Days Of Water Storage Research Articles

Effects of solvent evaporation on water sorption/solubility and nanoleakage of adhesive systems

ObjectiveTo evaluate the influence of solvent evaporation in the kinetics of water diffusion (water sorption-WS, solubility-SL, and net water uptake) and nanoleakage of adhesive systems. Material and MethodsDisk-shaped specimens (5.0 mm in diameter x 0.8 mm in thickness) were produced (N=48) using the adhesives: Clearfil S3 Bond (CS3)/Kuraray, Clearfil SE Bond - control group (CSE)/Kuraray, Optibond Solo Plus (OS)/Kerr and Scotchbond Universal Adhesive (SBU)/3M ESPE. The solvents were either evaporated for 30 s or not evaporated (N=24/per group), and then photoactivated for 80 s (550 mW/cm2). After desiccation, the specimens were weighed and stored in distilled water (N=12) or mineral oil (N=12) to evaluate the water diffusion over a 7-day period. Net water uptake (%) was also calculated as the sum of WS and SL. Data were submitted to 3-way ANOVA/Tukey's test (α=5%). The nanoleakage expression in three additional specimens per group was also evaluated after ammoniacal silver impregnation after 7 days of water storage under SEM. ResultsStatistical analysis revealed that only the factor "adhesive" was significant (p<0.05). Solvent evaporation had no influence in the WS and SL of the adhesives. CSE (control) presented significantly lower net uptake (5.4%). The nanoleakage was enhanced by the presence of solvent in the adhesives. ConclusionsAlthough the evaporation has no effect in the kinetics of water diffusion, the nanoleakage expression of the adhesives tested increases when the solvents are not evaporated.

Zirconia-composite bonding after plasma of argon treatment.

To compare the shear bond strength (SBS) values of resin cement to zirconia treated with a new activating method. Forty-five zirconia specimens were divided into three groups: no treatment (group 1), plasma of argon cleaning for 375 seconds (group 2), and plasma of argon cleaning for 750 seconds (group 3). Composite cylinders were bonded with a self-adhesive cement. After 40 days of water storage, specimens were subjected to the SBS test. Data were analyzed with one-way analysis of variance and the Neuman-Keuls multiple comparison test. Test groups obtained SBS values significantly higher (101% for group 2 and 81% for group 3) than controls. Plasma of argon appeared to improve bonding between zirconia and resin cement.

Effect of Water Storage on the Flexural Strength of Four Self-etching Adhesive Resin Cements and on the Dentin-titanium Shear Bond Strength Mediated by Them

The aim of this study was to evaluate the effect of water storage on the flexural strength (σf) of four self-etching adhesive resin cements (SEARC) and on the dentin-titanium shear bond strength (SBS) mediated by them. The selected SEARC were Rely X Unicem, G-Cem, Maxcem, and SmartCem2. For each material, 50 bars (2×2×25 mm) were made and stored in water at 37°C for 1 hour, 1 day, 7 days, 30 days, and 60 days before σf was determined via a three-point bend test. Titanium cylinders were bonded to freshly exposed human dentin surfaces using the selected cements. Fifty samples were obtained for each SEARC and were stored in water at 37°C for 1 hour, 1 day, 7 days, 30 days, and 60 days before SBS was determined. The results were statistically analyzed using two-way analysis of variance followed by Scheffé multiple means comparisons (α=0.05). Pearson's correlation coefficient between σf and SBS was determined. Significantly different σf and SBS values were obtained for the four cements. With regards to the effect of water storage, the σf of all materials increased during the first 7 days, was not significantly different between materials by 30 days, and then remained relatively constant or decreased for SmartCem2; SBS was not affected by water storage, with the exception of Maxcem, where a significant drop in SBS was detected after 1 day and no deterioration thereafter. No correlation was found between σf and SBS. Under the experimental conditions of this study, 60 days of water storage negatively affected the σf of SmartCem2 but did not negatively affect the SEARC-mediated dentin-titanium SBS (Maxcem showed a significant drop in SBS after 1 day but no deterioration thereafter). The dentin-titanium adherence afforded by Rely X and G-Cem was significantly higher than that of Maxcem and SmartCem2.

Evaluation of a commercial primer for bonding of zirconia to two different resin composite cements.

To evaluate the effects of a commercial zirconia primer (Choice or RelyX Unicem) on shear bond strength (SBS) of two different resin composite cements - Choice (a conventional bis-GMA-based resin cement) and RelyX Unicem (self-adhesive resin cement) - to zirconia. Zirconia blocks were manufactured and randomly divided into 5 main groups (n = 20) that received surface treatments and cements as follows: no surface treatment, Choice and RelyX Unicem (groups C and U, resp.); tribochemical silica coating followed by silanization, Choice (group SSC); application of a zirconia primer, Choice and RelyX Unicem (groups ZC and ZU, resp.). Light-curing composite resin cylinders were prepared and bonded on the prepared zirconia blocks using the two different resin cements. Half of the specimens in each group were stored in water for 24 h, and half were aged by 50 days of water storage followed by thermocycling (12,000 cycles between 5°C and 55°C). Thereafter, all of them were submitted to the SBS test. Fourier transmission infrared (FT-IR) spectrum analysis and gas mass spectrometry (MS) analysis were adopted for characterization of the zirconia primer. Statistical analysis of the SBS test showed that group C presented the lowest SBS values and group SSC the highest (p < 0.01). Artificial aging exerted no influence on the SBS of groups U, SSC, ZC, or ZU. FT-IR analysis suggested that benzene rings and carboxylic groups exist in the zirconia primer. MS analysis detected that 2-hydroxyethyl methacrylate, triethylamine, ethyl-4-dimethylaminobenzoate, ethanol, and water are contained in the primer. The zirconia primer and self-adhesive resin cement increased the SBS of zirconia.

Efficient immobilization of mushroom tyrosinase utilizing whole cells from Agaricus bisporus and its application for degradation of bisphenol A

A simple and efficient procedure for preparation and immobilization of tyrosinase enzyme was developed utilizing whole cells from the edible mushroom Agaricus bisporus, without the need for enzyme purification. Tyrosinase activity in the cell preparation remained constant during storage at 21 °C for at least six months. The cells were entrapped in chitosan and alginate matrix capsules and characterized with respect to their resulting tyrosinase activity. A modification of the alginate with colloidal silica enhanced the activity due to retention of both cells and tyrosinase from fractured cells, which otherwise leached from matrix capsules. The observed activity was similar to the activity that was obtained with immobilized isolated tyrosinase in the same material. Mushroom cells in water were susceptible to rapid inactivation, whereas the immobilized cells maintained 73% of their initial activity after 30 days of storage in water. Application in repeated batch experiments resulted in almost 100% conversion of endocrine disrupting bisphenol A (BPA) for 11 days, under stirring conditions, and 50–60% conversion after 20 days, without stirring under continuous usage. The results represent the longest yet reported application of immobilized tyrosinase for degradation of BPA in environmental water samples.

Mechanical properties and modeling of drug release from chlorhexidine-containing etch-and-rinse adhesives

ObjectivesTo evaluate the effects of chlorhexidine (CHX) addition in different concentrations into simplified etch-and-rinse adhesives on the ultimate tensile strength (UTS), water sorption (WS), solubility (SO) and the rate of CHX release over time. MethodsWe added CHX diacetate to Ambar [AM] (FGM) and XP Bond [XP] (Dentsply) in concentrations of 0, 0.01, 0.05, 0.1 and 0.2wt%. For UTS (n=10 for each group), adhesive specimens were constructed in an hourglass shape metallic matrix with cross-sectional area of 0.8mm2. Half of specimens were tested after 24h and the other half after 28 days of water storage in tension of 0.5mm/min. For WS and SO (n=10 for each group), adhesive discs (5.8mm×1.0mm) were prepared into a mold. After desiccation, we weighed and stored the cured adhesive specimens in distilled water for evaluation of the WS, SO and the cumulative release of CHX over a 28-day period. For CHX release (n=10 for each group), spectrophotometric measurements of storage solution were performed to examine the release kinetics of CHX. We subjected data from each test to ANOVA and Tukey’ test (α=0.05). ResultsXP Bond adhesive showed significantly more WS and SO and lower UTS than Ambar. In general, the addition of CHX did not alter WS, SO and UTS of the adhesives. XP showed a higher CHX release than AM (p<0.05) in all concentrations and the final amount of CHX release was directly proportional to the initial CHX concentration added to the adhesives. After 28 days of water storage, approximately 20% of CHX was released from XP and 8.0–12.0% from AM. ConclusionsAddition of CHX to commercial adhesive is a feasible method to provide a controlled release of CHX over time without jeopardizing WS, SO and UTS of the adhesives. SignificanceManufacturers should consider adding CHX to commercial adhesives to provide a controlled release of CHX over time.

Survival and Growth of Vibrio cholerae, Escherichia coli, and Salmonella Spp. in Well Water Used for Drinking Purposes in Garoua (North Cameroon).

The ability of strains of faecal bacteria (Vibrio cholerae, Escherichia coli ATCC 25922, and four strains of Salmonella isolated, resp., from well water, pig, poultry, and human urine in Garoua) to survive or grow in well water microcosms was compared. Water samples were obtained from two wells in Garoua (north Cameroun). Autoclaving at 121°C for 15 min and filtration through 0.2 µm filter were used to make microcosms. Microcosms were constituted of unfiltered-autoclaved, filtered-nonautoclaved, and filtered-autoclaved well waters. Bacterial strains were inoculated at initial cell concentration of 3 Log10CFU/mL. All strains were able to survive/grow in used microcosms, and a maximal concentration of 5.61 Log10CFU/mL was observed. Survival abilities were strain and microcosm dependent. The declines were more pronounced in filtered-nonautoclaved water than in the other microcosms. E. coli and Salmonella sp. (poultry strain) lowered to undetectable levels (<1 Log10CFU/mL) after two days of water storage. V. cholera decreased over time, but surviving cells persisted for longer period in filtered-nonautoclaved water from well W1 (1.91 Log10CFU/mL) and well W2 (2.09 Log10CFU/mL). Competition for nutrients and/or thermolabile antimicrobial substances synthesized by “ultramicrocells” or by the autochthonous bacteria retained by the filter might affect the bacterial survival.

Silane-Treated E-Glass Fiber-Reinforced Telechelic Macromer-Based Polymer-Matrix Composites

The aim of this in vitro study was to investigate the water sorption and flexural properties of fiber reinforced composites (FRC) prepared from telechelic macromer extended urethane dimethacrylate (PEG-400-E-UEDMA)(PEG), hydroxypropyl methacrylate (HPMA) and E-glass fibers. Three experimental groups of test specimens based on poly(PEG-400-E-UEDMA-HPMA) polymer matrices and continuous unidirectional E-glass fibers were light polymerized and stored in deionized water for 0, 4, 12 or 24 weeks. The weight ratios (%) of PEG-HPMA were 27.5–70.5, 49.0–49.0 and 70.5–27.5 with an initiator-activator percentage of 1.0–1.0. After each time period of storage the water absorption and flexural properties were measured. There were six test specimens in each of the test groups (N = 6) and the specimen’s fracture surfaces were analyzed using scanning electron microscopy (SEM). All the PEG-HPMA groups exhibited the highest water absorption at the time point of two days (5.5 to 6.4 %), which thereafter decreased to the level of 3.8–4.7 % at the time point of 30 days. The flexural strength varied from dry specimens’ 128 to 283 MPa to the 30 days water-stored specimens’ of 30 to 49 MPa. The flexural modulus exhibited values from 7.9 to 14.8 GPa (dry specimens) and ca. 0.5 to 1.8 GPa after 30 days of water-storage. Both the flexural strength and modulus decrease dramatically with a longer water storage time. The SEM images showed good adhesion between the fibers and the resin matrix. In the wet conditions, the telechelic macromer based hydrophilic PEG polymer-matrix FRCs formed a plasticized composite that decreased the flexural properties.

Effects of Mesoporous Silica Coating and Postsynthetic Treatment on the Transverse Relaxivity of Iron Oxide Nanoparticles

Mesoporous silica nanoparticles have the capacity to load and deliver therapeutic cargo and incorporate imaging modalities, making them prominent candidates for theranostic devices. One of the most widespread imaging agents utilized in this and other theranostic platforms is nanoscale superparamagnetic iron oxide. Although several core-shell magnetic mesoporous silica nanoparticles presented in the literature have provided high T2 contrast in vitro and in vivo, there is ambiguity surrounding which parameters lead to enhanced contrast. Additionally, there is a need to understand the behavior of these imaging agents over time in biologically relevant environments. Herein, we present a systematic analysis of how the transverse relaxivity (r2) of magnetic mesoporous silica nanoparticles is influenced by nanoparticle diameter, iron oxide nanoparticle core synthesis, and the use of a hydrothermal treatment. This work demonstrates that samples which did not undergo a hydrothermal treatment experienced a drop in r2 (75% of original r2 within 8 days of water storage), while samples with hydrothermal treatment maintained roughly the same r2 for over 30 days in water. Our results suggest that iron oxide oxidation is the cause of the r2 loss, and this oxidation can be prevented both during synthesis and storage by the use of deoxygenated conditions during nanoparticle synthesis. The hydrothermal treatment also provides colloidal stability, even in acidic and highly salted solutions, and a resistance against acid degradation of the iron oxide nanoparticle core. The results of this study show the promise of multifunctional mesoporous silica nanoparticles but will also likely inspire further investigation into multiples types of theranostic devices, taking into consideration their behavior over time and in relevant biological environments.

Influence of heat treatment on the sorption and solubility of direct composite resins

Heat treatment allows the use of direct composite resins for fabrication of inlays/onlays restorations because it improves some mechanical and physical properties. The aim of this study is to analyze the influence of heat treatment on the water sorption and solubility of direct composite resins compared with an indirect composite resin. A total of 50 cylindrical specimens were fabricated (6 mm diameter × 2 mm high) and divided into five groups (n = 10): G1 (FillMagic without heat treatment-control 1), G2 (heat-treated FillMagic), G3 (P60 without heat treatment-control 1), G4 (heat-treated P60) and G5 (indirect resin Epricord-control 2). After fabrication, the specimens were placed in a desiccator containing silica gel and maintained at 37°C for 24 h. This cycle was repeated until a constant weight was achieved (m1). Following, the specimens were stored in individual flasks containing 2 ml of distilled water in an oven at 37°C. The specimens were weighed after intervals of 1, 7 and 21 days of immersion in water (m2). After 21 days of storage in water, the specimens were once again desiccated until a constant weight was achieved (m3). The mean diameter and thickness of specimens were obtained using a digital pachymeter. Two - way analysis of variance and Tukey's test were used to compare the sorption and solubility (α = 0.05). The type of resin significantly influenced the sorption (P = 0.01) and solubility (P = 0.00). The heat treatment also significantly influenced the sorption (P = 0.026) and solubility (P = 0.01). It was concluded that the heat treatment is an additional curing method that improves strength to the sorption and solubility of composite resins.

Experimental adhesives with different hydrophilicity: microshear test in after 1, 7, and 90 days' storage.

To assess the microshear bond strength of 3 experimental adhesives with different degrees of hydrophilicity after 1, 7 and 90 days of storage. The bonding effectiveness of three experimental two-step etch-and-rinse adhesives (bis- GMA, bis-EMA/bis-GMA, polybutadiene [C6H12]) and one commercial adhesive (Single Bond) to sound hydrated dentin was determined using the microshear test with delimitation of the adhesive area after 1, 7, and 90 days of storage in water at 37°C. Two-way ANOVA was performed at the 0.05 probability level. The fractures were classified as adhesive, cohesive in dentin, cohesive in resin, and mixed. The experimental adhesives showed values in the range of 11.31 to 12.96 MPa, with polybutadiene (PBH) showing the lowest bond strengths, bis-GMA the highest, and bis-EMA/bis-GMA intermediary values. Single Bond yielded bond strengths of approximately 24 MPa. Water storage decreased the bond strength in all adhesives. Adhesive fractures were predominant in experimental adhesives, while mixed fractures were the most frequent type in the Single Bond group. The experimental dentin adhesives of this study were able to form resin tags, but they could not penetrate into the collagen fibers and form hybrid layers. The resulting low bond strength decreased with increasing length of storage.

Effect of different palatal vault shapes on the dimensional stability of glass fiber-reinforced heat-polymerized acrylic resin denture base material

The aim of this study was to determine the effect of different palatal vault shapes on the dimensional stability of a glass fiber reinforced heat polymerized acrylic resin denture base material. Three edentulous maxilla with shallow, deep and medium shaped palatal vaults were selected and elastomeric impressions were obtained. A maxillary cast with four reference points (A, B, C, and D) was prepared to serve as control. Point (A) was marked in the anterior midline of the edentulous ridge in the incisive papillary region, points (B) and (C) were marked in the right and left posterior midlines of the edentulous ridge in the second molar regions, and point (D) was marked in the posterior palatal midline near the fovea palatina media (Figure 2). To determine linear dimensional changes, distances between four reference points (A-B, A-C, A-D and B-C) were initially measured with a metal gauge accurate within 0.1 mm under a binocular stereo light microscope and data (mm) were recorded. No significant difference of interfacial distance was found in sagittal and frontal sections measured 24 h after polymerization and after 30 days of water storage in any of experimental groups (P>.05). Significant difference of linear dimension were found in all experimental groups (P<.01) between measurements made 24 h after polymerization of specimens and 30 days after water storage. Palatal vault shape and fiber impregnation into the acrylic resin bases did not affect the magnitude of interfacial gaps between the bases and the stone cast surfaces.

Bond Strength and Interfacial Micromorphology of Etch‐and‐Rinse and Self‐Adhesive Resin Cements to Dentin

To evaluate the microtensile bond strength and interfacial micromorphology of indirect composite restorations to dentin using three commercial resin cements after 24 hours and 30 days of water storage. The medium dentin of third human molars was exposed (N = 30, n = 10 per group). Three commercial resin cements were used to cement indirect resin composite restorations to dentin: the auto-cured C&B Cement/All Bond 2, the dual-cured RelyX ARC/Adper Single Bond 2, and the self-adhesive dual-cured RelyX Unicem. Teeth were sectioned after water storage at 37°C (24 hours and 30 days) to obtain beams with a bonded area of 0.8 mm(2) . The specimens were tested in a universal testing machine at a 0.5 mm/min crosshead speed. Scanning electron microscopic fractographic and interfacial micromorphology analyses were performed. Data were analyzed using two-way ANOVA and Tukey's test (α= 0.05). Mean bond strength (MPa) after 24 hours: C&B Cement 19.5 ± 3.8, RelyX ARC 40.8 ± 9.4, RelyX Unicem 31.3 ± 7.4; after 30 days: C&B Cement 24.5 ± 5.1, RelyX ARC 44.2 ± 8.5, RelyX Unicem 28.3 ± 7.1. The mean bond strengths of both dual-cure cements were significantly higher than that obtained with C&B Cement after 24 hours. A significant increase in the bond strength of C&B Cement was verified after 30 days, reaching values statistically equivalent to those produced by RelyX Unicem and RelyX ARC. The self-adhesive cement preserved the same level of bond strength after 30 days. Fractographic analysis revealed a prevalence of cohesive fractures in the hybrid layer for C&B Cement, mixed (cohesive in the cement, hybrid layer, and adhesive) for RelyX ARC, and cohesive in the cement for RelyX Unicem. No distinguishable hybrid layer or resin tags were observed in the interaction of RelyX Unicem with dentin. The particular interaction of each cement with dentin results in specific bond strength and failure patterns that varied among groups in both evaluation times. Even though the self-adhesive cement tested exhibited no authentic hybrid layer, it was able to promote reliable adhesion with the underlying dentin.

Effect of silica coating on fracture strength of glass-infiltrated alumina ceramic cemented to dentin.

To examine the availability of sol-gel processed silica coating for alumina-based ceramic bonding, and determine which silica sol concentration was appropriate for silica coating. Sixty disks of In-Ceram alumina ceramic were fabricated and randomly divided into 5 main groups. The disks received 5 different surface conditioning treatments: Group Al, sandblasted; Group AlC, sandblasted + silane coupling agent applied; Groups Al20C, Al30C, and Al40C, sandblasted, silica coating via sol-gel process prepared using 20 wt%, 30 wt%, and 40 wt% silica sols, and then silane coupling agent applied. Before bonding, one-step adhesives were applied on pre-prepared ceramic surfaces of all groups. Then, 60 dentin specimens were prepared and conditioned with phosphoric acid and one-step adhesive. Ceramic disks of all groups were cemented to dentin specimens with dual-curing resin cements. Fracture strength was determined at 24 h and after 20 days of storage in water. Groups Al20C, Al30C, and Al40C revealed significantly higher fracture strength than groups Al and AlC. No statistically significant difference in fracture strength was found between groups Al and AlC, or among groups Al20C, Al30C, and Al40C. Fracture strength values of all the groups did not change after 20 days of water storage. Sol-gel processed silica coating can enhance fracture strength of In-Ceram alumina ceramic after bonding to dentin, and different silica sol concentrations produced the same effects. Twenty days of water storage did not decrease the fracture strength.

The Effect of Dentin Desensitizer on Shear Bond Strength of Conventional and Self-adhesive Resin Luting Cements After Aging

This study tested the impact of Gluma Desensitizer on the shear bond strength (SBS) of two conventional (RelyX ARC, Panavia 21) and two self-adhesive (RelyX Unicem, G-Cem) resin luting cements after water storage and thermocycling. Human third molars (N=880) were embedded in acrylic resin. The buccal dentin was exposed. Teeth were randomly divided into four main groups, and the following cements were adhered: 1) RelyX ARC, 2) Panavia 21, 3) RelyX Unicem, and 4) G-Cem. In half of the teeth in each group, dentin was treated with Gluma Desensitizer. In the conventional cement groups, the corresponding etchant and adhesive systems were applied. SBS of the cements was tested after 1 hour (initial); at 1, 4, 9, 16, and 25 days of water storage; and at 1, 4, 9, 16, and 25 days of thermocycling. SBS data were analyzed by one-way analysis of variance (ANOVA); this was followed by the post hoc Scheffé test and a t-test. Overall, the highest mean SBS (MPa) was obtained by RelyX ARC (ranging from 14.6 ± 3.9 to 17.6 ± 5.2) and the lowest by Panavia 21 in combination with Gluma Desensitizer (ranging from 0.0 to 2.9 ± 1.0). All tested groups with and without desensitizer showed no significant decrease after aging conditions compared with baseline values (p>0.05). Only the Panavia 21/Gluma Desensitizer combination showed a significant decrease after 4 days of thermocyling compared with initial values and 1 day thermocycling. Self-adhesive cements with Gluma Desensitizer showed increased SBS after aging conditions (ranging from 7.4 ± 1.4 to 15.2 ± 3) compared with groups without desensitizer (ranging from 2.6 ± 1.2 to 8.8 ± 2.9). No cohesive failures in dentin were observed in any of the test groups. Although self-adhesive cements with and without desensitizer presented mainly adhesive failures after water storage (95.8%) and thermocyling (100%), conventional cement (RelyX ARC) showed mainly mixed failures (90.8% and 89.2%, after water storage and thermocyling, respectively). Application of the Gluma Desensitizer to dentin before cementation had a positive effect on the SBS of self-adhesive cements.

Influence of NaOCl irrigation and water storage on the degradation and microstructure of the resin/primary dentin interface.

To evaluate the influence of NaOCl irrigation and water storage on the degradation and microstructure of the resin/dentin interface of primary teeth bonded with three different adhesive systems using the microtensile bond strength test (μTBS) and scanning electron microscopy (SEM). Ninety sound primary molars were used. Eighteen groups were formed according to different adhesive systems (Adper Single Bond 2, SB; Clearfil Protect Bond, CP; Adper Prompt L-Pop, APL) with or without 0.5% NaOCl irrigation and water-storage time (24 h, 45 days, 90 days). The middle dentin was exposed. In the NaOCl group, NaOCl irrigation was performed for 30 min, and all groups were restored with composite (Charisma). Sticks with a 1-mm2 cross-sectional area were prepared for the μTBS test. The data were analyzed by ANOVA and Tukey's test (p < 0.05). The failure modes, presence or absence of resin tags, and the resin/ dentin interface were evaluated by SEM, and data were analyzed using Cochran-Mantel-Haenszel statistics (p < 0.05). The μTBS of APL was significantly lower than the other groups regardless of treatment and storage time. A significant decrease of μTBS values after 90 days of water storage occurred only in the non-NaOCl irrigation groups. After 90 days of storage, resin tags partially disappeared in APL and CP, and in SB, 100% of the resin tags remained. The choice of adhesive system is one of the factors when bonding to primary dentin is considered. In this study, the etch-and-rinse and the two-bottle self-etching adhesive system produced the highest μTBS values irrespective of prior NaOCl irrigation even up to 90 days of water storage.

Enamel Margin Integrity of Class I One-bottle All-in-one Adhesive-based Restorations

To evaluate marginal adaptation of Class I restorations in enamel using contemporary one-bottle all-in-one adhesives, stressed by thermocycling (TC) and mechanical loading (ML). Ninety-six extracted human molars were prepared (standard Class I cavities: 3 mm deep, 6 mm wide mesio-distally, and 4 mm wide bucco-lingually). Twelve adhesive systems were used: OptiBond FL (OPT), Clearfil SE Bond (CSE) and Adper Prompt L-Pop (PLP) as controls, compared with nine one-bottle all-in-one adhesives - AdheSe One (AHO), Adper Easy Bond (EB), Bond Force (BF), G-Bond (GB), iBond Self Etch (IB), One Coat 7.0 (OC), OptiBond All-in-one (OPA), Clearfil Tri-S-Bond (TSB), Xeno V (XV). All teeth were restored using Filtek Z250 placed in three (one horizontal, two oblique) increments. Enamel margins were evaluated following 21 days of water storage, after thermocycling (2000 cycles: 5°C to 55°C), and after mechanical loading (150,000 cycles, 50 N). After each step, replicas were produced and quantitative SEM margin analysis was performed (200X) using defined criteria. The median values of % "continuous margin" following TC and ML, respectively, were: OPT(98.6/96.2), CSE(95.4/90.9), BF(81.7/68.1), GB(81.1/65.0), OPA(83.0/68.1), OC(64.1/41.3), TSB(59.3/42.2), EB(57.1/42.6), IB(38.4/27.6), PLP(36.6/21.5), XV(45.0/30.0), AHO(17.7/5.4). Statistical evaluation (Kruskal-Wallis test with Bonferroni adjustment, p < 0.05) revealed the following ranking for ML: OPT=CSE>BF=OPA=GB>OC=EB=TSB=XV =IB=PLP>AHO. All one-bottle all-in-one adhesives exhibited statistically significant lower marginal qualities in enamel compared to the etch-and-rinse system OPF and the two-step self-etching system CSE. The results obtained for GB, OPA and BF, however, were better than for the other all-in-one adhesives.

Bond strength of three luting agents to zirconia ceramic - influence of surface treatment and thermocycling

ObjectiveThis in vitro study aimed to evaluate the influence of different surface treatments, 3 luting agents and thermocycling on microtensile bond strength (µTBS) to zirconia ceramic. Material and MethodsA total of 18 blocks (5x5x4 mm) were fabricated from zirconia ceramic (ICE Zirkonia) and duplicated into composite blocks (Alphadent). Ceramic blocks were divided into 3 groups (n=6) according to the following surface treatments: airborne-particle abrasion (AA), silica-coating, (SC) (CoJet) and silica coating followed by silane application (SCSI) (ESPE Sil). Each group was divided into 3 subgroups (n=2) according to the 3 luting agents used. Resin-modified glass-ionomer cement (RMGIC, Ketac Cem Plus), self-adhesive resin cement (UN, RelyX Unicem) and adhesive resin cement (ML, MultiLink Automix) were used for bonding composite and zirconia blocks. Each bonding assembly was cut into microbars (10 mm long and 1±0.1 mm2). Seven specimens of each subgroup were stored in water bath at 37ºC for 1 week. The o ther 7 specimens were stored in water bath at 37ºC for 30 days then thermocycled (TC) for 7,500 cycles. µTBS values were recorded for each specimen using a universal testing machine. Statistical analyses were performed using a 3-way ANOVA model followed by serial 1-way ANOVAs. Comparison of means was performed with Tukey's HSD test at (α=0.05). ResultsµTBS ranged from 16.8 to 31.8 MPa after 1 week and from 7.3 to 16.4 MPa after 30 days of storage in water and thermocycling. Artificial aging significantly decreased µTBS (p<0.05). Considering surface treatment, SCSI significantly increased µTBS (p<0.05) compared to SC and AA. Resin cements (UN and ML) demonstrated significantly higher µTBS (p<0.05) compared to RMGIC cement. ConclusionsSilica coating followed by silane application together with adhesive resin cements significantly increased µTBS, while thermocycling significantly decreased µTBS.

Effects of Different Silane Coupling Agent Monomers on Flexural Strength of an Experimental Filled Resin Composite

The hydrolytic stability of various silane combinations and their effects on biomechanical properties and water sorption of an experimental dental composite made of bis-GMA and TEGDMA and silane-treated fillers were evaluated. Four silane coupling agents and their blends with a cross-linker silane were used as coupling agents for the 0.7-μm BaSiO3 fillers. The silanization was carried out in toluene containing 1% (v/v) of one of the four following organofunctional silane coupling agents: 3-acryloxypropyltrimethoxysilane, 3methacryloxypropyltrimethoxysilane, 3-styrylethyltrimethoxysilane and 3-isocyanatopropyltriethoxysilane. Blends of these functional silanes with 1% (v/v) of a cross-linker silane, 1,2- bis -(triethoxysilyl)ethane were also used for silanization. Composites were prepared by mixing 5.00 g Ba-glass filler with 2.00 g of a resin mixture consisting of bis-GMA (58.8 wt%) and TEGDMA (39.2 wt%) in a high-speed mixer. Threepoint bending test specimens (2.0 mm × 2.0 mm × 25.0 mm) were fabricated (n= 8) in a mould and photo-polymerized. The degree of conversion was measured with FT-IR. Biomechanical testing was carried out according to the ISO 10477 standard. Specimens were tested (flexural strength) after 30 days of water storage (37° C, distilled water). Water sorption and solubility (in wt%) were also measured on 1, 2, 3, 5, 7, 14, 21 and 30 days in water storage. Statistical analysis with ANOVA showed that the highest flexural strength was obtained when 3-acryloxypropyltrimethoxysilane + 1,2- bis -(triethoxysilyl)ethane (100.5 MPa; SD, 25.7 MPa) was used in the silanization step, and the lowest was obtained when 3isocyanatopropyltriethoxysilane + 1,2- bis-(triethoxysilyl)ethane (28.9 MPa; SD, 8.8 MPa) was used. The three-point bending strength was significantly affected by the functionality of the main silane tested (p< 0.05), but not by the addition of the cross-linker silane ( p> 0.05). The composite that had been silanized with 3-isocyanatopropyltriethoxysilane had the greatest amount of water uptake (1.75%), and the composite silanized with 3-methacryloxypropyltrimethoxysilane + 1,2- bis-(triethoxysilyl)ethane had the least (1.08%). In conclusion, selection of the functional silane monomer can be a significant factor in developing filled resin composites in dentistry.

Differential hydrolytic degradation of dentin bonds when luting carbon fiber posts to the root canal

The purpose of the study was to evaluate the effect of water storage, adhesive system and root canal region on the hydrolytic degradation of dentin bonds to carbon fiber posts. Fiber posts were bonded to the root canals using different adhesive systems and composites: SB1 XT group (Scotchbond 1 XT/RelyX ARC), OBF group (One Up Bond F Plus/Ionotite F), and AB2 group (All Bond 2/C&B) After water storage (10 days), all roots were sectioned into 1 mm beams and divided into coronal or apical group. The specimens were stored in water at 22-26 °C temperature for 15 or 60 days and tested for microtensile bond strength at a crosshead speed of 0.9 mm/min after the calculation of the bonding area. Statistical analysis was performed with ANOVA followed by Tukey test to detect differences between groups (α=0.05). SEM investigation was performed to determine the mode of fracture. Bond strength at coronal and apical half showed significant differences between experimental groups both after 15 and 60 days of water storage. Premature failures were observed in 16-20% of specimens before storage in water. For the bonding systems tested, clinicians should consider that bond strength inside the root canal at apical half is lower than at coronal half irrespective of the adhesive system. The adhesion within the root canal is possible for SB1 XT and OBF groups unlike the AB2 group where adhesion to root canal dentine is not reliable. Nevertheless, apical half represents the worst scenario in which is possible to obtain a durable adhesion.