Changes in the properties of bulk-fill resins under conditions of gastroesophageal reflux and bulimia

Aim: Evaluate the roughness, microhardness and color change of different Bulk Fill resins when submitted to the condition of gastroesophageal reflux and bulimia. Methods: 60 specimens (n = 10) of Bulk-Fill composite resins were made: M1 ­ Filtek™; M2 ­ Tetric N-Ceram and M3 ­ OPUS, through a matrix 2x6 mm and light cured by the VALO light source. After polishing, initial analyzes (48 hours - T0) of surface roughness (Ra), microhardness (VHN) and color change (ΔE) were performed. To simulate the oral condition of severe gastroesophageal reflux and bulimia, the specimens were immersed in hydrochloric acid (S1) (pH 1.7) 4 minutes a day, for 7 days. Control group specimens were immersed in artificial saliva (S2). Subsequently to immersions, mechanical brushing was performed for 3 minutes, three times a day, simulating 7 days of brushing. And again, the analyzes of Ra, VHN and ΔE were performed (7 days - T1). Thus, hydrochloric acid immersion, mechanical brushing and Ra analysis were repeated at 14 days (T2) and 21 days (T3); and T2, T3 and T4 (3 years) for VHN and ΔE. Results: After Shapiro-Wilk statistical test, ANOVA and Tukey test with Bonferroni adjustment (p>0.05), M3 showed the lowest Ra at all times compared to the other resins, while the highest Ra was at T0. M1 and T1 showed higher VHN. And M2 and T4 showed higher ΔE. Conclusion: Bulk Fill resins can be indicated for patients with Gastroesophageal Reflux and Bulimia, nonetheless, Tetric N-Ceram resin showed the worst results

Assessment of influence of LED curing units used on microhardness of resin-modified glass ionomer sealants

Aim: Resin modified glass ionomer (RMGI) is class of material that can be used as sealant for preventing and arresting the progression of caries in pits and fissures. As these are hybrid materials, their properties can be affected by factors related to the polymerization process. Therefore, this study aimed to evaluate the influence of different generations of LED curing units (Elipar DeepCure-L and VALO Grand) on Knoop microhardness values (KHN) of RMGI sealants (Clinpro XT and Vitremer). Methods: Forty cylindrical specimens (6mm ø x 1 mm high) were prepared according to the manufacturer's instructions and divided into four groups (n=10) according to the type of RMGI and LED used. The KHN of the top surface of each sample was calculated 7 days after light-curing. Data were submitted to two-way ANOVA (α = 0.05). Results: Vitremer had higher KHN values than Clinpro XT after using both LEDs (p<0.0001), but especially when light-cured with the use of VALO Grand (p<0.0001). Whereas the KHN value of Clinpro was not influenced by the LED device (p>0.05). Conclusions: Top surface microhardness values of RGMI sealants were affected by both material composition and generations of LED curing units used. Third generation LED curing units seemed to be more efficient for the polymerization of RMGI-based sealants

Effect of conventional and power office bleaching with diode laser and led light on enamel microhardness

Aim: The present study aimed to asses enamel microhardness after office bleaching with diode laser and LED light compared to the conventional bleaching procedure. Methods: Thirty-nine human premolar teeth were collected and randomly divided into three groups regarding of the bleaching technique. Group 1: Snow O bleaching gel with LED light-curing unit; Group 2: Snow L bleaching gel with diode laser irradiation; and Group 3: Opalescence Boost bleaching gel with no light source in group 3. Enamel surface changes were evaluated in one tooth in each study group and one intact tooth as a reference under a scanning electron microscope (SEM). In the remaining samples (n=12), enamel microhardness was determined by Vickers microhardness test before and after bleaching. Data were analyzed with repeated-measures ANOVA to compare microhardness changes, followed by post hoc Tukey tests at the 0.05 significance level. Results: Enamel microhardness decreased in all the groups after bleaching, with the maximum decrease in microhardness in the Snow O bleaching group with LED light, which was significantly higher than the other groups (P=0.002). The two other groups did not exhibit any significant difference in microhardness decrease (P>0.05). Conclusion:Based on the limitations of this study, it can be concluded power bleaching with 980nm diode laser was less time-consuming compare to conventional bleaching procedure and yielded better outcomes in terms of enamel surface microhardness compared to the use of an LED light-curing unit

Influência da profundidade e de um processo de envelhecimento acelerado em propriedades de resinas bulk fill / Influence of depth and an accelerated aging process on bulk fill resin properties

O presente estudo teve como objetivo avaliar o desempenho de quatro resinas bulk fill (Filtek Bulk Fill (FBF), Opus Bulk Fill (OBF), Sonicfill (SF) e Tetric N-Ceram Bulk Fill (TNBF)) e uma resina convencional (Charisma Diamond (CD)) quanto às seguintes propriedades: resistência à flexão (RF), módulo de elasticidade (ME) e dureza Knoop (KHN) em função da profundidade e após a realização de um envelhecimento acelerado. Corpos de prova em formato de barra foram confeccionados simultaneamente em diferentes profundidades (1, 2, 3, 4 e 5 mm) para realização dos testes de resistência à flexão (n=10), módulo de elasticidade (n=10) e dureza Knoop (n=3). Os testes foram realizados em dois momentos, previamente e após a realização de um envelhecimento acelerado, que consistiu na realização de uma termociclagem com banhos alternados em água a 5 e 55ºC, com 1 min de imersão em cada, por 2000 ciclos. Os resultados para o teste de RF e ME mostraram que os valores para estas duas propriedades diminuíram em função da profundidade e após a realização da termociclagem para todas as resinas estudadas. Apenas a resina TNBF não apresentou diferença estatística para valores de ME após o envelhecimento acelerado. Quanto à dureza, os valores também diminuíram em função da profundidade, porém aumentaram após a realização do envelhecimento acelerado. Apenas a resina SF não apresentou diferença estatística entre os valores de dureza antes e após o envelhecimento. A resina convencional CD após a ciclagem térmica foi a única que apresentou relação base/topo (2 mm) acima de 80%. Nenhuma das resinas do tipo bulk fill apresentou uma relação base/topo acima de 80% para a dureza quando avaliadas na espessura máxima recomendada. Com base nos resultados obtidos, pode-se afirmar que, quando fotoativadas na espessura máxima recomendada, apenas a resina convencional CD apresentou resultados condizentes com a homogeneidade esperada em todas as condições deste estudo. Entretanto, para as resinas do tipo bulk fill, pode-se observar que as propriedades estudadas, de modo geral, sofreram uma diminuição significativa em função da profundidade. Para o envelhecimento, a dureza, diferentemente dos outros parâmetros, mostrou uma tendência de aumento.

Como as características dos LEDs de segunda e terceira geração podem influenciar a dureza de compósitos restauradores: uma revisão da literatura / How the second and third LED generation features can influence the hardness of restorative composites: a review of the literature.

Objetivo: Várias fontes de luz têm sido utilizadas desde que os materiais fotoativados foram introduzidos na odontologia. Diodos emissores de luz (LEDs) se popularizaram como a principal opção para a polimerização dos materiais restauradores. O objetivo nessa revisão da literatura foi avaliar a influência das fontes de luz emitidas por diodo (LEDs) de segunda e terceira geração sobre a dureza de compósitos restauradores. Revisão de literatura: Nas bases de dados PubMed e Google Scholar foram pré-selecionados 239 artigos na língua inglesa entre os anos de 2010 e 2020, utilizando os termos: lightcuring, LED light sources, and dental LEDs. Dos 239 artigos inicialmente selecionados, 37 artigos foram avaliados devido aos critérios de inclusão/exclusão no estudo. Considerações finais: Vários estudos apontaram diferenças importantes na dureza dos compósitos restauradores testados, tanto na superfície de topo quanto na base. No entanto, essas diferenças estavam mais associadas a características como: estado de conservação do LED, irradiância, tempo de ativação, espectro de emissão dos aparelhos e sua compatibilidade ao fotoiniciador presente no compósito. Assim, podemos considerar que o monitoramento das condições do aparelho, e a escolha correta da fonte de luz de acordo com o compósito a ser utilizado são essenciais para maximizar a dureza dos compósitos restauradores, pois embora os aparelhos de terceira geração sejam preferencialmente indicados para compósitos com fotoiniciadores alternativos, os aparelhos que emitem luz azul apresentam vantagens quando o compósito é ativado apenas pela Canforoquinona.(AU)

Objective: Several light sources have been used since the light-curing materials were introduced in dentistry. Light-emitting diodes (LEDs) have become popular as the main option for the polymerization of restorative materials. This literature review aimed to evaluate the influence of second and third generation Light-emitting Diode (LEDs) sources on the hardness of restorative composites. Literature Review: In the PubMed and Google Scholar databases, 239 scientific papers in English were pre-selected between 2010 and 2020 using light-curing, LED light sources, and dental LEDs. After reading, 37 articles were selected to compose the review. Several studies have pointed out significant differences in the hardness of the tested restorative composites, both on the top and base surfaces. However, these differences were more associated with characteristics such as: LED conservation conditions, irradiance, curing time, the emission spectrum of the devices and their compatibility with the photoinitiator used in the composite. Final Considerations: Thus, it can be considered that monitoring the condition of the device and the correct choice of light sources according to the composite to be used is essential to maximize the hardness of the restorative composites, because although third-generation devices are preferably indicated for composites with alternative photoinitiators, devices that emit blue light have advantages when the composite is activated only by Camphorquinone.(AU)

Light transmittance and depth of cure of a bulk fill composite based on the exposure reciprocity law

Abstract The objective of this study was to evaluate the effect of the exposure reciprocity law of a multi-wave light-emitting diode (LED) on the light transmittance (LT), depth of cure (DOC) and degree of conversion in-depth (DC) of a bulk fill composite. A bulk fill composite (EvoCeram® bulk fill, Ivoclar Vivadent) was photoactivated using the multi-wave LED (VALO™ Cordless, Ultradent). The LED was previously characterized using a spectrophotometer to standardize the time of exposure when using the Standard or Xtra-Power modes with the same radiant exposure of 20J/cm2. LT was evaluated through samples of the bulk fill composite every millimeter till 4 mm in-depth. DOC was evaluated according to the ISO 4049. DC of the central longitudinal cross-section from each sample of the DOC test was mapped using FT-NIR microscopy. Data were statistically analyzed according to the experimental design (α=0.05; ß=0.2). The radiant exposure in the violet wavelength range for Standard and Xtra-Power was 4.5 and 5.0 J/cm2, respectively; for the blue wavelength range the radiant exposure for Standard and Xtra-Power was 15.5 and 15.0 J/cm2, respectively. There was no statistical difference in the DOC using Standard or Xtra-Power light-curing modes, but the DOC was lower than the claimed by the manufacturer (4 mm). The DC was not significantly affected by the light-curing mode up to 4 mm in depth (p>0.05). According to exposure reciprocity law, the reduction in exposure time using the same radiant exposure did not affect the depth of cure of the bulk fill composite.

Resumo O objetivo deste estudo foi avaliar o efeito da lei de reciprocidade de um diodo emissor de luz (LED) multi-wave na transmitância de luz (LT), profundidade de cura (DOC) e grau de conversão em profundidade (DC) de um compósito bulk fill. Material e Métodos: Um compósito bulk fill (EvoCeram®, Ivoclar Vivadent) foi fotoativado utilizando um LED multi-wave (VALO ™ Cordless, Ultradent). O LED foi previamente caracterizado usando um espectrofotômetro para padronizar o tempo de exposição utilizando os modos Standard ou Xtra-Power com a mesma dose de energia de 20 J/cm 2. A LT foi avaliada através de amostras do compósito bulk fill a cada milímetro até 4 mm de profundidade. O DOC foi avaliado de acordo com a ISO 4049. O DC foi realizado em forma de mapeamento da seção transversal longitudinal central de cada amostra do teste de DOC utilizando microscopia FT-NIR. Os dados foram analisados estatisticamente de acordo com o delineamento experimental (α=0,05; ß=0,2). A exposição radiante na faixa de comprimento de onda violeta para os modos Standard e Xtra-Power foi de 4,5 e 5,0 J/cm2, respectivamente; e para a faixa de comprimento de onda azul, a exposição radiante para os modos Standard e Xtra-Power foi de 15,5 e 15,0 J/cm2, respectivamente. Não houve diferença estatística no DOC utilizando os modos de fotopolimerização Standard ou Xtra-Power, mas o DOC foi menor do que o reivindicado pelo fabricante (4 mm). O DC não foi afetado significativamente pelo modo de fotopolimerização até 4 mm de profundidade (p>0,05). De acordo com a lei de reciprocidade da exposição, a redução no tempo de exposição utilizando a mesma exposição radiante não afetou a profundidade de cura do compósito bulk fill.

Effect of Protein-Based Treatment on Chemical Composition, Hardness and Bond Strength of Remineralized Enamel

Abstract This study evaluated the chemical composition and microhardness of human enamel treated with an Enamel Matrix Derivative (EMD) solution, and the bond strength between composite resin and this enamel. Thirty human enamel samples were randomly divided into three groups: Untouched Enamel (UE), Demineralized Enamel (DE) and Demineralized Enamel Treated with EMD (ET). DE and ET groups were subjected to acid challenge and ET treated with EMD (EMD was directly applied over conditioned enamel and left for 15 min). Samples from each group (n=4) had chemical composition assessed through to attenuated total reflectance Fourier transform infrared (ATR-FTIR). Knoop microhardness of enamel samples from each group (n=10) was measured. For the microshear bond strength, the samples were etched for 30 s, and the adhesive was applied and cured for 10 s. Two matrixes were placed on the samples, filled with Filtek Z350 XT composite and cured for 20 s, each. The matrix was removed, and the microshear bond strength of each group (n=10) was tested. Data were subjected to Kruskal-Wallis test (for microhardness), to analysis of variance and to Tukey's test (for microshear bond strength); (α=0.05). FTIR results have shown phosphate (hydroxyapatite indicator) in 900-1200 cm-1 bands in the UE and ET groups, which were different from the DE group. Microhardness and microshear analyses recorded higher statistical values for the UE and ET groups than for DE. EMD application to demineralized enamel seems to have remineralized the enamel; thus, the microhardness and bond strength was similar between UE and ET groups.

Resumo Este estudo avaliou a composição química e microdureza do esmalte humano tratado com solução de Derivados da Matriz do Esmalte (EMD) e a resistência de união entre compósito e este esmalte. Trinta amostras de esmalte humano foram aleatoriamente divididas em três grupos: Esmalte Intocado (UE), Esmalte Desmineralizado (DE) e Esmalte Desmineralizado Tratado com EMD (ET). Os grupos DE e ET foram submetidos a desafio ácido e ET tratado com EMD (O EMD foi aplicado diretamente sobre esmalte condicionado e deixado por 15 minutos). Amostras de cada grupo (n = 4) tiveram composição química avaliada através de espectroscopia no infravermelho por transformada de Fourier com reflectância total atenuada (FTIR-ATR). A microdureza Knoop das amostras de esmalte de cada grupo (n=10) foi mensurada. Para a resistência ao microcisalhamento, as amostras foram condicionadas por 30 s, o adesivo aplicado e foto-ativado por 10 s. Duas matrizes plásticas (1 mm de comprimento) foram posicionadas sobre as amostras, preenchidas com compósito Filtek Z350 XT e foto-atiavadas por 20 s cada. As matrizes foram removidas e a resistência ao microcisalhamento de cada grupo (n=10) foi testada. Os dados foram submetidos ao teste de Kruskal-Wallis (para análise da microdureza), à análise de variância e ao teste de Tukey (para análise da resistência ao microcisalhamento); (α=0.05). Os resultados do FT-IR mostraram fosfato (indicador de hidroxiapatita) na banda entre 900-1200 cm-1 nos grupos UE e ET, diferentemente do grupo DE. Análises de microdureza e microcisalhamento demonstraram resultados estatisticamente superiores para os grupos UE e ET quando comparados ao DE. A aplicação de EMD ao esmalte desmineralizado parece ter remineralizado o esmalte; assim, a microdureza e a resistência de união foram semelhantes entre os grupos UE e ET.

Influence of radiant exposure values from two third generation LED curing units on polymerization profile and microhardness of orthodontic composite under ceramic and metallic brackets

ABSTRACT Introduction: Third generation of LED light curing units might be used in short exposure periods for orthodontic brackets bonding. Objective: This study evaluated the effect of the different radiant exposure (RE) values: Manufacturers' instructions (MI), ½ MI, 1/4 MI and Turbo mode. Two third-generation LED curing units were used: VALO® and Bluephase 20i® . The degree of conversion (DC) and Vickers hardness (VHN) of an orthodontic composite (OC) (Transbond XT) under metallic (MB) or ceramic brackets (CB) were measured. Methods: OC was applied to the bracket base, which was then placed over an attenuated total reflectance (ATR) table coupled to an infrared light spectroscope, or to a glass surface for the VHN analysis. The specimens were light-cured and DC values were calculated. The VHN was obtained in a microhardness tester. The data were analyzed with 2-way ANOVA followed by Tukey's post-hoc test (pre-set α=0.05). Linear regression analysis evaluated the relationship between RE values and dependent variables. Results: CB allowed higher DC and VHN values than MB (p< 0.001). No significant difference was noted among groups when CB were used. For MB, MI groups showed the highest DC and VHN values. A significant, but weak relationship was found between delivered RE values and dependent variables. Conclusions: The decrease in RE values from third generation LED CU did not jeopardize the DC values when CB were used, but can compromise DC and VHN values when MB are used.

RESUMO Introdução: A terceira geração de LEDs fotopolimerizadores pode ser utilizada em curtos períodos de exposição para a colagem de braquetes ortodônticos. Objetivo: O presente estudo avaliou o efeito dos diferentes valores de irradiância (IR): instruções do fabricante (IF), ½ IF, » IF e modo Turbo. Dois fotopolimerizadores LED de terceira geração (VALO® e Bluephase20i®) foram utilizados. Foram mensurados o grau de conversão (GC) e a dureza Vickers (VHN) de um compósito ortodôntico (CO) (Transbond XT) sob braquetes metálicos (BM) ou cerâmicos (BC). Métodos: O compósito ortodôntico foi aplicado na base do braquete e foi posicionado sobre uma mesa de refletância total atenuada (ATR) acoplada a um espectroscópio de infravermelho ou a uma superfície de vidro para análise de VHN. As amostras foram fotopolimerizadas e os valores de GC foram calculados. O VHN foi obtido em um microdurômetro. Os dados foram analisados com ANOVA de 2 fatores seguida do teste post-hoc de Tukey (predefinido α = 0,05). A análise de regressão linear avaliou a relação entre os valores de IR e as variáveis dependentes. Resultados: BC permitiu valores maiores de GC e VHN do que BM (p<0,001). Nenhuma diferença significativa foi observada entre os grupos quando BC foi utilizado. Para BM, os grupos de IF mostraram os maiores valores de GC e VHN. Uma relação significativa, mas fraca, entre os valores de IR entregue e as variáveis dependentes foi encontrada. Conclusões: A diminuição dos valores de IR dos fotopolimerizadores LED de terceira geração não prejudicou os valores de GC quando BC foram utilizados, mas pode comprometer os valores de GC e VHN quando BM são utilizados.

Effect of antioxidant agents after dental bleaching on luting of ceramic laminates / Efeito de agentes antioxidantes pós-clareamento na cimentação de laminados cerâmicos

O objetivo deste estudo in vitro foi avaliar o efeito da aplicação de agentes antioxidantes após o clareamento dentário e previamente à cimentação de laminados cerâmicos na estabilidade cromática do conjunto restaurador, assim como nas propriedades mecânicas de nanodureza (HIT), módulo de elasticidade (Eit*), grau de conversão, resistência de união e morfologia da interface adesiva. Ademais, a neutralização de peróxido de hidrogênio e a caracterização superficial do esmalte, como ângulo de contato, energia de superfície, energia livre total de interação, microscopia eletrônica de varredura e espectroscopia de energia dispersiva do substrato submetido à ação das soluções antioxidantes e do agente clareador também foram analisados. Duzentos e quarenta e dois blocos de esmalte dentário (7x8x0,6mm) foram utilizados para o processo de cimentação e distribuídos em grupos experimentais de acordo com os métodos de procedimentos (grupo não clareado, grupo clareado com Whiteness HP Maxx 35%), tipos de antioxidantes adotados (controle; ácido ascórbico 10% e α-tocoferol 10%) e períodos de cimentação (após 24 horas e 14 dias do processo de cimentação) (n = 22). Foi utilizado o sistema adesivo Tetric N Bond Universal e o cimento resinoso Variolink Esthetic LC (Ivoclar Vivadent) como agentes cimentantes. Os dados foram submetidos a testes estatísticos de normalidade e analisados por ANOVA e teste de Tukey (α = 0,05). Os dados da morfologia da interface adesiva, obtidas pela microscopia confocal a laser, foram submetidas ao teste Kappa inter-examinadores e os dados foram submetidos aos testes Kruskal-Wallis e Dunn (α = 0,05). Os resultados mostraram que, de modo geral, a utilização da solução antioxidante α-tocoferol 10% pós-clareamento no período mediato promoveu resultados satisfatórios com relação à estabilidade cromática do conjunto restaurador, assim como para as propriedades mecânicas, grau de conversão, resistência de união e morfologia da interface adesiva comparado ao grupo clareado sem associação dos agentes antioxidantes, tanto para o período mediato, quanto para o período de 14 dias (p< 0,05). A solução de αtocoferol 10% apresentou maiores valores de neutralização do peróxido de hidrogênio e maiores valores de molhabilidade do esmalte em relação aos grupos controle e ácido ascórbico (p< 0,05). A energia de superfície e energia livre total de interação do esmalte dentário foi significativamente influenciada pelo tratamento clareador (p< 0,05). Dessa forma, conclui-se que o emprego da solução antioxidante α-tocoferol 10% promoveu resultados promissores, sugerindo que o mesmo poderia ser utilizado mediatamente após o clareamento dental na cimentação de laminados cerâmicos(AU)

The aim of this in vitro study was to evaluate the effect of antioxidant agents application after tooth bleaching and prior to luting of ceramic veneers on color stability of the restorative set, as well as on mechanical properties of nanohardness (HIT), elastic modulus (Eit*), degree of conversion, bond strength and morphology of the adhesive interface. Furthermore, the hydrogen peroxide neutralization and surface characterization of enamel, such as contact angle, surface energy, total free energy of interaction, scanning electron microscopy and energy-dispersive spectroscopy of the substrate submitted to the action of antioxidant solutions and bleaching agent were also analyzed. Two hundred forty two dental enamel blocks (7 x 8 x 0.6 mm) were used for the luting process and distributed into experimental groups according to the procedure methods (unbleached group, bleached group with Whiteness HP Maxx 35%), types of antioxidants adopted (control; 10% ascorbic acid and 10% α-tocopherol) and the luting periods (24 hours and 14 days after the luting process) (n = 22). Tetric N Bond Universal adhesive system and Variolink Esthetic LC resin cement (Ivoclar Vivadent) were used as luting agents. Data were submitted to statistical tests of normality and analyzed by ANOVA and Tukey tests (α = 0.05). The adhesive interface morphology data, obtained by confocal laser microscopy, were submitted to the interexaminer Kappa test and the data were submitted to Kruskal-Wallis and Dunn´s tests (α = 0.05). The results showed that, in general, the use of 10% α-tocopherol antioxidant solution after bleaching in mediate period promoted satisfactory results regarding the color stability of the restorative set, as well as for the mechanical properties, degree of conversion, shear bond strength and adhesive interface morphology compared to the bleached group without antioxidant agents association, both for the mediate and 14-day period (P < 0.05). The 10% αtocopherol solution showed higher hydrogen peroxide neutralization values and higher enamel wettability values compared to the control and ascorbic acid groups (P < 0.05). Surface energy and total free energy of interaction of tooth enamel were significantly influenced by the bleaching treatment (P < 0.05). Thus, it is concluded that the use of 10% αtocopherol antioxidant solution promoted promising results, suggesting that it could be used mediately after tooth bleaching on luting of ceramic laminates(AU)

Análise in vitro da capacidade de soluções contendo fluoreto e/ou hexametafosfato na remineralização da dentina / In vitro analysis of the capacity of solutions containing fluoride and/or hexametaphosphate on the remineralization of dentin

O objetivo do presente estudo foi avaliar a capacidade de soluções contendo HMP e F, sozinhos ou em associação, em induzir a remineralização dentinária em um protocolo in vitro. Blocos de dentina radicular bovina (4 × 6 cm, n = 100) foram preparados e submetidos à indução de lesões de cárie artificiais em dois terços da superfície; cada bloco foi utilizado como seu próprio controle. Em seguida, os blocos foram divididos em 10 grupos experimentais (n=10/grupo), de acordo com as soluções a serem testadas: (1) Placebo (sem F ou HMP); (2) 0,5% HMP; (3) 0,75% HMP; (4) 1% HMP; (5) 250 ppm F; (6) 500 ppm F; (7) 1100 ppm F; (8) 250 ppm F + 0,5% HMP; (9) 500 ppm F + 0,75% HMP e (10) 1100 ppm F + 1% HMP. Os blocos foram tratados por um minuto, duas vezes ao dia com as respectivas soluções, e submetidos a uma ciclagem de pH durante 7 dias. Em seguida, foram determinadas a porcentagem de recuperação da dureza de superfície (%RDS) e a área integrada da lesão de subsuperfície (ΔKHN). Os dados foram submetidos a ANOVA e teste de Fisher LSD (p<0.05). Uma relação dose-reposta foi observada entre as concentrações de F nas soluções sem HMP e as variáveis %RDS e ΔKHN; quanto às soluções contendo apenas HMP, uma relação dose-resposta foi observada somente para ΔKHN. Em relação à %RDS, os grupos placebo e 0,5% HMP, e os grupos 0,75% e 1% HMP não apresentaram diferenças significativas entre si. Quando associado ao F, o HMP aumentou a capacidade de remineralização da superfície e subsuperfície dentinária, visto que os grupos contendo F + HMP apresentaram resultados significativamente melhores em relação aos grupos contendo F sozinho. Em acréscimo, a solução contendo 250 ppm F + 0,5% HMP promoveu um efeito remineralizador semelhante à solução contendo 500 ppm F. Já em relação à ∆KHN, diferenças estatísticas foram observadas entre todos os grupos na área tratada, sem diferenças significativas quanto às áreas controle e desmineralizada. Os resultados permitem concluir que a adição de HMP às soluções fluoretadas potencializou o efeito destas sobre a remineralização das lesões artificiais de cárie em dentina, tanto na superfície quanto em profundidade(AU)

The present study aimed to investigate the ability of solutions containing HMP and F, alone or in association, in promoting dentin remineralization in an in vitro protocol. Bovine root dentin blocks (4 × 6 cm, n = 100) were prepared, and caries-like lesions were induced in two thirds of the surface; each block served as its own control. Then, blocks were divided into 10 experimental groups (n = 10 / group), according to the solutions to be tested: (1) Placebo (without F or HMP); (2) 0.5% HMP; (3) 0.75% HMP; (4) 1% HMP; (5) 250 ppm F; (6) 500 ppm F; (7) 1100 ppm F; (8) 250 ppm F + 0.5% HMP; (9) 500 ppm F + 0.75% HMP and (10) 1100 ppm F + 1% HMP. Specimens were treated for one minute, twice a day with the respective solutions, and subjected to a pH-cycling regime for 7 days. Next, the percentage of the superficial hardness recovery (%SHR) and integrated loss of subsurface hardness (ΔKHN) were determined. Data were submitted to ANOVA and Fisher LSD's test (p<0.05). A dose-response relationship was observed between F concentrations in solutions without HMP and the variables %SHR and ΔKHN; as for the solutions containing HMP alone, a dose-response relationship was only observed for ΔKHN. Regarding %SHR, no significant differences were observed Placebo and 0.5% HMP groups, nor between 0.75% and 1% HMP groups. When associated with F, HMP was shown to increase the remineralizing capacity of the solutions both at the surface and the subsurface of dentin specimens, since the groups containing F + HMP showed significantly superior results compared to groups containing F alone. In addition, the solution containing 250 ppm F + 0.5% HMP promoted a remineralizing effect similar to that containing 500 ppm F. Regarding ∆KHN, significant differences were observed among all groups in the treated area, while no significant differences were observed among the groups in the control and demineralized areas. The results allowed the conclusion that the addition of HMP to fluoridated solutions significantly enhanced their remineralizing potential on dentin artificial caries lesions, both at the surface and in depth(AU)

A influência do eugenol na microdureza de duas resinas compostas comerciais / The influence of eugenol on the microhardness of two commercial composite resins

Objetivo: avaliar, in vitro, a dureza superficial e profunda de dois tipos diferentes de resina composta, quandoem contato com o cimento de óxido de zinco e eugenol (IRM®). Métodos: foram selecionadas as resinasCharisma® e Vittra® e confeccionados 80 corpos de prova, sendo 40 para cada marca de compósito, queforam divididos em oito grupos (n=10) conforme o contato (imediato, 7 dias, 14 dias) ou não (grupo controle)com o eugenol. Colocou-se num pote dappen uma porção de IRM e um espécime de resina pronto, que,após a presa do material restaurador temporário e a remoção do exemplar colocado, gerou o molde pararealização das amostras em contato com o eugenol, sendo armazenado em água em temperatura ambiente,para os subgrupos 7 e 14 dias. Em sequência, foi inserido um único incremento de resina composta e polimerizadopor 40 segundos, gerando os espécimes que foram armazenados em local seco para serem submetidosao teste de microdureza Vickers sob uma carga de 300 gramas, com tempo de penetração de 10 segundos.Os dados obtidos foram analisados pelo teste ANOVA, a um nível de significância de p<0,05. Resultados:somente o grupo da resina Charisma® que teve contato imediato com eugenol não atingiu 80% de durezaprofunda em relação à superficial. Entretanto, para todos os grupos analisados, tanto a dureza superficialquanto a profunda aumentaram após o contato com o eugenol em relação ao grupo controle. Conclusão: oeugenol não influenciou negativamente a dureza das resinas compostas.(AU)

Objective: to evaluate, in vitro, the superficial and deep hardness of two different types of composite resin when in contact with zinc oxide eugenol cement (IRM). Method: Charisma® and Vittra® resins were selected and 80 specimens were made, 40 for each composite brand that were divided into eight groups (n = 10) according to contact (immediate, 7 days, 14 days) or no (control group) with eugenol. A portion of IRM and a ready-made resin specimen were placed in a dappen pot, which after setting the temporary restorative material and removing the placed specimen, generated the template for making the samples in contact with eugenol, being stored in water in room temperature for subgroups 7 and 14 days. In sequence, a single increment of composite was inserted and polymerized resin for 40 seconds, generating specimens that were stored in a dry place to be submitted to the Vickers microhardness test under a load of 300 grams, with a penetration time of 10 seconds. The data obtained were analyzed by the ANOVA test, at a significance level of p <0.05. Results: only the Charisma® resin group that had immediate contact with eugenol did not reach 80% deep hardness in relation to superficial hardness. However, for all groups analyzed, both superficial and deep hardness increased after contact with eugenol compared to the control group. Conclusion: eugenol did not negatively influence the hardness of composite resins.(AU)

Physical-mechanical properties of bulk fill composites submitted to biodegradation by streptococcus mutans

Abstract The aim of this study was to evaluate the Streptococcus mutans biofilm influence on the roughness (Ra), gloss (GU), surface hardness (KHN) and flexural strength (FS) of high viscosity bulk fill composites. Filtek Bulk Fill (FBF), Tetric N Ceram Bulk Fill (TNC), X-tra fil Bulk Fill (XF) and Filtek Z350 (FZ) were used. Ten discs of each composite were prepared for Ra, KHN and GU and 20 bars for the FS. After 24 h, specimens were polished and initial analyzes performed. Samples were sterilized and subjected to biodegradation for 7 days and final analyzes performed. Representative samples of each group were evaluated in Scanning Electron Microscope. Data were submitted to ANOVA two factors and Tukey test. XF presented the highest values (p<0.05) of Ra before and after biodegradation (0.1251; 0.3100), and FZ (0.1443) the lowest after biodegradation (p<0.05). The highest GU values (p<0.05) were observed for FZ (71.7; 62) and FBF (69.0; 64.6), and the lowest (p<0.05) for TNC (61.4; 53.3) and XF (58.5; 53.5), both before and after biodegradation. For KHN the highest values were obtained by XF (151.7; 106), and the (p< 0.05) lowest values for TNC (62.2; 51.8), both before and after biodegradation. The highest values (p<0.05) of FS were observed for FZ (127.6) and the lowest (p<0.05) for TNC (86.9); after biodegradation, XF (117.7) presented the highest (p<0.05) values compared to TNC and FZ." In conclusion, biodegradation increased Ra and decreased GU and KHN for all. Concerning FS, degradation provided a significant decreased value only for FZ.

Resumo O objetivo deste estudo foi avaliar a influência do biofilme de S. mutans na rugosidade (Ra), brilho (GU), dureza superficial (KHN) e resistência à flexão (FS) de compósitos de Bulk Fill de alta viscosidade. Foram utilizados Filtek Bulk Fill (FBF), Tetric N Ceram Bulk Fill (TNC), X-tra fil Bulk Fill (XF) e Filtek Z350 (FZ). Dez discos de cada compósito foram preparados para Ra, KHN e GU e 20 barras para o FS. Após 24 h, os espécimes foram polidos e as análises iniciais realizadas. As amostras foram esterilizadas e submetidas a biodegradação por 7 dias e as análises finais foram realizadas. Amostras representativas de cada grupo foram avaliadas no Microscópio Eletrônico de Varredura. Os dados foram submetidos à ANOVA dois fatores e teste de Tukey. XF apresentou os maiores valores (p<0,05) de Ra antes e após a biodegradação (0,1251; o00,3100) e FZ (0,1443) os menores após a biodegradação (p<0,05). Os maiores valores de GU (p<0,05) foram observados para FZ (71,7; 62) e FBF (69,0; 64,6), e os mais baixos (p<0,05) para TNC (61,4; 53,3) e XF (58,5; 53,5), ambos antes e depois da biodegradação. Para KHN, os valores mais altos foram obtidos por XF (151,7; 106), e os (p<0,05) valores mais baixos para TNC (62,2; 51,8), antes e depois da biodegradação. Os maiores valores (p <0,05) de FS foram observados para a FZ (127,6) e os menores (p<0,05) para a TNC (86,9); após biodegradação, o XF (117,7) apresentou os maiores valores (p<0,05) em comparação ao TNC e FZ. Em conclusão, a biodegradação aumentou o Ra e diminuiu a GU e a KHN para todos. Em relação à FS, a degradação promoveu uma diminuição significativa apenas para a FZ.

Surface deterioration of indirect restorative materials

Abstract The objective of this work was to evaluate the effects of in vitro and in situ biodegradation on the surface characteristics of two resin cements and a hybrid ceramic system. One hundred and eighty specimens (4X1.5mm) of each material (Maxcem Elite, NX3 Nexus and Vita Enamic) were made and randomly distributed in twelve groups (n=15) according to the material and biodegradation method. The specimens were then submitted to the following challenges: storage in distilled water 37 ºC for 24 h or 7 days, storage for 7 days, at 37 ºC, in stimulated saliva or in situ. The in situ stage corresponded to the preparation of 15 intraoral palatal devices, used for 7 days. Each device presented 3 niches, where a sample of each materials was accommodated. Specimens from both saliva and in situ groups suffered a cariogenic challenge, corresponding to the application of a solution of 20% of sucrose, 10 times throughout each day. After each biodegradation method, the surface roughness (Ra), Vickers hardness (VHN) and scanning electron microscopy (SEM) analyzes were performed. The data collected were evaluated by Levene test, two-way ANOVA and Tukey`s test (α=5%). The in situ challenge promoted the greater biodegradation, regardless of the material. Regarding the materials, the Vita Enamic VHN was negatively affected by all biodegradation methods and the Nexus NX3 presented better performance than the self-adhesive cement tested. Therefore, within the conditions of this work, it was concluded that in situ biodegradation can affect negatively the surface characteristics of indirect restorative materials.

Resumo O objetivo deste trabalho foi avaliar os efeitos da biodegradação in vitro e in situ nas características superficiais de dois cimentos resinosos e de um sistema cerâmico híbrido. Cento e oitenta espécimes (4X1,5mm) de cada material (Maxcem Elite, NX3 Nexus e Vita Enamic) foram distribuídos aleatoriamente em doze grupos (n=15) de acordo com o material e o método de biodegradação. Os espécimes foram então submetidos aos seguintes desafios: armazenamento em água destilada 37ºC por 24 horas ou 7 dias, armazenamento por 7 dias, a 37ºC, em saliva estimulada ou in situ. O estágio in situ correspondeu à preparação de 15 dispositivos intra-orais palatinos, utilizados por 7 dias. Cada dispositivo apresentou 3 nichos, onde uma amostra de cada material foi acomodada. As amostras dos grupos saliva e in situ sofreram um desafio cariogênico, correspondendo à aplicação de uma solução de 20% de sacarose, 10 vezes ao longo de cada dia. Após cada método de biodegradação, foram realizadas as análises de rugosidade superficial (Ra), dureza Vickers (VHN) e microscopia eletrônica de varredura (MEV). Os dados coletados foram analisados por meio do teste de Levene, ANOVA two-way e teste de Tukey (α=5%). O desafio in situ promoveu maior degradação, independentemente do material. Em relação aos materiais, a VHN do Vita Enamic foi afetada negativamente por todos os métodos de degradação e o Nexus NX3 apresentou melhor desempenho que o cimento autoadesivo testado. Portanto, dentro das condições deste trabalho, concluiu-se que a biodegradação in situ pode afetar negativamente as características superficiais de materiais restauradores indiretos.

Influence of cavo superficial enamel acid-etching on the microtensile bond strength of low-shrinkage composite resin / Influência do condicionamento ácido do ângulo cavo superficial na resistência adesiva de restaurações em um compósito de baixa contração de polimerização

Introduction: To prevent the shrinkage stresses produced during polymerization, composite resins of low polymerization shrinkage were developed. Objective: To evaluate the microtensile bond strength in class I cavities restored by acid-etching the cavosurface angle and with composite resins indicated for posterior teeth. Material and method: 48 healthy molars were selected and divided into six groups (n = 8), considering that the cavosurface enamel of three groups was etched with 35% phosphoric acid. The teeth were restored with the Clearfil SE Bond adhesive system and Filtek Z350 XT, Empress Direct, and Charisma Diamond composite resins, which were light-cured for 40 seconds. After 24 hours, the teeth were taken to a cutting machine, which produced sections in the buccolingual and mesiodistal directions. This resulted in toothpicks of 0.9×0.9 mm that were taken to the universal testing machine for the microtensile bond strength test. Statistical analysis was performed with ANOVA and Tukey's test (p < 0.05). Result: There was no statistically significant difference between the groups evaluated. Conclusion: Acid-etching the cavosurface angle did not affect the performance of restorations, probably due to the adhesive system used.

Introdução: Com o intuito de se evitar as tensões geradas durante a contração de polimerização das resinas compostas, foram desenvolvidas as resinas compostas de baixa contração de polimerização. Objetivo: Avaliar a resistência à microtração em cavidades classe I restauradas com tratamento ácido do ângulo cavo superficial e resina composta indicada para dentes posteriores. Material e método: Foram selecionados 48 molares hígidos que foram divididos em 6 grupos (n=8), sendo que 3 desses tiveram o esmalte cavo superficial condicionado com ácido fosfórico a 35%. Os dentes foram restaurados com o sistema adesivo Clearfil SE Bond e as resinas compostas Filtek Z350 XT, Empress Direct e Charisma Diamond, fotoativadas por 40 segundos. Após 24 horas, os dentes foram levados para máquina de corte, na qual foram realizados cortes no sentido vestíbulo-lingual e no sentido mésio-distal obtendo - se palitos de 0,9×0,9 mm que foram levadas para a máquina de ensaio universal para a realização do teste de microtração. Para análise estatística foi realizado análise de variância e teste de Tuckey (p < 0,05). Resultado: Não houve diferença estatística significante entre os grupos avaliados. Conclusão: O condicionamento ácido do ângulo cavo superficial não influenciou no desempenho das restaurações provavelmente devido ao sistema adesivo utilizado.

Effect of CPP-ACP on remineralization of artificial caries-like lesion: an in situ study

Abstract The purpose of this double-blind, randomized, crossover in situ study is to compare remineralization of preformed enamel lesions by casein phosphopeptide-stabilized amorphous calcium phosphate (CPP-ACP) and fluoride dentifrice products. During each of four 10-day experimental legs, 10 participants wore intraoral removable palatal acrylic appliances with four human enamel slabs with preformed lesions. A 0.03-mL treatment paste was dripped extraorally onto the enamel blocks once a day for 3 min. The four randomly allocated treatments were as follows: CO- Control: silica dentifrice without fluoride; MP: MI Paste; MPP: MI Paste Plus and FD: Fluoride dentifrice - 1100 ppm F as NaF). Knoop surface hardness (SH) test was performed in three stages (T0 - sound enamel, T1 - after preformed lesion, and T2 - after treatment) and the cross-sectional hardness (CSH) test was performed after treatment using a 50-gram Knoop load for 15 s. Knoop hardness number (KHN) was similar between treatments. %SHr was significantly higher in the MP, FD, and MPP when compared to CO group (Kruskal-Wallis and Mann-Whitney tests, p < 0.05). Harder enamel was found in MP (75 μm) and FD groups at 75 to 175 μm. Treatment with DF, MP, and MPP promoted an increase of 20.27%, 19.24%, and 14.71%, respectively, in Integral Hardness Change (ΔIHC) when compared to CO (p<0.05). Remineralizing agents (MP, MPP, and DF) were able to inhibit demineralization of human enamel subjected to high cariogenic challenge in situ. DF had the greatest preventive potential against the progression of carious lesions.

Atenolol increases dental mineralization in male offspring of treated hypertensive rats and normotensive rats

Abstract This study evaluates how atenolol affects dental mineralization in offspring of female spontaneously hypertensive rats (fSHR) and normotensive Wistar rats (fW). fSHR and fW were treated with atenolol (100 mg/Kg/day, orally) during pregnancy and lactation. Non-treated fSHR and fW were the control groups. Enamel and dentin hardness were analyzed (Knoop, 15 g load, 10s) in mandibular incisor teeth (IT) and molar teeth (MT) obtained from the male offspring of atenolol-treated and non-treated fWistar and fSHR. Data were analyzed by ANOVA, followed by Tukey post hoc test (p < 0.05). Atenolol reduced the arterial blood pressure (SBP) in fSHR, but it did not change the SBP in fW. The offspring of non-treated fSHR had lower enamel (IT and MT) and dentin (IT) hardness than the offspring of non-treated fW (p < 0.05). Atenolol increased enamel and dentin hardness in the IT obtained from the offspring of fSHR and fW (p<0.05), but the offspring of fSHR presented higher values (p < 0.05). Atenolol did not alter enamel width in the IT obtained from any of the groups, but it increased enamel and dentin hardness in the IT obtained from the offspring of fSHR and fW. Atenolol affected the IT obtained from the offspring of fSHR. Atenolol increased only enamel hardness in the MT obtained from the offspring of fW. In conclusion, maternal hypertension reduces tooth hard tissues, and treatment with atenolol increases tooth hardness in male offspring of hypertensive and normotensive female rats.

Influence of salivary conditioning and sucrose concentration on biofilm-mediated enamel demineralization

Abstract The acquired pellicle formation is the first step in dental biofilm formation. It distinguishes dental biofilms from other biofilm types. Objective To explore the influence of salivary pellicle formation before biofilm formation on enamel demineralization. Methodology Saliva collection was approved by Indiana University IRB. Three donors provided wax-stimulated saliva as the microcosm bacterial inoculum source. Acquired pellicle was formed on bovine enamel samples. Two groups (0.5% and 1% sucrose-supplemented growth media) with three subgroups (surface conditioning using filtered/pasteurized saliva; filtered saliva; and deionized water (DIW)) were included (n=9/subgroup). Biofilm was then allowed to grow for 48 h using Brain Heart Infusion media supplemented with 5 g/l yeast extract, 1 mM CaCl2.2H2O, 5% vitamin K and hemin (v/v), and sucrose. Enamel samples were analyzed for Vickers surface microhardness change (VHNchange), and transverse microradiography measuring lesion depth (L) and mineral loss (∆Z). Data were analyzed using two-way ANOVA. Results The two-way interaction of sucrose concentration × surface conditioning was not significant for VHNchange (p=0.872), ∆Z (p=0.662) or L (p=0.436). Surface conditioning affected VHNchange (p=0.0079), while sucrose concentration impacted ∆Z (p<0.0001) and L (p<0.0001). Surface conditioning with filtered/pasteurized saliva resulted in the lowest VHNchange values for both sucrose concentrations. The differences between filtered/pasteurized subgroups and the two other surface conditionings were significant (filtered saliva p=0.006; DIW p=0.0075). Growing the biofilm in 1% sucrose resulted in lesions with higher ∆Z and L values when compared with 0.5% sucrose. The differences in ∆Z and L between sucrose concentration subgroups was significant, regardless of surface conditioning (both p<0.0001). Conclusion Within the study limitations, surface conditioning using human saliva does not influence biofilm-mediated enamel caries lesion formation as measured by transverse microradiography, while differences were observed using surface microhardness, indicating a complex interaction between pellicle proteins and biofilm-mediated demineralization of the enamel surface.

Physicomechanical properties of different nanohybrid composites after aging: color stability, flexural strength, and microhardness

Aim: To evaluate the physicomechanical properties of different hybrid composites (Charisma Diamond - CD, Aura - AU, NT Premium - NT, Opallis - OP, Filtek Z250 ­ Z250) after 6 months of aging in distilled water. Methods: Discs were fabricated and color measurements were performed after 24 hours and at 7, 30, and 180 days. Flexural strength was determined using the three-point bending test. For the microhardness test, the specimens were flattened to obtain polished and flat surfaces and indentations. The results for ∆E and microhardness were analyzed by two-way repeated-measures ANOVA and Tukey's HSD test. The flexural strength results were analyzed by two-way ANOVA and Tukey's test (α=0.05). Results: The ∆E values for composite resins varied in the following order: CD (3.54)a < Z250 (4.70)ab < AU (4.95)ab < OP (5.20)ab < NT (6.23)b. ∆E values were lower for 24 h (3.84)a < 7 days (4.43)ab < 30 days (4.93)b. The highest values were observed after 180 days (ΔE = 6.54)c. The flexural strength of composite resins varied in the following order: CD (89.17 MPa)a < Z250 (73.06 MPa)b < OP (60.30 MPa)c < NT (51.28 MPa)c < AU (23.77 MPa)d. Flexural strength values were significantly higher for 24 h (68.62 MPa)a < 180 days (51.40 MPa)b. The microhardness of composite resins varied in the following order: Z250 (112.05)a < CD (102.15)ab < OP (92.04)bc < NT (87.77)d < AU (87.68)d. Microhardness was significantly higher for 180 days (113.44)a < 24 h (78.21)b. Conclusion: The microhybrid (Z250) and one of the nanohybrid composites (CD) performed better. The color stability and flexural strength of all tested composites decreased with storage time

Effect of modified 45s5 bioglass on physical and chemical properties of bleached enamel

Aim: The purpose of this study was to evaluate of the effects of modified 45S5 bioglass (BG) before, after, and during the bleaching procedure with 35% hydrogen peroxide (HP) on the tooth colour change and physicochemical and morphological properties of human enamel. Methods: Forty-two human premolar enamel samples were prepared and randomly divided into six groups as G1: control (deionized distilled water for 20 min), G2: BG (Bioglass suspension for 20 min), G3: HP (hydrogen peroxide 35% for 20 min), G4: BG before HP (Bioglass suspension for 20 min followed by hydrogen peroxide 35%) , G5: BG after HP (hydrogen peroxide 35% followed by Bioglass suspension for 20 min), and G6: BG during HP (Bioglass in hydrogen peroxide 35% suspension for 20 min). The treatment procedure was performed on the whole enamel surface. Colorimetry was done before and after the treatment procedure. Two specimens from each group were selected for morphological analysis with scanning electron microscope (SEM). Microhardness analysis was performed after the treatment procedure and chemical analysis of BG dissolution was done for BG+DDW and BG+HP suspensions. Results: No statistically significant difference in colour was observed among different groups (P= 0.073133) and the yellowness index decreased in all of the four HP groups. The greatest reduction in microhardness occurred in groups HP and BG before HP (P<0.001) while the BG group showed increased microhardness measurements (P<0.001). Statically significant differences in microhardness were found among the groups. Elemental analysis showed significantly increased levels of Ca and P in BG after HP and BG before HP groups when compared to the HP group. Ionic release of BG was significantly greater in HP when compared to DDW. Conclusion: Using BG before HP had a greater protective effect since it increased microhardness more effectively, decreased mineral loss, and retained the integrity of the enamel surface. The HP group had the lowest microhardness and BG during HP showed less protective effects compared to BG before HP