Impact and fracture resistance of an experimental acrylic polymer with elastomer in different proportions

The purpose of this study was to evaluate the impact and fracture resistance of acrylic resins: a heat-polymerized resin, a high-impact resin and an experimental polymethyl methacrylate with elastomer in different proportions (10, 20, 40 and 60%). 120 specimens were fabricated and submitted to conventional heat-polymerization. For impact test, a Charpy-type impact tester was used. Fracture resistance was assessed with a 3-point bending test by using a mechanical testing machine. Ten specimens were used for each test. Fracture (MPa) and impact resistance values (J.m-1) were submitted to ANOVA - Bonferroni's test - 5% significance level. Materials with higher amount of elastomer had statistically significant differences regarding to impact resistance (p < 0.05). Fracture resistance was superior (p < 0.01) for high-resistance acrylic resin. The increase in elastomer concentration added to polymethyl methacrylate raised the impact resistance and decreased the fracture resistance. Processing the material by injection decreased its resistance to impact and fracture

Color stability, surface roughness and microhardness of composites submitted to mouthrinsing action

OBJECTIVE:The purpose of this study was to evaluate the effect of mouth rinse solutions on color stability, surface roughness and microhardness of two composite resins. MATERIAL AND METHODS: Fifty test specimens of each composite (Filtek Z250 and Z350; 3M ESPE) were made using a teflon matrix (12x2 mm). Color, surface roughness and Knoop microhardness baseline measurements of each specimen were made and specimens (n=10) were immersed in 5 mouth rinse solutions: G1: distilled water (control), G2: Plax Classic, G3: Plax alcohol-free; G4: Periogard, and G5: Listerine. Final measurements of color, roughness and microhardness were performed and the results submitted to statistical analysis (2-way ANOVA, Bonferroni s test;

Polymerization shrinkage stress of composites photoactivated by different light sources

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.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

Uso de uma técnica histológica adequada para análise microscópica dos tecidos corono-radiculares de dentes permanentes, variando-se a solução descalcificadora

The choice of the fixative, the time of fixation, the decalcification technique ant the solutions used are important factors in order to obtain a preparation appropriate for diverse light microscopy analyses. The objective of the present study was to identify the most adequate histological technique for recently extracted  permanent teeth by varying the decalcification solutions. For this purpose, 8 third molars were fixed in 10% formalin for 7 days and then decalcified. Four of these teeth were decalcified in 4% nitric acid solution (Group I), for 27 days. The other four teeth were decalcified in a solution containing equal parts of 20% sodium citrate and 30% formic acid (Group II), for 42 days. The specimens were embedded in parafinn in the horizontal position, cut into 5 micrometers thick sections with a microtome, and stained with hematoxylin-eosin and Gomori’s trichrome. The histological sections obtained were analyzed microscopically, selected and photomicrographed. The histological technique using 20% sodium citrate and 30% formic acid as decalcification solution provided the best results, preserving in a more satisfactory manner the crown-root tissues of the permanent teeth analyzed.A escolha do fixador e do tempo de fixação, a técnica de descalcificação e as soluções usadas com esse objetivo são fatores importantes na obtenção de uma preparação correta para as mais diversas análises ao microscópio de luz. Assim, no presente trabalho de pesquisa, foi selecionada a técnica mais adequada de preparo de cortes histológicos para dentes permanentes, variando-se as soluções descalcificadoras. Para tanto, 8 terceiros molares humanos recém-extraídos, divididos randomicamente em 2 grupos de 4 dentes, foram fixados durante 7 dias em uma solução de Formol à 10% e, em seguida, descalcificados por um período de 27 dias em uma solução de Ácido Nítrico a 4% (Grupo I) e 42 dias em uma solução de Citrato de Sódio a 20% + Ácido Fórmico a 30%, em partes iguais (Grupo II). As etapas laboratoriais seguintes foram àquelas utilizadas rotineiramente e a coloração, segundo as técnicas da Hematoxilina-Eosina e do Tricrômico de Gomori. Os cortes histológicos assim obtidos foram selecionados, analisados microscopicamente e fotografados. Pôde-se, assim, concluir, a partir dos resultados obtidos pela análise microscópica, que a técnica Histológica com a solução descalcificadora constituída pelo Citrato de Sódio a 20% + Ácido Fórmico a 30% obteve melhor desempenho, pois apresentou uma preservação mais satisfatória dos tecidos dentais observados

Systemic effect of mineral aggregate-based cements: histopathological analysis in rats

Objective: Several studies reported the local tissue reaction caused by mineral aggregate-based cements. However, few studies have investigated the systemic effects promoted by these cements on liver and kidney when directly applied to connective tissue. The purpose of this in vivo study was to investigate the systemic effect of mineral aggregate-based cements on the livers and kidneys of rats. Material and Methods: Samples of Mineral Trioxide Aggregate (MTA) and a calcium aluminate-based cement (EndoBinder) containing different radiopacifiers were implanted into the dorsum of 40 rats. After 7 and 30 d, samples of subcutaneous, liver and kidney tissues were submitted to histopathological analysis. A score (0-3) was used to grade the inflammatory reaction. Blood samples were collected to evaluate changes in hepatic and renal functions of animals. Results: The moderate inflammatory reaction (2) observed for 7 d in the subcutaneous tissue decreased with time for all cements. The thickness of inflammatory capsules also presented a significant decrease with time (

In vitro study of the effect of Er: YAG laser irradiation on the apical sealing of different root canal sealers

OBJECTIVES: The aim of this study was to determine the effect of Er:YAG laser irradiation used to clean dentinal walls on the apical sealing of root canals filled with different types of sealers. Background Data: Laser application to the dentinal walls removed debris, rendering the root canals free of smear layers and leaving the dentinal canaliculi open. METHODS: Sixty-four maxillary canines obtained from laboratory files were instrumented with K-files (Dentsply, Maillefer, Ballaigues, Switzerland) using the crown-down technique, and irrigated with a 0.5% sodium hypochlorite solution. The specimens were divided into two groups of 32 teeth each. In group I, the teeth were instrumented and irrigated with sodium hypochlorite solution, and divided into four subgroups to be sealed with the different materials (Endofill, N-Rickert, Sealapex and Sealer 26). In group II, the root canals were subjected to Er:YAG laser irradiation (200 mJ, 7 Hz and 60 J total energy), followed by root canal sealing as in group I. RESULTS: The data showed lower levels of apical microleakage in the teeth filled with N-Rickert, Sealapex and Sealer 26 cements than in those sealed with Endofill (p ; 0.05). CONCLUSIONS: The Er:YAG laser irradiation applied to the root canal walls was not able to prevent apical microleakage.OBJETIVOS: Avaliou-se a infiltração marginal apical em caninos superiores, obturados com quatro tipos diferentes de cimento, os quais foram imersos em tinta nanquim e mantidos a uma temperatura de 37º C por 96 horas, descalcificados em solução de ácido clorídrico a 5%, desidratados em série crescente de álcoois e diafanizados em salicilato de metila. MÉTODOS: Para isto, 64 dentes de estoque foram instrumentados pela técnica "crown-down", irrigados com solução de hipoclorito de sódio a 0,5% e divididos em dois grupos experimentais. Os dentes do Grupo I foram subdivididos em quatro sub-grupos de oito elementos e obturados cada um deles com os cimentos Endofill®, N-Rickert®, Sealapex® e Sealer 26®. Os dentes do Grupo II receberam aplicação adicional de laser Er:YAG, tendo seus canais radiculares obturados como aqueles do grupo I. RESULTADOS: A infiltração marginal apical apresentou valores estatisticamente maiores e significantes (p ; 0,05), quanto à infiltração marginal apical, nos dentes do Grupo I, preparados somente com a solução de hipoclorito de sódio a 0,5%, e naqueles do Grupo II, que foram irradiados com laser Er: YAG. CONCLUSÕES: A irradiação de laser Er:YAG aplicada nas paredes do canal radicular não foi capaz de prevenir a infiltração marginal apical

Synthesis and biocompatibility of an experimental glass ionomer cement prepared by a non-hydrolytic sol-gel method

The aims of this study were to demonstrate the synthesis of an experimental glass ionomer cement (GIC) by the non-hydrolytic sol-gel method and to evaluate its biocompatibility in comparison to a conventional glass ionomer cement (Vidrion R). Four polyethylene tubes containing the tested cements were implanted in the dorsal region of 15 rats, as follows: GI - experimental GIC and GII - conventional GIC. The external tube walls was considered the control group (CG). The rats were sacrificed 7, 21 and 42 days after implant placement for histopathological analysis. A four-point (I-IV) scoring system was used to graduate the inflammatory reaction. Regarding the experimental GIC sintherization, thermogravimetric and x-ray diffraction analysis demonstrated vitreous material formation at 110oC by the sol-gel method. For biocompatibility test, results showed a moderate chronic inflammatory reaction for GI (III), severe for GII (IV) and mild for CG (II) at 7 days. After 21 days, GI presented a mild reaction (II); GII, moderate (III) and CG, mild (II). At 42 days, GI showed a mild/absent inflammatory reaction (II to I), similar to GII (II to I). CG presented absence of chronic inflammatory reaction (I). It was concluded that the experimental GIC presented mild/absent tissue reaction after 42 days, being biocompatible when tested in the connective tissue of rats.O objetivo deste estudo foi demonstrar a sinterização pelo método sol-gel não-hidrolítico de um cimento de ionômero de vidro experimental (CIV) e avaliar sua biocompatibilidade em relação a um cimento de ionômero de vidro convencional (Vidrion R). Quatro tubos de polietileno contendo os cimentos testados foram implantados no dorso de 15 ratos, da seguinte maneira: GI - CIV Experimental e GII - CIV Convencional. A lateral do tubo foi considerada Grupo Controle. Os ratos foram sacrificados em 7, 21 e 42 dias pós-implantação para análise histopatológica. Uma escala de I a IV foi utilizada como sistema de score para graduar a reação inflamatória. Em relação à sinterização do CIV experimental, as análises termogravométrica e por difração de raio-x demonstraram a formação de material vítreo aos 110oC pelo método sol-gel. Para o teste de biocompatibilidade, os resultados mostraram uma reação inflamatória moderada para o GI (III), severa para o GII (IV) e branda para o Grupo Controle (II) aos 7 dias. Após 21 dias, GI apresentou uma reação branda (II); GII, moderada (III) e Grupo Controle, branda (II). Aos 42 dias, GI apresentou uma reação inflamatória branda/ausente (II a I), similar ao GII (II a I). O Grupo Controle demonstrou ausência de reação inflamatória (I). Concluiu-se que o CIV Experimental apresentou reação tecidual branda/ausente após 42 dias, sendo biocompatível quando testado em tecido conjuntivo de ratos