Resumo O objetivo deste estudo foi avaliar a dureza Knoop de diferentes cores de um cimento resinoso fotoativado diretamente ou através da interposição de um disco de cerâmica, medindo 15 min ou 24 h após exposição à luz, em diferentes profundidades. Amostras do cimento resinoso (Variolink Veneer) em sete cores foram fabricados num molde de elastômero, coberto com tira de poliéster, seguido de um disco cerâmico (IPS e.max Press) com 0.7 mm de espessura e fotoativado por 20 s com o aparelho LED (IPS e.max Press). O cimento resinoso fotoativado foi transversalmente desgastado na porção média e os valores de microdureza Knoop foram obtidos após 15 min após exposição à luz e após armazenagem em água deionizada à 37 °C por 24 h. Cinco penetrações foram feitas na secção transversal à 100 e 700 μm da superfície de topo. Dez amostras foram confeccionadas para cada condição de teste. Os dados foram submetidos à Análise de Variância em esquema de parcelas subdivididas (cor, tempo pós-ativação, modo de ativação e profundidade), seguido pelo teste de Tukey post hoc (α=0,05). Diferença significante para a cor (p<0,0001), modo de ativação (p<0,001), tempo pós-ativação (p<0,0001) e profundidade (p<0,0001) foi detectada. Nenhuma interação significante foi encontrada (p>0,05), exceto para a interação cor x tempo pós-ativação (p<0,0045) e modo de ativação x tempo pós-ativação (p<0,0003). A cor do cimento resinoso teve significante efeito na dureza Knoop. A ativação indireta através do material cerâmico reduziu significativamente a dureza Knoop. A dureza Knoop aumentou significativamente após 24 h em todas as cores do cimento comparados aos valores obtidos após 15 min. A profundidade do cimento resinoso reduziu significativamente os valores de dureza Knoop.

Abstract The aim of this study was to evaluate Knoop hardness of different shades of a resin cement light-cured directly or through ceramic discs, measured 15 min or 24 h after light exposure, and at different depths. Specimens of a commercial resin cement (Variolink Veneer) in seven shades, were fabricated in an elastomeric mold, covered with a mylar strip, a 0.7 mm thick ceramic disc (IPS e.max Press) was placed and the cement was light-activated for 20 s using a blue LED (Radii-Cal). The cured resin cement specimens were transversely wet-flattened to their middle portion and microhardness (Knoop) values were recorded at 15 min after light exposure and after deionized water storage at 37 ºC for 24 h. Five indentations were made in the cross-sectional area at 100 and 700 μm depths from the top surface. Ten specimens were made for each test conditions. Data were submitted to ANOVA split-plot design (shade, post-cure time, mode of activation and depth), followed by Tukey post hoc test (α=0.05). Significant differences for shade (p<0.0001), mode of activation (p<0.001), post-cure time (p<0.0001) and depth (p<0.0001) were detected. No significant interactions (p>0.05) were found, except for shade x post-cure time (p<0.0045) and mode of activation x post-cure time (p<0.0003). Resin cement shade has a significant effect on Knoop hardness. Indirect activation through a ceramic material reduced significantly Knoop hardness. Hardness Knoop significantly increased after 24 h in all cements shades compared to values obtained after 15 min. Resin cement depth significantly reduced Knoop hardness.

Resumo O objetivo deste estudo foi avaliar a eficácia da aplicação de energia sônica sobre a resistência de união à microtração e a microdureza após o processo de restauração. Um total de 40 terceiros molares humanos foram extraídos. Cavidades Classe II foram preparadas e restauradas com os compósitos SonicFill ou Filtek Z350 XT com e sem a aplicação de energia sônica. Após os dentes serem armazenados em água durante 24 h, foram seccionados em palitos (1,0 mm2) e submetidos a ensaio de tração. Para um ensaio de dureza Knoop de profundidade, as amostras foram cortadas e as penetrações foram feitas sequencialmente a partir da superfície para o fundo das amostras em três intervalos de 1 mm cada. As amostras foram então submetidas a uma carga de 50 g durante 10 s. Os resultados dos testes de tração (fatores: sistema de inserção e compósito) e dureza (fatores: sistema de inserção x compósito x profundidade) foram submetidos ao teste de normalidade Kolmogorov-Smirnov, seguido da análise de variância e do teste de Tukey (significância de 5%). Para o fator sistema de inserção, observou-se maior resistência de união para as cavidades que foram restauradas com energia sônica (p < 0,001). Para a dureza Knoop de profundidade, a dureza a 1 mm de profundidade foi significativamente maior do que a profundidade de 3 mm apenas para as restaurações com o compósito Filtek Z350 XT sem a aplicação de energia sônica. Portanto, o uso de energia sônica durante o processo restaurador melhorou a união, mas não afetou acentuadamente a dureza de profundidade para ambos os compósitos.

Abstract The aim of this study was to evaluate the efficacy of applying sonic energy on microtensile bond strength and microhardness after the restoration process. A total of 40 human third molars were extracted. Class II cavities were prepared and restored with composite SonicFill or Filtek Z350 XT with and without the application of sonic energy. After the teeth were stored in water for 24 h, the teeth were sectioned into sticks (1.0 mm2) and subjected to tensile testing. For a depth Knoop hardness test, the samples were cut and indentations were made sequentially from the surface of the samples to the bottom of the samples in three intervals of 1 mm each. The samples were then subjected to a load of 50 g for 10 s. The results from the tensile (factors: placement system and composite) and hardness (factors: placement system, composite and depth) tests were subjected to the Kolmogorov-Smirnov normality test, followed by analysis of variance and Tukey’s test (5% significance). For the placement system factor, higher bond strength was observed for the cavities that were restored with sonic energy (p < 0.001). For depth Knoop hardness, the hardness at 1 mm depth was significantly greater than that at 3 mm depth just for the restorations with Filtek Z350 XT composite without the application of sonic energy. Therefore, the use of sonic energy during the restorative process improved bonding, yet it did not markedly affect the depth hardness for both composites.

Resumo Este estudo avaliou os efeitos de três primers para metais e um sistema adesivo multi-mode na resistência da união por cisalhamento (SBS) de um compósito resinoso de baixa viscosidade a uma liga niquel-cromo (Ni-Cr). Noventa placas Ni-Cr foram divididas em 9 grupos (n=10). As superfícies foram jateadas com Al2O3 e condicionadas com três primers adesivos: Alloy Primer (AP), Universal Primer (TP) e Rely X Ceramic Primer (CP) e um adesivo multi-mode (Scotchbond Universal, SU). Os adesivos Adper Single Bond Plus (SB) e SU foram combinados com os primers para metais. O grupo controle não recebeu nenhum tipo de tratamento superficial. Os grupos foram: AP, AP+SB, AP+SU, TP+SB, TP+SU, CP+SB, CP+SU e SU. Cilindros de resina foram construídos na superfície da liga. Após 24 h, metade dos espécimes foi submetido ao SBS, a outra metade foi termociclada previamente. Os dados foram analisados pelos testes ANOVA dois fatores e Tukey (a=0.05). Os tipos de fraturas foram determinados utilizando microscopia eletrônica de varredura (MEV). Os maiores valores de SBS foram obtidos com AP e TP combinados com adesivos após 24 h e o menor valor foi obtido no grupo controle. A ciclagem térmica reduziu a SBS para AP, CP+SU e SU. Combinação entre TP e SU resultou em altos valores de SBS após termociclagem. Os grupos TP apresentaram todos os modos de fratura e alta incidência de fraturas mistas. O uso dos primers AP e UP para metais antes da aplicação dos sistemas adesivos SU e SB aumentou a SBS entre o Ni-Cr e a resina composta. Essa combinação entre primers e adesivos mostrou os maiores valores de SBS após a termociclagem.

Abstract This study evaluated the effects of three metal primers and one multi-mode adhesive system on the shear bond strength (SBS) of a flowable composite resin to nickel-chrome metal alloy (Ni-Cr). Ninety plates were cast from Ni-Cr and divided in nine groups (n=10). The surfaces were sandblasted with Al2O3 and primed with three adhesive primers: Alloy Primer (AP), Universal Primer (TP) and RelyX Ceramic Primer (CP), and a multi-mode adhesive (Scotchbond Universal, SU). The Adper Single Bond Plus (SB) and SU adhesives were also combined with adhesive primers. Control group did not have any surface treatment. The groups were: AP, AP+SB, AP+SU, TP+SB, TP+SU, CP+SB, CP+SU and SU. Composite cylinders were built on alloy surface. After 24 h, half the specimens were subjected to SBS and the other half to thermal cycling before testing. Data were analyzed by two-way ANOVA and Tukey’s test (a=0.05). Failure modes were assessed by SEM observation. Higher SBS were obtained with AP and TP combined with adhesives at 24 h and the lowest one for control group. Thermocycling reduced SBS for AP, CP+SU and SU. Combination between TP and SU resulted in the highest SBS after the thermocycling. TP groups showed all types of failures and high incidence of mixed failures. The use of AP and UP metal primers before application of SU and SB adhesive systems increased the SBS of composite to Ni-Cr. These combinations between metal primers and adhesives had the highest SBS after thermocycling.

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.

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.

Este estudo avaliou a variação de temperatura na câmara pulpar durante a fotoativação de duas resinas compostas (Filtek P90 – compósito à base de silorano e Heliomolar – compósito à base de metacrilato) com as unidades foto-ativadoras (UFs) luz de quartzo-tungstênio-halogênio (QTH) ou diodo emissor de luz (LED) e utilizando espessuras de dentina (0,5 e 1,0 mm). Cavidades padronizadas (2×2×2 mm) foram preparadas em 80 incisivos bovinos, as quais foram aleatoriamente divididas em 8 grupos de acordo com os métodos de fotoativação e espessura da dentina. Filtek P90 e Heliomolar (ambos na cor A3) foram utilizadas com seus respectivos sistemas adesivos (Primer P90 auto-condicionante / adesivo P90 e adesivo Excite). Todos os experimentos foram realizados em um ambiente controlado (37°C). As variações de temperatura (°C) foram mensuradas usando um termômetro digital conectado a um termopar tipo-K. Os resultados foram analisados estatisticamente por ANOVA e teste de Tukey (α=0,05). Para interação compósito/espessura de dentina, o aumento da temperatura foi estatisticamente superior para a espessura de dentina de 0,5 mm (40,07°C) quando comparado com a espessura de dentina de 1,0 mm (39,61°C) para a Filtek P90. Para a interação compósito/UFs, o aumento de temperatura foi estatisticamente superior para o Filtek P90 (39,21°C – QTH e 40,47°C – LED) quando comparado ao Heliomolar (38,40°C – QTH e 39,30°C – LED). Compósitos à base de silorano promovem maior aumento da temperatura na câmara pulpar em relação aos compósitos à base de metacrilato.

This study evaluated the temperature variation in the pulp chamber during photoactivation of two restorative composite resins (Filtek P90 silorane-based composite and Heliomolar methacrylate-based composite) with either a quartz-tungsten-halogen (QTH) or light-emitting diodes (LED) light-curing unit (LCU) and using dentin thicknesses (0.5 and 1.0 mm). Standardized cavities (2x2x2 mm) were prepared in 80 bovine incisors, which were randomly assigned to 8 groups according to the photoactivation method and dentin thickness. Filtek P90 and Heliomolar (both in shade A3) were used with their respective adhesive systems (P90 self-etch primer / P90 adhesive bond and Excite adhesive). All experiments were carried out in a controlled environment (37°C). The temperature variations (°C) were recorded using a digital thermometer attached to a K-type thermocouple. The results were analyzed statistically by ANOVA and Tukey's test (α=0.05). For composite/dentin thickness interaction, temperature increase was significantly higher in 0.5 mm dentin thickness (40.07°C) compared with 1.0 mm dentin thickness (39.61°C) for Filtek P90. For composite/LCU interaction, the temperature increase was significantly higher for Filtek P90 (39.21°C - QTH and 40.47°C - LED) compared with Heliomolar (38.40°C - QTH and 39.30°C - LED). The silorane-based composite promoted higher temperature increase in the pulp chamber than the methacrylate-based composite.

This study evaluated an alternative method for thermal cycling test on the microleakage and bond strength of the polymer-dentin bond. For the microleakage test the cavities were restored with a TEGDMA+UDMA+bis-EMA composite polymer light cured for 20 s. Samples were immersed in 2% methylene blue solution for 2 h and sectioned. Microleakage scores were submitted to Kruskal-Wallis test. For the shear bond strength test the adhesive was applied to dentin, photoactivated for 10 s and the composite polymer incrementally photoactivated. Samples were submitted to shear bond strength test in a machine with a cross-head speed of 0.5 mm/min and data were submitted to ANOVA and Tukey's test. Studied groups were: 1 - without thermocycling; 2 - thermocycled at 5 ºC and 55 ºC with intermediate bath at 37 ºC; 3 - thermocycled at 5 ºC and 37 ºC; 4 - thermocycled at 37 ºC and 55 ºC; 5 - thermocycled at 5 ºC and 55 ºC (traditional test). Cold baths promoted greater microleakage when compared to control and hot bath, whereas control and hot bath were similar. Cold baths presented significant lower shear bond strength than those submitted to hot bath and control. It was concluded that the alternative method for thermal cycling test showed that cold temperatures increased the microleakage and decreased the bond strength of the polymeric adhesive.

The type IV dental stone is widely used for the fabrication of dyes and master casts for fixed and removable partial prostheses. It is typically normal to wait at least 24 hours for the casts to dry prior to beginning the laboratory procedures. The waiting time has been shown to be greatly reduced by using microwave drying. OBJECTIVE: This study evaluated the influence of drying techniques at room temperature and microwave oven on the linear dimensional change, compressive strength and detail reproduction in type IV dental stones. MATERIAL AND METHODS: Three type IV dental stone brands were selected; elite Rock, Shera Premium and Durone IV. Two different drying protocols were tested in 4 groups (n=10); G1 - room temperature (25±4ºC) dried for 2 hours; G2 - room temperature dried for 24 hours; G3 - room temperature dried for 7 days and G4 - microwave oven dried at 800 W for 5 minutes and after 2 hours at room temperature. After drying, the samples were assayed for dimensional charges. The sample surface was submitted to the ImageTool 3.0 software for compressive strength in a universal testing machine with a cell load of 50 KN at a crosshead speed of 0.5 mm/minutes and the detail reproduction was analyzed with a stereomicroscope at 25x magnification. The statistical analysis of the linear dimensional change and compressive strength data were conducted by the ANOVA test followed by the Tukey test (p<0.05). Detailed reproduction values were reported in percentages. RESULTS: For the compressive strength test, Elite Rock and Durone IV did not present significant differences between G2 and G4, while Shera Premium did not present differences between G3 and G4. The best reproduction levels were observed for G3. CONCLUSIONS: Dental stone microwave oven drying showed a linear dimensional change similar to after room temperature drying for 24 hours and 7 days. The compressive strength of the stone dried in the microwave oven was similar to those dried at room temperature for 24 hours, with the exception of Shera Premium, which had similar results for microwave and room temperature drying for 7 days. For the microwave drying method the detail reproduction levels for samples dried at room temperature for 24 hours and 7 days were similar, except for the Durone IV.

We compared polymerization stress in two commercial composites and three experimental composites made using camphorquinone (CQ) and/or phenylpropanedione (PPD) as photoinitiators. The internal surfaces of photoelastic resin discs with cylindrical cavities were roughened and treated with adhesive. Composites were divided into five groups: two commercial composites (Filtek Silorane and Filtek Z250) and three experimental composites with CQ/amine, CQ/PPD/amine, and PPD/amine. Composites were photopolymerized inside cavities, and subjected to photoelastic analysis immediately and at 24 hours and 7 days later using a plane polariscope. Stress created by Silorane (3.08 ± 0.09 MPa) was similar to that of Z250 (3.19 ± 0.13 MPa) immediately after photopolymerization (p > 0.05). After 24 hours and 7 days, Z250 (3.53 ± 0.15 and 3.69 ± 0.10 MPa, respectively) showed higher stress than Silorane (3.19 ± 0.10 and 3.16 ± 0.10 MPa, respectively). Qualitative analysis immediately after photopolymerization showed composite/CQ promoted higher stress than PPD, but stress levels at other evaluated times were statistically similar, varying between 3.45 ± 0.11 MPa and 3.92 ± 0.13 MPa. At 24 hours and 7 days, Silorane created the lowest stress. All photoinitiators created comparable tensions during polymerization.

O objetivo neste estudo foi avaliar a tensão de contração de polimerização e o grau de conversão de uma resina composta submetida a vários protocolos de fotoativação. O compósito Filtek Z350 foi inserido na perfuração central de um disco de resina fotoelástica e polimerizado usando uma unidade de fotoativação LED (BluePhase II - IvoclarVivadent) com as doses de energia de 12, 24 or 36 J/cm² usando os seguintes protocolos de polimerização: contínuo de alta intensidade (HI: 1200 mW/cm² durante 10, 20 ou 30s), contínuo de baixa intensidade (LI: 650 mW/cm² durante 18, 36 ou54s) e "soft-start" (SS: 150 mW/cm² durante 5 s + 1200 mW/cm² durante 9, 19 ou 29s) (n=5). Análise fotoelástica e Espectroscopia Infravermelha Transformada de Fourier (FTIR) foram usados para avaliar a tensão de contração de polimerização e grau de conversão do compósito respectivamente. O teste ANOVA três fatores foi usado para determinar os principais efeitos e interações das variáveis e seguidamente, ANOVA 2 fatores para ver a diferença entre os grupos (p<0.05). A tensão de contração aumentou com valores maiores de energia. Não foram observadas diferenças estatisticamente significantes para a tensão de contração entre os modos de alta e baixa intensidade. O modo "soft-start" gerou menor tensão que os modos contínuos, exceto quando 12 J/cm² foi aplicado. Similar grau de conversão foi observado para os modos de fotoativação usados, com exceção do modo "soft-start" com 12, 24 e 36 J/cm² que mostraram níveis menores de conversão. A dose de energia e modo de ativação influenciam a tensão de contração de polimerização, porém nenhum benefício no grau de conversão foi observado.

The aim of this study was to evaluate the polymerization stress and degree of conversion of a composite submitted to different photoactivation protocols. The composite Filtek Z350 was placed in the central perforation of a photoelastic disc and polymerized using a LED-based curing unit (BluePhase II - IvoclarVivadent) with energy density of 12, 24 or 36 J/cm² using the following photopolymerization protocols: continuous high intensity (HI: 1200 mW/cm² during 10, 20 or 30s), continuous low intensity (LI: 650 mW/cm² during 18, 36 or 54s) and soft-start (SS: 150 mW/cm² during 5 s + 1200 mW/cm² during 9, 19 or 29s) (n=5). Photoelastic analysis was used to evaluate polymerization shrinkage stress and FTIR was performed to determine the degree of conversion of the composite. ANOVA 3-way procedure was used to determine the significance of the main effects and their interactions followed by two-way ANOVA for each time was performed (p<0.05). Shrinkage stress increased with higher values of energy. No statistically significant differences on polymerization shrinkage stress were found between high and low intensity activation modes. Softstart method generated stresses that were statistically lower than continuous modes except when 12 J/cm² was applied. Similar degree of conversion was observed for photoactivation modes used, except for soft-start mode with 12, 24 and 36 J/cm² that showed lowest levels of conversion. Energy density and activation mode influenced polymerization shrinkage stress, but no benefit on degree of conversion was observed.

A discrepância entre a expansão e a contração térmica dos materiais restauradores e o dente podem causar estresse na sua interface, podendo levar a uma microinfiltração. O presente trabalho determinou e comparou o coeficiente de expansão térmica (CET) com o comportamento termo mecânico dos dentes humanos e bovinos e determinou se o CET é um parâmetro adequado para descrever o comportamento dental. 15 fatias (6×5×2 mm) de terceiros molares humanos e 15 de incisivos bovinos foram divididos em 3 grupos de acordo com o ambiente testado: G1 - condição ambiente, G2 - 100% de umidade, G3 - dissecado e testado em condição seca. Cada espécime foi pesado, aquecido de 20 a 70<img border=0 width=32 height=32 src="../../../../../../img/revistas/bdj/v23n1/car01.jpg">C a 10ºC min-1 e pesados novamente. O CET foi mensurado entre 20 e 50ºC. Dentina fresca (humana -0,49% ± 0,27, bovina -0,22% ± 0,16) contrai no aquecimento sobre condição seca. Em condição úmida, somente dente humano (-0,05% ± 0,04) mostrou contração (bovina 0,00% ± 0,03) acompanhado por uma significante (p<0.05) perda de massa que os espécimes secos. A dentina dissecada expande no aquecimento sem mudanças óbvias de peso (0,00% ± 0,00). O CET encontrado foi, respectivamente, em condições seca, úmida e dissecada em ºC-1: humana (-66,03×10-6, -6,82×10-6, 5,52×10-6) e bovina (-33,71×10-6, 5,47×10-6, 4,31×10-6). De acordo com sua condição de umidade, a dentina mostrou diferentes CETs. O comportamento de expansão térmica de dentes humanos e bovinos é similar. Uma simples avaliação do coeficiente de expansão térmica da estrutura dental pelo seu valor de CET pode não ser apropriada para uma consideração significativa dos efeitos na interface dente-material restaurador.

The mismatch of thermal expansion and contraction between restorative materials and tooth may cause stresses at their interface, which may lead to microleakage. The present work compared the coefficient of thermal expansion (CTE) with the thermomechanical behavior of human and bovine teeth and determined if the CTE is a suitable parameter to describe tooth behavior. Fifteen human third molar and 15 bovine incisor tooth slices (6×5×2 mm) were allocated to 3 groups according to the test environment: G1 - room condition, G2 - 100% humidity, G3 - desiccated and tested in dry condition. Each specimen was weighed, heated from 20 to 70ºC at 10ºC min−1 and reweighed. The CTE was measured between 20 and 50ºC. Fresh dentin (human -0.49% ± 0.27, bovine -0.22% ± 0.16) contracted on heating under dry condition. Under wet conditions, only human teeth (-0.05% ± 0.04) showed contraction (bovine 0.00% ± 0.03) accompanied by a significantly lower (p<0.05) weight loss than in dry specimens (human 0.35% ± 0.15, bovine 0.45% ± 0.20). The desiccated dentin expanded on heating without obvious weight changes (0.00% ± 0.00). The CTE found was, respectively, in dry, wet and dissected conditions in ºC-1: human (-66.03×10-6, -6.82×10-6, 5.52×10-6) and bovine (-33.71×10-6, 5.47×10-6, 4.31×10-6). According to its wet condition, the dentin showed different CTEs. The thermal expansion behavior of human and bovine dentin was similar. A simple evaluation of the thermal expansion behavior of tooth structure by its CTE value may not be appropriate as a meaningful consideration of the effects on the tooth-material interface.

O propósito neste estudo foi verificar a movimentação linear de dentes em prótese total superior confeccionada com resina acrílica, proporcionada com conteúdo de monômero indicado pelo fabricante, com 25% de excesso ou com 25% a menos de monômero, nas técnicas de polimerização convencional e por microondas. Foram confeccionados 30 modelos, representando uma arcada maxilar desdentada com rebordo normal. As bases de prova e os planos de orientação foram confeccionados em cera e o conjunto montado em articulador semi-ajustável relacionado com um modelo inferior dentado. Depois da montagem dos dentes artificiais, a prótese foi moldada com silicone para duplicação das demais próteses. Foram confeccionados pontos referenciais para mensurações das distâncias entre os dentes, as quais foram analisadas com microscópio comparador linear antes e depois da desinclusão das próteses. As resinas acrílicas foram prensadas de modo convencional, alterando somente o conteúdo de monômero na proporção monômero-polímero recomendada pelo fabricante. Os dados da distância entre os dentes foram submetidos à análise de variância e ao teste de Tukey (5%). Não houve diferença estatística entre os grupos com quantidade de monômero recomendada pelo fabricante e os grupos com 25% a mais ou 25% a menos de monômero, tanto na polimerização convencional como por microondas. A alteração do conteúdo de monômero e o tipo de polimerização (convencional ou por microondas) não exerceram influência na movimentação dental nas distâncias transversal e ântero-posterior.

The purpose of the study was to verify the linear displacement of teeth in maxillary complete dentures influenced by different monomer-polymer ratios - according to the manufacturer's instructions, with 25% excess or 25% less monomer content - in the conventional and microwaved polymerization techniques. Wax base plates and wax planes were made on edentulous maxillary stone casts according to traditional method. The set was assembled in semi-adjustable articulator with a lower toothed stone cast as guide to mounting of the maxillary artificial teeth. Impressions were taken from this tooth arrangement with silicone and the mold was used to standardize the mounting of the teeth of all dentures. Referential points were made on the artificial teeth for linear measurements with optical microscope before processing of the dentures and after deflasking. Denture bases were conventionally packed with acrylic resin according to the monomer-polymer ratio protocol. Tooth displacement data were submitted to ANOVA and Tukey test (α=0.05). There were no statistically significant differences (p>0.05) between the group with monomer content recommended by the manufacturer and groups with 25% more and 25% less monomer, in both conventional and microwaved polymerizations. Excess or less monomer in the monomer-polymer ratio and polymerization types did not change the linear distance between teeth.

O objetivo deste estudo foi avaliar a influência da diferença entre a dureza do topo e da base em compósitos restauradores. Foram utilizados os compósitos restauradores Filtek P90 (compósito à base de silorano) e Heliomolar (compósito à base de metacrilato). A irradiância da unidade foto-ativadodora (UF) foi mensurada com um potenciômetro Ophir Optronics (900 mw/cm2) e o espectro de luz foi obtido usando um espectrofotômetro (USB 2000). Vinte espécimes cilíndricos padronizados (2 mm de espessura por 7 mm de diâmetro) foram obtidos pela fotoativação utilizando UF (40 s) para cada compósito. A irradiância que passou através do compósito foi mensurada (n=10). O número de dureza Knoop para cada superfície foi calculado pela média de 3 penetrações. A diferença da dureza Knoop entre o topo e base (DDK) de um mesmo espécime foi calculada (n=10). A irradiância que passou através da Filtek P90 (272 mW/cm2) não foi estatisticamente superior a Heliomolar (271 mW/cm2). A DDK da Filtek P90 (25%) foi estatisticamente superior a Heliomolar (12%). O compósito a base de metacrilato apresentou melhor grau de polimerização na base quando comparado ao compósito à base de silorano.

The aim of this study was to investigate the influence of different composite resins - Filtek P90 (silorane-based composite) and Heliomolar (methacrylate-based composite) - on light transmission and decrease in Knoop hardness between the bottom and top of cured specimens. The irradiance of a light-curing unit (LCU) was measured with a power meter (Ophir Optronics; 900 mw/cm2) and spectral distributions were obtained using a spectrometer (USB 2000). Twenty standardized cylindrical specimens (2 mm thick x 7 mm diameter) of each composite resin were obtained by curing using the LCU for 40 s. Light energy transmission through the composite was calculated (n=10). The Knoop hardness number for each surface was recorded as the mean of 3 indentations. The difference in Knoop hardness between the top and bottom (DKH) of the same specimen was calculated (n=10). The irradiance of light that passed through Filtek P90 (272 mW/cm2) was not significantly greater than that the passed through Heliomolar (271 mW/cm2). The DKH of Filtek P90 (25%) was significantly higher than that of Heliomolar (12%). There was a greater degree of subsurface polymerization of the methacrylate-based composite compared to the silorane-based composite.

OBJECTIVE: The aim of this study was to determine the influence of different energy densities on the heat generated during photoactivation of Filtek Z250 (3M/ESPE) and Z100 (3M/ESPE) composite resins with different dentin and composite thickness. MATERIAL AND METHODS: The temperature increase was registered with a type-K thermocouple connected to a digital thermometer (Iopetherm 46). A chemically polymerized acrylic resin base was prepared to serve as a guide for the thermocouple and as a support for 0.5-, 1.0-, and 1.5-mm-thick bovine dentin discs. Circular elastomer molds (1.0 mm-height x 3.0-mm diameter or 2.0-mm height x 3.0-mm diameter) were adapted on the acrylic resin base to standardize the composite resin thickness. A conventional halogen light-curing unit (XL 2500, 3M/ESPE) was used with light intensity of 700 mW/cm². Energy density was calculated by the light intensity applied during a certain time with values of 28 J/cm² for Z100 and 14 J/cm² for Filtek Z250. The temperature change data were subjected to three-way ANOVA and Tukey's test at 5% level. RESULTS: The higher energy density (Z100) promoted greater temperature increase (p<0.05) than the lower energy density (Filtek Z250). For both composites and all composite thicknesses, the lowest dentin thickness (0.5 mm) yielded significantly higher (p<0.05) temperature increase than the other two dentin thicknesses. The 1-mm-thick composite resin layer yielded significantly higher (p<0.05) temperature changes for both composites and all dentin thicknesses. CONCLUSIONS: Temperature increase was influenced by higher energy density and dentin/composite thickness.

The aim of this study was to verify the influence of investment granulometry on the castability and surface roughness of Ni/Cr castings. Four investments were selected for casting according to decreasing order of granulometry: Heat Shock > Micro Fine 1700 > Gilvest HS > Castotal. Castability was verified by means of 40 specimens made with a polyester screen and determined from the number of segments completely filled by the cast alloy. To analyze the roughness, 40 disk-shaped wax patterns were made (15 x 3 mm), and after inclusion in the investments, they were cast and analyzed, before and after polishing (Mitutoyo SJ-201). The measurements were statistically analyzed (1-ANOVA - Tukey - p < 0.05) and it was verified that Heat Shock provided the worst castability with significant difference (p < 0.05) when compared with other investments. This material and Castotal presented similar roughness before and after polishing, with statistically significant difference (p < 0.05) between them and Gilvest and Micro Fine. It was concluded that investments with smaller granulometry provided castings that were more complete, but not smoother.

Este estudo comparou a contração de polimerização de resinas compostas fotoativadas por luz halógena (QTH) e diodo emissor de luz (LED). Foram confeccionados bastões de vidro (5,0 mm x 5,0 cm), e uma de suas extremidades sofreu jateamento com óxido de alumínio, sobre a qual foi aplicado um adesivo e fotoativado com luz halógena. Os bastões de vidro foram acoplados verticalmente, em pares, em uma máquina universal de ensaios (EMIC DL-2000) e as resinas compostas aplicadas no bastão inferior. A distância entre os bastões foi padronizada em 2 mm e um extensômetro foi acoplado a eles. As resinas foram fotoativadas (n=20), sendo 10 por QTH e 10 por LED utilizando dois aparelhos posicionados em lados opostos, acionados simultaneamente por 40 s. A tensão de contração foi analisada em dois momentos: logo após a polimerização (t40s) e 10 min após (t10min). A tensão de contração apresentada por todas as resinas foi maior em t10min do que em t40s, independente da fonte ativadora. A resina de micropartículas apresentou menores valores de tensão de contração com valores estatisticamente significantes em relação às demais resinas. Para as resinas híbrida e microhíbrida não houve influência da unidade ativadora sobre a tensão de contração, com exceção para a resina de micropartículas em t10min. Concluiu-se que a composição da resina composta foi o fator que mais interferiu na tensão de contração da resina composta.

The purpose of this study was to compare the polymerization shrinkage stress of composite resins (microfilled, microhybrid and hybrid) photoactivated by quartz-tungsten halogen light (QTH) and light-emitting diode (LED). Glass rods (5.0 mm x 5.0 cm) were fabricated and had one of the surfaces air-abraded with aluminum oxide and coated with a layer of an adhesive system, which was photoactivated with the QTH unit. The glass rods were vertically assembled, in pairs, to a universal testing machine and the composites were applied to the lower rod. The upper rod was placed closer, at 2 mm, and an extensometer was attached to the rods. The 20 composites were polymerized by either QTH (n=10) or LED (n=10) curing units. Polymerization was carried out using 2 devices positioned in opposite sides, which were simultaneously activated for 40 s. Shrinkage stress was analyzed twice: shortly after polymerization (t40s) and 10 min later (t10min). Data were analyzed statistically by 2-way ANOVA and Tukey's test (a=5%). The shrinkage stress for all composites was higher at t10min than at t40s, regardless of the activation source. Microfilled composite resins showed lower shrinkage stress values compared to the other composite resins. For the hybrid and microhybrid composite resins, the light source had no influence on the shrinkage stress, except for microfilled composite at t10min. It may be concluded that the composition of composite resins is the factor with the strongest influence on shrinkage stress.