Análisis In vitro de yesos dentales de alta resistencia y baja expansión disponibles en Perú / In vitro analysis of high resistance and low expansion dental plasters available in Peru

Objetivo. Comparar la dureza, estabilidad dimensional y resistencia a la compresión de los yesos dentales de alta resistencia y baja expansión disponibles en el Perú. Métodos. Se realizó un estudio descriptivo, observacional y transversal. Se confeccionaron muestras de forma cilíndrica (8) y rectangular (8), de siete yesos dentales de alta resistencia y baja expansión. Se evaluó la dureza utilizando el Durómetro Universal Identec, la estabilidad dimensional con un calibrador digital y la resistencia a compresión con la Máquina de Ensayo Universal. Para determinar si hay diferencia en cada una de estas propiedades se empleó el análisis de varianza, la prueba F y la prueba de Duncan. Además, se empleó la prueba de comparación de medias, t de Student, para evaluar si difieren con los valores de la ADA (Asociación Dental Americana). Resultados. La dureza, estabilidad dimen-sional y resistencia a la compresión promedio de los yesos dentales presentó diferencias significativas (p<0.05) entre cada uno con los promedios estándares establecidos por la ADA. Conclusiones. En relación resistencia a la compresión el 100% de los yesos analizados cumplen con los parámetros establecidos por la ADA, en relación estabilidad dimensional solo el 28.6% y el 100% no alcanzan los estándares de dureza promedio establecidos por la ADA.

Objective. To compare the hardness, dimensional stability, and compressive strength of high-strength, low-expansion dental plasters available in Peru, according to ADA criteria. Methods. A descriptive, observational and cross-sectional study was developed. A selection of 8 cylindrical-shaped samples and 8 rectangular- shaped ones, from seven high-resistance, low-expansion dental plasters were fabricated. The hardness was evaluated using the Identec Universal Durometer. Dimensional stability was evaluated with a digital caliper and compressive strength was evaluated with the Instron Universal Testing Machine. To determine if there is a difference in each of these properties, the analysis of variance, F test, and the Duncan's test were used. In addition, to assess whether these values differ from those of the ADA, the mean comparison test, student's t table, were used. Results. The hardness, dimensional stability and average compressive strength of the high-strength, low-expansion dental plasters showed that there are significant di-fferences (p<0.05) between each of the dental plasters and with the standard averages established by the American Dental Association. (ADA). Conclusions. 100% of the high-strength, low-expansion dental casts meet the parameters established by the ADA in terms of their compressive strength, only 28.6% of these comply with the ADA in terms of dimensional stability and that 100% of these do not meet the average hardness standards established by the ADA.

Influence of paper mixing pads thickness on the compressive strength of glass ionomer cement / 北京大学学报(医学版)

OBJECTIVE@#To explore the influence of the thickness of mixed cardboard on the compressive strength of glass ionomer cement and the associated factors.@*METHODS@#Three different types of glass ionomer cements were mixed on the top of 60, 40, 20 and 1 pieces of paper (P60, P40, P20 and P1), respectively. The compressive strength of the materials was tested after solidification, and the bubble rate was calculated with the assistance of scanning electron microscope.@*RESULTS@#(1) Compressive strength: ① ChemFil Superior glass ionomer (CF): The average compressive strength of P1 group was the highest, which was significantly different from that of P40 and P60 groups (P values were 0.041 and 0.032 respectively); ② To Fuji IX GP glass ionomer (IX): The average compressive strength of P1 group was the highest, which was statistically different from that of P40 and P60 groups (P values were 0.042 and 0.038 respectively); ③ Glaslonomer FX-Ⅱ glass ionomer cement (FX): The average compressive strength of P1 group was the highest, which was statistically different from that of P20, P40 and P60 groups (P values were 0.031, 0.040 and 0.041 respectively), but there was no statistical difference among the other groups. All the three materials showed that the compressive strength of glass ions gradually increased with the decrease of the thickness of the blended paperboard, and the two materials had a highly linear negative correlation, the correlation coefficients of which were CF-0.927, IX-0.989, FX-0.892, respectively. (2) Scanning electron microscope: P1 group had the least bubbles among the three materials.@*CONCLUSION@#It indicates that the thickness of mixed cardboard has a negative correlation with the compressive strength of glass ions. The thicker the mixed cardboard is, the greater the elasticity is. Excessive elasticity will accelerate the mixing speed when the grinding glass ions. Studies have shown that the faster the speed of artificial mixing is, the more bubbles is produced.The thicker ther mixed cardboard is, the more bubblesn are generated by glass ionomer cement, and the higher the compressive strength is. Using one piece of paper board to mix glass ionomer cement has the least bubbles and can obtain higher compressive strength.

Novel pulp capping material based on sodium trimetaphosphate: synthesis, characterization, and antimicrobial properties

Abstract Objectives: To evaluate the mechanical, physicochemical, and antimicrobial properties of four different formulations containing micro- or nanoparticles of sodium trimetaphosphate (mTMP and nTMP, respectively). Methodology: Four experimental groups were used in this investigation: two mTMP groups and two nTMP groups, each containing zirconium oxide (ZrO2), and solution containing either chitosan or titanium oxide (TiO2) nanoparticles (NPs). Setting time, compression resistance, and radiopacity were estimated. The agar diffusion test was used to assess the antimicrobial activity of the formulations against five different microbial strains: Streptococcus mutans, Lactobacillus casei, Actinomyces israelii, Candida albicans, and Enterococcus faecalis. Parametric and nonparametric tests were performed after evaluating homoscedasticity data (p<0.05). Results: From the properties evaluated, nTMP cements required less setting time and showed greater resistance to compression. Cements containing TiO2 showed greater radiopacity for both nTMP and mTMP. All four cement formulations showed antimicrobial activity against S. mutans and L. casei Conclusion: Formulations containing nTMP have shorter setting times and higher compressive strength, and those with TiO2 nanoparticles showed antimicrobial activities. Clinical relevance: The cement containing nTMP, ZrO2, and TiO2 could be an alternative material for protecting the pulp complex.

Molars Fracture Resistance with Class II Cavities Restored with Different Resin - Based Materials / Resistência à Fratura de Molares com Cavidades Classe II Restauradas com Diferentes Materiais à Base de Resina

The teeth weakening due to the preparation of class II mesio-occluso-distal cavities is a challenge for the clinician. The objective of this study was to evaluate the molars fracture resistance with class II mesio-occluso distal cavities restored with different restorative techniques and materials. Forty extracted molars were divided into 5 groups: Group 1 ­ intact healthy teeth (positive control); Group 2 ­ unrestored teeth with mesio-occluso distal class II cavities (negative control); Groups 3 to 5 ­ restored teeth with standardized dimensions. In groups 3 to 5, the cavities were restored with flow resin only, flow resin coated with a nano-hybrid resin, and nano-hybrid resin only, respectively. All specimens were tested for resistance to fracture using an axial compressive load, a metallic sphere measuring 8 mm in diameter on a universal testing machine EMIC DL-2000. A 10 kN load cell operated at a speed of 5 mm/min until the tooth fracture. Data were subjected to analysis of variance and Tukey's tests (α = 0.05). Group 3 showed higher fracture strength (2243.1 ± 473.7N) when compared to groups 2, 4 and 5. This difference was statistically significant (p<0.05). The fracture strength of teeth restored with flow mesio occluso-distal restorations was similar to that of intact natural teeth. (AU)

O enfraquecimento dos dentes devido às preparações de cavidades mesio-ocluso-distal é um desafio para o clínico. O objetivo deste estudo foi avaliar a resistência à fratura de molares com cavidades mesio-ocluso-distais classe II restauradas com diferentes técnicas e materiais restauradores. Quarenta molares extraídos foram divididos em 5 grupos: Grupo 1 ­ dentes saudáveis intactos (controle positivo); Grupo 2 ­ dentes não restaurados com cavidades mesio-occluso-distais classe II (controle negativo); Grupos 3 a 5 ­ dentes restaurados com dimensões padronizadas. Nos grupos 3 a 5, as cavidades foram restauradas apenas com resina flow, resina flow recoberta com uma resina nanohíbrida e somente resina nano-híbrida, respectivamente. Todas as amostras foram testadas quanto à resistência à fratura usando uma carga compressiva axial, usando uma esfera metálica medindo 8 mm de diâmetro em uma máquina de teste universal EMIC DL-2000. Uma célula de carga de 10 kN operava a uma velocidade de 5 mm/min até a fratura do dente. Os dados foram submetidos à análise de variância e testes de Tukey (α = 0,05). O grupo 3 apresentou maior resistência à fratura (2243,1 ± 473,7N) quando comparado aos grupos 2, 4 e 5. Essa diferença foi estatisticamente significante (p <0,05). A resistência à fratura dos dentes restaurados com resina flow foi semelhante à dos dentes naturais intactos. (AU)

Creating Antibacterial Properties in Flowable Dental Composites by Incorporation of 3, 4-dihydropyrimidin-2(1H)-ones

ABSTRACT Objective: To investigate the antibacterial, mechanical, physical properties and water sorption of flowable dental composites containing 3,4-dihydropyrimidin-2(1H)-ones. Material and Methods: 3,4-dihydropyrimidin-2(1H)-ones was synthesized and the antibacterial activity of flowable dental composites containing 0-5 wt% 3,4-dihydropyrimidin-2(1H)-ones and also of their mechanical and physical properties on flowable dental composites were investigated. Flexural strength was measured by a three-point bending test. Compressive strength (CS), Water sorption (WS) and depth of cure (DOC) were investigated. The data were analyzed by One-way ANOVA test. The level of significance was determined as p<0.01. Results: The direct contact test demonstrates that by increasing the 3,4-dihydropyrimidin-2(1H)-ones content, the bacterial growth is significantly diminished (p<0.001). The average flexural strength results show that with increasing 3,4-dihydropyrimidin-2(1H)-ones until 3% in the composite, no significant difference was observed in flexural strength (p>0.001) and the mean of compressive strength results show no significant difference between 0-4% groups (p>0.001). The mean of water sorption and depth of cure results shows no significant difference between groups (p>0.001). Conclusion: Incorporation of 3,4-dihydropyrimidin-2(1H)-ones into flowable resin composites in 3% wt can reduce the activity of Streptococcus mutans.

Mechanical and bonding properties of different combinations of nanohybrid and bulk-fill composites / Propiedades mecánicas y adhesión entre diferentes combinaciones composite Nanohíbrido-Bulkfill

ABSTRACT The aim of this research was to determine compressive and shear bond strength of blocks prepared with bulk-fill and nanofill composite resin combinations. Materials used were Filtek Bulk Fill (FBF) and Z350 (both 3M-ESPE) and Surefil SDR flow (SFF) - Dentsply. To determine shear bond strength, cylindrical specimens 10 mm thick were prepared with composite consisting of thicknesses of 6 mm of one material and 4 mm of the other, in the following combinations: G1: FBF- FBF; G2: Z350-Z350, G3: FBF-Z350, G4: Z350-SFF and G5: SFFSFF. Materials were cured using a 1100 mw/cm2 light for 20 seconds for each layer. Samples were stored for 24 hours at 37 °C in distilled water and shear bond strength was determined. To assess compressive strength, cylindrical samples 4 mm diameter and 6 mm thick consisting of 4 mm + 2 mm were used in the same combinations as described above, stored in distilled water at 37 °C for 24 hours, after which compressive strength was determined. Both tests were performed with a Universal testing machine at a cross head speed of 1 mm/min. Results were analyzed with ANOVA and Tukey's test. Means and standard deviations in MPa for each group were the following: Shear bond strength: G1: 435.87 (65.86), G2: 233.6 (108.15), G3: 279.2 (22.05), G4:449.1 (109.35) and G5: 196.6 (51.16). Compressive strength: G1:160.07(4.27), G2: 149.49 (14.06), G3: 156.10 (29.99), G4: 199-30(39.28), G5: 171.23 (28.71). Evaluation with ANOVA showed no significant differences among combinations for compressive strength (p>0.05) and significant differences for bond strength (p<0.05). Tukey's test showed three homogeneous groups. Under these experimental conditions, it can be concluded that the study combinations have adequate mechanical behavior, equivalent to materials used individually. However, shear bond strength was affected by the combinations analyzed.

RESUMEN El objetivo de este trabajo fue determinar la resistencia compresiva (RC) y la resistencia adhesiva al corte (RAC) en bloques preparados con combinaciones de composites bulk-fill y nanoparticulados. Los materiales usados fueron Filtek Bulk Fill (FBF) y Z350 (ambos de 3M-ESPE) y Surefil SDR flow (SFF) - Dentsply. Para medir la RAC, se prepararon probetas cilindricas de 10 mm de espesor consistentes en 6 mm de un material y 4 mm del otro con las siguientes combinaciones: G1: FBF- FBF; G2: Z350-Z350, G3: FBF-Z350, G4: Z350-SFF y G5: SFF-SFF. Se curaron a 1100 mw/cm2 durante 20 segundos cada capa. Se conservaron 24 horas a 37 °C en agua destilada antes de determinar la RAC. Para medir la RC se prepararon probetas de 4 mm de diametro y 6 mm de espesor (4 mm + 2 mm de cada material), con las mismas combinaciones. Se conservaron en agua destilada a 37 °C durante 24 horas y se midió la RC. Ambos ensayos se realizaron con una máquina universal para ensayos mecánicos a 1 mm/min de velocidad de desplazamiento de cabezal. Los resultados se evaluaron con ANOVA y prueba de Tukey. Las medias y desviaciones estándar (MPa) para cada grupo fueron: RAC: G1: 435.87 (65.86), G2: 233.6 (108.15), G3: 279.2 (22.05), G4:449.1 (109.35) y G5: 196.6 (51.16). RC: G1:160.07(4.27), G2: 149.49 (14.06), G3: 156.10 (29.99), G4: 199-30(39.28), G5: 171.23 (28.71). ANOVA no mostró diferencias estadísticamente significativas para RC (p>0.05) y diferencias significativas para RAC (p<0.05). La prueba de Tukey mostró tres grupos homogéneos. En las condiciones experimentales de este trabajo puede concluirse que las combinaciones evaluadas tienen un comportamiento mecánico adecuado equivalente al de los materiales individuales. Sin embargo, la adhesión entre materiales se vio afectada por las combinaciones realizadas.

Study on injectable calcium sulfate bone cement rich in bioactivity / 中华骨科杂志

Objective:To explore the effect of decalcified bone matrix (DBM) rich in biological activity on surgical-grade medical calcium sulfate, and to observe the change of different content of DBM on the physical and chemical properties of calcium sulfate, which provide theoretical basis for the preparation of calcium sulfate bone cement with osteogenic and injectable properties.Methods:DBM with weight content of 0, 5%, 10%, 20%, 30%, 40% was fully mixed with CSH. Dissolve 0.3 g of methyl cellulose in 10 ml of deionized water to prepare a 3% methyl cellulose solution. Methylcellulose solution was added according to the liquid-solid ratio of 0.4. The mixture was evenly stirred to form slurry, then the degradation rate, compressive strength, setting time and and pH value of calcium sulfate in vitrowas measured.Results:The initial setting time and final setting time of calcium sulfate were 4.96±0.20 and 5.83±0.12 min respectively. With the increase of DBM content, the initial setting time and final setting time increased significantly ( F=49.275, P<0.05; F=124.859, P<0.05). The compressive strength of pure calcium sulfate is 23.33±6.35 MPa; when the content is 40%, the compressive strength is only 3.33 MPa. With the increase of DBM content, the compressive strength first increased and then decreased; the content of 5%, 10%, 20% DBM had little effect on the compressive strength ( P>0.05), while the compressive strength of 30% and 40% groups decreased significantly ( t=3.259, P<0.05). DBM with different contents can significantly change the degradation rate of calcium sulfate complex. When the content of DBM is 30% and 40%, the complete degradation time in vivo is only 10 d, while the degradation rate of calcium sulfate is 63% in 30 d. At any time point in vitro degradation, DBM had no significant effect on the pH value of calcium sulfate complex culture medium, and the change law was consistent with that of pure calcium sulfate. Conclusion:With the increase of DBM content, the degradation rate is gradually accelerated, the compressive strength is reduced, and the setting time is prolonged, which is not conducive to the preparation of injectable calcium sulfate cement.

Physical properties of glass ionomer cement containing pre-reacted spherical glass fillers

Abstract The aim of this study was to assess the effect of different commercial liquid phases (Ketac, Riva, and Fuji IX) and the use of spherical pre-reacted glass (SPG) fillers on cement maturation, fluoride release, compressive (CS) and biaxial flexural strength (BFS) of experimental glass ionomer cements (GICs). The experimental GICs (Ketac_M, Riva_M, FujiIX_M) were prepared by mixing SPG fillers with commercial liquid phases using the powder to liquid mass ratio of 2.5:1. FTIR-ATR was used to assess the maturation of GICs. Diffusion coefficient of fluoride (DF) and cumulative fluoride release (CF) in deionized water was determined using the fluoride ion specific electrode (n=3). CS and BFS at 24 h were also tested (n=6). Commercial GICs were used as comparisons. Riva and Riva_M exhibited rapid polyacrylate salt formation. The highest DF and CF were observed with Riva_M (1.65x10-9 cm2/s) and Riva (77 ppm) respectively. Using SPG fillers enhanced DF of GICs on average from ~2.5x10-9 cm2/s to ~3.0x10-9 cm2/s but reduced CF of the materials on average from ~51 ppm to ~42 ppm. The CS and BFS of Ketac_M (144 and 22 MPa) and Fuji IX_M (123 and 30 MPa) were comparable to commercial materials. Using SPG with Riva significantly reduced CS and BFS from 123 MPa to 55 MPa and 42 MPa to 28 MPa respectively. The use of SPG fillers enhanced DF but reduced CF of GICs. Using SPG with Ketac or Fuji IX liquids provided comparable strength to the commercial materials.

Resumo O objetivo deste estudo foi avaliar o efeito de diferentes fases líquidas comerciais (Ketac, Riva e Fuji IX) e o uso de partículas esféricas de vidro pré-reagido (SPG) na maturação do cimento, liberação de flúor, força de compressão (CS) e resistência biaxial à flexão (BFS) de cimentos de ionômero de vidro (GICs) experimentais. Os GICs experimentais (Ketac_M, Riva_M, FujiIX_M) foram preparados pela mistura de partículas SPG com fases líquidas comerciais usando a proporção de pó para massa líquida de 2,5: 1. O FTIR-ATR foi usado para avaliar a maturação dos GICs. O coeficiente de difusão do flúor (DF) e a liberação cumulativa de flúor (CF) em água deionizada foram determinados usando o eletrodo específico do íon fluoreto (n = 3). CS e BFS em 24 h também foram testados (n = 6). GICs comerciais foram usados como comparações. Riva e Riva_M exibiram rápida formação de sal de poliacrilato. Os maiores DF e CF foram observados com Riva_M (1,65x10-9 cm2/s) e Riva (77 ppm), respectivamente. O uso de partículas SPG melhorou o DF de GICs em média de ~ 2,5x10-9 cm2/s a ~ 3,0x10-9 cm2/s, mas reduziu o CF dos materiais em média de ~ 51 ppm a ~ 42 ppm. O CS e BFS de Ketac_M (144 e 22 MPa) e Fuji IX_M (123 e 30 MPa) foram comparáveis aos materiais comerciais. Usar SPG com Riva reduziu significativamente CS e BFS de 123 MPa para 55 MPa e 42 MPa para 28 MPa, respectivamente. O uso de SPG partículas melhorou o DF, mas reduziu o CF dos GICs. O uso de partículas SPG com líquidos Ketac ou Fuji IX proporcionou resistência comparável aos materiais comerciais.

Correlation between mechanical properties and stabilization time of chemical bonds in glass-ionomer cements

Abstract The objective was to evaluate the compressive strength (CS), diametral tensile strength (DTS), flexural strength (FS), and Knoop microhardness (KH) of different conventional restorative glass-ionomer cements (GICs) and to correlate these mechanical properties (MP) with the stabilization time (ST) of their chemical bonds. Eighteen GICs were tested: Bioglass [B], Chemfil Rock [CR], Equia Forte [EF], Gold Label 2 [GL2], Gold Label 9 [GL9], Glass Ionomer Cement II [GI], Ionglass [IG], Ion Z[ IZ], Ionomaster [IM], Ionofil Plus [IP], Ionostar Plus [IS], Ketac Molar Easymix [KM], Magic Glass [MG], Maxxion R [Ma], Riva Self Cure [R], Vidrion R [V], Vitro Fil [VF] and Vitro Molar [VM]. The mechanical strength tests were performed in a universal testing machine. KH readings were done with a diamond indenter. STs were examined by Fourier Transform Infrared spectroscopy (FTIR). Data were analyzed with ANOVA and Tukey test (p<0.05). The Spearman rank test was used to evaluate the dependence between the MPs and ST results. The highest MP values were EF, GL2, GL9, GI and KM and the lowest for MG, MA, B, VF and IM. The longest ST was for GL2 and the shortest was for B. ST correlated positively with MP. GICs with longer chemical bonds ST are generally stronger and the ST value obtained from FTIR was useful in predicting the strength of GICs tested.

Resistência à fratura de dentes tratados endodonticamente reforçados com pinos customizados de fibra de vidro e carbono / Fracture resistance of endodontically treated teeth reinforced with customized glass and carbon fiber posts

Objetivo: o objetivo do presente estudo foi comparar a resistência à fratura de quatro tipos de pinos intrarradiculares pré-fabricados: fibra de vidro, fibra de vidro customizado com resina composta, fibra de carbono e fibra de carbono customizado com resina, em dentes bovinos. Métodos: foram utilizados 60 dentes bovinos unirradiculares, que receberam tratamento endodôntico e foram divididos nos seguintes grupos: FV = pino de fibra de vidro; FVP = pino de fibra de vidro customizado; FC = pino de fibra de carbono; FCP = pino de fibra de carbono customizado; e Controle = restauração coronária com resina composta. Os dentes foram inseridos em blocos de resina acrílica, a 2 mm da junção amelocementária, simulando a interface dente-osso. Os espécimes foram submetidos ao teste de resistência à fratura em máquina de ensaio universal, sob uma carga de 0,5mm/min, até a fratura do corpo de prova. Os valores obtidos foram submetidos ao teste ANOVA, com pós-teste de Tukey. Foi realizada, também, uma análise dos padrões de fratura, por meio do teste Kruskal- -Wallis. Resultados: o grupo FCP mostrou os maiores valores de resistência à fratura, seguido pelos grupos FV, FVP e FC. O grupo controle mostrou menor resistência do que os demais, que receberam pinos intrarradiculares. Os pinos de FVP apresentaram o maior número de fraturas reparáveis, em contraste ao controle, no qual houve o maior número de fraturas desfavoráveis. Conclusão: o uso de pinos customizados reduziu a incidência de fraturas catastróficas. A ausência de pino intrarradicular ocasionou a maior incidência de fraturas irreparáveis. (AU)

Objective: The aim of this study was to compare the fracture resistance of four types of prefabricated intraradicular posts - glass fiber, glass fiber customized by composite resin, carbon fiber, and customized carbon fiber - on bovine teeth. Methods: Sixty bovine teeth were submitted to endodontic treatment and divided into the following groups: GF - glass fiber post; CGF - customized glass fiber post; CF - carbon fiber post; CCF - customized carbon fiber post; control - composite resin restoration. The teeth were embedded in acrylic resin blocks at 2 mm from the cement-enamel junction, simulating the teeth-bone interface. The specimens were submitted to a fracture resistance test in a universal test machine under a 0.5 mm/min load until the fracture of the specimen. The values obtained were submitted to ANOVA and Tukey tests. The analysis of the fracture patterns was performed by the Kruskal-Wallis test. Results: The CCF group presented the highest values of fracture resistance, followed by GF, CGF, and CF posts. The control group offered less resistance than the other groups that received intraradicular posts. The CGF presented the highest number of favorable fractures, in contrast to the control group, which presented the highest number of unfavorable fractures. Conclusion: The use of customized posts reduced the incidence of catastrophic fractures. The lack of intracanal posts led to a higher incidence of irreparable fractures (AU).

Knowledge And Awareness Of Diabetic Retinopathy Among Diabetic Patients, Al-Ahsaa, Saudi Arabia

Introduction: Saudi Arabia is a country with high prevalence of diabetes. The prevalence of diabetic retinopathy is 19.7%. To decrease the incidence of diabetic retinopathy and to improve quality of life, our study aims to assess the knowledge of diabetic retinopathy among diabetic patients. Objectives: The primary objective is to assess the knowledge of diabetic patients about DR. Methods: Cross-sectional study, conducted in PHC centers. Data was collected using an interviewer-administered questionnaire to study the relationship between socio-demographic factors and knowledge about DR. Results: Atotal of 383 adult diabetic subjects participated in the. The association between socio-demographic factors and the knowledge of DR showed that, females, elderly, illiterate and those attained high school education or less showed significantly poor level of knowledge (p<0.05). Conclusion: lack of knowledge was associated with low levels of education, female and older ages.

Mechanical Characteristics of (TiO2-ZnO)/PMMA Nanocomposites for Dentures

Mechanical properties (impact strength, compressive strength and flexural strength) have been studied for (Polymethyl-methacrylate (PMMA)) polymer reinforced with nano (TiO2+ZnO) (0 v%, 1 v%, 2 v%, 3 v%, 4 v% and 5 v%). Ultrasonic dispersion technique was used to prepare the nanocomposites samples, follow with cold casting technique using Teflon molds standard conditions. Charpy impact instrument was used to measure the impact strength, the compressive strength of each sample which was tested in newton units using digital compression tester (TinusOlsen: H50KT, England), while flexural strength can be found from mathematical formulas which depend on the impact strength, compressive strength and flexural strength. Results show that values increase in 1 v%, then decrease alternately by (2 v%, 3 v%, 4 v%, and 5 v%), while 0 v% is the less value of volume fraction of fillers. Young modules values increase alternately by the volume fraction of fillers until 2 v%, while if it is higher and lower than 2 v% it decreases the modulus of elasticity.

Mechanical properties of bulk-fill versus nanohybrid composites: effect of layer thickness and application protocols / Propriedades mecânicas de compósitos de resina bulk versus nano-híbrida: efeito da espessura da camada e protocolos de aplicação

Objective: The objective of this study was to evaluate the compressive strength, flexural strength and flexural modulus of high-viscosity, low-viscosity bulk-fill, and conventional nanohybrid resin composite materials alone and when covered with nano-hybrid resin composite at different incremental thicknesses on the bulk-fill composites. Material and Methods: Specimens (N=60) were fabricated from the following materials or their combinations (n=10 per group): a) conventional nano-hybrid composite Z550 (FK), b) high-viscosity bulk-fill composite (Tetric N Ceram-TBF), c) low-viscosity bulk-fill composite SDR (SDR), d) Sonicfill (SF), e) SDR (2 mm)+FK (2 mm), f) SDR (4 mm)+FK (4 mm). After 24 h water storage, compressive strength was measured in a universal testing machine (1 mm/min). Additional specimens (N=40) (25x2x2 mm3) were made from FK, TBF, SDR and SF in order to determine the flexural strength and the flexural modulus, (n=10) and subjected to three-point bending test (0.5 mm/min). Data were analyzed using one-way ANOVA and Tamhane's T2 post-hoc tests (p p<0.05). Results: The mean compressive strength (MPa) of the nano-hybrid composite (FK) was significantly higher (223.8±41.3) than those of the other groups (123±27 - 170±24) (p <0.001). SDR (4 mm)+FK (2 mm) showed significantly higher compressive strength than when covered with 4 mm (143±30) or when used alone (146±11) (p <0.05). The mean flexural strength (159±31) and the flexural modulus of FK (34±7) was significantly higher than that of the high- or low-viscosity bulk-fill composites (p<0.001). The mean flexural strength of SF (132±20) was significantly higher compared to TBF (95±25) (p <0.05). Conclusion: Bulk-fill resin composites demonstrated poorer mechanical properties compared to nano-hybrid composite but similar to that of SF. Increasing the thickness of low-viscosity bulk-fill composite (SDR) from 2 to 4 mm underneath the nano-hybrid composite (FK) can improve the mechanical properties of the bulk-fill composites.(AU)

Objetivo: O objetivo deste estudo foi avaliar a resistência à compressão, resistência à flexão e módulo de flexão de materiais compósitos de alta viscosidade, baixa viscosidade e compósitos nanohíbridos convencionais e quando cobertos com resina composta nano-híbrida em diferentes espessuras incrementais sobre os compósitos de resina tipo bulkfilll. Material e Métodos: Os espécimes (N = 60) foram fabricados a partir dos seguintes materiais ou suas combinações (n = 10 por grupo): a) compósito nano-híbrido convencional Z550 (FK), b) compósito de bulk-fill de alta viscosidade (Tetric N CeramTBF), c) compósito SDR (SDR) de bulk-fill de baixa viscosidade, d) Sonicfill (SF), e) SDR (2 mm) + FK (2 mm), f) SDR (4 mm) + FK (4 mm). Após 24 h de armazenamento em água, a resistência à compressão foi medida em uma máquina universal de ensaios (1 mm / min). Espécimes adicionais (N = 40) (25x2x2 mm3) foram confeccionados com FK, TBF, SDR e SF para determinação da resistência à flexão e do módulo de flexão, (n = 10) e submetidos ao teste de flexão de três pontos (0,5 mm / min). Os dados foram analisados utilizando one-way ANOVA e testes post-hoc T2 de Tamhane (p <0,05). Resultados: A resistência média à compressão (MPa) do compósito nano-híbrido (FK) foi significativamente maior (223,8 ± 41,3) que os demais grupos (123 ± 27 - 170 ± 24) (p <0,001). SDR (4 mm) + FK (2 mm) apresentou resistência à compressão significativamente maior do que quando coberta com 4 mm (143 ± 30) ou quando usada sozinha (146 ± 11) (p <0,05). A resistência à flexão média (159 ± 31) e o módulo de flexão de FK (34 ± 7) foram significativamente maiores do que os compósitos do tipo bulk-fill de alta ou baixa viscosidade (p <0,001). A resistência à flexão média do FS (132 ± 20) foi significativamente maior em comparação ao TBF (95 ± 25) (p <0,05). Conclusão: Os compósitos de resina do tipo bulk-fill demonstraram propriedades mecânicas mais insatisfatórias em comparação com o compósito nano-híbrido, mas semelhantes aos do SF. O aumento da espessura do composto de bulkfilll de baixa viscosidade (SDR) de 2 a 4 mm sob o compósito nano-híbrido (FK) pode melhorar as propriedades mecânicas dos compósitos de bulk-fill.(AU)

Resin-modified glass ionomer containing calcium glycerophosphate: physico-mechanical properties and enamel demineralization

Abstract Sources of calcium and phosphate have been added to dental restorative materials to improve their anticaries effect. Objective This study evaluated the effect of adding calcium glycerophosphate (CaGP) to resin-modified glass ionomer cement (RMGIC) on the physico-mechanical properties, ion release, and enamel demineralization. Material and Methods: Specimens were fabricated for each experimental group: RMGIC without CaGP (Control), RMGIC with 1, 3 and 9% CaGP. To determine the release of fluoride (F), calcium (Ca) and phosphorus (P), six specimens were immersed in demineralization and remineralization solutions for 15 days. In another experimental trial, the following physico-mechanical properties were evaluated at time intervals of 1 and 7 days after fabrication: compressive strength (n=12), diametral tensile strength (n=12), surface hardness of material (n=6) and the degree of conversion of monomers (n=8). To study enamel demineralization, specimens (n=12) were attached to enamel blocks and submitted to pH-cycling. Subsequently, surface and cross-sectional hardness and the concentration of F, Ca and P in enamel were determined. Results The addition of CaGP to RMGIC led to higher mean release of F, Ca and P when compared with control (p<0.001). Mechanical properties were within the range of those of the ionomer cements after addition of 1% and 3% CaGP. The degree of conversion did not differ between groups at the 1st and the 7th day (p>0.439). The addition of 3% and 9% CaGP reduced mineral loss and increased F, Ca and P in the enamel when compared with control (p<0.05). Conclusion The addition of 3% CaGP in RMGIC increased the release of F, P and Ca, reduced enamel demineralization, and maintained the physico-mechanical properties within the parameters for this material.

Compressive Strength of a Glass Ionomer Cement Under the Influence of Varnish Protection and Dietary Fluids / Resistencia a la compresión de un cemento de ionómero de vidrio bajo la influencia de la protección del barniz y diversos productos alimenticios

RESUMEN El objetivo de este estudio fue evaluar la resistencia a la compresión de un cemento de ionómero de vidrio (GIC) bajo la influencia de la protección del barniz y alimentos. Ochenta muestras cilíndricas de GIC fueron realizadas y se distribuyeron en cuatro grupos (G1, G2, G3, G4) de acuerdo con el alimento. Cada grupo se sub-dividió además en A y B, de acuerdo con la presencia o ausencia de protección de barniz. Las ocho muestras de cada subgrupo se almacenaron en agua destilada durante 30 días y recibieron los siguientes tratamientos durante 14 días: G2A: protección del barniz e inmersión en gaseosas, G2B: sin barniz e inmersión en gaseosas, G3A: protección del barniz e inmersión en jugo de naranja, G3B: sin protección de barniz e inmersión en jugo de naranja, G4A: protección de barniz e inmersión en yogurt, G4B: sin protección de barniz e inmersión en yogur. El procedimiento de inmersión se realizó tres veces al día, durante 15 minutos por 14 días. Las muestras del Subgrupo G1A (con barniz) y G1B (sin barniz) se usaron como controles y se almacenaron en agua destilada. Las muestras se sometieron a una prueba de resistencia a la compresión después del período de inmersión. Los resultados se analizaron usando ANOVA 2, prueba de Tukey (5%) y T de Student (5%). No hubo diferencias significativas entre los subgrupos, a excepción del subgrupo con protección de barniz e inmersión en jugo de naranja, que mostró una resistencia a la compresión GIC reducida.

ABSTRACT The objective of this study was to evaluate the compressive strength of a glass ionomer cement (GIC) under the influence of varnish protection and dietary fluids. Eighty cylindrical test specimens were made from GIC and distributed into four groups (G1, G2, G3, G4) according to the dietary fluid. Each group was further divided into subgroups A and B according to the presence or absence of varnish protection. The eight subgroup samples were stored in distilled water for 30 days and received the following treatments for 14 days: G2A: varnish protection and immersion in soft drink, G2B: no varnish protection and immersion in soft drink, G3A: varnish protection and immersion in orange juice, G3B: no varnish protection and immersion in orange juice, G4A: varnish protection and immersion in yogurt, G4B: no varnish protection and immersion in yogurt. The immersion procedure was performed three times a day, for 15 minutes at a time, for a total of 14 days. The samples from subgroups G1A (with varnish) and G1B (without varnish) were used as controls and stored in distilled water only for 30 days. The samples were submitted to a compressive strength test after the immersion period. The results were analyzed using the ANOVA 2, Tukey test (5%) and Student's t-test (5%). There were no significant differences between the subgroups, except for the subgroup with varnish protection and immersion in orange juice, which showed reduced GIC compressive strength.

Comparação da resistência à compressão entre materiais restauradores provisórios na endodontia: estudo in vitro / Comparison of compressive strength between temporary restorative materials in endodontics: in vitro study

Objetivo: este trabalho avaliou in vitro a resistência à compressão (RC) de diferentes materiais restauradores provisórios utilizados na endodontia: G1 (Vitremer®), G2 (Bioplic®), G3 (Coltosol ®) e G4 (IRM®). Material e método: Foram feitos 8 corpos de prova (n=8) de cada material totalizando 32 amostras (n=32) em matriz de silicone altura de 3,5mm e 6 mm de largura. Metade das amostras (n=16) foram mantidas 7 dias em soro fisiológico em estufa a 37ºC e a outra metade (n=16) mantidas por 14 dias e então foram submetidos ao ensaio de resistência a compressão, em uma máquina de Ensaios Universal (Emic 200) à velocidade de 0,5mm/min com uma célula de capacidade de carga de 200 kgf. Os dados obtidos em Mpa foram submetidos ao teste ANOVA a um critério, Tukey para comparações múltiplas (p<0,05) e por último T-test para amostras pareadas. Resultados: houve diferença estatisticamente significativa entre os grupos em 7 dias (p=0,000) sendo os grupos G1 e G2 iguais entre si (420,72 Mpa e 396,50 Mpa), porém em 14 dias não houve diferença entre os 4 grupos (p=0,104). O T-test mostrou a diferença entre os diferentes períodos de tempo dos grupos sendo G1 e G2 sem diferença estatística (p=0,178 e p=0,066), mas entre os grupos G3 e G4 houve diferença estatística (p=0,001 e p=0,000). Conclusão: O material a base de ionômero de vidro (Vitremer®) e a base de resina (Bioplic®) apresentaram os maiores valores em 7 dias. Em 14 dias os grupos não apresentaram diferenças estatísticas entre si, tiveram o mesmo comportamento apesar dos materiais à base de óxido de zinco (IRM® e Coltosol®) apresentarem maiores valores de resistência a compressão.

Objective: this study compared in vitro the compreesive strengt (CS) of the diferents materials used in endodontics: G1 (Vitremer®), G2 (Bioplic®), G3 (Coltosol®) e G4 (IRM®). Were made 8 specimens (n= 8) of each material, totalizing 32 samples (n=32) in a silicone matrix of 3,5mm height and 6mm diameter. Half the samples (n=16) was held 7 days in saline solution in an oven at 37ºC, and the other half (n=16) in 14 days and then subjected to the CS test in a universal machine (Emic 200), at a crosshead spreed of 0,5mm/min. Data in Mpa were submitted to one-way ANOVA, Tukey test for multiplex comparisons (p<0,05) and finally T-test for paired samples. Results: there was a statistically significant difference between the groups in 7 days (p=0,000), being the G1 and G2 equal to each other (420,72 Mpa e 396,50 Mpa), but in 14 days there was not a statically significant difference between the 4 groups (p=0,104). The T-test showed the difference between the different periods of the groups being G1 and G2 without statically difference (p=0,178 and p=0,066), between G3 and G3 groups there was significant differences (p=0,001 e p=0,000). Conclusion: materials based on glass ionomer (Vitremer®) and resinous (Bioplic®) showed higher values in 7 days. In 14 days the groups did not show statistically differences each other, had the same behavior dispite the fact that zinc oxide materials (Coltosol® and IRM®) had higher valuer of compressive strenght.

Avaliação da deformação de agulhas gengivais e análise fractal / Evaluation of dental needle deformation and fractal analysis

Introdução: A fratura da agulha na anestesia odontológica é rara, mas sua ocorrência tem sérias complicações e deve ser evitada. Objetivo: O objetivo deste estudo foi avaliar a deformação de agulhas dentárias após a aplicação de forças de compressão. Material e método: Agulhas das marcas Dencojet e Septoject XL nos calibres 27G e 30G (quatro grupos) foram dobradas em dois sentidos opostos em máquina de ensaio mecânico DL200 - EMIC, com base na ISO 7885:2010. A resistência à compressão das agulhas foi medida em cada dobra. Ao final, foi realizada inspeção visual em uma lupa EK3ST em aumento de 40×, para análise da integridade das agulhas. Resultado: As agulhas de calibre 30G não apresentaram diferenças significativas entre elas. As agulhas de maior calibre (27G) apresentaram diferenças no primeiro (p = 0,0001) e no segundo dobramento (p = 0,0016). As agulhas Septoject XL 27G demonstraram ser muito menos flexíveis, fornecendo valores mais altos de resistência à dobra. No grupo Septoject XL 30G, 70% das agulhas fraturaram próximo ao canhão. Todas as amostras do grupo Septoject XL 27G apresentaram fraturas após a segunda dobra. Conclusão: Todas as agulhas gengivais testadas apresentaram comportamento aceitável, mesmo quando submetidas a situações críticas. As agulhas Dencojet 27G demonstraram ser mais flexíveis quando dobradas. Todas as agulhas Septoject XL 27G fraturaram após a segunda dobra. Não é aconselhável dobrar as agulhas dentárias.

Introduction: Needle fracture in dental anesthesia is rare, but its occurrence has serious complications and should be avoided. Objective: The objective of this study was to evaluate the deformation of dental needles after the application of compression forces. Material and method: Needles of the Dencojet and Septoject XL brands in the 27G and 30G gauges (4 groups) were folded in two opposite directions in a mechanical test machine DL200 - EMIC, based on ISO 7885: 2010. The compressive strength of the needles was measured at each fold. At the end, visual inspection was performed on an EK3ST magnifying glass in a magnification of 40× for analysis of needle integrity. Result: 30G needles did not present significant differences between them. The largest gauges (27G) presented differences in the first (p = 0.0001) and in the second folding (p = 0.0016). Septoject XL 27G needles have been shown to be much less flexible, providing higher values ​​of resistance to folding. Seventh percent of the Septoject XL 30G group fractured near the cannon. All samples from the Septoject XL 27G group showed fractures after the second fold. Conclusion: All the gingival needles tested presented acceptable behavior, even when submitted to critical situations. Dencojet 27G needles have been shown to be more flexible when folded. All Septoject XL 27G needles fractured after the second fold. It is not advisable to bend the dental needles.

Influence of Functional Clinical Temperature over Compressive Strength and Diametral Tensile Strength of Various Luting Cements

Objective: To estimate the effect of temperature over the physical properties of commonly used luting cements. Material and Methods: The two set of cylindrical shaped cement samples measuring 12mm X 6mm and 4mm X 8mm were fabricated from non-eugenol zinc oxide, glass ionomer, zinc phosphate, Zinc polycarboxylate, resin cements. These two sets of samples were utilized to test compressive and diametral tensile strength respectively. Forty cement samples from each mold were fabricated and distributed between 14, 22, 37 and 550C (N=10). The samples were tested under universal testing machine, and data subsequently analyzed using One-way ANOVA and Tukey multiple comparison's statistical methods at p > 0.05. Results: The higher temperature resulted in noticeable reduction in the compressive strength of non-eugenol -zinc oxide, Zinc-phosphate, Zinc poly carboxylate cements. The highest compressive strength was recorded for non-eugenol zinc oxide (8.08 Mpa) at 370C, Zinc phosphate (91.01Mpa) at 140C, and for zinc polycarboxylate (83.06 Mpa) at 370C. The comparative values for respective cements at 550C were 6.40Mpa, 59.80Mpa, and 52.88 Mpa. The higher temperature had insignificant effect on the compressive strength of glass ionomer cement, while composite resin cement indicated minor deterioration. Conclusion: The relative mouth temperature influences the physical properties of the luting cements.

Preparation technology of oyster hydroxyapatite porous material for bone repair / 国际生物医学工程杂志

Objective To verify the feasibility of applying hydrothermal synthesis for preparing oyster hydroxyapatite(HA) and to develop a preparation method of oyster HA porous material for bone repair.Methods Hydrothermal synthesis was applied for preparing oyster HA,and the reaction condition was 220 ℃ for 6 h.Then,the prepared oyster HA was used as the raw material for porous scaffold preparation by sponge-soaking and sintering,successively.The porosity and compressive strength of the scaffold were adjusted by controlling the soaking time and absorbed HA slurry of the sponges.Results Hydrothermal synthesis was an effective method for preparing oyster HA.When the volume of the sponge cube was 1 cm3,the material absorbed by one to three times sponge-soaking were 0.184 8 g,0.318 1 g and 0.426 1 g,respectively,the corresponding porosity were 91.5％,82.9％ and 78.5％,and the compressive strength were 1.06 MPa,3.99 MPa and 8.49 MPa.Conclusion The oyster shell powder can be effectively converted into HA under the hydrothermal reaction condition of 220 ℃ for 6 h.The preparation of HA porous bone repair material by sponge-soaking method can obtain ideal porosity and mechanical strength.However,in this preparation process,the number of sponge-soaking and the weight of the absorbed HA slurry should be exactly controlled in order to obtain desired properties.

Influence of elastic modulus of intraradicular posts on the fracture load of roots restored with full crowns / Influência do modulo de elasticidade de retentores intrarradiculares na carga para fratura de raízes restauradas com coroas totais

Objective: This study aimed to evaluate the fracture load and displacement of roots restored with posts of different elastic modulus. Material and method: Thirty-six replicas of epoxy resin mixed with glass microfibers were made from an endodontically-treated human premolar root prepared to a length of 12 mm with a custom drill, leaving the apical 4 mm unprepared. Replicas were randomly restored with (n = 12): FP-LM (fiber post with low elastic modulus- 50 GPa), FP-HM (fiber post with high elastic modulus - 67 GPa) and MP (metallic post - 208 GPa), using self-curing adhesive and dual resin cement. Cores were built up with composite resin and metallic crowns were cemented in all the roots with self-adhesive resin cement with self-curing mode. Specimens were subjected to a fracture load test (45° inclination/0.5 mm/min) and displacement was registered at 100 N. Result: One-way ANOVA showed that elastic modulus of the post did not affect the fracture load means (p = 0.203) (FP-LM: 237.4 ± 65.11 N; FP-HM: 236.7 ± 92.85 N; MP: 295.8 ± 108.7 N) but was statistically significant for the displacement (p < 0.00): Tukey's test showed that FP-LM displacement mean (0.81 ± 0.15 mm) was significantly higher than those for FP-HM (0.46 ± 0.26 mm; p = 0.00) and MP (0.62 ± 0.07 mm; p = 0.04). Conclusion: Posts with different elastic modulus exhibit similar fracture loads, but a lower displacement is achieved when fiber posts with a high elastic modulus and metallic posts are used.

Objetivo: Este trabalho avaliou a carga para fratura e deslocamento de raízes restauradas com pinos de diferentes módulos de elasticidade. Material e método: Trinta e seis réplicas de microfibras de vidro embutidas em resina epóxi foram fabricadas a partir de uma raiz de um pré-molar tratado endodonticamente preparado em 12 mm de comprimento com brocas customizadas, deixando 4 mm apicais sem preparo. As raízes foram randomicamente restauradas com (n = 12): FP-LM (pino de fibra com um baixo módulo de elasticidade - 50 GPa), FP-HM (pino de fibra com um alto módulo de elasticidade - 67 GPa) e MP (pinos metálicos - 208 GPa), usando adesivo autopolimerizável e cimento resinoso dual. Núcleos foram confeccionados com resina composta e coroas metálicas foram cimentadas em todas as raízes com cimento resinoso autoadesivo com modo de polimerização químico. Os espécimes foram submetidos ao teste de fratura em 45° (inclinação de 45° / 0,5 mm/min) e o deslocamento foi registrado aos 100 N. Resultado: Anova 1 fator mostrou que o módulo de elasticidade dos retentores não afetou as médias de fratura (p = 0,203) (FP-LM: 237,4 ± 65,11 N; FP-HM: 236,7 ± 92,85 N; MP: 295,8 ± 108,7 N) mas foi estatisticamente significante para o deslocamento (p < 0,00): o teste de Tukey mostrou que a média de deslocamento do grupo FP-LM (0,81 ± 0,15 mm) foi significativamente maior do que o grupo FP-HM (0,46 ± 0,26 mm; p = 0,00) e MP (0,62 ± 0,07 mm; p = 0,47). Conclusão: Pinos com diferentes módulos de elasticidade mostram resistência similar, porém um menor deslocamento é obtido quando pinos de fibra com alto módulo de elasticidade (FP-HM/MP) são usados.