Biological and mechanical properties of an experimental glass-ionomer cement modified by partial replacement of CaO with MgO or ZnO

AbstractSome weaknesses of conventional glass ionomer cement (GIC) as dental materials, for instance the lack of bioactive potential and poor mechanical properties, remain unsolved.Objective The purpose of this study was to investigate the effects of the partial replacement of CaO with MgO or ZnO on the mechanical and biological properties of the experimental glass ionomer cements.Material and Methods Calcium fluoro-alumino-silicate glass was prepared for an experimental glass ionomer cement by melt quenching technique. The glass composition was modified by partial replacement (10 mol%) of CaO with MgO or ZnO. Net setting time, compressive and flexural properties, and in vitrorat dental pulp stem cells (rDPSCs) viability were examined for the prepared GICs and compared to a commercial GIC.Results The experimental GICs set more slowly than the commercial product, but their extended setting times are still within the maximum limit (8 min) specified in ISO 9917-1. Compressive strength of the experimental GIC was not increased by the partial substitution of CaO with either MgO or ZnO, but was comparable to the commercial control. For flexural properties, although there was no significance between the base and the modified glass, all prepared GICs marked a statistically higher flexural strength (p<0.05) and comparable modulus to control. The modified cements showed increased cell viability for rDPSCs.Conclusions The experimental GICs modified with MgO or ZnO can be considered bioactive dental materials.

Shear bond strength of three self-adhesive resin cements to dentin.

Context: The result of the studies concerning the bonding of self-adhesive resin cements to dentin is controversial. Aims: To assess in vitro shear bond strength (SBS) of three self-adhesive dual-cured resin cements to dentin compared to a currently used dual-cured resin cement, using SBS test. Settings and Design: The extant study is an experimental in vitro one on extracted human third molars dentin. Material and Methods: 40 intact human third molars were selected and randomly divided into 4 groups of 10. Buccal dentin surfaces were exposed perpendicular to the long axis and prepared with SiC papers. A translucent plastic ring, was placed over the dentin surfaces. Group I (Control group): After 15 s of etching and application of Excite DSC Bond (Ex), Variolink II (Var II) resin cement was injected into the plastic ring and was light cured for 40 s. Group II: RelyX Unicem (RX) was injected into the plastic ring and after 30 s, was light cured for 40 s. Group III: Maxcem (Mc) was injected into the plastic ring and after 30 s, was light cured for 40 s. Group IV: Multilink Sprint (MS) was injected into the plastic ring and after 30 s, was light cured for 40 s. After thermal cycling, SBS were measured with a universal testing machine. Statistical Analysis Used: Statistical computations were conducted according to Student's t-test. Results: The mean SBS and standard deviations (in parentheses) for groups I, II, III, and IV were 12.95 (2.64), 6.73 (0.79), 3.01 (0.90), 4.60 (0.75) MPa, respectively. Statistical analysis, revealed that: (1) the mean SBS of Var II were significantly higher than the other groups (P<0.05). (2) The mean SBS of Mc and MS were significantly lower than RX (P<0.05). (3) The mean SBS of Mc and MS did not show significant difference (P>0.05). Conclusion: Bond strength of three self-adhesive resin cements was significantly lower than the conventional total-etch resin cement. RX significantly performed better SBS than Mc and MS to dentin.

The effect of urea on the corrosion behavior of different dental alloys.

Objective: Intraoral corrosion of dental alloys has biological, functional, and esthetic consequences. Since it is well known that the salivary urea concentrations undergo changes with various diseases, the present study was undertaken to determine the effect of salivary urea concentrations on the corrosion behavior of commonly used dental casting alloys. Materials and Methods: Three casting alloys were subjected to polarization scans in synthetic saliva with three different urea concentrations. Results: Cyclic polarization clearly showed that urea levels above 20 mg/100 ml decreased corrosion current densities, increased the corrosion potentials and, at much higher urea levels, the breakdown potentials. Conclusion: The data indicate that elevated urea levels reduced the corrosion susceptibility of all alloys, possibly through adsorption of organics onto the metal surface. This study indicates that corrosion testing performed in sterile saline or synthetic saliva without organic components could be misleading.

Changes in surface roughness and color stability of two composites caused by different bleaching agents

The objective of this study was to evaluate the effect of two bleaching agents (10% and 35% hydrogen peroxide) on the color stability and surface roughness of two composites, one nanohybrid and one nanoparticle. Specimens were polished, aged, stained, bleached and polished again. The action of the bleaching agents on the composites was analyzed using a profilometer (surface roughness) and a spectrophotometer (color stability). The effect of polishing the composites on the surface roughness and the resumption of the composite color was also evaluated. The results were analyzed statistically by ANOVA and Tukey's test at 5% significance level. The analysis indicated that the nanohybrid composite was more affected by staining. The bleaching agents were not able to promote bleaching of either composite over the evaluation period. Surface polishing returned nanohybrid composite to its original color condition, which did not occur for the nanoparticle composite. Additionally, polishing did not return the surface roughness of either composite to its original value. It may be concluded that polishing surface after bleaching should not be the treatment of choice, as it was not possible to reverse the roughness of the composites to their original values, suggesting that a more extensive and irreversible degradation might have occurred.

O objetivo deste estudo foi avaliar o efeito de dois agentes clareadores (peróxido de hidrogênio a 10% e 35%) sobre a estabilidade de cor e rugosidade superficial de dois compósitos, um nanohíbrido e um nanoparticulado. Os espécimes foram polidos, envelhecidos, manchados, clareados e polidos novamente. A ação dos agentes clareadores sobre os compósitos foi analisada em perfilômetro (rugosidade) e um espectrofotômetro (estabilidade de cor). A ação de polimento dos compósitos sobre a rugosidade superficial e a retomada da cor dos compósitos também foi avaliada. Os resultados foram analisados estatisticamente por ANOVA e teste de Tukey (5% de significância). A análise indicou que o compósito nanohíbrido foi mais afetado pelo manchamento. Os agentes clareadores não foram capazes de promover o clareamento dos compósitos ao longo do período de avaliação. O polimento da superfície retornou o compósito nanohíbrido à sua condição de cor original, o que não foi observado para o nanoparticulado. Além disso, o polimento não retornou a rugosidade de superfície dos compósitos para os valores originais. Os autores concluíram que o polimento da superfície após o clareamento não deve ser a opção de tratamento, uma vez que não foi possível inverter a rugosidade dos compósitos à sua rugosidade original, sugerindo que uma degradação mais extensa e irreversível pode ter ocorrido.

Effect of filler particles on surface roughness of experimental composite series

OBJECTIVE: The purpose of this study was to evaluate the effect of different filler sizes and shapes on the surface roughness of experimental resin-composite series. MATERIAL AND METHODS: Thirty-three disc-shaped specimens of the series (Spherical-RZD 102, 105, 106, 107, 114 and Irregular-RZD 103, 108, 109, 110, 111, 112) were prepared in a split Teflon mold and irradiated with an halogen light-curing unit (450 mW/cm² for 40 s) at both top and bottom surfaces. The specimens were stored for 3 months in distilled water. The surface roughness values in form of surface finish-vertical parameter (Ra), maximum roughness depth (Rmax) and horizontal roughness parameter (Sm) were recorded using a contact profilometer. The data were analyzed by one-way ANOVA and the means were compared by Scheffé post-hoc test (a=0.05). RESULTS: The lowest surface roughness (Ra) was observed in S-100 (0.079±0.013), while the roughest surface was noted in I-450/700/1000 (0.125±0.011) and I-450/1000 (0.124±0.004). The spherical-shape series showed the smoothest surface finish compared to the irregular-shape ones with higher significant difference (p>0.05). The vertical surface roughness parameter (Ra) values increased as the filler size increased yielding a linear relation (r²=0.82). On the contrary, the horizontal parameter (Sm) was not significantly affected by the filler size (r²=0.24) as well as the filler shape. CONCLUSIONS: Filler particle's size and shape have a great effect on the surface roughness parameters of these composite series.

Effect of temperature variation on the cytotoxicity of cast dental alloys and commercially pure titanium

Cell culture system has been used to evaluate alloy cytotoxicity under different environments, testing the extracts, but the effect of temperature variation on the cytotoxicity of dental alloys has not been analyzed. OBJECTIVE: The aim of the present study was to investigate if temperature variation could affect dental alloy cytotoxicity, testing alloy extracts in an epithelial cell culture system. MATERIAL AND METHODS: Discs of Ni-Cr, Co-Cr-Mo, Ni-Cr-Ti, Ti-6Al-4V and commercially pure titanium (cp Ti) were cast by arc melting, under argon atmosphere, injected by vacuum-pressure. Discs were immersed in artificial saliva and subjected to different temperatures: 37ºC and thermocycling (37ºC/5ºC/37ºC/55ºC/37ºC). After thermocycling, extracts were put in a subconfluent culture during 6 h, and the number of cells and their viability were used to evaluate cytotoxicity in these temperatures. For each alloy, data from temperature conditions were compared by Student's t-test (α=0.05). RESULTS: The cytotoxicity tests with alloy/metal extracts showed that Ni-Cr, Co-Cr-Mo, Ti-6Al-4V and cp Ti extracts (p>0.05) did not affect cell number or cell viability, while Ni-Cr-Ti (p<0.05) extract decreased cell number and viability when the alloy was subjected to thermocycling. CONCLUSION: Within the limitations of the present study, the Ni-Cr-Ti alloy had cell number and viability decreased when subjected to temperature variation, while the other alloys/metal extracts did not show these results.

promotion effect of cerment dust for the Ca [oH] 2-Sio2 Hydrothermal reaction

Understanding of the chemistry of the Ca[OH]2-SiO2 hydrothermal reaction put the bases of the manufacture of sand-lime brick and autoclaved building materials. The effect of partial or complete substitution of Ca [OH]2 with cement dust on the lime-silica hydrothermal reaction was investigated. The pressed samples were prepared by using Ca [OH]2; silica ratio of 10: 90 by wt in which 20, 40, 60, 80 and 100% Ca [OH]2 was substituted by cement dust. The hydrothermal conditions were 10 bar [180 degree] and different periods from 4-24 hour. Major attention focused on the kinetic of the reactions, while other properties such as strength, density and porosity were also studied. The extent of hydration as measured by the chemically combined water, free lime and reacted silica, is enhanced due to the cement dust substitution. The reaction products as characterized by x-ray diffraction analysis and scanning electron microscopy [SEM] are CSH [1] and 11 A tobermorite. The results indicate that the substitution of Ca [OH]2 with cement dust accelerate the tobermorite formation and improve its crystallinity. For industry the results revealed that the substitution of lime with cement dust [by-product of cement industry] up to 50% can be used to prepare sand- lime brick with higher strength and lower cost