Aging studies of light cured dimethacrylate-based dental resins and a resin composite in water or ethanol/water.

OBJECTIVE: To study the aging of neat resins, prepared from bis-GMA, UDMA, D(3)MA or a mixture of bis-GMA/UDMA/D(3)MA (65/20/15 w/w/w), in water or 75% (v/v) ethanol/water 37 degrees C. Also the study of aging of Heliomolar RO, which is a radiopaque, microfilled, light cured composite, the resin matrix of which is the copolymer of bis-GMA/UDMA/D(3)MA (65/20/15 w/w/w). METHODS: Samples of neat resins and Heliomolar RO prepared by light curing were immersed in water or 75% (v/v) ethanol/water 37 degrees C, for 1, 7 or 30 days. Then the flexural and tensile strength were determined. The fractured surface of samples after the flexural tests was observed by scanning electron microscopy. RESULTS: Bis-GMA and copolymer resin did not showed any significant change in mechanical properties after immersion in water or 75% (v/v) ethanol/water 37 degrees C, for 30 days. On the contrary UDMA, D(3)MA and the composite Heliomolar RO showed a significant decrease. SIGNIFICANCE: The results obtained showed that the effect of aging in water or ethanol/water solution on mechanical properties of a light cured dimethacrylate resin depends on the chemical structure of resin. In the case of resin composite this effect depends on the filler-matrix bond strength.     

Dynamic thermomechanical properties and sorption characteristics of two commercial light cured dental resin composites.

OBJECTIVES: The first objective of this work is the study by DMTA of viscoelastic properties (E', E', tandelta, Tg) of two current dental resin composites Tetric EvoCeram (nanohybrid) and Heliomolar (microfilled) in dry condition and in water for up to 30 days. The second objective is to determine the sorption characteristics of these composites in water and ethanol/water solution 75vol.%. METHODS: For DMTA the bar-shaped specimens divided into five groups of three samples each. The first group consisted of dry samples measured 1h after curing. The second and third group consisted of samples, which had been heated in air at 80+/-1 degrees C for 1 day or had been stored in distilled water at 80+/-1 degrees C for 1 day. The fourth and fifth group consisted of samples, which had been stored in distilled water at 37+/-1 degrees C for periods 1 and 7 days correspondingly. Also specimen discs (15mm in diameter and 1mm in thickness) were immersed in water or a 75vol.% ethanol/water solution at 37+/-1 degrees C. At fixed time intervals they were removed, blotted dry to remove excess liquid, weighted and returned to the liquid. This process continued for 30 days. RESULTS: The viscoelastic properties (E', E', tandelta, Tg) of the two composites treated under different conditions were recorded and compared. Also the mass uptake, diffusion coefficient, solubility and volumetric changes for immersion of composites in water and ethanol/water solution 75vol.% at 37+/-1 degrees C were determined. SIGNIFICANCE: Tetric EvoCeram a nanohybrid composite with similar about resin matrix with Heliomolar which is a microfilled showed better dynamic thermomechanical properties and sorption characteristics than Heliomolar.     

Effects of ethanol addition on the water sorption/solubility and percent conversion of comonomers in model dental adhesives

ObjectivesThis study evaluated the kinetics of water uptake and percent conversion in neat versus ethanol-solvated resins that were formulated to be used as dental bonding agents.MethodsFive methacrylate-based resins of known and increasing hydrophilicities (R1, R2, R3, R4 and R5) were used as reference materials. Resins were evaluated as neat bonding agents (100% resin) or they were solvated with absolute ethanol (95% resin/5% ethanol or 85% resin/15% ethanol). Specimens were prepared by dispensing the uncured resin into a circular mold (5.8 mm × 0.8 mm). Photo-activation was performed for 80 s. The water sorption/diffusion/solubility was gravimetrically evaluated, while the degree of conversion (DC) was calculated by Fourier-transform infrared spectroscopy.ResultsWater sorption increased with the hydrophilicity of the resin blends. In general, the solvated resins exhibited significantly higher water sorption, solubility and water diffusion coefficients when compared to their corresponding neat versions (p < 0.05). The only exception was resin R1, the least hydrophilic resin, in which neat and solvated versions exhibited similar water sorption (p > 0.05). Addition of ethanol increased the DC of all resins tested, especially of the least hydrophilic, R1 and R2 (p < 0.05). Despite the increased DC of ethanol–solvated methacrylate-based resins, it occurs at the expense of an increase in their water sorption/diffusion and solubility values.SignificanceNegative effects of residual ethanol on water sorption/solubility appeared to be greater as the hydrophilicity of the resin blends increased. That is, the use of less hydrophilic resins in dental adhesives may create more reliable and durable bonds to dentin.     

Water sorption of resin-modified glass-ionomer cements photoactivated with LED

The Light Emitting Diodes (LED) technology has been used to photoactivate composite resins and there is a great number of published studies in this area. However, there are no studies regarding resin-modified glass-ionomer cements (RMGIC), which also need photoactivation. Therefore, the aim of this study was to evaluate water sorption of two RMGIC photoactivated with LED and to compare this property to that obtained with a halogen light curing unit. A resin composite was used as control. Five specimens of 15.0 mm in diameter x 1.0 mm in height were prepared for each combination of material (Fuji II LC Improved, Vitremer, and Filtek Z250) and curing unit (Radii and Optilight Plus) and transferred to desiccators until a constant mass was obtained. Then the specimens were immersed into deionized water for 7 days, weighed and reconditioned to a constant mass in desiccators. Water sorption was calculated based on weight and volume of specimens. The data were analyzed by two-way ANOVA and Tukey test (p < 0.05). Specimens photocured with LED presented significantly more water sorption than those photocured with halogen light. The RMGIC absorbed statistically significant more water than the resin composite. The type of light curing unit affected water sorption characteristics of the RMGIC.     

Effect of light source and solvent on the sorption and solubility of two dual-cured cements photocured through ceramic

The purpose of this study was to verify the polymerization efficiency of two curing units through a ceramic barrier. Forty specimens apiece of two resin luting cements (AllCem and RelyX U100) were made in a stainless steel mold. The experimental group was photocured through a ceramic barrier, while the control group was photocured without a barrier. The specimens were stored in deionized water or 75% ethanol for 28 days and submitted to tests of sorption and solubility (ISO 4049:2000). Values obtained were subjected to ANOVA and Tukey multiple comparison tests (P < 0.05). RelyX U100 suffered more sorption and solubility than AllCem. The light sources did not influence sorption and solubility values, except for the specimens of RelyX U100 that were photocured with an LED unit through ceramic and stored in ethanol; these specimens demonstrated higher values than those photocured using a halogen lamp.     

Hardness and diametral tensile strength of a hybrid composite resin polymerized with different modes and immersed in ethanol or distilled water media

OBJECTIVES: The aim of this in vitro study was to evaluate the microhardness and diametral tensile strength of a hybrid composite resin (Z250, 3M ESPE) polymerized with four different modes of light exposure and immersed in two different media. METHODS: Composite resin specimens were randomly polymerized according to the experimental groups (conventional, 550 mW/cm(2)/30 s; soft start, 300 mW/cm(2)/10 s + 550 mW/cm(2)/20 s; high intensity, 1060 mW/cm(2)/10 s; pulse delay, 550 mW/cm(2)/1 s + 60 s of waiting time + 550 mW/cm(2)/20 s) and immersed in one of two media (distilled water or absolute ethanol) for 24 h. After that, microhardness (M) and diametral tensile strength (DTS) tests were performed. RESULTS: For DTS, there were no statistical differences among the polymerization modes, however, ethanol medium groups presented statistically lower DTS (p < 0.05) than water medium. For the M test, samples immersed in ethanol medium presented lower M for almost all groups. Conventional mode presented higher M values for the groups immersed in water medium. In ethanol medium, conventional and pulse delay groups presented higher M values, statistically different (p < 0.05) from the high intensity group. For all experimental conditions, the top surface showed higher M than the bottom surface. SIGNIFICANCE: Different polymerization modes can be related to the different polymer structures formed, and consequently with different physical properties of resin composite. The immersion media can alter the physical properties of resin composites of different polymer structures.     

Effect of water on the physical properties of resin-modified glass ionomer cements.

OBJECTIVES: Resin-modified glass ionomer cements (GIC) are available for clinical use as restorative materials or as liners and bases. This work was conducted to study the effect of water sorption on the physical properties of several resin-modified GIC, by changing the samples' storage conditions. METHODS: The water sorption, the flexural strength, the flexural elastic modulus, the Vickers hardness and the dimensional changes of five resin-modified GICs were measured using specimens aged for 24 h to 3 mon. The specimens were stored at 37 degrees C, either in a dry environment (A), immersed in water (B), stored in a humid environment (C), stored in a humid environment for 1 h and then immersed in water (D), or immersed in water and subsequently dried (B + A). An analysis of variance was used to compare the results. RESULTS: The resin-modified GIC absorb during the first 24 h large amounts of water (114-172 mg/cm3) compared to the conventional GIC (30-63 mg/cm3). Water alters the physical properties of resin-modified GICs: With regard to dry specimens, a decrease in the flexural strength of 20 to 80% was observed for samples immersed in water. Decreases in their flexural elastic modulus (50 to 80%) and in their hardness (approximately 50%) were also observed. Water sorption also provoked an expansion in volume of the immersed specimens, ranging from 3.4 to 11.3% after 24 h. SIGNIFICANCE: The flexural strength and Vickers hardness of the resin-modified GICs are sensitive to the water contained in the tested specimens. A correlation was established between the decrease in their physical properties and the water uptake. However, it should not be concluded that these materials are not adequate for use in applications in direct contact with oral fluids. Probably, resin-modified GIC placed in oral cavities would not be affected to the same extent as in in vitro tests. In an oral environment, the constituents of saliva will certainly decrease the rate of water sorption and will hence delay its effects.     

Water sorption and dimensional changes of denture base polymer reinforced with glass fibers in continuous unidirectional and woven form

PURPOSE: The aim of this study was to determine the dimensional accuracy and water sorption of a denture base polymer that was reinforced with glass fibers in continuous unidirectional and woven form in different weight fractions. MATERIALS AND METHODS: Ten rhombic brass plates were prepared with reference points, and 70 heat-cured denture base polymer specimens were produced using these brass models. Ten of 70 were used for controls, and 60 were reinforced with glass fibers in continuous parallel and woven form. The dimensional changes of polymer and fiber-reinforced composite specimens after processing, drying for 4 days at 37 degrees C, and storage in 37 degrees C water for 90 days were calculated by the change of the distance vector. The measurements were made between the reference points on the specimens and were compared with those on the brass model at 4 different stages. The water sorption calculations were made at 10 different time intervals on 70 specimens, which were immersed in a 37 degrees C distilled water bath and weighed. RESULTS: The polymerization shrinkage and water sorption of denture base polymers is lower when the specimens are reinforced with glass fibers in continuous unidirectional and woven form. The highest fiber content showed the smallest dimensional change (0.069 mm, or 0.25%), and the unreinforced group showed the largest change (0.139 mm, or 0.54%). Water sorption occurred mainly during the first 14 days. CONCLUSION: As the fiber content increases, the dimensional change and water sorption decrease.     

Difference in water accumulation patterns between solid and closed hollow obturators under a thermal cycle

ABSTRACT: Water accumulation in the hollow space of a maxillary obturator is a continuing problem, and it is unclear whether the porosity of acrylic resin is involved in the mechanism. The purposes of the study were to evaluate the effect of a hollow space in the resin obturator on water sorption under a thermal cycle and to determine factors associated with water accumulation in the obturator. Twenty solid spheres (30-mm diameter) and 40 hemispheres (30-mm diameter, 1.5 mm thickness) were fabricated from heat-polymerized acrylic resin. Closed hollow specimens consisted of 2 hemispheres joined with autopolymerizing resin. Ten solid and 10 closed hollow specimens were immersed in distilled water, whereas the other specimens were stored at 100% relative humidity. Each specimen was thermocycled (5°C-37°C) with a dwell time of 12 hours and weighed every 12 hours for 180 days. Of the 20 closed hollow specimens, 16 showed no water accumulation (8 in distilled water, 8 at 100% humidity). The weight of these specimens became saturated by day 90, with increases from the initial weight of 1.41% at 5°C and 1.36% at 37°C. By day 180, the weights of the solid specimens had increased by 0.96% at 5°C and 0.94% at 37°C. Weight fluctuation associated with temperature was observed for both types of specimens and for all storage conditions. It is concluded that water accumulation inside a closed hollow obturator is not directly related to the water absorption properties of the acrylic resin but is related to thermal damage of the obturator.     

Influence of chain extender length of aromatic dimethacrylates on polymer network development.

OBJECTIVE: To investigate the role of chain extender size from Bis-EMA monomers on the polymerization profiles and properties of the crosslinked polymers. Additionally, the influence of Bis-GMA was also evaluated. METHODS: The polymer network from homopolymers Bis-EMA4, Bis-EMA10 and Bis-EMA30 was characterized, as well as copolymers formed among these monomers and Bis-GMA. The degree of conversion from neat and blended monomers as a function of photo-activation time was evaluated by FTIR. Rate of polymerization, network parameter and cross-link density from materials were demonstrated. Water sorption and solubility were determined according to ISO 4049 specification and the data obtained were analyzed by two-way ANOVA/Tukey's test (alpha=0.05). Flexural strength and Young's modulus from polymerized monomers/co-monomers were measured after 24h water storage at 37 degrees C and the results were analyzed by one-way ANOVA/Tukey's test (alpha=0.05). RESULTS: Monomers with larger ethylene oxide units presented the highest values regarding the degree of conversion and cross-link density. The effect of the chain extender length was also observed in water sorption and solubility polymer characteristics, with Bis-EMA4 being the most hydrophobic polymer. Bis-EMA10 and Bis-EMA30 homopolymers were not able to be tested with the three point bending test due to their great flexibility. The addition of Bis-GMA produced stronger and more rigid Bis-EMA polymers (p<0.05). SIGNIFICANCE: Aromatic dimethacrylates with different chain extender lengths can be a useful alternative in controlling the properties of a dental material, adjusting those to specific applications.     

The diffusion kinetics of a nanofilled and a midifilled resin composite immersed in distilled water,artificial saliva,and lactic acid

This study investigated the diffusion kinetics of a nanofilled (Filtek Z350) and a midifill (Filtek P60) resin composite immersed in distilled water, artificial saliva and lactic acid. Resin composite specimens were desiccated, immersed in the media, weighed at suitable time intervals until they reached sorption equilibrium and were then desiccated again. Sorption and solubility (μg/mm³) were calculated based on ISO 4049:2000(E). The diffusion coefficient (m².s⁻¹) was determined according to Flick’s second law. The degree of conversion (DC%) was evaluated by FT-IR and the action of the media on the surfaces of the resin composite was evaluated by SEM. Z350 immersed in lactic acid presented the highest sorption (25.9 ± 1.3). The highest solubility was presented by Z350 immersed in lactic acid (5.6 ± 0.9), followed by P60 immersed in lactic acid (4.4 ± 0.5). The other groups presented no significant difference among them. The diffusion coefficients of both resin composites immersed in lactic acid and that of Z350 immersed in artificial saliva were significantly higher. The lowest diffusion coefficient was presented by P60 immersed in distilled water. The DC% was not significant, (p > 0.05). The SEM analysis showed that the effect of lactic acid on the resin composites was more deleterious than those of water and artificial saliva.     

Sorption and solubility of luting cements in different solutions

This study examined the solubility, sorption, and dimensional change of eight luting cements in two different solutions: 50% ethanol:water and distilled water. Ten disk specimens were prepared of each material following the manufacturers instructions, and then ground with silicone carbide paper. Sorption and solubility were calculated by weighing the specimens before and after immersion and desiccation. Data were analyzed by two-way ANOVA, Tukey's HSD and Fisher's PLSD tests. GC Fuji Plus and RelyX Luting2 showed the highest values of sorption and solubility both in water and ethanol:water. The percentage changes in volume for Maxcem, Nexus 2, Panavia F, RelyX Veneer, and VariolinkII were considerably smaller than for GC Fuji Plus, RelyX Luting2, and seT in both water and ethanol:water and after desiccation. Stability occurred within 2 weeks for all the eight materials when in water, while GC Fuji Plus, Maxcem, Panavia F and seT took 3 to 4 weeks to stabilize in ethanol:water.     

Water sorption and dimensional stability of three glass fiber-reinforced composites

PURPOSE: Water sorption and dimensional stability of three fiber-reinforced composites were studied. Two composites (Vectris, FibreKor) were resin impregnated industrially, and one composite (Stick) was polymer preimpregnated but required further manual impregnation. MATERIALS AND METHODS: Bar-shaped specimens of each material were prepared according to manufacturers' instructions. The water sorption and dimensional change of each specimen were calculated according to the change in its weight and dimension before and after immersion. Specimens were immersed in distilled water for 1, 7, 60, and 180 days. SEMs were taken to examine the quality of the fiber-matrix interface. The volume percentage of fiber content of each fiber-reinforced composite was experimentally estimated. RESULTS: A general trend of increasing water sorption for each immersion period according to the material type was: Vectris < FibreKor < Stick. There were no significant differences in dimensional change among the materials and immersion periods. CONCLUSION: The preimpregnated fiber-reinforced composite (Stick) showed higher water sorption than the industrially impregnated fiber-reinforced composites (Vectris, FibreKor). Despite a variation in the water sorption of the fiber-reinforced composites studied, all were within a 32 microg/mm3 criterion established by the ISO. The magnitude of dimensional change was small enough that it should not raise any significant clinical concern.     

INFLUENCE OF PULSE-DELAY CURING ON SORPTION AND SOLUBILITY OF A COMPOSITE RESIN

The purpose of this study was to evaluate the sorption and solubility of a composite resin (TPH³; Dentsply) cured with halogen light due to different storage media and curing modes. The methodology was based on the ISO 4049 standard. Two independent groups were established according to the storage time (7 days-G1; 60 days-G2). A stainless steel mould (2 mm x 8 mm ø) was used. The selected curing modes were: I (Conventional - C): 40s - 600 mW/cm²; II (Pulse I - PD): 3 s - 200 mW/cm² + 2 min (delay) + 39 s - 600 mW/cm²; III (Pulse II): 10 s - 200 mW/cm² + 2 min (delay) + 37 s - 600 mW/cm²; IV (Pulse III): 3 s- 600 mW/cm² + 2 min (delay) + 37 s -600 mW/cm². The media used were: distilled water, 75% ethanol and 100% chlorophorm. Five repetitions were made for each group. The specimens were placed in a desiccator at 37°C for 24 h and, after that, at 23°C for 1 h to be weighed until a constant mass (m₁) was obtained. The discs were immersed separately into the 3 media for 7 days (G1) and 60 days (G2), and thereafter reweighed (m₂). The reconditioning in the desiccator was done until a constant mass (m₃) was obtained. Sorption and solubility were calculated and the data of G1 and the sorption data of G2 were subjected to two-way ANOVA and Tukey''s tests (p=0.05). The solubility data of G2 were analyzed by Kruskal-Wallis test (p=0.05). For G1 and G2, no statistically significant differences were found in sorption among curing techniques (p>0.05). The solubility values were negative, which means that there was mass gain. Regarding the storage media, in G2 chlorophorm had the highest sorption values. It may be concluded that the curing modes (C and PD I, II and III) did not affect the sorption of the tested composite resin. However, different storage media influenced sorption behavior. The solubility test demonstrated negative data, masking the real solubility.     

载银软衬材料颜色稳定性、吸水性和溶解性的体外研究

目的：研究冷热循环对载银软衬材料颜色稳定性、吸水性和溶解性影响。方法：Sofreliner Tough和Silagum软衬材料各制作10mm×10mm×3mm试件50个,各试件含质量分数为5%的纳米银。每种材料的样本随机分为5组：对照组于37℃蒸馏水浸泡24h;实验组分别冷热循环1000、2000、3000、4000次。结果：冷热循环次数增加,吸水率和溶解率增高;仅Sofreliner Tough循环1000次组和Silagum循环1000、2000次组色差值≤3。结论：冷热循环增加载银软衬材料的吸水率和溶解率,并对载银软衬材料颜色稳定性有明显影响。     

Dimensional change of a calcium aluminate cement for posterior restorations in aqueous and dry media.

OBJECTIVES: A calcium aluminate cement has recently been developed, with claims of being an alternative to dental amalgam and resin composites in posterior cavities. However, its' mechanical properties are not well evaluated and the aim of the study was therefore, to evaluate its' dimensional stability over time. METHODS: The dimensional changes of the cement, Doxadent, and two composite resins, Esthet-X and InTen-S, were tested during 360 d. The specimens were stored at 37+/-1 degrees C either in 100% air humidity (dry) or immersed in distilled water (wet), except for the first 24h when all specimens were stored at 100% air humidity and 37+/-1 degrees C. RESULTS: During the first 24h, Doxadent decreased in volume with 0.04%, while InTen-S and Esthet-X decreased with 1.60 and 1.75%, respectively. From d 1-360, the dry Doxadent specimens increased in volume with 2.0% and in weight with 5.5%, while the corresponding increase for the wet specimens were 4.1 and 6.3%, respectively. The volume of both composites increased 0.8% or less in dry and wet conditions, while the increase in weight for InTen-S was 1.2% for the wet specimens and 0.6% for the dry. The corresponding figures for Esthet-X were 0.7 and 0.2%. SIGNIFICANCE: Doxadent was less dimensionally stable than the composites tested. Doxadent increased 2 times more in volume immersed in water than in 100% air humidity, while the increase in weight was almost similar. The clinical implications of the results found in the present study are uncertain. A material that continues to absorb water during prolonged periods and continues to react is questionable for clinical use.     

Chlorhexidine release and water sorption characteristics of chlorhexidine-incorporated hydrophobic/hydrophilic resins

OBJECTIVES: The aim of this study was to evaluate chlorhexidine release from unfilled non-solvated methacrylate-based resins of increasing hydrophilicity and to examine relationships among Hoy's solubility parameters, water sorption, solubility and the rate of chlorhexidine release. METHODS: Resin discs were prepared from light-cured, experimental resin blends (R1, R2, R3, R4 and R5) containing 0.0, 0.2, 1.0 and 2.0wt.% chlorhexidine diacetate (CDA). Discs were immersed in distilled water at 37 degrees C, and mass changes were recorded at different periods. Spectral measurements were made to follow change in optical densities of storage solution to examine chlorhexidine release kinetics. After a 28-day period, water sorption, solubility, and the cumulative chlorhexidine release were obtained. Additionally, antibacterial study was performed by observing the presence of inhibition zone against Streptococcus mutans. RESULTS: The most hydrophilic resin (R5) exhibited the highest chlorhexidine release rate. The most hydrophobic resin (R1) exhibited the lowest rate. However, no inhibition zone was produced by any specimens stored in water for 2 weeks. The addition of CDA increased solubility significantly but had no effect on water sorption. Significant positive correlations were seen between water sorption and the cumulative chlorhexidine release. SIGNIFICANCE: Chlorhexidine release from resins may be related to water-induced swelling, which in turn is enhanced by the hydrophilicity of cured polymer matrix.     

The Effect of Repeated Microwaving Disinfection on the Dimensional Stability of Acrylic Dentures

Objective

The aim of this study was to evaluate the effect of repeated microwave disinfections on the dimensional stability of acrylic dentures.

Materials and Methods

Three groups of dentures made of a heat polymerized acrylic resin were tested. I: dentures kept in water (control group). II: dentures microwaved daily while being immersed into water (wet disinfection). III: dentures microwaved daily without being immersed into water (dry disinfection).
Measurements were taken across three reference points, on two occasions: after curing and immersion in water for 24 hours, and one week later.
Data obtained were analyzed using one-way analysis of variance (ANOVA) and Scheffe’s multiple range test.

Results

The results showed that the microwave disinfection provokes dimensional changes of the same pattern (shrinkage). The dentures which underwent wet disinfection exhibited the greatest shrinkage (p<0.05).

Conclusions

Disinfection using microwave energy may cause dimensional changes (shrinkage) of complete dentures.
The microwave “dry disinfection” method can be safely applied in everyday practice since the dimensional changes which occurred seem to be of no clinical significance.Key words: Complete Dentures, Acrylic Resins, Disinfection, Microwaves, Dimensional Measurement Accuracy     

The Effect of Polymerization Cycles on Color Stability of Microwave-Processed Denture Base Resin

Purpose: This study evaluated the effect of different microwave polymerization cycles on the color changes of a microwave-processed denture base resin after accelerated aging and immersion in beverages.
Materials and Methods: Specimens of light pink acrylic resin were divided into three groups according to polymerization cycle: (A) 500 W for 3 minutes, (B) 90 W for 13 minutes + 500 W for 90 seconds, and (C) 320 W for 3 minutes + 0 W for 4 minutes + 720 W for 3 minutes. Control groups were a heat-processed acrylic resin (T) and a chemically activated denture repair resin (Q). Eight specimens per group were aged in an artificial aging chamber and evaluated at 20, 192, and 384 hours. Another series of 40 specimens per group were immersed in water, coffee, tea, cola, or red wine and evaluated at 1, 12, and 36 days. Color was measured by a spectrophotometer before and after aging or immersion. Color changes (ΔE) were analyzed by ANOVA/Bonferroni t -test (α= 0.05).
Results: Mean ΔE (±SD) after 384 hours of accelerated aging were (A) 2.51 ± 0.50; (B) 3.16 ± 1.09; (C) 2.89 ± 1.06; (T) 2.64 ± 0.34; and (Q) 9.03 ± 0.40. Group Q had a significantly higher ΔE than the other groups. Color changes of immersed specimens were significantly influenced by solutions and time, but the five groups showed similar values. Mean ΔE at 36 days were (water) 1.4 ± 0.8; (coffee) 1.3 ± 0.6; (tea) 1.7 ± 0.5; (cola) 1.4 ± 0.7; and (red wine) 10.2 ± 2.7. Results were similar among the five test groups.
Conclusions: Color changes of the microwave-polymerized denture base resin tested were not affected by different polymerization cycles after accelerated aging or immersion in beverages. These changes were similar to the conventional heat-polymerized acrylic resin test, but lower than the repair resin after accelerated aging.     

Effect of light sources and curing mode techniques on sorption, solubility and biaxial flexural strength of a composite resin

Adequate polymerization plays an important role on the longevity of the composite resin restorations.

Objectives

The aim of this study was to evaluate the effect of light-curing units, curing mode techniques and storage media on sorption, solubility and biaxial flexural strength (BFS) of a composite resin.

Material and Methods

Two hundred and forty specimens were made of one composite resin (Esthet-X) in a stainless steel mold (2 mm x 8 mm Ø), and divided into 24 groups (n=10) established according to the 4 study factors: light-curing units: quartz tungsten halogen (QTH) lamp and light-emitting diodes (LED); energy densities: 16 J/cm² and 20 J/cm²; curing modes: conventional (CM) and pulse-delay (PD); and permeants: deionized water and 75% ethanol for 28 days. Sorption and solubility tests were performed according to ISO 4049:2000 specifications. All specimens were then tested for BFS according to ASTM F394-78 specification. Data were analyzed by three-way ANOVA followed by Tukey, Kruskal-Wallis and Mann-Whitney tests (α=0.05).

Results

In general, no significant differences were found regarding sorption, solubility or BFS means for the light-curing units and curing modes (p>0.05). Only LED unit using 16 J/cm² and PD using 10 s produced higher sorption and solubility values than QTH. Otherwise, using CM (16 J/cm²), LED produced lower values of BFS than QTH (p<0.05). 75% ethanol permeant produced higher values of sorption and solubility and lower values of BFS than water (p<0.05).

Conclusion

Ethanol storage media produced more damage on composite resin than water. In general the LED and QTH curing units using 16 and 20 J/cm² by CM and PD curing modes produced no influence on the sorption, solubility or BFS of the tested resin.