Search

Zahra Jowkar,1 Zahra Fattah,1 Saeedreza Ghanbarian,2 Fereshteh Shafiei1 1Oral and Dental Disease Research Center, Department of Operative Dentistry, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran; 2Department of Operative Dentistry, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, IranCorrespondence: Fereshteh Shafiei Tel +98-71-36263193Fax +98-71-36280804Email shafief@sums.ac.irAim: This study was conducted to evaluate the effects of three nanoparticle solutions used as dentin pretreatments on the microshear bond strength (μSBS) of a conventional glass ionomer cement (GIC) to dentin.Materials and Methods: Ninety intact human molars were used after sectioning their occlusal surfaces to expose flat dentin surfaces. The specimens were randomly assigned to nine groups (n = 10). Group A was the control group (without using the cavity disinfectant). In groups B, C, D, and E, the prepared dentin surfaces were treated with 1 cc 2% chlorhexidine (CHX), 0.1% silver nanoparticle (SNP), 0.1% titanium dioxide nanoparticle (TNP), and 0.1% zinc oxide nanoparticle (ZNP) solutions for 1 minute, respectively, before applying the conditioner. CHX, SNPs, TNPs, and ZNPs were applied for 1 minute after applying the conditioner in groups F, G, H, and I, respectively. The specimens were restored with a conventional GIC and underwent μSBS testing after 24 hours. The data were analyzed using the one-way analysis of variance and Tukey’s test (p=0.05).Results: The applications of the nanoparticles (SNP, TNP, and ZNP) after the conditioner were associated with significantly greater μSBS values compared to that of the control group (p values < 0.05). Significantly higher μSBS values were observed when TNP or ZNP was applied after the conditioner compared to their applications before the conditioner (p values < 0.05). The highest μSBS values were observed when TNP was applied after the conditioner.Conclusion: Dentin pretreatment with the nanoparticles after applying the conditioner enhanced the bond strength of the GIC to dentin compared with the control group. The best results were obtained for the TNPs applied after the conditioner.Keywords: glass ionomer cement, microshear bond strength, nanoparticles

Zahra Jowkar,1 Seyed Ahmadreza Hamidi,2 Fereshteh Shafiei,1 Yasamin Ghahramani3 1Oral and Dental Disease Research Center, Department of Operative Dentistry, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran; 2Department of Operative Dentistry, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran; 3Department of Endodontics, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, IranCorrespondence: Fereshteh Shafiei Tel +98 71-36263193Email shafief@sums.ac.irAim: This study was conducted to evaluate the effect of three nanoparticle solutions used as final root canal irrigants on the fracture resistance of endodontically treated roots.Materials and Methods: Sixty intact single-rooted premolar teeth were used after removing the crowns below the cementum–enamel junction to standardize the length of the remaining roots to 13 mm. After instrumenting the roots using ProTaper Universal rotary instruments up to size F4, the roots were randomly divided into six groups (n=10) according to the final irrigating solutions: Group 1: normal saline; Group 2: 2% chlorhexidine (CHX); Group 3: 17% EDTA+2.5% NaOCl; Group 4: 17% EDTA+0.1% silver nanoparticle (SNP) solution; Group 5: 17% EDTA+0.1% titanium dioxide nanoparticle (TNP) solution; Group 6: 17% EDTA+0.1% zinc oxide nanoparticle (ZNP) solution. After filling the root canals with gutta-percha and AH Plus sealer, the fracture resistance (FR) values were measured. The data were subjected to the one-way analysis of variance and the Tamhane post hoc test (p=0.05).Results: EDTA + NaOCl had the lowest FR value, followed by normal saline and CHX (p values < 0.05). No significant difference was found between the FR of roots irrigated with CHX and normal saline (p > 0.05). The application of nanoparticles (SNP, TNP, and ZNP) was associated with a significantly greater FR than that of other irrigation solutions (p values < 0.05).Conclusion: The final irrigation of root canals with nanoparticles enhanced the fracture resistance of the endodontically treated roots. The lowest FR value was observed for NaOCl.Keywords: fracture resistance, nanoparticles, root canal irrigants

Statement of problem: Secondary dental caries is a common clinical finding in composite restoration. The development of a bactericidal dental adhesive provides a promising method to reduce the risk of secondary caries. Objectives: This study aimed to assess the antibacterial activity of silver (Ag) and titanium dioxide (TiO2) nanoparticles incorporated into an experimental dentin bonding agent formulation. Materials and Methods: Ag and TiO2 nanoparticles at 0.05, 0.1, 0.2, 0.5, and 1 wt% concentrations were incorporated into the adhesives. The suspensions were sonicated to ensure homogenous dispersion of nanoparticles in the adhesive system. Formulation was composed of acetone, 2,2-bis[4-(2-hydroxy-3-methacryloxypropoxy)phenyl]propane (Bis-GMA), 1,6-bis-[2-methacryloyloxyethyl carbonyl amino]-2,4,4-trimethylhexane (UDMA), trimethylolpropane trimethacrylate (TMPTMA), 2-hydroxyethyl methacrylate (HEMA), and photoinitiator, with polyvinylpyrrolidone (PVP) as the stabilizer. We counted the colony-forming units (CFU%) of two cariogenic bacteria, Streptococcus mutans (S. mutans) and Lactobacillus acidophilus (L. acidophilus), that were exposed to the powdered light cured adhesive specimens. The effects of various concentrations of each nanoparticle were compared by one-way ANOVA, followed by the post hoc Bonferroni test. Results: All samples exhibited definite antibacterial activity (P

Background and Aim: Although the use of adhesive systems can be effective in decreasing microleakge, it is still a major problem in composite resin restorations. The aim of the present study was to evaluate the marginal sealing ability of resin composite restorations using four dentin bonding systems in both primary and permanent teeth. Materials and Methods: In this experimental study, one hundred and sixty extracted human teeth (80 primary and 80 permanent) were selected. All of the samples received a class V cavity preparation on the buccal surfaces (The coronal half in enamel and the gingival half in cementum or dentin). Each group was then divided into four subgroups each containing 20 teeth. Four different dentin bonding systems (Scotchbond Multipurpose, Single Bond, Clearfil SE Bond and Prompt L-Pop) were used in each subgroup. Then the cavities were filled with composite resin (Z100 for SBMP and Clearfil AP-X for Clearfil SE Bond). Samples were thermocycled, immersed in 0.5% basic fuschin, cut faciolingually and evaluated for dye penetration using a binocular stereomicroscope. Kruskal-Wallis and Dunn tests were used for comparison of microleakage between groups with p

A novel double network (DN) hydrogel nanocomposite with good compressive strength has been prepared by using Carboxymethyl Cellulose-g-Acrylic acid-Iron Oxides Nanoparticles (CMC-g-AA-IONs) as the primary network and polyacrylamide as the secondary network. The structure of the synthesized DN hydrogel nanocomposite was investigated by Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), thermogravimetric analysis (TGA), and mechanical strength measurement. The synthesized DN hydrogel showed high mechanical strength (σ of 0.238 MPa), despite the water content of 90%. Its biocompatibility effect on sensitive nerve cells was evaluated by the 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) test. The results showed that the DN hydrogel nanocomposite has no cytotoxicity on these cells and did not cause any disturbance or inhibit their growth and proliferation. [ABSTRACT FROM AUTHOR]

Aim: To assess the effect of acid‐etching duration time on the compressive strength, microstructure and shear bond strength of All‐Bond Universal adhesive to MTA‐Angelus (AMTA), and Biodentine (BD). Methodology: Forty‐eight cylindrical specimens (4 mm in diameter, 6 mm in height) of AMTA in four groups and 48 specimens of BD in four groups (n = 12) were prepared and stored for 72 h. The control groups were unetched whilst the three experimental groups were acid‐etched for 5, 10 and 15 s, respectively, followed by compressive strength testing. The effect of the various acid‐etching times on surface micromorphology was evaluated under a scanning electron microscope. Similar groups were bonded using All‐Bond Universal and Aelite Flo and shear bond strength was tested. Data were analysed using two‐way ANOVA and Tukey tests. Results: 10‐s and 15‐s acid‐etching reduced the compressive strength of AMTA and BD (P < 0.001), while 5‐s etching did not (P ≤ 0.86). In all the groups, BD had greater compressive strength compared to AMTA. Contrary to BD, the three etched AMTA groups had significantly higher shear bond strength compared to the control group (P < 0.001), with no significant differences between them. The etched groups of AMTA had shear bond strengths comparable to all the BD groups. Scanning electron microscope observations indicated variable surface morphologies such as remnant crystals and cracking/eroding in all our groups of AMTA; though these differences were less prominent for BD. Conclusions: Shortening the acid‐etching time to 5 s resulted in a beneficial effect in terms of resin bonding for AMTA while preventing the detrimental effect of 10‐s and 15‐s etching on the compressive strength of AMTA and BD. However, the three etching times had no effect on resin–BD bond. [ABSTRACT FROM AUTHOR]

The morphologies of the copper deposits obtained by pulsating overpotential regime with prolonged pulse and pause durations from the solution of 0.15 M CuSO4 in 0.50 M H2SO4 at overpotentials lower, higher and belonging to the plateau of limiting diffusion current density were compared with those obtained by the same electrodeposition regime from solutions of 0.075 and 0.30 M CuSO4 in 0.50 M H2SO4 and 0.15 M CuSO4 in 0.25 and 1.00 M H2SO4 at overpotentials outside the plateau of limiting diffusion current density. These samples were characterized by scanning electron microscopic (SEM) analysis and the cathodic polarization characteristics from solutions compared. Increasing the Cu(II) concentration led to an increase in the limiting diffusion current density. Decreasing the H2SO4 concentration shifts both beginning and the end of the plateau of the limiting diffusion current density towards higher electrodeposition overpotentials. Also, electrodeposition in solutions of 0.15 M CuSO4 in 0.25 and 1.00 M H2SO4 led to the formation of morphological forms of copper deposits characteristic for electrodeposition of copper from higher CuSO4 or lower H2SO4 in solution at some higher overpotentials.