submitted to two-way ANOVA, microharness test was adjusted by gamma distribution to be a non-parametric analyses (p=0.05), and surface morphology as qualitative analyses. Loss percentage of microhardness was observed only in groups submitted to erosion. Bond strength was statistically similar between all groups. The most prevalent failure pattern was of adhesive type. Morphological analysis of dentin showed obliterated tubules in groups submitted to cigarette smoke exposure. Cigarette smoke exposure did not promote any effect in the percentage of microhardness loss, as in sound dentin as in eroded dentin. Cigarette smoke, erosion, and association of both, did not alter the bond strength of self-etching adhesives to dentin. (AU)

Objetivo: Este estudo teve como objetivo avaliar a microdureza (% perda de dureza) e morfologia de superfície (MS), assim como a resistência de união (RU) de um adesivo autocondicionante (Clearfil SE, Kuraray) à uma dentina erodida, exposta ou não à fumaça de cigarro. Material e Métodos: Quarenta coroas dentais de terceiros molares foram seccionadas da raiz e polidas até a exposição dentinária, sendo aleatoriamente divididas em 4 grupos (n=10): sem tratamento (controle), erosão (E), erosão+ exposição a fumaça de cigarro (ES); exposição a fumaça de cigarro (S).O ciclo erosivo foi realizado 5 vezes/dia por 30s, com 60 minutos de intervalo entre eles. Os grupos ES e S foram exposto à fumaça de cigarro produzida por 20 cigarros/dia, durante 5 dias. A avaliação da microdureza foi realizada antes e após os tratamentos, enquanto a resistência da união por microcisalhamento foi realizada após os tratamentos Os padrões de fratura representativos e a MS dentinária foram avaliados por microscopia eletrônica de varredura (MEV). Os dados de RU foram analisados por ANOVA dois fatores, enquanto a análise de microdureza foi ajustada por distribuição gama por ser uma análise não-paramétrica (p=0.05). A MS foi analisada qualitativamente. Resultados: Os grupos expostos aos ciclos erosivos (E e ES) apresentaram % de perda de dureza significativamente menor que os grupos não expostos (Controle e S. aos ciclos erosivos (E e ES). Para RU, não houve diferença estatística significativa entre os grupos. O padrão de fratura mais observado foi do tipo adesivo, e através das imagens obtidas por MEV, observou-se a obliteração de túbulos dentinários no grupo exposto à fumaça de cigarro, enquanto os grupos submetidos aos ciclos erosivos (E e ES) apresentaram maior exposição e diâmetro de túbulos dentinários. Conclusão: A exposição à fumaça de cigarro não promove nenhum efeito quanto a perda de porcentagem de dureza dentinária, assim como em dentina erodida e saudável. A fumaça de cigarro, o processo erosivo, e a associação de ambos, não altera a resistência da união de adesivos autocondicionantes à dentina. (AU)

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)