Comparative study on radio-opacity of dental composite resin materials'determination using film imaging and digital imaging / 北京大学学报(医学版)

OBJECTIVE@#To compare the effects of different imaging methods on radio-opacity. Digital imaging and traditional film imaging were used to determine the radio-opacity of dental composite resin materials.@*METHODS@#Fourteen dental composite resins commonly used in clinic were prepared for disc samples with thickness of 1 mm and diameter of 15 mm respectively. The aluminum step wedge was used as the reference and the disc samples were irradiated with X-rays by the traditional film imaging, phosphor imaging plate and charge-coupled device(CCD) intra-oral X-ray sensor respectively. Exposure was set at 65 kV and 7 mA, with 300 mm focus to film distance and the exposure time was 0.25 s. After developing and fixing the film, the optical density of the image of the sample and that of each step of the aluminum step wedge were measured using the densitometer. The digital image file was exported to grey scale analysis software of Adobe Photoshop® to measure the average grey value in the sample image and aluminum step wedge image. The curves were drawn corresponding to the optical density/gray value of each step of the aluminum step wedge and its thickness, and the equivalent thickness of the aluminum plate was calculated according to the optical density/gray value of the actual measured thickness of the sample, so as to evaluate the radio-opacity of dental composite resin material.@*RESULTS@#For the same sample, the aluminum equivalent measured by traditional film imaging and two other digital imagings had significant differences among the 14 composite resins (P < 0.05), and the aluminum equivalent measured by the two digital imagings were greater than that of the traditional film. Moreover the aluminum equivalent measured by the two digital imagings was also different, and the aluminum equivalent measured by the CCD intra-oral X-ray sensor in most composite resins was larger than that measured by phosphor imaging plate. The same sample was photographed with the same imaging method, and the aluminum equivalent was different after three exposures. The standard deviation of aluminum equivalent measured by phosphor imaging plate was the largest, while that measured by CCD intra-oral X-ray sensor was the smallest. Among the 14 dental composite resin materials, the aluminum equivalent of Tetric N-Ceram and Te-Econom Plus measured by traditional film imaging and phosphor imaging plate was significantly higher than other composite resins.@*CONCLUSION@#Based on clinical significance, three kinds of sensors designed to measure the radio-opacity of dental composite resin, the value of aluminum equivalent will change according to different types of sensors. The aluminum equivalent measured by CCD intra-oral X-ray sensor was higher than that measured by phosphor imaging plate, and the aluminum equivalent measured by phosphor imaging plate was higher than that measured by traditional film imaging. Moreover, even though the same sensor was used, the aluminum equivalent measured by multiple exposures was different. The standard deviation of the aluminum equivalent measured by phosphor imaging plate was greater than that measured by traditional film imaging and CCD intra-oral X-ray sensor. The three sensors in this study could be used for evaluating the radio-opacity of dental composite resin materials. But no matter what kind of sensor was used to measure the radio-opacity of dental composite resin, it complied to ISO 4049: 2019 standard, the materials were suitable for clinical use.

Shear Bond Strength and Failure Mode of Different Dental Adhesive Systems

@#The study aimed to evaluate the shear bond strength (SBS) and to analyse the failure mode at the resindentine interface of different dental adhesive systems. A total of 75 sound premolar teeth were selected and randomly assigned into five different adhesive groups (n=15): OptiBond Solo (OBS, total-etch), OptiBond Versa (OBV, two-bottles, self-etch), Adhe SE Ivoclar (ADHE, two-bottles, self-etch), G-Bond (GB, one-bottle, selfetch), and OptiBond All in One (OBO, one-bottle, self-etch). The occlusal surface of each tooth was flattened and composite resin cylinder (4x2 mm) was built up on the flat dentine surface using a custom made mould. The specimens were then subjected to 500 thermal cycles between 5 °C and 55 °C and dwell time of 20s. The SBS test was conducted using a universal testing machine at a crosshead speed of 0.5 mm/min. Data were analyzed using one-way ANOVA and Dunnett T3 Test. Failure mode was determined as adhesive, cohesive or mixed mode using a stereomicroscope and the data were analyzed using Fisher's exact test. The total-etch (OBS) had significantly higher value of SBS than the two self-etch (ADHE and GB) adhesive systems. Within the self-etch systems, OBV showed significantly higher SBS value compared to ADHE and GB. There were no statistically significant differences between types of failure mode (p > 0.05) and adhesive group. It can be concluded that the different compositions in the self-etch adhesive materials may contribute to the different SBS value. The failure modes detected within all tested groups did not show clinically important differences

Evaluation of Mechanical Properties of Various Nanofibre Reinforced Bis-GMA/TEGDMA Based Dental Composite Resins / Evaluación de las propiedades mecánicas de varias resinas compuestas dentales basadas en Bis-GMA/TEGDMA reforzadas con nanofibras

ABSTRACT Objective: To investigate the mechanical properties of various mass fractions of Nylon 6 (N6), polymethyl-metacrylate (PMMA) and polyvinylidene-difluoride (PVDF) nanofibres reinforced bisphenol A-glycidyl methacrylate (Bis-GMA) and tri-ethylene glycol dimethacrylate (TEGDMA) based dental composite resins and to evaluate the penetration characteristics of the nanofibres into the resin. Methods: Nylon 6, PMMA and PVDF nanofibres were produced using the electrospinning method. The morphologies of the fabricated nanofibres were evaluated with a scanning electron microscope (SEM). The nanofibres were placed into the resin matrix at different mass fractions (3%, 5% and 7%). The three-point bending test was applied to nanofibre-reinforced dental composite resins and neat resin specimens. The flexural strength (Fs), flexural modulus (EY) and work of fracture (WOF) of the groups were found. The analysis of variance was used for the statistical analysis of the acquired data. Tukey 's multiple test was performed to compare the Fs, EY and WOF means. Fractured surfaces of the samples were observed by SEM, and fracture morphologies were evaluated. Results: Polymethyl-metacrylate nanofibres dissolved in the matrix, and a polymer alloy took place in the matrix. Fibre pull-out and fibre bridging mechanisms were observed by SEM images of the N6 and PVDF nanofibre-reinforced dental composites. The produced nanofibres enhanced the mechanical properties of the dental composite resins. Conclusion: Fibre pull-out and fibre bridging mechanisms on the fractured surfaces of samples may play a key role in the reinforcement of dental composite resins. However, polymer alloy of PMMA nanofibres increased the mechanical properties of the resin matrix.

RESUMEN Objetivo: Investigar las propiedades mecánicas de resinas compuestas dentales basadas en bisfenol A-diglicidildimetacrilato (Bis-GMA) y dimetacrilato trietilen-glicol (TEGDMA) reforzadas con nanofibras de fracciones de masa de Nylon 6 (N6), polimetilmetacrilato (PMMA) y fluoruro de polivinilideno (PVDF), y evaluar las características de la penetración de las nanofibras en la resina. Métodos: Se produjeron nanofibras de Nylon 6, PMMA y PVDF utilizando el método de electrohilado (electrospinning). Las morfologías de las nanofibras fabricadas fueron evaluadas con un microscopio electrónico de barrido (MEB). Las nanofibras fueron introducidas en la matriz de resina en diferentes fracciones de masa (3%, 5% y 7%). La prueba de flexión de tres puntos fue aplicada a las resinas compuestas dentales reforzadas por nanofibras y a las muestras de resina pura. La resistencia a la flexión (Rf), el módulo de flexión (EY) y el trabajo de fractura (WOF) de los grupos fueron halladas. El análisis de varianza se usó para el análisis estadístico de los datos adquiridos. Se realizó la prueba de comparaciones múltiples de Tukey con el propósito de comparar las medidas de Rf, EY y WOF. Las superficies fracturadas de las muestras fueron observadas mediante un MEB, y se evaluaron las morfologías de fractura. Resultados: Las nanofibras de polimetilmetacrilato se disolvieron en la matriz, y tuvo lugar una aleación de polímeros en la matriz. Los mecanismos de desprendimiento de fibras y puenteo de fibras fueron observados mediante imágenes de MEB de los compuestos dentales reforzados con nanofibras de N6 y PVDF. Las nanofibras producidas realzaron las propiedades mecánicas de las resinas compuestas dentales. Conclusión: Los mecanismos de desprendimiento de fibras y puenteo de fibras en las superficies fracturadas de las muestras pueden desempeñar un papel clave en el reforzamiento de las resinas de los compuestos dentales. Sin embargo, la aleación polimérica de las nanofibras de PMMA aumentó las propiedades mecánicas de la matriz de resina.

Microhybrid versus nanofill composite in combination with a three step etch and rinse adhesive in occlusal cavities: five year results

OBJECTIVES: The aim of the study was to evaluate the 5-year clinical performance of occlusal carious restorations using nanofill and microhybrid composites, in combination with 3-step etch-and-rinse adhesives, in patients who were going to commence orthodontic treatment. MATERIALS AND METHODS: A total of 118 restorations for occlusal caries were conducted prior to orthodontic treatment. Occlusal restorations were performed both with Filtek Supreme XT (3M ESPE) and Filtek Z250 (3M ESPE) before beginning orthodontic treatment with fixed orthodontic bands. Restorations were clinically evaluated at baseline and at 1, 2, 3, 4, and 5-year recalls. RESULTS: None of the microhybrid (Filtek Z250) and nanofill (Filtek Supreme XT) composite restorations was clinically unacceptable with respect to color match, marginal discoloration, wear or loss of anatomical form, recurrent caries, marginal adaptation, or surface texture. A 100% success rate was recorded for both composite materials. There were no statistically significant differences in any of the clinical evaluation criteria between Filtek Z250 and Filtek Supreme XT restorations for each evaluation period. CONCLUSIONS: The composite restorations showed promising clinical results relating to color matching, marginal discoloration, wear or loss of anatomical form, recurrent caries, marginal adaptation, and surface texture at the end of the 5-year evaluation period.

Repair Strength in Simulated Restorations of Methacrylate- or Silorane-Based Composite Resins

Abstract The study verified the bond strength in simulated dental restorations of silorane- or methacrylate-based composites repaired with methacrylate-based composite. Methacrylate- (P60) or silorane-based (P90) composites were used associated with adhesive (Adper Single Bond 2). Twenty-four hemi-hourglass-shaped samples were repaired with each composite (n=12). Samples were divided according to groups: G1= P60 + Adper Single Bond 2+ P60; G2= P60 + Adper Single Bond 2 + P60 + thermocycling; G3= P90 + Adper Single Bond 2 + P60; and G4= P90 + Adper Single Bond 2 + P60 + thermocycling. G1 and G3 were submitted to tensile test 24 h after repair procedure, and G2 and G4 after submitted to 5,000 thermocycles at 5 and 55 ?#61616;C for 30 s in each bath. Tensile bond strength test was accomplished in an universal testing machine at crosshead speed of 0.5 mm/min. Data (MPa) were analyzed by two-way ANOVA and Tukey's test (5%). Sample failure pattern (adhesive, cohesive in resin or mixed) was evaluated by stereomicroscope at 30?#61655; and images were obtained in SEM. Bond strength values of methacrylate-based composite samples repaired with methacrylate-based composite (G1 and G2) were greater than for silorane-based samples (G3 and G4). Thermocycling decreased the bond strength values for both composites. All groups showed predominance of adhesive failures and no cohesive failure in composite resin was observed. In conclusion, higher bond strength values were observed in methacrylate-based resin samples and greater percentage of adhesive failures in silorane-based resin samples, both composites repaired with methacrylate-based resin.

Resumo O objetivo neste estudo foi verificar a resistência de união em restaurações simuladas de compósitos baseados em metacrilato ou silorano reparadas com compósito à base de metacrilato. Compósitos baseados em metacrilato (Filtek P60; 3M ESPE) ou silorano (Filtek P90; 3M ESPE) foram associados com adesivo (Adper Single Bond 2; 3M ESPE). Vinte e quatro amostras em forma de semi-ampulhetas foram reparadas com cada material (n=12), conforme os grupos experimentais: G1- P60 + Adper Single Bond 2 + P60; G2- P60 + Adper Single Bond 2 + P60 + termociclagem; G3- P90 + Adper Single Bond 2 + P60; e G4- P90 + Adper Single Bond 2 + P60 + termociclagem. Os grupos G1 e G3 foram submetidos ao ensaio de tração após 24 horas do procedimento de reparo e os grupos G2 e G4 depois de submetidos a 5.000 ciclos térmicos de 5 e 55 ?#61616;C por 30 s em cada banho. O teste de resistência à tração foi efetuado em máquina universal atuando numa velocidade de 0,5 mm/min. Os dados (MPa) foram submetidos a ANOVA a dois fatores e teste de Tukey (5%). O padrão de fratura das amostras (adesivo, coesivo em resina ou misto) foi avaliado em estereomicroscópio com aumento de 30x e imagens representativas foram obtidas em MEV. Os valores de resistência à tração das amostras feitas com compósito à base de metacrilato e reparadas com compósito à base de metacrilato (G1 e G2) foram maiores do que nas amostras feitas com compósito à base de silorano e reparadas nas mesmas condições (G3 e G4). A termociclagem diminuiu os valores de resistência à tração para ambos os compósitos. Todos os grupos mostraram predominância de fraturas adesivas e nenhuma falha coesiva foi observada em compósito. Em conclusão, valores maiores de resistência à tração foram observados em amostras de resina à base de metacrilato e maior porcentagem de fraturas adesivas nas amostras de resina à base de silorano, ambos os compósitos reparados com resina à base de metacrilato.

Recomendaciones para el empleo práctico de resinas compuestas en restauraciones estéticas / Recommendations for the use of composite resins in esthetic restorations

Introducción: la población, solicita con frecuencia restauraciones compatibles con los estándares de la estética dental y ello en ocasiones se dificulta dada la diversidad de materiales restauradores existentes y técnicas para su aplicación. Objetivo: proponer recomendaciones para el empleo práctico de las resinas compuestas fotopolimerizables en restauraciones estéticas de dientes anteriores y posteriores. Métodos: se realizó un estudio de revisión bibliográfica sobre técnicas para el empleo de resinas compuestas en restauraciones estéticas. Esto se llevó a cabo a través de Scopus, SciELO, Hinari, Medline y 45 revistas científicas indexadas de manera manual. El estudio se circunscribió a 89 artículos y 3 libros que enfocaron esta temática de manera más integral. Se reagruparon todos los documentos revisados y se procesaron según revista científica de origen y año de publicación. Integración de la información: las recomendaciones incluyeron la valoración individual de la estética del paciente, selección del tipo de resina a emplear, selección del color, profilaxis y pulido de la superficie de trabajo, preparaciones cavitarias con o sin confección de biseles, protección o no del complejo dentino pulpar, grabado ácido, lavado y enjuague del ácido grabador, aplicación del adhesivo, inserción y manipulación de la resina compuesta, polimerización y acabado de la restauración. Consideraciones finales: los tratamientos curativos y estéticos son muy variado en el campo de las resinas compuestas fotopolimerizables, por lo cual resulta útil seguir, entre otras, las recomendaciones de realizar limpieza de la superficie de trabajo, seleccionar el color y tipo de resina indicados en cada caso, realizar preparaciones cavitarias mínimas con biseles (si es necesario), emplear incrementos en la realización de las restauraciones, polimerizar evitando grandes reacciones de contracción, y pulir adecuadamente las restauraciones(AU)

Introduction: patients often request the performance of restorations compatible with the standards of dental esthetics. This is sometimes hampered by the great variety of restoring materials and techniques for their application. Objective: propose recommendations for the use of photopolymerizable composite resins in esthetic restorations of anterior and posterior teeth. Methods: a bibliographic review was performed about techniques for the use of composite resins in esthetic restorations. The search was conducted in the databases Scopus, SciELO, Hinari and Medline, as well as 45 manually indexed scientific journals. The reviewers selected the 89 papers and 3 books which approached the topic in a more comprehensive manner. All the documents reviewed were arranged and processed by scientific journal and year of publication. Data integration: recommendations included the following topics: individual assessment of the patient's esthetic considerations, selection of the resin type to use, selection of color, prophylaxis and polishing of the work surface, cavity preparation with or without beveling, protection or not of the dentin-pulp complex, acid engraving, washing and rinsing of the engraving acid, application of the adhesive, insertion and manipulation of the composite resin, polymerization and finishing of the restoration. Final considerations: there is a great variety of curative and esthetic treatments based on the use of photopolymerizable composite resins. Therefore, it would be advisable to follow these recommendations, among others: clean the work surface, select the appropriate resin color and type, perform as few beveled cavity preparations as possible (only if required), apply increments while carrying out the restoration, polymerize avoiding great contraction reactions, and polish the restorations appropriately(AU)

Análisis comparativo in vitro del grado de filtración marginal de restauraciones de resina compuesta realizadas con dos métodos de grabado ácido distintos / In vitro comparative analysis of microleakage in composites resin restorations made with a conventional and a modified acid etch technique

La técnica de grabado ácido en esmalte representa el hito que marca la puerta de entrada para el establecimiento de la odontología adhesiva. Producto de que el sustrato adamantino pudiese presentar comportamiento refractario a la técnica convencional de grabado ácido es que se plantea una técnica en dos tiempos operatorios, la cual pudiese disminuir dicho comportamiento resistente al grabado ácido y combatir así el fenómeno de la filtración marginal de las resinas compuestas. En este estudio se utilizaron 30 terceros molares sanos, en los cuales se realizaron cavidades clases V en las caras vestibulares y linguales/palatinas, las cuales fueron obturadas con resina compuestas utilizando técnica de grabado ácido convencional y técnica de grabado ácido en dos tiempos operatorios, respectivamente. Estos especímenes fueron sometidos a un proceso de termociclado en presencia de un agente colorante marcador. Luego de un proceso de termociclado, las muestras fueron cortadas transversalmente para evaluar el porcentaje de penetración del agente marcador. El análisis de los resultados demostró que las restauraciones realizadas con técnica de grabado ácido en dos tiempos operatorios presentaron menores valores de filtración marginal, existiendo diferencias significativas entre ambos grupos estudiados.

The acid etch technique is the fact that marks the starting point for the establishment of the adhesive dentistry era. But as the enamel structure may have a resistant behavior towards the conventional acid etch technique ,a two-step acid etch technique is presented. This would diminish the aforementioned resistant behavior of enamel to the conventional acid etch technique, and minimize as well, the marginal leakage phenomenon of the composite materials. In this study 30 sound recently extracted molars were used. Equal class V cavities preparations were made in the buccal and palatal/lingual faces of each tooth. Buccal cavities were filled with composite before the use of the conventional acid etch technique, as adhesive method, while in the lingual/palatal faces the two-step acid etch technique was used. The samples were subjected to thermal cycles in the presence of a dying agent. After the thermocycling process, the samples were cut transversely to assess the percentage of penetration of the staining agent. The analysis of the results showed that there was a significant statistical difference between both groups. Moreover the restorations made with the two-step acid etch technique presented lower values of marginal leakage.

Síntese e análise de compósitos experimentais para uso odontológico reforçados com nanoargila / Synthesis and analysis of experimental composites for dentistry use reinforced with nanoclay

O objetivo do presente estudo foi de avaliar os efeitos de diferentes frações de partículas de nanoargila modificadas do tipo montmorilonita Cloisite® 20A em propriedades físicas, mecânicas e biológicas de resinas experimentais do tipo nanohíbrida. Compósitos dentais foram preparados através da mistura de 30% de matriz resinosa (BisGMA/TEGDMA) em 70% de partículas de carga (vidro de bário silicato silanizado ­VB, dióxido de silício ­ SD, partículas de nanoargila MMT). Quatro grupos de compósitos experimentais foram formados, variando o percentual de nanoargila empregada (0%, 5%, 7,5%, 10%). O processamento foi realizado em uma máquina de dupla mistura (SpeedMixer DAC, Germany, 3500 rpm). A citotoxicidade in vitro do material foi avaliada baseada nas normas ISO 10993- 5-2009 e comparado com compósito comercial. Ensaios mecânicos para cálculo de Resistência à Flexão e Módulo de Elasticidade foram realizados em máquina de ensaios universal EMIC. O aparelho Acuvol® foi utilizado para o ensaio de contração de polimerização. A sorção e solubilidade dos compósitos foram calculadas baseadas nas normas ISO 4049. Os dados foram analisados estatisticamente, utilizando-se a tabela ANOVA e o Teste de Tukey para comparação dos grupos de dois em dois. O nível de significância utilizado foi de 95% (p< 0,05). Por meio do exame dos resultados, concluiu-se que foi possível esfoliar 5 e 7,5% de partículas de MMT satisfatoriamente na matriz BisGMA/TEGDMA, porém, o inserção de 10% de MMT na matriz orgânica não trouxe vantagens ao compósito, certamente por não permitir a total exfoliação de suas partículas. A inserção de 5 e 7,5% de nanoargila ao compósito dental experimental possibilitou uma diminuição da contração de polimerização do material em 22,13 e 17,4%, respectivamente. Além disso, esses dois grupos permaneceram com suas propriedades mecânicas e de absorção e solubilidade satisfatórias, além de apresentar ausência de citotoxicidade para as células fibroblasticas L929 testadas

The aim of the present study was to evaluate the effect of different weight fractions of modified montmorillonite nanoclay fillers Cloisite ® 20A on mechanical, physical and biological properties of nanohybrid experimental resins. Dental composites were prepared by mixing 30% of resin matrix (BisGMA / TEGDMA) to 70% of particulate fillers (Silanized barium silicate particles - BS, silicone dioxide - SD, montmorillonite nanoclay cloisite 20AMMT). Four groups of experimental composite were formed with various fractions of the nanoclay fillers (0%; 5%; 7,5%; 10% ). Processing was performed using a dual high speed mixing machine (SpeedMixer DAC, Germany, 3500 rpm). In vitro citotoxicity of the material was calculated based on standards ISO 10993-5-2009 and compared to a comercial composite. Tensile strenght and elastic modulus were performed using an universal test machine EMIC. The volumetric shrinkage was calculated by Acuvol® machine. Water sorption and solubility were measured based on International Standard ISO 4049. Data were statistically analyzed by ANOVA and Tukey Test for multiple comparisons. The significance level utilized was 95% (p < 0,05). By the results, it was concluded that it is possible to exfoliate nicely 5 and 7.5% of MMT particles inside Bis-GMA/TEGDMA matrix. However, insertion of 10% of MMT did not improve composite, certainly, because the total exfoliation of particles did not occured. Insertion of 5 and 7.5% of nanoclay in dental composite diminished polymerization shrinkage in 22,13% and 17,4% , respectively. Furthermore, these two groups maintained their mechanical properties, satisfactory sorption and solubility and also presented no citotoxicity for L929 fibroblastic cells

Effects of heat treatment on the microhardness of direct composites at different depths of restoration / Efeito do tratamento térmico na microdureza de resinas compostas diretas em diferentes profundidades de restauração

PURPOSE: The mechanical properties of direct composites may be improved by heat treatment. This study aimed to verify whether heat treatment influences the Knoop microhardness (KHN) of direct composites and whether there are differences among photoactivated areas before and after the application of heat. METHODS: A total of 84 rectangular cross-sectional specimens (10 × 2 × 2 mm) was prepared, 14 per composite. After photoactivation (600 mW/cm² - 40 s), seven specimens per composite were heat-treated (170 ºC/10 min), whereas the others remained unheated (control). KHN values were obtained for three sites on each specimen at specified distances from the irradiated surface (0.2, 1.0, and 2.0 mm). The data were analyzed by two-way ANOVA and Tukey's test at with a significance level set to 5%. RESULTS: The improvement in the KHN values depended on the composites studied. The KHN values of TE-Economic, Natural Look, and Prisma were significantly improved by heat treatment (P < 0.05), whereas FillMagic and Glacier remained unchanged (P > 0.05) after heating. The distance from the irradiated area significantly influenced the KHN of all of the composites, regardless of heating application (P < 0.05). Sites that were closer to the irradiated surface exhibited a higher KHN (P < 0.05). CONCLUSION: The choice of the composite is important when intending to improve the KHN by heating. Sites that are closer to the irradiation source exhibit greater hardness, even after thermal treatment.

OBJETIVO: Este estudo procurou verificar se o tratamento térmico influencia na microdureza Knoop (KHN) de resinas compostas, e observar se existem diferenças entre áreas fotoativadas antes e depois da aplicação do calor. METODOLOGIA: Oitenta e quatro amostras retangulares transversais (10 × 2 mm × 2 mm) foram preparadas, 14 por resina composta. Após fotoativação (600 mW/cm² - 40), sete espécimes por compósito foram tratados termicamente (170 ºC/10 min), enquanto os demais permaneceram sem tratamento térmico (controle). Os dados de KHN foram obtidos em três áreas de cada amostra, de acordo com a distância a partir da superfície irradiada (mais próxima, intermediária e mais distante). Os dados foram analisados por ANOVA a dois critérios e teste de Tukey a 5%. RESULTADOS: O aumento da KHN foi dependente dos compósitos estudados. Os valores da KHN da TE-Econômico, Natural Look e Prisma foram significativamente melhorados por tratamento térmico (P < 0,05), enquanto que na FillMagic e Glacier permaneceram inalterados (P > 0,05) após o aquecimento. A área mais distante irradiada influenciou significativamente a KHN para todos os compósitos, independentemente da aplicação de tratamento térmico (P < 0,05). Quanto mais próximo da superfície irradiada, maior foi a KHN observada (P < 0,05). CONCLUSÃO: A escolha do compósito é importante quando é proposta a melhora da KHN por aquecimento. Quanto mais próximo da fonte de irradiação, maior a dureza mesmo após tratamento térmico.

Thermal behavior of direct resin composites: glass transition temperature and initial degradation analyses / Comportamento térmico de resinas compostas de uso direto: temperatura de transição vítrea e temperatura de degradação inicial

PURPOSE: The association of direct resin composites with simple thermal treatments may improve the mechanical properties of these materials. However, the ideal temperature for heat application depends on the thermal behavior of each material, such as glass transition (Tg) and initial degradation temperatures. To propose a heat treatment methodology, this study evaluated the thermal behavior of five commercial direct resin composites using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). METHODS: Photo-irradiation was achieved in cylindrical specimens (3×2 mm) using a photo-activator source (600 mW/cm² for 40 s). Thermal analyses were performed by DSC and TGA using a temperature range from 25 ºC to 900 ºC. RESULTS: Tg values obtained by DSC were 130.6 ºC for FillMagic, 129 ºC for Glacier, 143.5 ºC for Te-Econom, 147.5 ºC for Prisma APH and 143.7 ºC for Natural Look. A moderate weight loss began at around 270 ºC for all materials, which represented the initial degradation temperature. Conclusion: Regarding the heat treatment itself, it was concluded that the effective temperature for heat treatment is material dependent.

OBJETIVO: A associação de resinas compostas de uso direto com tratamentos térmicos pode melhorar as propriedades mecânicas destes materiais. No entanto, a temperatura ideal de aplicação está na dependência do comportamento térmico individual, como a temperatura de transição vítrea (Tg) e a temperatura inicial de degradação. Com o objetivo de propor uma metodologia de aplicação do tratamento térmico, o objetivo deste trabalho foi caracterizar cinco resinas compostas de uso direto usando calorimetria exploratória diferencial (DSC) e termogravimetria (TGA). METODOLOGIA: Corpos-de-prova cilíndricos (3×2 mm) foram fotoirradiados utilizando um aparelho de fotopolimerização (600 mW/cm² - 40s). As análises térmicas foram realizadas nas temperaturas de 25 ºC a 900 ºC. RESULTADOS: Os valores de Tg após análise de DSC foram: 130,6 ºC para FillMagic, 129 ºC para Glacier, 143,5 ºC para Te-Econom, 147,5 ºC para Prisma APH e 143,7 ºC para Natural Look. Para todos os materiais estudados a degradação iniciou-se por volta de 270 ºC. CONCLUSÃO: Considerando a aplicação do tratamento térmico em resinas compostas de uso direto, é possível sugerir que a temperatura efetiva é dependente do material em uso.

Understanding of the color in composite resin / 대한치과보존학회지

In clinic, esthetic restoration of a defective natural tooth with composite resin is challenging procedure and needs complete understanding of the color of tooth itself and materials used. The optical characteristics of the composites are different because the chemical compositions and microstructures are not same. This review provided basic knowledge of the color and the color measurement devices, and analyze the color of the natural tooth. Further, the accuracy of the shade tab, color of the composite resins before and after curing, effect of the water, food and bleaching agent, and translucency, opalescence, and fluorescence effects were evaluated.

The evaluation of surface roughness and polishing time between polishing systems / 대한치과보존학회지

OBJECTIVES: The purpose of this experiment was to evaluate four different polishing systems of their polishability and polishing time. MATERIALS AND METHODS: 4 mm diameter and 2 mm thickness Teflon mold was made. Z-250 (3M ESPE) hybrid composite resin was slightly overfilled and pressed with slide glass and cured with Optilux 501 for 40 sec each side. Then the surface roughness (glass pressed: control group) was measured with profilometer. One surface of the specimen was roughened by #320 grit sand paper and polished with one of the following polishing systems; Sof-Lex (3M ESPE), Jiffy (Ultradent), Enhance (Dentsply/Caulk), or Pogo (Dentsply/Caulk). The surface roughness and the total polishing time were measured. The results were analyzed with one-way ANOVA and Duncan's multiple range test. RESULTS: The surface roughness was lowest in Pogo, and highest in Sof-Lex. Polishing times were shortest with Pogo, and followed by the Sof-Lex, Enhance and Jiffy. CONCLUSIONS: One-step polishing system (Pogo) is very effective to get the smooth surface in a short time, therefore it can be recommended for final polishing system of the restoration.

Tensile bond strength and SEM analysis of enamel etched with Er:YAG laser and phosphoric acid: a comparative study In vitro

Er:YAG laser has been studied as a potential tool for restorative dentistry due to its ability to selectively remove oral hard tissue with minimal or no thermal damage to the surrounding tissues. The purpose of this study was to evaluate in vitro the tensile bond strength (TBS) of an adhesive/composite resin system to human enamel surfaces treated with 37 percent phosphoric acid, Er:YAG laser (lambda=2.94 mum) with a total energy of 16 J (80 mJ/pulse, 2Hz, 200 pulses, 250 ms pulse width), and Er:YAG laser followed by phosphoric acid etching. Analysis of the treated surfaces was performed by scanning electron microscopy (SEM) to assess morphological differences among the groups. TBS means (in MPa) were as follows: Er:YAG laser + acid (11.7 MPa) > acid (8.2 MPa) > Er:YAG laser (6.1 MPa), with the group treated with laser+acid being significantly from the other groups (p=0.0006 and p= 0.00019, respectively). The groups treated with acid alone and laser alone were significantly different from each other (p=0.0003). The SEM analysis revealed morphological changes that corroborate the TBS results, suggesting that the differences in TBS means among the groups are related to the different etching patterns produced by each type of surface treatment. The findings of this study indicate that the association between Er:YAG laser and phosphoric acid can be used as a valuable resource to increase bond strength to laser-prepared enamel.

A tecnologia a laser tem sido estudada como uma ferramenta potencial para uso em odontologia devido à sua habilidade em remover tecido ósseo com um mínimo ou nenhum dano aos tecidos vizinhos. O objetivo deste estudo é comparar in vitro a resistência à tração do sistema adesivo em esmalte tratado com ácido fosfórico a 37 por cento, laser Er:YAG (lambda=2,94 mim) com energia total de 16 J (80 mJ/pulso, 2 Hz, 200 pulsos e largura de pulso de 250 ms) e com a combinação laser Er:YAG seguido por ácido fosfórico. O teste de resistência à tração foi usado para comparar a resistência à tração em cada grupo. Foi também realizada microscopia eletrônica de varredura para permitir a análise das diferenças morfológicas entre os grupos. Foram obtidos os seguintes valores médios de resistência para os grupos tratados com: laser (6,1 MPa), ácido fosfórico (8,2 MPa) e laser mais ácido (11,7 Mpa). Amostras tratadas com laser e ácido apresentaram valores maiores de resistência do que amostras com laser ou ácido isoladamente. A análise da microscopia eletrônica revelou diferenças que corroboram os resultados, demonstrando que diferenças de resistência entre os grupos são devidas às diferenças entre os padrões superficiais resultantes. Nossos resultados sugerem que a combinação do laser Er:YAG com ácido fosfórico pode ser usada como um método para aumentar a resistência à tração do sistema esmalte resina.

Effect of different modes of light modulation on the bond strength and knoop hardness of a dental composite

This study evaluated the bond strength and Knoop hardness of Z250 composite resin, light activated with XL2500 curing unit, using different protocols: continuous mode - high intensity (CH) (700 mW/cm²) for 20 s; continuous mode - low intensity (CL) (150 mW/cm²) for 20 s; and pulse-delay with 150 mW/cm² for 2(P2), 3(P3), 5(P5), 10(P10) or 15 s (P15), with a 1-min delay, followed by 700 mW/cm² for 20 s. For the push-out test (n=10), the bond strength values were obtained using a universal test machine at a crosshead speed of 0.5 mm/min. For Knoop hardness (n=5), the specimens were made using the same light-activation protocols. The hardness measurements were made with a hardness tester at six depths (top, 1, 2, 3, 4, and 5 mm). The data were subjected to ANOVA and Tukey's test at 5 percent significance level. For bond strength, CL and P5 presented significantly higher mean values (p<0.05) than the other groups. There was no statistically significant difference (p>0.05) between P2, P3, P10, P15 and CH. For Knoop hardness, CH and P15 presented the highest mean values from top surface up to 4 mm depth , while CL presented the lowest hardness mean values (p<0.05). From the depth of 3 mm to 5 mm, the mean values of all groups were significantly lower (p<0.05) than those recorded on top surface. In conclusion, for the pulse-delay method, the initial exposure time can influence bond strength and Knoop hardness of composites.

Este estudo verificou a resistência de união e a dureza Knoop do compósito Z250 (3M/ESPE), fotoativado com luz de lâmpada halógena (XL2500, 3M/ESPE), utilizando diferentes protocolos: modo contínuo alta intensidade (CH) (700mW/cm²) por 20s; modo contínuo baixa intensidade (CL) (150mW/cm²) por 20s; pulse-delay com 150mW/cm² por 2(P2), 3(P3), 5(P5), 10(P10) ou 15(P15) segundos, com 1 min de espera, seguido por 700mW/cm² por 20s. Para o teste de união push-out (n=10), os valores de resistência de união foram obtidos em máquina de ensaio universal Instron. Para o ensaio de dureza Knoop (n=5) os espécimes foram fotoativados pelos mesmos protocolos utilizados no ensaio de resistência de união. As medidas de dureza foram realizadas em um microdurômetro (Shimadzu) em 6 profundidades (topo, 1, 2, 3, 4 e 5 mm). Os dados foram submetidos à Análise de Variância e ao teste de Tukey com nível de significância de 5 por cento. Os resultados mostraram que P5 e CL apresentaram resistência de união estatisticamente superior a todos os grupos. Não houve diferença entre os grupos P2, P3, P10, P15 e CH. Para dureza Knoop, CH apresentou os maiores valores, estatisticamente superiores a P2 e CL até 4 mm. A partir de 3 mm, a dureza de todos os grupos foi inferior a dureza do topo. O tempo de exposição inicial para o modo pulse-delay pode influenciar a resistência de união e a dureza Knoop.

Comparison of the residual stress of the nanofilled composites / 대한치과보존학회지

"Residual stress" can be developed during polymerization of the dental composite and it can be remained after this process was completed. The total amount of the force which applied to the composite restoration can be calculated by the sum of external and internal force. For the complete understanding of the restoration failure behavior, these two factors should be considered. In this experiment, I compared the residual stress of the recently developed nanofilled dental composite by ring slitting methods. The composites used in this study can be categorized in two groups, one is microhybrid type-Z250, as control group, and nanofilled type-Grandio, Filtek Supreme, Ceram-X, as experimental ones. Composite ring was made and marked two reference points on the surface. Then measure the change of the distance between these two points before and after ring slitting. From the distance change, average circumferential residual stress (sigmatheta) was calculated. In 10 minutes and 1 hour measurement groups, Filtek Supreme showed higher residual stress than Z250 and Ceram-X. In 24 hour group, Filtek showed higher stress than the other groups. Following the result of this experiment, nanofilled composite showed similar or higher residual stress than Z250, and when comparing the Z250 and Filtek Supreme, which have quite similar matrix components, Filtek Supreme groups showed higher residual stress.

Effect of different initial light intensity by the soft-start photoactivation on the bond strength and Knoop hardness of a dental composite

This study evaluated the bond strength (push-out method) and Knoop hardness of Z250 composite resin, photoactivated with XL 2500 curing unit, using different protocols: continuous mode (700mW/cm² for 20s) (CO); soft-start (50 mW/cm² for 5 s, followed by 700 mW/cm² for 15 s) (SS1); soft-start (100 mW/cm² for 5 s, followed by 700 mW/cm² for 15 s) (SS2); soft-start (150 mW/cm² for 5 s, followed by 700mW/cm² for 15s) (SS3); soft-start (200mW/cm² for 5s, followed by 700mW/cm² for 15s) (SS4); soft-start (250mW/cm² for 5 s, followed by 700 mW/cm² for 15 s) (SS5); soft-start (300 mW/cm² for 5 s, followed by 700 mW/cm² for 15 s) (SS6). For the push-out test, the specimens were tested in a universal testing machine at a crosshead speed of 0.5 mm/min. For the hardness test, the specimens were polished for the hardness measurements, using a 50 g load for 15 s. Data were submitted to ANOVA and Tukey's test (alpha=5 percent). The results of bond strength showed that the SS3 group obtained the highest bond strength when compared to the CO group. There were no significant differences among the other modes in relation to the other groups. Regarding the other results in hardness, there were no significant differences among the groups in the surface region and up to 4 mm depth.

Este estudo avaliou a resistência de união (push-out) e a dureza Knoop do compósito Z250, fotoativado por luz de lâmpada halógena XL2500, com diferentes modos: Contínuo (700 mW/cm²/20 s) (CO); Soft-start (50 mW/cm²/5 s + 700 mW/cm²/15 s) (SS1), (100 mW/cm²/5 s + 700 mW/cm²/15 s) (SS2), (150 mW/cm²/5 s + 700 mW/cm²/15 s) (SS3), (200 mW/cm²/5 s + 700 mW/cm²/15 s) (SS4), (250 mW/cm²/5 s + 700 mW/cm²/15 s) (SS5), (300 mW/cm²/5 s + 700 mW/cm²/15 s) (SS6). Para o ensaio de resistência de união, os espécimes foram testados em máquina de ensaio universal com velocidade de 0,5 mm/min. Para o teste de dureza, os espécimes foram polidos para a realização das leituras de dureza, realizadas com carga de 50 g por 15 s. Os dados foram submetidos a ANOVA e ao teste de Tukey (alfa=5 por cento). Os resultados de resistência da união mostraram que o grupo SS3 apresentou maior resistência da união quando comparado ao grupo CO. Não houve diferença entre os demais grupos testados. O teste de dureza Knoop mostrou que não houve diferença entre os grupos até 4 mm de profundidade.