Amelogenin-inspired peptide, calcium phosphate solution, fluoride and their synergistic effect on enamel biomimetic remineralization: an in vitro pH-cycling model.

BACKGROUND: Several methods were introduced for enamel biomimetic remineralization that utilize a biomimetic analogue to interact and absorb bioavailable calcium and phosphate ions and induce crystal nucleation on demineralized enamel. Amelogenin is the most predominant enamel matrix protein that is involved in enamel biomineralization. It plays a major role in developing the enamel's hierarchical microstructure. Therefore, this study was conducted to evaluate the ability of an amelogenin-inspired peptide to promote the remineralization potential of fluoride and a supersaturated calcium phosphate solution in treating artificially induced enamel carious lesions under pH-cycling regimen. METHODS: Fifty enamel slices were prepared with a window (4*4 mm2 ) on the surface. Five samples were set as control healthy enamel and 45 samples were subjected to demineralization for 3 days. Another 5 samples were set as control demineralized enamel and 40 enamel samples were assigned into 8 experimental groups (n=5) (P/I, P/II, P/III, P/AS, NP/I, NP/II, NP/III and NP/AS) according to peptide treatment (peptide P or non-peptide NP) and remineralizing solution used (I; calcium phosphate solution, II; calcium phosphate fluoride solution, III; fluoride solution and AS; artificial saliva). Samples were then subjected to demineralization/remineralization cycles for 9 days. Samples in all experimental groups were evaluated using Raman spectroscopy for mineral content recovery percentage, microhardness and nanoindentation as healthy, demineralized enamel and after pH-cycling. Data were statistically analysed using two-way repeated measures Anova followed by Bonferroni-corrected post hoc test for pairwise multiple comparisons between groups. Statistical significance was set at p= 0.05. Additionally, XRD, FESEM and EDXS were used for crystal orientation, surface morphology and elemental analysis after pH-cycling. RESULTS: Nanocrystals clumped in a directional manner were detected in peptide-treated groups. P/II showed the highest significant mean values in mineral content recovery (63.31%), microhardness (268.81±6.52 VHN), elastic modulus (88.74±2.71 GPa), nanohardness (3.08±0.59 GPa) and the best crystal orientation with I002/I300 (1.87±0.08). CONCLUSION: Despite pH changes, the tested peptide was capable of remineralizing enamel with ordered crystals. Moreover, the supplementary use of calcium phosphate fluoride solution with peptide granted an enhancement in enamel mechanical properties after remineralization.

Regenerative potential of a novel aloe vera modified tricalcium silicate cement as a pulp capping material: An animal study.

This study compared the histologic response of a pulp capping material Matreva MTA modified with different concentrations of aloe vera (AV) solutions to Biodentine cement. Ninety dogs' teeth were included and categorized according to the capping material into five groups (18 teeth each); Group I (Biodentine), group II (Matreva MTA), group III (Matreva MTA 10% AV), group IV (Matreva MTA 20% AV) and group V (Matreva MTA 30% AV). The histopathological findings were recorded at 2, 4, and 8 weeks. Matreva MTA and Biodentine groups showed the highest inflammatory cell count compared to the AV-modified Matreva MTA groups at 2- and 4-week intervals (p>0.05). Moreover, the AV-modified Matreva MTA and Biodentine groups showed higher dentin bridge thickness compared to unmodified Matreva MTA at different follow-up periods (p<0.05). AV can significantly enhance the in vivo bioactivity of Matreva MTA, inducing mild inflammation and good dentine bridge formation comparable to Biodentine.

Effect of incorporation of nano-graphene oxide on physicochemical, mechanical, and biological properties of tricalcium silicate cement.

OBJECTIVE: Evaluation of setting time, compressive strength, pH, calcium ion release, and antibacterial activity of mineral trioxide aggregate (MTA) after modification with three different concentrations of nano-graphene oxide (GO) powder compared to unmodified Biodentine as a commercial control. METHODS: GO powder, unhydrated and hydrated cements were characterized using Environmental Scanning Electron Microscope (ESEM) with Energy Dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Raman Spectroscopy, and Fourier Transform Infrared spectroscopy (FTIR). GO was also analyzed using Scanning Transmission Electron Microscope (STEM) to determine average lateral dimensions. Specimens were prepared and grouped according to the concentration of GO added to Rootdent MTA (control, 1, 3, and 5 wt%) and the material used (MTA and unmodified Biodentine) into five groups. Setting time was evaluated using Gillmore penetrometer (n = 5). Compressive strength was evaluated using universal testing machine (n = 7). pH and calcium ion release were assessed using pH meter and Induced Coupled Plasma-Optical Emission Spectroscopy (ICP-OES) at 1, 7, 14, and 28 days (n = 7). Antibacterial activity was evaluated against Streptococcus mutans using direct contact test (n = 7). One-way and repeated measures ANOVA followed by Tukey's post hoc test were used for data analysis with significance level set at p ≤ 0.05. RESULTS: Addition of GO to MTA reduced both initial and final setting time. GO modified MTA groups and unmodified Biodentine showed significantly increased calcium ion release at 14 and 28 days. All cements showed alkaline pH of the storage media at all tested time intervals. 1 wt% GO recorded the highest compressive strength values in MTA modified groups. The increased concentration of GO from 1 to 5 wt% successively increased antibacterial activity of MTA, with Biodentine showing the lowest significant value. CONCLUSION: Addition of 1 wt% GO can significantly improve the tested properties of tricalcium silicate-based cements without compromising their compressive strength. CLINICAL SIGNIFICANCE: GO is a promising modification for tricalcium silicate cements to improve setting time, compressive strength, and antibacterial activity to provide a variety of materials for different clinical situations. This in turn can reduce the risk of reinfection and allow placement of the final restoration in a single visit.

Effect of dentin biomodification using natural collagen cross-linkers on the durability of the resin-dentin bond and demineralized dentin stiffness.

OBJECTIVE: The purpose of this study was to evaluate the effect of using natural cross-linkers as sumac and curcumin on the durability of the resin-dentin bond and stiffness of demineralized dentin matrix. METHODS: Thirty sound molars were divided into 5 groups: Control (CO), Grape Seed extract (GSE), Cacao seed extract (CSE), Sumac extract (SE) and Curcumin extract (CE). The teeth had their coronal dentin exposed, etched, and pre-treated for 1 min with the extracts. Teeth were then bonded using Single-Bond II adhesive and 4 mm composite was built up on dentin surface. Teeth were sectioned into 1 × 1 × 8mm beams and their micro-tensile bond strength (µTBS) was tested after 24 h and 6 months of water storage. For stiffness testing, 15 teeth were sectioned to obtain dentin beams (1 × 1 × 6.5 mm), the beams were demineralized in 10% phosphoric acid then rinsed and divided into 5 groups. Beams were then immersed in their respective extract solution for 1 min after which they were subjected to a 3- point loading test using a universal testing machine to calculate their modulus of elasticity. RESULTS: After 24 h, no significant difference in µTBS was shown between all groups. After 6 Months, GSE, CE, and SE showed significantly higher µTBS compared to CO (p ≥ 0.05). For the modulus of elasticity; only GSE showed a significantly higher modulus compared to other groups. CLINICAL RELEVANCE: The application of grape seed extract, curcumin and sumac extract as dentin pre-treatments appear to be a promising approach to enhance the durability of the resin-dentin bond in a clinically relevant application time.

Effect of Ionizing Radiation on the Mechanical Properties of Two Dental Materials Commonly Used in Primary Teeth.

Aim: The purpose of this in vitro study was to evaluate the effect of radiotherapy on flexural strength, microhardness, and surface roughness of bulk fill composite (X-tra fil) and glass ionomer (EQUIA Forte HT). Materials and methods: A total of 40 specimens were prepared for each test and were divided into two groups according to the material used (composite or glass ionomer cement), and each group was divided into two subgroups (n = 10) according to radiation condition, irradiated subgroup, subjected to 50 Gy by multienergy linear accelerator delivered in one shot and control subgroup. Results: Control samples of flexural strength and microhardness had a significantly higher value than irradiated samples in both materials. Regarding the surface roughness, irradiated samples had a significantly higher value than the control samples in both materials. Conclusion: Irradiation with a linear accelerator had a negative impact on the flexural strength and microhardness of both materials. Moreover, it increased the surface roughness for both materials. Bulk fill composite is the dental restorative material of choice in head and neck cancer patients undergoing radiotherapy due to its high mechanical properties before and after radiation. How to cite this article: Nagi BM, El-Korashy DI, Amin A El-S, et al. Effect of Ionizing Radiation on the Mechanical Properties of Two Dental Materials Commonly Used in Primary Teeth. Int J Clin Pediatr Dent 2023;16(5):758-762.

Effect of different surface treatments on the bonding potential and physical and mechanical properties of ultratranslucent zirconia.

STATEMENT OF PROBLEM: Studies to determine a suitable surface treatment that improves bonding without compromising the strength or translucency of ultratranslucent zirconia are scarce. PURPOSE: The purpose of this in vitro study was to evaluate the effect of different surface treatments on translucency, surface topography, phase transformation, biaxial flexural strength, bond strength, and durability. MATERIAL AND METHODS: A total of 169 ultratranslucent zirconia disks were randomly divided into 4 groups according to the surface treatment applied: airborne-particle abrasion (APA) (n=46), tribochemical silica airborne-particle abrasion (TS) (n=46), nonthermal oxygen plasma (NTP) (n=46), and no treatment, control (C) (n=31). The translucency parameter (ΔTP00) was evaluated with a spectrophotometer (n=15), phase transformation was assessed with an X-ray diffractometer (n=5), surface topography was evaluated with a scanning electron microscope (SEM) (n=3), and biaxial flexural strength (BFS) was tested with a universal testing machine (n=15). For the microshear bond strength (µSBS) test, 40 composite resin specimens were attached to 8 disks and tested with a universal testing machine; 20 specimens were tested after 24 hours, and 20 specimens after hydrothermal aging in a thermocycler (TC). The data were analyzed with ANOVA followed by the Tukey post hoc test (α=.05). Weibull analysis was performed for the flexural strength and µSBS results. RESULTS: Significant ΔTP00 differences were found among all groups and were highest for the APA group (7.33) and lowest for the NTP group (4.79). The NTP group had a significantly higher monoclinic weight fraction value (4.54%) than other groups. The NTP group had significantly higher BFS (581.31) than other groups, while the APA group showed significantly lower values than other groups (340.43). The APA group had significantly higher µSBS values after 24 hours (13.51 MPa) and after TC (13.68 MPa) than the other groups (P<.05). CONCLUSIONS: Although APA and TS are effective techniques for improving resin-zirconia bonding, they result in significantly higher deterioration of translucency and strength. NTP significantly improved the BFS of zirconia; however, it showed lower bond strength values than other methods.

Durability of bond strength to dentin using two universal adhesives in different etching modes

Aim. To evaluate the bond durability of two universal adhesives; mild and ultra-mild in both etch-and-rinse and self-etch modes after simulated in-vitro degradation by long-term water storage or thermocycling. Methods. A total of 144 specimens were used in this study; 120 specimens (prepared from 30 teeth) for microshear bond strength testing and fracture mode assessment, and 24 specimens for scanning electron microscopic evaluation (prepared from 24 teeth). Specimens were prepared from 54 recently extracted caries free third molars and randomly divided into 12 groups, according to the adhesive treatment (All Bond or Scotchbond Universal), etching mode (etch-andrinse or self-etch) and aging method (thermocycling or water storage). Each tooth was sectioned mesio-distally into two halves exposing free dentin surface for bonding where dentin substrate 1 mm below the dentino-enamel junction was used. After adhesive application and composite build up, specimens were tested in shear mode after storing in distilled water at 37˚C for 24 hours or 1 year, or after being thermocycled between 5 and 55 °C for 10,000 cycles (n=10). Microshear bond strength (µSBS) was tested using a universal testing machine. Adhesive-dentin interface was examined using scanning electron microscope (SEM) (n=2). Data were analyzed using 3 way AN0VA and pairwise comparisons was performed using Bonferroni correction at significance level of α ≤0.05. Results. Statistical analysis revealed non-significant difference for etching mode in both adhesives (p=0.596). After aging, the bond strength was only reduced in Scotchbond Universal after one year of water storage in both modes (p<0.001). SEM evaluation revealed intact hybrid layer and longer resin tags for etch-and-rinse mode than selfetch mode of both adhesives. Conclusion. The bond strength of universal adhesives is not affected by the etching mode, however its durability was shown to be material dependent

Electrospun nano-fibrous bilayer scaffold prepared from polycaprolactone/gelatin and bioactive glass for bone tissue engineering.

This work is focused on integrating nanotechnology with bone tissue engineering (BTE) to fabricate a bilayer scaffold with enhanced biological, physical and mechanical properties, using polycaprolactone (PCL) and gelatin (Gt) as the base nanofibrous layer, followed by the deposition of a bioactive glass (BG) nanofibrous layer via the electrospinning technique. Electrospun scaffolds were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy. Surface area and porosity were evaluated using the nitrogen adsorption method and mercury intrusion porosimetry. Moreover, scaffold swelling rate, degradation rate and in vitro bioactivity were examined in simulated body fluid (SBF) for up to 14 days. Mechanical properties of the prepared scaffolds were evaluated. Cell cytotoxicity was assessed using MRC-5 cells. Analyses showed successful formation of bead-free uniform fibers and the incorporation of BG nanoparticles within fibers. The bilayer scaffold showed enhanced surface area and total pore volume in comparison to the composite single layer scaffold. Moreover, a hydroxyapatite-like layer with a Ca/P molar ratio of 1.4 was formed after 14 days of immersion in SBF. Furthermore, its swelling and degradation rates were significantly higher than those of pure PCL scaffold. The bilayer's tensile strength was four times higher than that of PCL/Gt scaffold with greatly enhanced elongation. Cytotoxicity test revealed the bilayer's biocompatibility. Overall analyses showed that the incorporation of BG within a bilayer scaffold enhances the scaffold's properties in comparison to those of a composite single layer scaffold, and offers potential avenues for development in the field of BTE.

Physical and mechanical evaluation of dental resin composite after modification with two different types of Montmorillonite nanoclay.

OBJECTIVES: Evaluation of degree of conversion (DC), flexural properties, micro-hardness and color change (ΔE00) of dental resin composite after modification with two types of organo-modified Montmorillonite (MMT) nanoclay; an experimentally synthesized polymethyl-methacrylate modified MMT nanoclay (PMMA/MMT), and a commercially available one (Cloisite20A). METHODS: MMT was synthesized by sol-gel technique, organo-modified with polymethyl-methacrylate and characterized using EDX, XRD and FTIR. PMMA/MMT and Cloisite20A nanoclay were added to flowable resin composite in 0.5, 1 and 1.5 wt% concentrations. Unmodified resin composite was used as control group. DC was assessed by FTIR, flexural properties were tested by three-point bending test using a universal testing machine, micro-hardness was analyzed by Vickers micro-hardness tester and color change (ΔE00) was evaluated using a reflective spectrophotometer. SEM and elemental mapping assessment were performed to evaluate nanoclay distribution in resin composite. Data were analyzed using One-way ANOVA followed by Tukey's post hoc test, in addition to Two-way ANOVA (p ≤ 0.05). Weibull analysis was used to analyze flexural strength results. RESULTS: Characterization results revealed successful preparation of PMMA/MMT. DC results showed insignificant difference up to 1 wt% of nanoclay concentration. Addition of 0.5 wt% of PMMA/MMT significantly increased flexural properties, while addition of 1.5 wt% of PMMA/MMT significantly decreased flexural properties. Micro-hardness results revealed a significant increase in PMMA/MMT groups in all tested concentrations. ΔE00 results showed that color change was clinically acceptable on adding 0.5 wt% nanoclay. CONCLUSION: PMMA/MMT in 0.5 wt% is a promising nanofiller for resin composite that significantly enhanced flexural strength and micro-hardness without compromising DC and color.

The polymerization efficiency of a bulk-fill composite based on matrix-modification technology.

OBJECTIVES: To evaluate the polymerization efficiency of a matrix-modified bulk-fill composite, and compare it to a conventional composite which has a similar filler system. The degree of conversion (DC%) and monomer elution were measured over different storage periods. Additionally, fillers' content was examined. MATERIALS AND METHODS: Cylindrical specimens were prepared, in bulk and incrementally, from Filtek Bulk Fill (B) and Filtek Supreme XTE (S) composites using a Teflon mold, for each test (n = 6). Using attenuated total reflection method of Fourier transformation infrared spectroscopy, DC% was measured after 24 hours, 7 days, and 30 days. Using high-performance liquid chromatography, elution of hydroxyethyl methacrylate, triethylene glycol dimethacrylate, urethane dimethacrylate, and bisphenol-A glycidyl dimethacrylate was measured after 24 hours, 7 days and 30 days. Filler content was examined by scanning electron microscopy (SEM). Data were analyzed using 2-way mixed-model analysis of variance (α = 0.05). RESULTS: There was no significant difference in DC% over different storage periods between B-bulk and S-incremental. Higher monomer elution was detected significantly from S than B. The elution quantity and rate varied significantly over storage periods and between different monomers. SEM images showed differences in fillers' sizes and agglomeration between both materials. CONCLUSIONS: Matrix-modified bulk-fill composites could be packed and cured in bulk with polymerization efficiency similar to conventional composites.

Evaluation of Two Resin Composites Having Different Matrix Compositions.

This study compared two resin composites with similar filler systems and different matrix compositions. The depth of cure (DoC), polymerization shrinkage, and marginal leakage were evaluated. A Filtek Bulk Fill resin composite (FB) and a Filtek Supreme resin composite (FS) were used. For the DoC and polymerization shrinkage, cylindrical specimens with different thicknesses were prepared. The DoC was attributed to the bottom/top ratios of Vickers microhardness numbers. For polymerization shrinkage, each specimen was firstly scanned using micro-computed tomography (µCT) then cured for 20 s, then for 10 s, and then for 10 s, and they were rescanned between each curing time. Data were processed using the Mimics software. For marginal leakage, standardized 5 mm cavities were prepared in 90 molars. After etching and bonding, materials were packed according to groups: FB-bulk, FB-incremental, and FS-incremental, which were cured for 20, 30, and 40 s, respectively. After thermo-cycling, teeth were stored in 1% methylene blue dye for 24 h and then sectioned and observed for dye penetration. The results showed insignificant differences in the shrinkage and leakage between the different packing techniques and curing times of both materials. In conclusion, the introduction of a novel matrix into resin composite composition enabled bulk-filling in one layer up to 5 mm deep while keeping a tolerable polymerization shrinkage.

Mechanical properties and bonding potential of partially stabilized zirconia treated with different chemomechanical treatments.

PURPOSE: To evaluate the effect of different chemomechanical surface treatments of zirconia on fracture toughness, flexural strength, bond strength of zirconia to composite cement, surface topography, and phase transformation. MATERIALS AND METHODS: Pre-sintered yttrium-stabilized zirconium oxide blocks (in Coris ZI) were used. Specimens were prepared using a milling machine (Cerec InLab). Specimens for each testing procedure were classified into 6 groups according to the surface treatment applied: group 1: air-borne particle abrasion (ABA); group 2: silica coating; group 3: hot etching solution; group 4: hot etching solution followed by ABA; group V: hot etching solution followed by silica coating; group 6: control. Fracture toughness, biaxial flexural strength, and shear bond strength were tested using a universal testing machine. Surface topography was evaluated using a surface roughness tester and scanning electron microscope. Phase transformation was examined using x-ray diffraction analysis. Data were subjected to one-way ANOVA followed by Tukey's HSD multiple comparisons test at p < 0.05. The strength reliability was analyzed using the Weibull distribution. RESULTS: Silica coating revealed the highest mean fracture toughness (9.18 ± 0.11 MPa • m½), biaxial flexural strength (1614.1 ± 124.6 MPa), and bond strength value (31.5 ± 5.06 MPa) among all tested groups. Surface topography evaluation revealed variations among the different surface-treated groups. CONCLUSIONS: Silica coating induced significant improvement in the tested properties compared to other treatments. The use of combined treatment of hot etching solution followed by either air-borne particle abrasion or silica coating of the zirconia surface did not provide an added advantage over silica coating alone.

Influence of shade and light-curing distance on the degree of conversion and flexural strength of a dual-cure core build-up resin composite.

PURPOSE: To investigate the influence of shade and light-curing distance on the degree of conversion (DC) and flexural strength (FS) of a dual-cure core build-up resin composite. METHODS: 135 specimens were prepared and divided into three main groups according to the shade of the composite core material; dentin, blue and white shades. Each group was further subdivided into three subgroups according to the light-curing distance; 0 mm, 3 mm and 5 mm. The DC was measured using FTIR spectrometer. For testing the FS, the mini flexural test specimens were prepared and subjected to three point bending test in a universal testing machine. The results were analyzed using two-way and one-way ANOVA followed by Duncan's Multiple Range Test. The significance level was set at P = 0.05. RESULTS: Both the DC and FS of the dual-cure core build-up material used in this study were influenced by the shade of the material and the light-curing distance. The blue shade exhibited the highest percentage DC values while the white shade revealed the lowest percentage DC. The dentin shade at 0 mm light-curing distance exhibited the highest mean FS value; however the 3 mm and 5 mm light-curing distance of the white shade showed the lowest mean FS values.

Post-gel shrinkage strain and degree of conversion of preheated resin composite cured using different regimens.

OBJECTIVES: This study investigated the influence of resin composite preheating temperature, light curing regimen (mode and duration) on post-gel shrinkage strain (PGSS) and degree of conversion (DC) of a restorative resin composite. METHODS: A hybrid resin composite preheated to three different temperatures (37 degrees C, 54 degrees C and 68 degrees C) was cured using a high intensity light emitting diode (LED) curing unit. The light source was used in 40- and 20-second continuous mode as well as soft start mode. The resin composite was monitored for PGSS during curing and 10 minutes following light irradiation using strain gauges. DC was measured using FTIR spectrometer. The results were analyzed using two-way ANOVA followed by the Duncan's Multiple Range Test for pairwise comparisons. The significance level was set at p < or = 0.05. RESULTS: Preheating of the resin composite significantly increased its PGSS and DC. The soft start groups revealed significantly lower PGSS values compared to the 20- and 40-second groups without altering the DC. CONCLUSIONS: Preheating of resin composite prior to curing increased its DC but also increased its PGSS. The soft-start mode decreased the PGSS of resin composite without altering the DC.

Effect of chlorhexidine concentrations on micro-shear bond strength of self-etch adhesive to normal and caries-affected dentin.

PURPOSE: To evaluate the effect of different chlorhexidine concentrations on bond strength of resin composite to normal and caries-affected dentin using a self-etch primer adhesive. METHODS: Thirty carious human molars were ground to expose flat dentin surfaces containing caries-affected surrounded by normal dentin. The teeth were divided into three groups. One group received no chlorhexidine pretreatment (control). The second and third groups received 2% or 5% chlorhexidine pretreatments, respectively before applying the self-etch primer adhesive (Clearfil SE Bond). Resin composite was applied to caries-affected dentin and to normal dentin on the same tooth with the aid of polyethylene tubes (0.9 mm diameter and 0.7 mm height). For micro-shear bond strength testing, each tooth was secured in a specially designed attachment jig to hold the specimens to the universal testing machine. Load was applied by the testing machine through a wire loop adjusted to the bonded interface at a crosshead speed of 0.5 mm/minute. Micro-shear bond strength was calculated and mode of failure was examined with a x40 stereomicroscope. RESULTS: Statistical analysis revealed insignificant differences between control, 2% and 5% chlorhexidine pretreatment for normal as well as for caries-affected dentin groups. Also, there were insignificant differences in bond strength values between normal and caries-affected dentin for each treatment modality. Adhesive failure was the most common mode of failure.

Phosphoric acid/sodium hypochlorite mixture as dentin conditioner: a new approach.

PURPOSE: To investigate the effect of a phosphoric acid/sodium hypochlorite (NaOCl) mixture as a dentin conditioner on shear bond strength, the resin/dentin interface, as well as the surface area and tubular diameter of dentin. MATERIALS AND METHODS: Thirty human molars were prepared for shear bond strength testing. The teeth were randomly divided into five groups according to the method of dentin conditioning. In group I, dentin was conditioned with 37% phosphoric acid, in group II dentin was conditioned with 37% phosphoric acid followed by application of 5.25% NaOCl, and in groups III, IV, and V, dentin was conditioned with a phosphoric acid/NaOCl mixture for 15, 30, and 60 s, respectively. A resin-based restorative composite disk was bonded to the occlusal surface of each tooth and shear bond strength was measured in a universal testing machine. The resin/dentin interface was evaluated using a scanning electron microscope (SEM). The surface area and tubular diameter for different conditioning methods were assessed using atomic force microscopy (AFM). The data were submitted to one-way ANOVA at a significance level of 0.05 followed by the Tukey-Kramer Multiple comparisons test. RESULTS: Group III showed the highest shear bond strength value (36 MPa), which was significantly higher than groups I and II. SEM micrographs revealed hybrid layer formation for all groups except group II. AFM results showed that groups II and V have significantly higher surface areas and dentinal tubular diameters than other groups. CONCLUSION: The use of a phosphoric acid/NaOCl mixture as dentin conditioner improved the bond strength of an etch-and-rinse single-bottle adhesive to dentin.

Effect of platform switching on strain developed around implants supporting mandibular overdenture.

PURPOSE: The aim of this study was to assess the effect of platform switching, using 3 different abutment sizes on the strain developed around implants supporting mandibular overdenture, using strain gages. MATERIALS: An implant-supported overdenture was constructed on an acrylic model with 2 implant fixtures placed at canine areas. Abutments of different sizes (5.5 mm, 4.5 mm, and 3.5 mm diameter) were screwed in the implant fixtures (platform switching). Anterior axial, anterior off-axis (lateral), and posterior load were applied on each abutment through a load applicator attached to the upper compartment of a universal testing machine until a load of 100 N, at which instant, the resultant strain on the implants was recorded using 4 strain gages connected to a 4-channel strain indicator. Data were analyzed by 1-way ANOVA at a significance level of 0.05, followed by Tukey-Kramer multiple comparisons test. RESULTS: Anterior axial load application and decreasing the abutment size lead to a decrease in the strain developed on the loaded abutment and to an increase in the strain developed on the unloaded abutment. Anterior off-axis load application and decreasing the abutment size lead to an increase in the strain developed on the loaded abutment and to a decrease on the unloaded abutment. On the other hand, posterior load application and decreasing the abutment size lead to an increase in the strain developed on the mesial side of the near abutment and a decrease in the strain developed on its distal side, where there was a significant increase in the strain developed on the mesial and distal sides of the far abutment. CONCLUSION: The distribution of the strain developed because of decreasing the abutment size does not favor the use of platform switching in an implant-supported mandibular overdenture.