Microtensile bond strength of resin-based composites to Ti–6Al–4V

ObjectiveThe purpose of this study was to determine the microtensile bond strength of various resin composite/adhesive systems to alumina particle abraded Ti–6Al–4V substrate after aging for 24 h, 10 days, and 30 days in distilled water at 37 °C.MethodsFour laboratory resin composite veneering systems (Gradia, GR; Solidex, SOL; Ceramage, CER; and Sinfony, SF) were bonded to 25 mm diameter machined disks of Ti–6Al–4V with their respective adhesive and methodology, according to the manufacturer's instructions. Microtensile bars of approximate dimensions 1 mm × 1 mm × 6 mm were prepared for each resin composite/adhesive system. After cutting, groups (n = 12) from each adhesive system were separated and either stored in water at 37 °C for 24 h (baseline) or aged for 10 or 30 days prior to loading to failure under tension at a cross head speed of 1.0 mm/min. Failure modes were determined by means of scanning electron microscopy (SEM). Statistical analysis was performed through one-way ANOVA and Tukey's test at 95% level of significance.ResultsSignificant variation in microtensile bond strength was observed for the different systems and aging times. SOL and GR showed the highest mean bond strength values followed by SF and CER at baseline. Aging specimens in water had an adverse effect on bond strength for SOL and CER but not for the SF and GR groups.SignificanceIn vitro bond strength of laboratory resin composites to Ti–6Al–4V suggests that strong bonds can be achieved and are stable for certain systems, making them useful as an alternative for esthetic fixed prosthetic restorations.     

Viscosity and stickiness of dental resin composites at elevated temperatures

ObjectiveTo investigate the influence of pre-heating different classes of dental resin composites on viscosity and stickiness at five different temperatures.MethodsSix flowable, five conventional packable, and one thermo-viscous bulk-fill resin composites were heated up to 54 °C in a plate-plate rheometer to determine their complex viscosity. Normal force measurements were carried out for the six packable materials to determine the unplugging force and unplugging work (stickiness) over the same temperature range. Data were analyzed using Kolmogorov–Smirnoff test, one-way ANOVA and Tukey Post Hoc test with α = 0.05 as level of significance.ResultsAt 23 °C packable composites showed viscosity between 6.75 and 19.14 kPa s, while flowable composites presented significantly lower viscosities between 1.31 and 2.20 kPa s. Pre-heating led to a drop of 30–82% in the viscosity of packable materials. The thermo-viscous material dropped to the level of flowables at 45 and 54 °C thus behaving as a packable composite at room temperature with flowable-like viscosity at higher temperatures. No statistically significant differences for viscosity were observed among flowable composites at any temperature.The unplugging force decreased for packable composites, while their unplugging work generally increased at elevated temperature. At 23 °C unplugging force was measured between 7.50 and 19.18 N, while pre-heating up to 54 °C led to values between 2.9 and 6.2 N. Regarding unplugging work at 23 °C the calculated values were between 3.0 and 8.9 × 10^?3 J and at 54 °C between 8.8 and 13.0 × 10^?3 J.SignificancePre-heating significantly reduced viscosity of highly viscous resin composites, while no influence was shown for flowable composites. In general stickiness, measured as unplugging work, increased at elevated temperatures. The thermo-viscous material showed low viscosity comparable to flowable composites at 45 and 54 °C, yet its stickiness did not increase significantly compared to the values at 23 °C.     

Influence of bonding surface and bonding methods on the fracture resistance and survival rate of full-coverage occlusal veneers made from lithium disilicate ceramic after cyclic loading

ObjectivesThe purpose of this laboratory study was to evaluate the influence of bonding method and type of dental bonding surface on fracture resistance and survival rate of resin bonded occlusal veneers made from lithium disilicate ceramic after cyclic loading.MethodsFourty-eight extracted molars were divided into three groups (N = 16) depending on the preparation: within enamel, within dentin/enamel or within enamel/composite resin filling. Lithium disilicate occlussal veneers were fabricated with a fissure-cusp thickness of 0.3–0.6 mm. Restorations were etched (5% HF), silanated and adhesively luted using a dual-curing luting composite resin. Test groups were divided into two subgroups, one using a only a self-etching primer, the other additionally etching the enamel with phosphoric acid. After water storage (37 °C; 21 d) and thermocycling (7500 cycles; 5–55 °C), specimens were subjected to dynamic loading in a chewing simulator (600,000 cycles; 10 kg/2 Hz). Surviving specimens were loaded until fracture using a universal testing machine.ResultsAll specimens survived artificial aging, several specimens showed some damage. ANOVA revealed that enamel etching provided statistically significantly (p ≤ 0.05) higher fracture resistance than self-etching when bonding to enamel and dentin. Self-etching provided statistically significant (p ≤ 0.05) higher fracture resistance for the enamel-composite group than for the enamel group. Enamel etching provided statistically significant (p ≤ 0.05) higher fracture resistance for the enamel and dentin group than for groups enamel and enamel-composite.SignificanceEtching enamel improved the fracture resistance of occlusal veneers when bonding to dentin and enamel and increased the survival rate when bonding to enamel.     

Streptococcal adhesion to novel low-shrink silorane-based restorative

ObjectivesThe aim of the present study was to compare the susceptibility of one novel silorane-based and four widely used conventional methacrylate-based resin composites to adhere oral streptococci and to relate any differences to surface roughness, hydrophobicity and type of matrix.MethodsSpecimens of restoratives Filtek Silorane, Filtek Z250, Tetric EvoCeram, Quixfil and Spectrum TPH were prepared (10.0-mm diameter, 2.0-mm height). Surface roughness was assessed by perthometer measurements and hydrophobicity according to water contact angles was determined by computerized image analysis. Bacterial suspensions of Streptococcus oralis, Streptococcus sanguinis, Streptococcus gordonii and Streptococcus mutans were incubated for 2.5 h at 37 °C with 15 test specimens for each material and adhesion was quantified with fluorescence dye Alamar Blue/Resazurin and an automated multi-detection reader. Glass served as reference. Statistical analysis was performed using the Mann–Whitney U-test (α = 0.05).ResultsMedian roughness values of all composites ranged between 0.04 and 0.11 μm, median contact angles between 59.7° and 92.1°. Significantly lowest fluorescence intensities of all test materials were found on Filtek Silorane for three of four streptococcal strains. The fluorescence intensities of the four conventional methacrylate resin composites were significantly higher and comparable among each other.SignificanceWhen compared against four conventional methacrylate composite resins, a general significance to a lower quantity of adhering streptococci was found on the novel silorane-based composite resin, which might result from its increased hydrophobicity. The low adhesion potential of the silorane-based composite may potentially improve the longevity of direct fillings and reduce recurrent caries.     

An in vitro comparison of four intra-oral ceramic repair systems

ObjectivesThis study evaluated the effect of different surface conditioning methods on the tensile bond strength (TBS) and integrity of the leucite-reinforced glass ceramic (Cerana^® inserts)–resin composite interface, using four commercially available ceramic repair systems.MethodsTwo hundred extra-large Cerana^® inserts were mechanically treated and stored in artificial saliva for 3 weeks and subsequently randomly assigned to one of the following ceramic repair systems (n = 40/group): Group 1, Ceramic Repair^® (Ivoclar Vivadent, Liechtenstein); Group 2, Cimara^® (Voco, Germany); Group 3, Clearfil Repair^® (Kuraray, Japan); Group 4, CoJet system^® (3M ESPE, Germany); and Group 5, no surface conditioning and no adhesive system applied: the control group. Subsequently, resin composite material was added to the substrate surfaces and the ceramic–resin composite specimens were subjected to TBS testing. Representative samples from the test groups were subjected to scanning electron microscopy (SEM) to determine the mode of failure. The data were analysed statistically using a one-way multivariate analysis of variance and Kruskal–Wallis test at a 95% confidence interval level.ResultsSurface conditioning with the CoJet^® system resulted in significantly higher bond strength values (5.2 ± 1.1 MPa) than surface conditioning with the other repair systems (p = 0.03). The SEM examination of the failed interfaces revealed that all the specimens examined failed adhesively.SignificanceWhilst highest bond strength values were observed with the CoJet^® system all tested repair systems resulted in relatively weak TBS values and, as a consequence, these repair systems may be indicated only as interim measures.     

Shear bond strength vs interfacial fracture toughness — Adherence to CAD/CAM blocks

ObjectiveTo compare shear bond strength (SBS) and interfacial fracture toughness (IK_IC) results when assessing the effect of surface roughness and thermocycling on the adherence of a resin composite luting agent (RCLA) to a CAD/CAM resin composite block (RCB).MethodsTetric CAD HT along with the recommended bonding system, Adhese Universal and Variolink Esthetic LC, were used. Surface roughness was achieved with 600/320/60 grit SiC papers. Samples were stored 24 h in 37 °C water or thermocycled 10000× (5 °C–55 °C) prior to testing. Results were analyzed by univariate ANOVA and Scheffé modified t-tests (α = 0.05). Fractured specimens were viewed with a stereo microscope and selected specimens with a scanning electron microscope.ResultsSBS results showed a significant difference between the 60 grit group and the other groups, both after 24 h and thermocycling. A large number of SBS samples showed cohesive fracture or subsurface damage in RCB. Thermocycling led to a significant decrease in SBS in all groups. IK_IC results showed no significant differences due to surface preparation after 24 h storage in 37 °C. After thermocycling, there was a significant difference between the 60 and the 600 grit groups. All K_IC samples fractured adhesively at the RCB surface. K_IC of the RCLA was significantly higher than IK_IC of all groups.SignificanceThe results endorse the use of fracture mechanics methodology for the assessment and characterization of adherence, while identifying difficulties in its implementation. The results suggest also that adherence to CAD/CAM RCB may be limited by the strength of the resin composite block — adhesive interface.     

Curing potential and color stability of different resin-based luting materials

PurposeTo determine the curing potential and color stability of resin-based luting materials for aesthetic restorations.Material and MethodsFour resin-based luting agents were tested: traditional dual-activated resin cement (RelyX ARC, ARC), amine-free dual-activated resin cement (RelyX Ultimate, ULT), light-activated resin cement (RelyX Veneer, VEN), and pre-heated restorative resin composite (Filtek Supreme, PHC). Degree of C = C conversion was determined by infrared spectroscopy (n = 3) with direct light exposure or with interposition of 1.5-mm-thick ceramic (e.max Press HT) between the luting material and light. The curing potential considered the ratio between these two scenarios. Color difference (n = 6) was determined by CIELAB (ΔE_ab) and CIEDE2000 (ΔE₀₀) methods, by spectrophotometer measurements made 24 h after photoactivation and 90 days after storage in water. Data was submitted to ANOVA and Tukey’s test (α = 0.05).ResultsThe luting agents affected both conversion and color stability. With ceramic, ARC produced the highest conversion among the tested groups (75 ± 1%) and the pre-heated composite (PHC) the lowest one (51 ± 3%), but the curing potential was similar for all materials. ULT produced lower ΔE_ab than ARC. PHC presented the lowest color difference when considered both CIELAB and CIE2000 methods (ΔE_ab 2.1 ± 0.4; ΔE₀₀ 1.6 ± 0.2).SignificanceAll luting strategies presented high curing potential. Amine-free dual-activated material was able to reduce color difference than that formulated with the amine component. Pre-heated composite produced the least color variation after storage.     

Evaluation of interface characterization and adhesion of glass ceramics to commercially pure titanium and gold alloy after thermal- and mechanical-loading

ObjectivesThis study evaluated the effect of thermal- and mechanical-cycling on the shear bond strength of three low-fusing glassy matrix dental ceramics to commercial pure titanium (cpTi) when compared to conventional feldspathic ceramic fused to gold alloy.MethodsMetallic frameworks (diameter: 5 mm, thickness: 4 mm) (N = 96, n = 12 per group) were cast in cpTi and gold alloy, airborne particle abraded with 150 μm aluminum oxide. Low-fusing glassy matrix ceramics and a conventional feldspathic ceramic were fired onto the alloys (thickness: 4 mm). Four experimental groups were formed; Gr1 (control group): Vita Omega 900–Au–Pd alloy; Gr2: Triceram–cpTi; Gr3: Super Porcelain Ti-22–cpTi and G4: Vita Titankeramik–cpTi. While half of the specimens from each ceramic–metal combination were randomly tested without aging (water storage at 37 °C for 24 h only), the other half were first thermocycled (6000 cycles, between 5 and 55 °C, dwell time: 13 s) and then mechanically loaded (20,000 cycles under 50 N load, immersion in distilled water at 37 °C). The ceramic–alloy interfaces were loaded under shear in a universal test machine (crosshead speed: 0.5 mm/min) until failure occurred. Failure types were noted and the interfaces of the representative fractured specimens from each group were examined with stereomicroscope and scanning electron microscope (SEM). In an additional study (N = 16, n = 2 per group), energy dispersive X-ray spectroscopy (EDS) analysis was performed from ceramic–alloy interfaces. Data were analyzed using ANOVA and Tukey's test.ResultsBoth ceramic–metal combinations (p < 0.001) and aging conditions (p < 0.001) significantly affected the mean bond strength values. Thermal- and mechanical-cycling decreased the bond strength (MPa) results significantly for Gr3 (33.4 ± 4.2) and Gr4 (32.1 ± 4.8) when compared to the non-aged groups (42.9 ± 8.9, 42.4 ± 5.2, respectively). Gr1 was not affected significantly from aging conditions (61.3 ± 8.4 for control, 60.7 ± 13.7 after aging) (p > 0.05). Stereomicroscope images showed exclusively adhesive failure types at the opaque ceramic–cpTi interfacial zone with no presence of ceramic on the substrate surface but with a visible dark titanium oxide layer in Groups 2–4 except Gr1 where remnants of bonder ceramic was visible. EDS analysis from the interfacial zone for cpTi–ceramic groups showed predominantly 34.5–85.1% O₂ followed by 1.1–36.7% Al and 0–36.3% Si except for Super Porcelain Ti-22 where a small quantity of Ba (1.4–8.3%), S (0.7%) and Sn (35.3%) was found. In the Au–Pd alloy–ceramic interface, 56.4–69.9% O₂ followed by 15.6–26.2% Si, 3.9–10.9% K, 2.8–6% Na, 4.4–9.6% Al and 0–0.04% Mg was observed.SignificanceAfter thermal-cycling for 6000 times and mechanical-cycling for 20,000 times, Triceram–cpTi combination presented the least decrease among other ceramic–alloy combinations when compared to the mean bond strength results with Au–Pd alloy–Vita Omega 900 combination.     

Effect of different composite modulation protocols on the conversion and polymerization stress profile of bulk-filled resin restorations

ObjectiveThe aim of this in vitro study was to test the effect of different composite modulation protocols (pre-heating, light-curing time and oligomer addition) for bulk filling techniques on resin polymerization stress, intra-pulpal temperature change and degree of conversion.MethodsClass I cavities (4 mm depth × 5 mm diameter) were prepared in 48 extracted third molars and divided in 6 groups. Restorations were completed with a single increment, according to the following groups: (1) Filtek Z250XT (room temperature – activated for 20 s); (2) Filtek Z250XT (at room temperature – activated for 40 s); (3) Filtek Z250XT (pre-heated at 68 °C – activated for 20 s); (4) Filtek Z250XT (pre-heated at 68 °C – activated for 40 s); (5) Filtek BulkFill (at room temperature – activated for 20 s); (6) Filtek Z250XT (modified by the addition of a thio-urethane oligomer at room temperature – activated for 40 s). Acoustic emission test was used as a real-time polymerization stress (PS) assessment. The intra-pulpal temperature change was recorded with a thermocouple and bottom/top degree of conversion (DC) measured by Raman spectroscopy. Data were analyzed with one-way ANOVA/Tukey's test (α = 5%).ResultsPre-heating the resin composite did not influence the intra-pulpal temperature (p = 0.077). The thio-urethane-containing composite exhibited significantly less PS, due to a lower number of acoustic events. Groups with pre-heated composites did not result in significantly different PS. Filtek BulkFill and the thio-urethane experimental composite presented significantly higher DC.SignificanceResin composite pre-heating was not able to reduce polymerization stress in direct restorations. However, thio-urethane addition to a resin composite could reduce the polymerization stress while improving the DC.     

Temperature change in pulp cavity in vitro during the polymerization of provisional resins

ObjectivesTo measure the temperature change in the pulp cavity of an extracted tooth during the polymerization of provisional resins within impression putty and polyethylene matrices. The effect of pre-cooling the putty matrix was also evaluated.MethodsA freshly extracted premolar tooth had putty impressions recorded prior to crown preparation. Putty matrices were stored at room temperature, 4 and ?12 °C prior to use. A thermocouple placed in the pulp chamber recorded the temperature change every 15 s for a 10-min duration during polymerization of three resins using putty and clear polyethylene matrices. Five recordings were made with each material at each storage temperature.ResultsThere is a temperature rise of 3.4–5.5 °C when the resins were autocured in a putty matrix. When the polyvinyl matrix was used the temperature rise increased to 4.0–8.2 °C (P < 0.001). The temperature rise was reduced to zero when the putty had been pre-cooled in the fridge (P < 0.001) and reduced further following pre-cooling in the freezer (P < 0.001).SignificanceThe use of a polyvinyl matrix allows higher pulp temperature rises to occur due to the exotherm from provisional resins. Lower temperatures were recorded when putty was used. The temperature rise could be eliminated when the putty was cooled at 4 °C prior to reinsertion.     

The effect of resin composite pre-heating on monomer conversion and polymerization shrinkage

ObjectivesTo determine monomer conversion and polymerization shrinkage of a resin composite after different pre-heating procedures and storage intervals.MethodsFor a commercial resin-based composite the immediate (5 min) and final (24 h) degree of conversion was measured on top and bottom surfaces utilizing FTIR spectroscopy. Composite pre-heating temperatures were selected between 10 and 68 °C. Polymerization shrinkage was measured according to Archimedes’ principles of buoyancy after 5 min at respective pre-heating temperatures and after 24 h dark and wet storage at 37 °C. Intra-cavity temperature development was monitored using a K-type thermocouple.ResultsNo significant increase in immediate as well as in final degree of conversion were measured from composite pre-heating at 68 °C compared to 54 and 39 °C. Linear correlations were detected immediately after photo-polymerization and on the top surface after 24 h storage. Polymerization shrinkage as a function of pre-heating temperatures exhibited a linear correlation after 5 min, but no statistically different behavior after 24 h.SignificancePre-heating of resin composites does not increase degree of conversion over time. It can be clinically beneficial, due to a superior marginal adaptation. This advantageous effect of reduced material paste viscosity has to be clinically addressed, since temperature rapidly drops to the physiological level upon removal from the pre-heating device.     

Shear bond strength between light polymerized hard reline resin and denture base resin subjected to long term water immersion

Statement of the problemThe effect of long-term water immersion on the shear bond strength between denture base resin and Triad visible-light-polymerized (VLP) direct hard reline resin is not known.PurposeThe aim of this study was to investigate the bonding characteristics of Triad VLP direct hard reline resin to heat-polymerized denture base resin subjected to long-term water immersion.Material and methodsNinety circular disks, 15 mm in diameter and 3 mm thick, of denture base resin were polymerized from a gypsum mold. Sixty specimens were subjected to water immersion and 30 were stored at ambient room temperature for 4 months. Thirty water-immersed specimens were dried with gauze (group 1), while the other 30 water-immersed specimens were dried with a hair dryer (group 2). The dry specimens (n = 30) represented the control group (group 3). All specimens were air abraded and painted with bonding agent before packing Triad VLP direct hard-reline resin. Specimens in each group were subjected to thermal cycling for 50,000 cycles between 4 °C and 60 °C water baths with 1-min dwell time at each temperature. The bond strength at which the bond failed under stress was recorded using a universal testing machine. One-way ANOVA and Tukey post hoc comparison were applied to find significant differences between groups (α = 0.05).ResultsSignificant differences in mean shear bond strength among the specimens existed because of variable water content in the denture base resin (P < 0.05). Group 3 (dry) was higher than group 2 (desiccated), and the lowest was group 1 (saturated).ConclusionThe shear bond strength of Triad VLP direct hard reline resin to denture base resin depended on the water content in the denture base resin. The dry denture base resin demonstrated superior bond strength compared with the desiccated and water-saturated denture base resins.     

Effects of aging procedures on the topographic surface,structural stability,and mechanical strength of a ZrO2-based dental ceramic

ObjectiveTo determine the effects of different aging methods on the degradation and flexural strength of yttria-stabilized tetragonal zirconia (Y-TZP)MethodsSixty disc-shaped specimens (∅, 12 mm; thickness, 1.6 mm) of zirconia (Vita InCeram 2000 YZ Cubes, VITA Zahnfabrik) were prepared (ISO 6872) and randomly divided into five groups, according to the aging procedures (n = 10): (C) control; (M) mechanical cycling (15,000,000 cycles/3.8 Hz/200 N); (T) thermal cycling (6,000 cycles/5–55 °C/30 s); (TM) thermomechanical cycling (1,200,000 cycles/3.8 Hz/200 N with temperature range from 5 °C to 55 °C for 60 s each); (AUT) 12 h in autoclave at 134 °C/2 bars; and (STO) storage in distilled water (37 °C/400 days). After the aging procedures, the monoclinic phase percentages were evaluated by X-ray diffraction (XRD), and topographic surface analysis was performed by 3D profilometry. The specimens were then subjected to biaxial flexure testing (1 mm/min, load 100 kgf, in water). The biaxial flexural strength data (MPa) were analyzed by 1-way ANOVA and Tukey's test (α = 0.05). The data for monoclinic phase percentage and profilometry (Ra) were analyzed by Kruskal–Wallis and Dunn's tests.ResultsANOVA revealed that flexural strength was affected by the aging procedures (p = 0.002). The M (781.6 MPa) and TM (771.3 MPa) groups presented lower values of flexural strength than did C (955 MPa), AUT (955.8 MPa), T (960.8 MPa) and STO (910.4 MPa). The monoclinic phase percentage was significantly higher only for STO (12.22%) and AUT (29.97%) when compared with that of the control group (Kruskal–Wallis test, p = 0.004). In addition, the surface roughnesses were similar among the groups (p = 0.165).SignificanceWater storage for 400 days and autoclave aging procedures induced higher phase transformation from tetragonal to monoclinic; however, they did not affect the flexural strength of Y-TZP ceramic, which decreased only after mechanical and thermomechanical cycling.     

Effect of water aging on microtensile bond strength of dual-cured resin cements to pre-treated sintered zirconium-oxide ceramics

ObjectivesTo evaluate the hydrolytic stability of different dual-cure resin cements when luted to zirconia ceramic.MethodsEighteen cylinder-shaped zirconia blocks (Cercon Zirconia, Dentsply) were conditioned with: Group 1, no treatment; Group 2, sandblasting (125 μm alumina–Al₂O₃-particles); Group 3, tribochemical silica coating (50 μm silica-modified Al₂O₃ particles). Ceramic blocks were duplicated in composite resin (Tetric Evo Ceram, Ivoclar-Vivadent). Composite disks were luted to pre-treated ceramic surfaces using: (1) Clearfil Esthetic Cement (CEC; Kuraray); (2) Rely X Unicem (RXU; 3M ESPE); (3) Calibra (CAL; Dentsply Caulk). After 24 h, bonded samples were cut into microtensile sticks (1 mm²). Half of the sticks were loaded in tension until failure (cross-head speed of 0.5 mm/min). The remaining half was tested after 6 months of water storage at 37 °C. Data was analyzed with three-way ANOVA and Tukey’s test (P <0.05). Fractographic analysis was performed by SEM.ResultsAfter 24 h, bond strength of CEC to zirconia was significantly higher than that of RXU and CAL, independently from the ceramic pre-treatment (P <0.001). Using CAL, all samples failed prematurely except when luting to sandblasted surfaces. After 6 months of water aging, bond strength of CEC significantly decreased. RXU did not significantly alter bond strengths. Adhesion of sandblasted specimens luted with CAL fell over time. Micromorphological alterations were evident after water storage.SignificanceResin–ceramic interfacial longevity depended on cement selection rather than on surface pre-treatments. CEC and RXU were both suitable for luting zirconia. Water aging played an important role in the durability of zirconia-to-composite chemical bonds.     

Effect of water-bath post-polymerization on the mechanical properties,degree of conversion,and leaching of residual compounds of hard chairside reline resins

ObjectivesThis study evaluated the effect of water-bath post-polymerization at 55 °C for 10 min (WB) on the content and leaching of residual compounds, degree of conversion, flexural strength, and hardness of hard chairside reline resins (Kooliner: K, New Truliner: N, Ufi Gel hard: U, and Tokuso Rebase Fast: T).MethodsLeaching experiments were made by storing specimens (n = 48) in artificial saliva at 37 ± 1 °C and analyzing residual monomers and plasticizer by HPLC. Analysis of residual monomer and plasticizer content (n = 48) was also made by HPLC. Degree of conversion (n = 40) was analyzed by using FT-Raman spectroscopy. A 3-point loading test was used to evaluate the flexural strength of the specimens (n = 80). One fragment of each flexural test specimen was then submitted to Vickers microhardness test.ResultsWB produced a significant decrease (p < 0.050) in the amount of residual compounds eluted from the materials within the first hour of immersion. With the exception of material U, WB decreased the duration of release of the residual compounds evaluated. All materials evaluated exhibited significantly (p < 0.050) lower values of residual monomer and plasticizer (material N) after WB compared with the control groups. WB increased the degree of conversion of K and T resins and the hardness of N, K, and T resins (p < 0.050). Only material K showed an increase in flexural strength after WB (p < 0.050).SignificanceImmersion of relined dentures in water at 55 °C for 10 min can be used to reduce the amounts and duration of release of residual compounds and improve mechanical properties of some of the materials evaluated.     

Detection of Bisphenol A in dental wastewater after grinding of dental resin composites

ObjectivesThis study evaluated the release of bisphenol A (BPA) in wastewater after grinding of resin composites and tested three filtration materials.MethodsThree resin composites (Ceram X, Filtek Supreme XTE and Core-X flow) were used. Samples (5 mm × 2 mm, n = 10) were prepared using a metal mold and were polymerized for 20 s according to manufacturers’ instructions. A dental unit was disconnected from wastewater circulation and composite samples were ground under standardized procedures (200,000 rpm; 90 s). Wastewater was collected in glass bottles. Water samples were collected as control by performing the same procedure without grinding resin composite. All samples were stored at 7 °C for 6 months to simulate storage. Then they were analyzed by HPLC–FLD. Three filtration materials (Zeosorb, Katalox Light and Catalytic Carbon) were used for water treatment to remove BPA. BPA-water solutions were prepared; corresponding to the highest amount released by the resin composites. These solutions were analyzed before and after filtration by HPLC–FLD and their efficacy (%) was calculated.ResultsBPA was detected in all composite solutions: Ceram X and Filtek Supreme XTE showed similar findings (p > 0.05) which were significantly higher than the control (p < 0.001) and Core-X flow (p = 0.001). The efficacy of the filtration materials was: Katalox Light (5.09%) < Zeosorb (7.91%) < Catalytic Carbon (99.38%). Only Catalytic Carbon caused a clinically significant reduction of BPA (p < 0.05).SignificanceBPA can be released in wastewater during dental procedures. This release seems to be material dependent. Among the filtration methods tested, Catalytic carbon seems to be effective for BPA reduction in water.     

Effect of delivering light in specific narrow bandwidths from 394 to 515 nm on the micro-hardness of resin composites

ObjectivesThis study investigated the wavelength-dependent photosensitivity of eleven resin composites (Admira A2, Heliomolar A2, Herculite XRV A2, Pyramid Dentin A2, Solitaire 2 A2, Z250 A2, Ælite LS A2, Vit-l-escence A2, Tetric Ceram Bleach XL, Tetric Ceram A2, Pyramid Enamel Neutral).MethodsResin composites 1.6 mm thick were exposed to narrow bandwidths of light at the following peak wavelengths: 394, 400, 405, 410, 415, 420, 430, 436, 442, 450, 455, 458, 467, 470, 480, 486, 493, 500, 505, and 515 ± 5 nm. A spectroradiometer was used to ensure that the same irradiance (mW/cm²) and total energy density (J/cm²) was delivered through each filter. For each resin composite, three specimens were exposed through each filter. The Knoop micro-hardness at the top and bottom of the composites was then measured. The wavelength-dependent photosensitivity of each resin composite was analyzed by plotting the mean hardness achieved at each wavelength.ResultsThe composites responded variably when they received light through the narrow bandpass filters. Six resin composites had a single peak of wavelength-dependent photosensitivity at ～470 nm. Four resin composites had two peaks of wavelength-dependent photosensitivity at ～470 and ～405 nm. One resin composite had a single peak of wavelength-dependent photosensitivity at ～405 nm and was only sensitive to light below 436 nm.SignificanceUsing light delivered through narrow bandpass filters is a convenient method to determine the wavelength-dependent photosensitivity of resins and can be used to predict the performance of dental curing lights.     

Temperature-dependence of creep behaviour of dental resin-composites

ObjectivesTo determine the effect of temperature, over a clinically relevant range, on the creep behaviour of a set of conventional and flowable resin-composites including two subgroups having the same resin matrix and varied filler loading.MethodsEight dental resin-composites: four flowable and four conventional were investigated. Stainless steel split moulds (4 mm × 6 mm) were used to prepare cylindrical specimens for creep examination. Specimens were irradiated in the moulds in layers of 2 mm thickness (40 s each), as well as from the radial direction after removal from the moulds, using a light-curing unit with irradiance of 650 mW/cm². A total of 15 specimens from each material were prepared and divided into three groups (n = 5) according to the temperature; Group I: (23 °C), Group II: (37 °C) and Group III: (45 °C). Each specimen was loaded (20 MPa) for 2 h and unloaded for 2 h. Creep was measured continuously over the loading and unloading periods.ResultsAt higher temperatures greater creep and permanent set were recorded. The lowest mean creep occurred with GS and GH resin-composites. Percentage of creep recovery decreased at higher temperatures. At 23 °C, the materials exhibited comparable creep. At 37 °C and 45 °C, however, there was a greater variation between materials. For all resin-composites, there was a strong linear correlation with temperature for both creep and permanent set.ConclusionsCreep parameters of resin-composites are sensitive to temperature increase from 23 to 45 °C, as can occur intra-orally. For a given resin matrix, creep decreased with higher filler loading.