Effect of chlorhexidine application on long-term shear bond strength of resin cements to dentin

PurposeThe purpose of this study was to investigate the effect of chlorhexidine [CH] on dentin bond strength of three resin cements after 1 year of water storage.MethodsA flat middle dentin surface was prepared on 120 extracted premolars. The teeth were randomly divided into 6 groups of 20 specimens each according to the resin cement used: Panavia F2.0, Variolink II, and RelyX Unicem, with or without CH application. After cementation of an indirect composite rod [Z250], one subgroup [n = 10] was tested after 24 h in water at 37 °C and the other subgroup [n = 10] was tested after 1 year storage in water plus thermocycling. A shear bond strength [SBS] test was performed. The data [in MPa] were analyzed with ANOVA and Tukey tests [P < 0.05].ResultsThree-way ANOVA [resin cement, CH and time] indicated that Variolink II had the highest strength [16.65 ± 3.60] and RelyX Unicem had the lowest strength [9.30 ± 4.07]. Chlorhexidine application increased SBS [13.31 ± 4.61] compared to samples without CH [12.16 ± 5.04] [P = 0.04]. Initial SBS [15.63 ± 4.37] was significantly higher than after 1 year of storage [9.85 ± 3.36] [P < 0.001]. Separate two-way ANOVA for 24-h and 1-year data showed that cement had a significant effect but CH and its interaction had no significant effect at 24 h, whereas at 1 year the two factors and their interaction differed significantly [P ≤ 0.001].ConclusionsChlorhexidine 2% can diminish the loss of bonding effectiveness over time associated to etch-and-rinse and self-etch cements, although it appears not have any effect on self-adhesive cement.     

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 surface treatments of monolithic zirconia in different sintering stages

Purpose

This study evaluated the effect of surface treatment of zirconia in pre-sintered and post-sintered stages on its surface roughness, phase transformation, and biaxial flexural strength (BFS).

The development and testing of glaze materials for application to the fit surface of dental ceramic restorations

ObjectivesThe aims of the study were to develop and test overglaze materials for application to the fit surface of dental ceramic restorations, which could be etched and adhesively bonded and increase the flexural strength of the ceramic substrate.MethodsThree glaze materials were developed using commercial glass powders (P25 and P54, Pemco, Canada). P25 (90 wt%) was mixed with P54 (10 wt%) to produce (P25/P54). P54 (90 wt%) was mixed with P25 (10 wt%) to produce (P54/P25). P25 (90 wt%) was mixed with 10 wt% of an experimental glass powder (P25/frit). Eighty-two disc specimens (14 mm × 2 mm) were produced by heat pressing a leucite glass–ceramic and were sandblasted with 50 μm glass beads. Group 1 control specimens (10) were sandblasted. Groups 2–4 (10 per group) were coated using P25/frit (Group 2), P25/P54 (Group 3) and P54/P25 (Group 4) overglazes before sintering. Groups 1–4 were etched for 2 min using 9.5% HF (Gresco, USA). Composite cylinders (Marathon^® v, Den-Mat) were light cured and bonded to the glazed and prepared disc surfaces and groups water stored for 8 days. Groups were tested using shear bond strength (SBS) testing at 0.5 mm/min. Disc specimens (42) were tested using the biaxial flexural strength (BFS) test at a crosshead speed of 0.15 mm/min. Group 1 was tested as sandblasted (21) and Group 2 (21) after coating the tensile surface with P25/frit. Xrd, Eds and Sem analyzes were carried out.ResultsMean SBS (MPa ± S.D.) were: Group 1: 10.7 ± 2.1; Group 2: 9.8 ± 1.9; Group 3: 1.8 ± 1.0 and Group 4: 2.6 ± 1.7. Groups 1 and 2 were statistically different to Groups 3 and 4 (p < 0.001), but there was no difference between Groups 1 and 2 and 3 and 4 (p > 0.05). The mean BFS (MPa ± S.D.) of the overglazed Group 2 (200.2 ± 22.9) was statistically different (p < 0.001) to Group 1 (150.4 ± 14.3).SignificanceThe P25/frit overglaze significantly (p < 0.001) increased the biaxial flexural strength of the leucite glass–ceramic substrate and produced comparable shear bond strengths to an etched and bonded control. The application of etched overglaze materials to dental glass–ceramic and ceramic substrates may be useful in adhesive dentistry.     

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.     

Evaluation of physical properties of fiber-reinforced composite resin

ObjectivesThis study aimed to investigate physical properties of a fiber-reinforced CAD/CAM resin disc, which included woven layers of multi-directional glass fibers.MethodsFiber orientations of CAD/CAM specimens (TRINIA, SHOFU) were specified as longitudinal (L), longitudinal-rotated (LR), and anti-longitudinal (AL). A fiber-reinforced composite (everX posterior, GC (E)) and a conventional composite (Beauti core flow paste, SHOFU (B)) were also tested.A three-point bending test and a tensile test with notchless prism-shaped specimens were conducted using a universal testing machine (AUTOGRAPH AG-IS, Shimadzu). A water absorption test was also carried out after the specimens were stored in water for 24 h or 1 week. Flexural strength and fracture toughness were obtained by conducting a three-point bending test.ResultsTRINIA L and LR groups showed significantly high flexural strength (254.2 ± 22.3 and 248.8 ± 16.7 MPa, respectively). Those were approximately 2.5 times higher than those in AL, E, and B groups (96.8–98.0 MPa) (p < 0.05, ANOVA and Tukey HSD test). No significant difference was shown in flexural modulus among the experimental groups. The fracture toughness in L group (9.1 ± 0.4 MPa/m^1/2) was found to be significantly higher than those in other groups (1.9–3.0 MPa/m^1/2; p < 0.05). TRINIA group demonstrated significantly lower water absorption (4.7 ± 1.9 μg/mm³) than did E (16.1 ± 3.1 μg/mm³) and B (17.3 ± 3.7 μg/mm³) groups (p < 0.05).SignificanceTRINIA demonstrated distinct anisotropy. TRINIA can be used as a superior restorative material when specifying directions of its fiber mesh layers.     

Effect of cleaning protocol on silica deposition and silica-mediated bonding to Y-TZP

ObjectivesTo evaluate the effect of cleaning methods on the deposition of silica on yttria-stabilized zirconium dioxide (Y-TZP) surface and on the silane-silica mediated bond strength between Y-TZP and resin cement.MethodsY-TZP slabs were air-abraded with 30 μm silica-coated alumina particles and distributed in three groups: no cleaning, cleaning with a stream of oil-free air/water spray for 5 s and cleaning with an ultrasonic bath in water for 10 min. The distribution of Si on the Y-TZP surfaces was recorded using energy dispersive spectroscopy (EDS). After the treatment was applied, Y-TZP slabs (n = 20) received a primer application and resin cement cylinders were built on the surface. After storage (24 h) in water storage or 3 months plus thermocycling; n = 10), microshear bond strength test (μSBS) was performed. X- ray Photoelectron Spectroscopy (XPS) characterized the chemical bonds between the silica layer and the silane-containing primer. Data were analyzed using ANOVA and Tukey test, as well as Weibull analysis (α = 0.05).ResultsCleaning method had a significant effect on the amount of Si deposited on zirconia surface (p < 0.001) and, consequently, on bond strength (p < 0.001). Storage/aging also had a significant effect on bond strength (p < 0.001). Low values of Weibull moduli for bond strength were observed for all groups after aging. XPS showed silane-silica chemical interaction for all groups.SignificanceThe silica deposited by tribochemical coating to Y-TZP was removed by the cleaning methods evaluated, compromising bond strength. Stability of the bonding is also a concern when no cleaning method is applied.     

Ultrashort-pulse laser as a surface treatment for bonding between zirconia and resin cement

ObjectivesTo evaluate ultrashort-pulse laser (UPL) as a surface treatment for improved bond strength to Yttria-tetragonal zirconia polycrystalline (Y-TZP).MethodsFully-sintered Y-TZP samples received either no treatment (CTL), or were treated by alumina blasting (ALB), tribochemical silica coating (SIL), or one of two UPL patterns: multiple pulses laser surface dots with 2.5 μm spacing (8 mJ, 10 kHz)(LSD); or single pulse laser surface lines with 2.5 μm spacing (4 mJ, 6.7 kHz)(LSL). Surface roughness, wettability (contact angle), and quantification of crystalline phases were evaluated for each group (n = 3/group). Y-TZP treated slabs were cemented to resin composite slabs using silane and 10-methacryloyloxydecyl dihydrogen phosphate (MDP)-containing adhesive. Beams from the Y-TZP/resin blocks were microtensile tested (n = 5/group) after 48 h water incubation (37 °C) with or without subsequent thermocycling (5–55 °C, 5000 cycles).ResultsAll surface treatments increased surface roughness values versus control (P < 0.001). Contact angles were lowest for SIL (6.57 ± 2.37°) and highest for control (50.97 ± 6.30°). LSL and LSD were the only treatments that did not increase the relative monoclinic phase. All surface treatments significantly increased microtensile bond strengths (μTBS) compared with the control group (P < 0.001), with highest values for UPL (LSD: 35.40 ± 4.53 MPa > LSL: 31.84 ± 8.46 MPa > SIL: 19.95 ± 3.99 MPa = ALB: 19.51 ± 2.55 MPa > CTL: 14.51 ± 2.23 MPa). Thermocycling significantly reduced bond strength for all treatments in a surface treatment-dependent manner.SignificanceThe ability of UPL to alter Y-TZP surface morphology, increase wettability and μTBS without increasing the monoclinic content suggests its potential to improve bonding to the underlying resin cement and tooth without compromising the strength of the restoration.     

Bis-GMA co-polymerizations: Influence on conversion,flexural properties,fracture toughness and susceptibility to ethanol degradation of experimental composites

ObjectivesThe aim of this study was to evaluate the influence of monomer content on fracture toughness (K_Ic) before and after ethanol solution storage, flexural properties and degree of conversion (DC) of bisphenol A glycidyl methacrylate (Bis-GMA) co-polymers.MethodsFive formulations were tested, containing Bis-GMA (B) combined with TEGDMA (T), UDMA (U) or Bis-EMA (E), as follows (in mol%): 30B:70T; 30B:35T:35U; 30B:70U; 30B:35T:35E; 30B:70E. Bimodal filler was introduced at 80 wt%. Single-edge notched beams for fracture toughness (FT, 25 mm × 5 mm × 2.5 mm, a/w = 0.5, n = 20) and 10 mm × 2 mm × 1 mm beams for flexural strength (FS) and modulus (FM) determination (10 mm × 2 mm × 1 mm, n = 10) were built and then stored in distilled water for 24 h at 37 °C. All FS/FM beams and half of the FT specimens were immediately submitted to three-point bending test. The remaining FT specimens were stored in a 75%ethanol/25%water (v/v) solution for 3 months prior to testing. DC was determined with FT-Raman spectroscopy in fragments of both FT and FS/FM specimens at 24 h. Data were submitted to one-way ANOVA/Tukey test (α = 5%).ResultsThe 30B:70T composite presented the highest K_Ic value (in MPa m^1/2) at 24 h (1.3 ± 0.4), statistically similar to 30B:35T:35U and 30B:70U, while 30B:70E presented the lowest value (0.5 ± 0.1). After ethanol storage, reductions in K_Ic ranged from 33 to 72%. The 30B:70E material presented the lowest reduction in FT and 30B:70U, the highest. DC was similar among groups (69–73%), except for 30B:70U (52 ± 4%, p < 0.001). 30B:70U and 30B:35T:35U presented the highest FS (125 ± 21 and 122 ± 14 MPa, respectively), statistically different from 30B:70T or 30B:70E (92 ± 20 and 94 ± 16 MPa, respectively). Composites containing UDMA or Bis-EMA associated with Bis-GMA presented similar FM, statistically lower than 30B:35T:35U.SignificanceComposites formulated with Bis-GMA:TEGDMA:UDMA presented the best compromise between conversion and mechanical properties.     

Response of composite resins to preheating and the resulting strengthening of luted feldspar ceramic

ObjectiveThis study evaluated the influence of preheating different composite resins on their viscosity and strengthening yielded to ceramic.MethodsModulus of elasticity, Poisson’s ratio, and degree of CC conversion were measured for three restorative composite resins (Z100–microhybrid; Empress Direct–nanohybrid; Estelite Omega–supranano) and one photoactivated resin cement (RelyX Veneer). Viscosity was measured during a heating-cooling curve (25 °C–69 °C–25 °C) and also using isothermal analyses at 25 °C and 69 °C. Feldspar ceramic disks simulating veneers were bonded with the luting materials. Biaxial flexural strength, characteristic strength, and Weibull modulus were calculated at axial positions (z = 0 and z = −t₂) of the bilayers. Film thickness was measured and morphology at the bonded interfaces was observed. Data were statistically analyzed (α = 0.05).ResultsA gradual decrease in viscosity was noticed as the rheometer temperature gradually increased. Viscosity differences between the composite resins were large at the beginning of the analysis, but minor at 69 °C. At 25 °C, the composites were up to 38 times more viscous than the resin cement; at 69 °C the difference was 5-fold. CC conversion was similar between all resin-based agents. The resin cement yielded lower film thickness than the composites. All resin-based agents were able to infiltrate the ceramic porosities at the interface and strengthen the ceramic. However, the magnitude of the strengthening effect was higher for the preheated composite resins, particularly at z = −t₂.SignificanceSelection of composite resin impacts its response to preheating and the resulting viscosity, film thickness, and magnitude of ceramic strengthening.     

Curing efficiency of four self-etching,self-adhesive resin cements

ObjectivesTo evaluate the degree of cure (%DC) of four self-etching, self-adhesive resin cements, and one conventional resin cement, in their self- and dual-curing mode.MethodsThe self-etching, self-adhesive resin cements studied were RelyX? Unicem (3M? ESPE? AG), Maxcem? (Kerr Corporation), Biscem? (Bisco, Inc.) and Multilink^® Sprint (Ivoclar Vivadent^® AG) and the classic resin cement was Multilink^® Automix (Ivoclar Vivadent^® AG). Twelve specimens of each material (1.8 mm × 4 mm × 4 mm) were prepared in room temperature (23 ± 1) °C following the manufacturers’ instructions. Six of them were treated as dual-cured, thus irradiated for 20 s with a halogen light curing unit and left undisturbed for 5 min. The other six were treated as self-cured and were not irradiated, but left in dark and dry conditions for 10 min. The assessment of the %DC was made using micro-ATR FTIR spectrometry.ResultsThe %DC in their self-curing mode was very low (10.82–24.93%), with Multilink Sprint exhibiting the highest values among the five. In the dual-curing mode the values obtained were also low (26.40–41.52%), with the exception of Multilink Automix (61.36%). Maxcem was found to have the lowest DC.SignificanceThe low %DC found raises questions as to whether these materials can be successfully used in clinical applications, where light attenuation takes place. Increased irradiation times could potentially lead to higher %DC, in applications where light is not completely blocked by the overlying restoration.     

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.     

Effect of platelet rich plasma on bone regeneration in maxillary sinus augmentation (randomized clinical trial)

This study evaluates bone quality in sinus augmented with autogenous bone with or without platelet rich plasma (PRP) mix. 15 partially edentulous patients requiring maxillary sinus floor augmentation, followed by implant insertion were studied. In Group I, 5 patients underwent maxillary sinus lifting with autogenous bone augmentation and implant insertion at 6 months post grafting. In Group II, 10 patients underwent maxillary sinus lifting with autogenous bone augmentation mixed with PRP prepared from the patient's own blood with implant insertion at 4 or 6 months post grafting (n = 5 for each implantation time). A core biopsy was taken at the time of implant placement for histological and histomorphometric evaluation. Immediately and 3 months after implantation, Group I showed the statistically significant highest mean bone density (p = 0.046 and 0.022, respectively). At 6 months post-implantation, Group II showed the statistically significant highest mean bone density (p = 0.041). Histomorphometric analysis showed that Group I had the statistically significant highest mean value (39.5 ± 7.4; p = 0.003). Enrichment with PRP did not significantly improve bone density or morphometric value at 3 months post grafting. PRP enriched bone grafts were associated with superior bone density at 6 months post grafting.     

Surface treatments of a glass-fiber reinforced composite: Effect on the adhesion to a composite resin

PurposeTo compare the effect of different surface treatments (pre-treatments and bonding agents) on the bond strength between glass-fiber post and composite resin, and the topographic alterations of the treated post surface.MethodsThirty-six glass-fiber blocks (12 mm × 10 mm × 8 mm) were specifically manufactured for this study and randomly assigned into 12 groups considering two factors: ‘pre-treatments’ (–cleaning with 70% alcohol; air-abrasion with silica-coated aluminum oxide particles; 35% hydrogen peroxide) and type of ‘bonding agent’ (no bonding agent; application of Monobond Plus; RelyX Ceramic Primer; Single Bond Universal). After that, 6 cylindrical templates ( 1mm high × 1 mm Ø) were fixed on each block, filled with composite resin (n = 18) and light-cured. Specimens were stored under 37 °C for 24 h and microshear tests (wire loop Ø = 0.2 mm) were performed. Topographic, roughness and failure analyses were also performed.ResultsDifferent surface pre-treatments led to different topographic and roughness alterations; a higher surface alteration was noted after silica particles air-abrasion, while a slight surface alteration in the hydrogen peroxide group and a smooth pattern were observed in the cleaning group. The factors ‘pre-treatments’ (p < 0.05), ‘bonding agent’ (p < 0.05) and their interaction (p < 0.05) influenced the bond strength. Silica coating, apart from bonding agent application, or Single Bond Universal application without pre-treatment promoted the highest bond values. The main failure type was adhesive at the resin-post interface.ConclusionsIn terms of pre-treatments, silica coating promotes the best bonding performance, but pre-treatments can be dispensable when applying Single Bond Universal.     

Effects of different abutment material and surgical insertion torque on the marginal adaptation of an internal conical interface: An in vitro study

PurposeTo evaluate the marginal adaptation at implant–abutment connection of an implant featuring a conical (45° taper) internal hexagonal abutment with a connection depth of 2.5 mm, comparing the performance of two identical abutments of different material (titanium grade-4 and Co-Cr-alloy).MethodsTwenty implants (3.75 mm × 15 mm) were connected to non-matching abutments (5.5 mm × 10 mm) of two different materials (titanium grade-4: n = 10; Co-Cr-alloy: n = 10). The specimens were separately embedded in epoxylite resin, inside copper cylinders, and submerged without covering the most coronal portion (5 mm) of the fixture. Five specimens per group were stressed simulating a surgical 100 Ncm insertion torque, while the others had no torque simulation. All specimens were subjected to a non-axial static load (100 N) in a universal testing machine, under an angle of 30° with respect to the implant axis. Once 100 N load was reached, low shrinkage self-curing resin was injected inside the cylinders, and load was maintained until complete resin polymerization. Specimens were cut and analyzed with optical and scanning-electron-microscope (SEM) to evaluate the marginal adaptation at the implant–abutment connection. Statistical analysis was performed using one-way ANOVA (p = 0.02).ResultsNone of the 20 samples failed. The implant–abutment connection was able to guarantee a good optical seal; SEM analysis confirmed the absence of microgaps.ConclusionsWithin the limits of this study (small sample size, limited time) the marginal adaptation of the implant–abutment connection was not affected by the abutment material nor by the application of surgical insertion torque.     

Graded structures for damage resistant and aesthetic all-ceramic restorations

ObjectivesClinical studies revealed several performance deficiencies with alumina- and zirconia-based all-ceramic restorations: fracture; poor aesthetic properties of ceramic cores (particularly zirconia cores); and difficulty in achieving a strong ceramic–resin-based cement bond. We aim to address these issues by developing a functionally graded glass/zirconia/glass (G/Z/G) structure with improved damage resistance, aesthetics, and cementation properties.MethodsUsing a glass powder composition developed in our laboratory and a commercial fine zirconia powder, we have successfully fabricated functionally graded G/Z/G structures. The microstructures of G/Z/G were examined utilizing a scanning electron microscopy (SEM). The crystalline phases present in G/Z/G were identified by X-ray diffraction (XRD). Young's modulus and hardness of G/Z/G were derived from nanoindentations. Critical loads for cementation radial fracture in G/Z/G plates (20 mm × 20 mm, 1.5 or 0.4 mm thick) bonded to polycarbonate substrates were determined by loading with a spherical indenter. Parallel studies were conducted on homogeneous yttria-stabilized tetragonal zirconia polycrystal (Y-TZP) controls.ResultsThe G/Z/G structure consists of an outer surface aesthetic glass layer, a graded glass–Y-TZP layer, and a dense Y-TZP interior. The Young's modulus and hardness increase from surface to interior following power-law relations. For G/Z/G plates of 1.5 and 0.4 mm thick, critical loads for cementation radial fracture were 1990 ± 107 N (mean ± S.D., n = 6) and 227 ± 20 N (mean ± S.D., n = 6), respectively, which were ～30 and 50% higher than those for their monolithic Y-TZP counterparts (1388 ± 90 N for 1.5 mm and 113 ± 10 N for 0.4 mm thick; mean ± S.D., n = 6 for each thickness). A 1-sample t-test revealed significant difference (p < 0.001) in critical loads for radial fracture of G/Z/G and homogeneous Y-TZP for both specimen thicknesses.SignificanceOur results indicate that functionally graded G/Z/G structures exhibit improved damage resistance, aesthetics, and potentially cementation properties compared to homogeneous Y-TZP.     

Adhesion procedures for CAD/CAM indirect resin composite block: A new resin primer versus a conventional silanizing agent

PurposeThe purpose of this study was to evaluate the effectiveness of both a resin primer containing methyl methacrylate (MMA) and a silanizing agent on bonding to indirect resin composite blocks, using two types of build-up hybrid resin composites.MethodsSHOFU BLOCK HC (Shofu) specimens were blasted with alumina, after which one of two surface treatments was applied: CERA RESIN BOND (Shofu, the Silane group) or HC primer (Shofu, the MMA group). Resin composites made using either Solidex Hardura (SDH, Shofu) or Ceramage Duo (CMD, Shofu) were built up and micro-tensile bond strength (μTBS) values were measured after storage in water for either 24 h or 6 months (n = 24 per group). The fracture surfaces after μTBS measurements and the resin block/build-up resin interfaces were observed by scanning electron microscopy (SEM).ResultsThe bond strength of the Silane/SDH group significantly decreased after 6 months (p < 0.001), whereas in the MMA group there was no significant loss after 24 h or 6 months (p = 0.99). In the CMD group, the bond strength after 6 months was significantly lowered in both the Silane group (p < 0.001) and the MMA group (p < 0.001), but the latter still showed greater adhesion. SEM images demonstrated that the matrix resin was partially destroyed at the fracture surfaces of the MMA group and fracture surface unevenness was observed.ConclusionsA primer containing MMA produced stronger bonding to CAD/CAM resin even after long-term aging compared to a silane treatment.     

Comparative effects of tungsten,diamond burs and laser for residual adhesive removal after orthodontic debonding on flexural strength,surface roughness and phase transformation of high-translucent zirconia: An in vitro study

ObjectivesInformation regarding the effects of orthodontic bracket debonding on zirconia restorations, and the preferred method for residual adhesive removal from the zirconia restoration surface is lacking. Thus, this study aimed to assess the effects of different methods of residual adhesive removal after orthodontic bracket debonding on flexural strength, surface roughness, and phase transformation of high-translucent (HT) zirconia.Materials and methodsThis in vitro study evaluated 72 bar-shaped HT zirconia specimens; 18 specimens were assigned to the control group. Metal brackets were bonded to the remaining specimens by resin cement. After bracket debonding, the residual adhesive on the surface of specimens was removed by three methods (n = 18): a 30-flute tungsten-carbide (TC) bur at low speed, an ultrafine diamond bur at high speed, and Er:YAG laser irradiation. The surface roughness (Ra and Rz) was measured. X-ray diffraction (XRD) analysis was carried out, and the flexural strength was measured as well. Data were statistically analyzed (α = 0.05).ResultsBefore polishing, all methods increased the Ra and Rz values (P < 0.05) except for the diamond bur yielding a Rz value comparable to that of the control group. The Ra values of the test groups were comparable after polishing, and still higher than that of the control group (P < 0.05). The flexural strength of all three test groups was comparable (P > 0.05), and significantly lower than that of the control group (P < 0.001). The monoclinic phase was not observed in any group.ConclusionsOrthodontic bracket debonding adversely affects the surface roughness and flexural strength of zirconia despite polishing.     

Effect of storage in artificial saliva and thermal cycling on Knoop hardness of resin denture teeth

PurposeThis study aimed to evaluate the effect of different storage periods in artificial saliva and thermal cycling on Knoop hardness of 8 commercial brands of resin denture teeth.MethodsEigth different brands of resin denture teeth were evaluated (Artplus group, Biolux group, Biotone IPN group, Myerson group, SR Orthosit group, Trilux group, Trubyte Biotone group, and Vipi Dent Plus group). Twenty-four teeth of each brand had their occlusal surfaces ground flat and were embedded in autopolymerized acrylic resin. After polishing, the teeth were submitted to different conditions: (1) immersion in distilled water at 37 ± 2 °C for 48 ± 2 h (control); (2) storage in artificial saliva at 37 ± 2 °C for 15, 30 and 60 days, and (3) thermal cycling between 5 and 55 °C with 30-s dwell times for 5000 cycles. Knoop hardness test was performed after each condition. Data were analyzed with two-way ANOVA and Tukey's test (α = .05).ResultsIn general, SR Orthosit group presented the highest statistically significant Knoop hardness value while Myerson group exhibited the smallest statistically significant mean (P < .05) in the control period, after thermal cycling, and after all storage periods. The Knoop hardness means obtained before thermal cycling procedure (20.34 ± 4.45 KHN) were statistically higher than those reached after thermal cycling (19.77 ± 4.13 KHN). All brands of resin denture teeth were significantly softened after storage period in artificial saliva.ConclusionStorage in saliva and thermal cycling significantly reduced the Knoop hardness of the resin denture teeth. SR Orthosit denture teeth showed the highest Knoop hardness values regardless the condition tested.     

Effect of propionaldehyde or 2,3-butanedione additives on the mechanical properties of Bis-GMA analog-based composites

ObjectivesThe purpose of this study was to evaluate the effect of two additives, propionaldehyde/aldehyde or 2,3-butanedione/diketone, on mechanical properties of Bis-GMA-based composites containing TEGDMA, propoxylated Bis-GMA (CH₃Bis-GMA) or propoxylated fluorinated Bis-GMA (CF₃Bis-GMA).MethodsThree control composites, Bis-GMA/diluent monomer (25/75 mol%), and six test composites, Bis-GMA/diluent monomer/aldehyde or diketone (17/51/32 mol%) were prepared. All composites contained hybrid treated filler (barium aluminosilicate glass/pyrogenic silica; 60 wt%), and 0.2 wt% each of camphorquinone and N,N-dimethyl-p-toluidine. Degree of conversion (DC%), flexural strength (FS), modulus of elasticity (E), modulus of resilience (R) and diametral tensile strength (DTS) were determined. DC% (n = 3) was investigated by FT-IR. For FS and E, beam-shaped specimens (25 mm × 2 mm × 2 mm) were prepared (n = 6), stored for 7 days in 37 °C deionized water and tested on an Instron utilizing a three-point loading jig (0.5 mm/min). The R-values were obtained from the following equation: R = (FS)²/2E. For DTS, cylindrical specimens (4 mm × 8 mm) were prepared (n = 6), stored for 7 days in 37 °C deionized water and diametrically loaded on an Instron (0.5 mm/min). Data were analyzed by one-way ANOVA and Tukey's test (α = 0.05).ResultsIncorporation of additives led to an increase in DC%, FS and E for Bis-GMA/TEGDMA and Bis-GMA/CH₃Bis-GMA systems. R-values for all systems were unaffected by addition of additives. They had no significant effect on DC% or mechanical properties of Bis-GMA/CF₃Bis-GMA.SignificanceThe findings correlate with the ability of additives to improve degree of conversion of some composite systems thereby enhancing mechanical properties.