Adhesion potential of relining materials to polyamide and PMMA-based denture base materials: effect of surface conditioning methods

This study evaluated the bond strength of relining materials to different denture base materials polyamide and polymethylmethacrylate denture base materials after various surface conditioning methods. Denture base resin specimens (N?=?128; n?=?8 per group) (10?×?10?×?2.5?mm³) were fabricated out of injection-moulded thermoplastic polyamide resin (POL) (Deflex) and heat-polymerized polymethylmethacrylate (PMMA, Dura Dent) (HC). The specimens were randomly divided into 4 main groups according to different surface conditioning methods: (a) No conditioning, control (C), (b) grinding with green stone (G), (c) application of primer (V), (d) silica coating with Al₂O₃ particles coated with SiO₂ (Rocatec) (R). Half of the specimens in each group received auto-polymerized hard relining resin (GC, GC Reline Hard) and the other half PMMA based relining resin (SC, Dura Dent). After thermocycling (×5000), the bonded specimens were tested under tensile forces (0.5?mm/min). Data (MPa) were analyzed using Mann–Whitney U and Kruskal–Wallis tests (alpha = 0.05). Bond strength of relining resins were significantly higher to PMMA than to POL, regardless of the conditioning method (p?<?0.05). While R positively affected the bond strength results (p?<?0.05) (4.99?±?1.65–3.27?±?1.31), application V or G did not show significant effect to POL-relining resin adhesion. After R conditioning, bond strength values were significantly higher in HC-GC group (7.48?±?2.32) than POL-GC group (3.27?±?1.31) (p?<?0.05). Adhesion of auto-polymerized relining materials to thermoplastic polyamide or polymethylmethacrylate denture resins could be improved after surface conditioning with silica-coating.     

A Comparative Study of Polyamide and PMMA Denture Base Biomaterials: I. Thermal,Mechanical, and Dynamic Mechanical Properties

The fracture of denture base materials usually occurs due to accidental dropping and mishandling of these materials. Repeated fracture of denture base materials could be a problem for denture materials made of acrylic resins due to lack of toughness of PMMA-based denture materials. Use of a material with higher toughness might eliminate this problem. Properties of heat-polymerized poly(methyl methacrylate) (PMMA) and high-impact polyamide denture base biomaterials were compared. The test results showed that polyamide samples were more resilient and tougher. Polyamide biomaterials might be good candidate as an alternative to denture base PMMA materials for clinical situations of repeated fractures.     

Fiber‐reinforced nanopigmented poly(methyl methacrylate) as improved denture base

Nanopigmented and fiber‐reinforced poly (methyl methacrylate) (PMMA) were synthesized for denture bases, by incorporating E‐glass fibers, flock fibers, or polyethylene fibers into the PMMA powder formulation to improve the flexural behavior and porosity; decreasing the Candida albicans adherence and being noncytotoxic. The commercial acrylic resin, Lucitone 199 was used as a control group. Scanning electron microscopy analysis was performed to the PMMA particles and the reinforcing fibers. Flexural strength increased by adding E‐glass fibers in the PMMA powder as compared to flock and polyethylene fibers. The reinforced PMMA with flock fibers showed the lower porosity even smaller than Lucitone 199. The synthesized PMMA and the fiber reinforced nanopigmented PMMA groups reduced significantly the C. albicans adherence when compared to the commercial acrylic resin. All the tested groups were found to be nontoxic materials after being in contact with mouse fibroblast culture during 24 h, showing that these novel nanostructured composites are suitable for producing adequate and nontoxic reinforced materials with antimicrobial properties for dentistry applications. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Analysis of Damage on the Streptococcus mutans Immersed in Ozonated Water: Preliminary Study for Application as Mouth Rinse

Ozonated water has been demonstrated to induce significant results in terms of the elimination of microorganisms. The present study assessed the damage to Streptococcus mutans after exposure to ozonated water; the ozone generator was adjusted to provide an outlet concentration of 60 mg/L, the samples were submitted to different ozonation times 1, 2, 4, 6, and 10 mi. Scanning electron microscopy and atomic force images were obtained to identify damage to the bacteria, followed by reactive oxygen species (ROS) evaluation and microbial viability. The results showed a significant reduction in viability and the images evidenced the generation of gaps on the microbial wall and surface layer alterations. Ozone can induce significant damage to S. mutans, thus suggesting that the use of ozonated water to prevent carious lesion formation is extremely promising.     

Antibacterial effect of dental cements evaluated using agar diffusion test

Purpose: Secondary caries can occur around the restoration, fixed prosthesis, and orthodontic band margins because of cariogenic bacteria. Long-lasting antibacterial effectiveness of dental cements used contemporarily can reduce this phenomenon. The purpose of this study was to examine the antibacterial activities of nine dental cements (BisCem^®, Super-Bond C&B, Rely X^TM, Panavia^TM F 2.0, Variolink^® II, Unitek^TM Multi Cure, Multilink^® Automix, Clearfil^TM Esthetic Cement, Transbond^TM LR) using agar diffusion test. Materials and methods: The test materials were inserted into the wells of Muller Hinton agar plates inoculated with Streptococcus mutans and Streptococcus salivarious. The diameters of the inhibition zones produced around the materials were measured after 24 h of incubation. Two-Way ANOVA, the Kruskal-Wallis, and the Mann–Whitney U tests at a significance level of p < 0.05 were analyzed for the results. Results: Unitek Multi Cure cement exhibited a significant difference from the control group against both S. mutans and S. salivarious (p < 0.05). While the zone of inhibition of Unitek Multi Cure cement was shorter (8.50 ± 1.77) than the control group (12.63 ± 1.30), Unitek Multi Cure had antibacterial effect against S. mutans and S. salivarious (p < 0.05). S. mutans displayed a significantly lower resistance to Unitek Multi Cure, BisCem, and Superbond C&B than S. salivarious (p < 0.05). Conclusion: Conventional glass ionomer cement, Unitek Multi Cure, exhibited greatest in vitro antibacterial activity against both S. mutans and S. salivarious. Formation of dental caries had been suppressed by the fluoride-releasing GICs.     

Are antibacterial component additions in etchants and adhesives effective against Streptococcus Mutans?

The aim was to investigate the antibacterial activity of various acids and adhesives with and without antibacterial components against Streptococcus mutans. The antibacterial activities of 35% phosphoric acid (Ultra-Etch), 37% phosphoric acid with benzalkonium chloride (Etch-37), adhesive with chlorhexidine (Peak Universal Bond) and without any agent (PQ1) were investigated by agar-diffusion test. The inhibition-zones were measured after 48 h of incubation. For the tooth-cavity model test; cylindrical cavities were prepared on occlusal dentin surfaces of human molars and divided into four groups (n = 10 cavity/group). Group 1: Ultra-Etch + Peak Universal Bond, Group 2: Ultra-Etch + PQ1, Group 3: Etch-37 + PQ1 were applied. The fourth group without any agent application served as control. The teeth were immersed in 5.8 × 10⁶ cfu/ml of S. mutans solution to infect the cavities for 72 h before the application of the groups. After 72 h, dentin chips were collected from the cavity walls with burs for bacterial counting. Statistical analysis was performed by ANOVA, Bonferroni and Dunnett C tests (p < 0.05). Ultra-Etch and Etch-37 performed similar antibacterial activities in agar-diffusion test. Both acids showed better antibacterial activity compared to adhesives (p < 0.05). The antibacterial activity of PQ1 and Peak Universal Bond was observed to be inactivated by light-polymerization. According to the tooth-cavity model; Group I, II, and III demonstrated reduction in bacterial number and there was no significant difference between them. Antibacterial component additions in etchant and adhesive did not show superior antibacterial activity against S. mutans in both in vitro tests.     

Tensile bond strengths of silicone soft liners to two chemically different denture base resins

Silicone-based soft liners can be useful for patients who have difficulty to tolerate the hard-based dentures. However lack of adhesion to the denture base resin can be a problem that limits their clinical use. This study evaluated the tensile bond strengths (TBS) of four silicone soft liners (GC Soft, GC XSoft, Silagum, Mollosil) to two chemically different denture base resins, polymethyl methacrylate (PMMA) and urethane dimethacrylate (UDMA). Specimen consisted of soft liner material self-cured between two square plates of cured denture base resin measuring 20×20×4 mm. The circular bonding area of soft liner to each plate was 10 mm in diameter. Proprietary primer was applied to the surface of the denture base specimens before bonding following the manufacturers' recommendations. Ten specimens for each denture base-soft liner combination were prepared and tested under tension on a Shimadzu Universal Testing Machine at a cross head speed of 5 mm/min. The mode of failure was determined using a stereo-microscope at magnification of 10x. Two- and one-way ANOVA and post-hoc Dunnett-T3 and t-test were used for statistical analysis. There were significant differences in TBS values for the effect of denture base resins, soft liner and their interaction (p<0.05). The TBS of soft liners to PMMA was significantly higher than to UDMA denture base resins except for Silagum where no significant difference was observed. A mixed mode of failure was more common for all soft liners bonded to PMMA except for Silagum while adhesive failure was more predominant in the UDMA group.     

A New Catechol Biosensor Immobilized Polyphenol Oxidase by Combining Electropolymerization and Cross-Linking Process

A highly stable and effective catechol biosensor was prepared by immobilizing polyphenol oxidase (PPO) into polyaniline (PANI) film by using the direct electropolymerization (one-step) process in conjunction with cross-linking with glutaraldehyde. The results of electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) confirmed that the immobilization of PPO was successful. The biosensor has a fast response to catechol (10 s) with a linear range of 1.0–100 µM and a detection limit of 0.01 µM. The maximum response current (I _max) and the Michaelis-Menten constant (k' _m) were found to be 7.94 µA and 81.32 µM, respectively. The activation energy (E _a) of the PPO catalytic reaction was 16.5 kJ/mol. The biosensor exhibited good stability by retaining 80% of its original activity when stored in a dry state at 4°C for up to 5 months.     

Design and development of a self-contained personal electrostatic bioaerosol sampler (PEBS) with a wire-to-wire charger

Here, we present a concept of a personal electrostatic bioaerosol sampler (PEBS), which is an open channel collector consisting of a novel wire-to-wire particle charger and a collection section housing a double-sided and removable metal collection plate and two quarter-cylinder ground electrodes. The charger consists of a tungsten wire (25.4 mm long and 0.076 mm in diameter) connected to high voltage and positioned in the center of the charging section (a cylinder 50.8 mm long and 25.4 mm in diameter); a ring of stainless steel wire 0.381 mm in diameter surrounds the hot electrode at its midpoint and is grounded. The newly designed wire-to-wire charger produces lower ozone concentrations compared to traditional wire-to-plate or wire-to-cylinder charger designs. The particles captured on the collection plate are easily eluted using water or other fluids. The sampler was iteratively optimized for optimum charging and collection voltages, and collection electrode geometry. When tested with polystyrene latex particles ranging from 0.026 µm to 3.1 µm in diameter and 10 L/min collection flow rate, the sampler's collection efficiency was approximately 70%–80% at charging and collection voltages of +5.5 kV and ?7 kV, respectively. The PEBS showed this collection efficiency at sampling times ranging from 10 min to 4 h. Preliminary tests with Bacillus atrophaeus bacterial cells and fungal spores of Penicillium chrysogenum showed similar collection efficiency. The use of a unique wire-to-wire charger resulted in ozone production below 10 ppb. Due to low ozone emissions, this sampler will allow maintaining desirable physiological characteristics of the collected bioaerosols, leading to a more accurate sample analysis.

© 2017 American Association for Aerosol Research     

Development of biocompatible and biofilm-resistant silver-poly(methylmethacrylate) nanocomposites for stomatognathic rehabilitation

Abstract

Recurrent prosthesis fracture and microbial contamination of the tissue bed or prosthetic materials remain the major clinical challenge for successful intraoral/faciomaxillary rehabilitation. Biocompatible and biofilm-resistant silver nanoparticle (AgNPs) based on poly(methyl methacrylate) was successfully developed by a compression-molding technique. The AgNP-loaded PMMA were characterized using TEM, SEM, FT-IR and XRD analysis. The nanocomposites were found to be biocompatible and biofilm-resistant against Streptococcus mutans and Candida albicans. Mechanical performance of the nanocomposite was statistically analysed and modulus of elasticity was theoretically predicted using four models. The biomaterial developed in this study can be effectively used for stomatognathic rehabilitation.     

Evaluation of antibacterial effects of contemporary orthodontic bonding materials

Aim: The aim of this study was to evaluate the antibacterial effects of five orthodontic bonding materials commonly used in orthodontics. Materials and Methods: The antibacterial effects of five orthodontic bonding materials were evaluated against Streptococcus mutans and Streptococcus salivarius by direct contact test (DCT). Using the DCT technique, quintet specimens of Transbond XT, Blugloo, Grengloo, Light Bond, and Opal Bond were applied to the bottom and the walls of the five wells of a 96-microtiter plate with a height of 2 mm. Samples were prepared in two sets: 1-day samples and 7-day samples. Ten microliters of bacterial suspension were added to each well for direct contact with each material for 1h at 37 °C. Bacterial growth was then measured in a microplate spectrophotometer hourly at 600 nm for 24 h. Five uncoated wells with identical inoculum sizes served as positive controls. The data obtained at the end of 24 h was statistically analyzed with one-way ANOVA, and post hoc comparisons were done using Tamhane’s T2 test. Results: Blugloo generally showed better antibacterial activity than the other materials. Transbond XT did not show any antibacterial activity. There was a statistically significant difference between Transbond XT and Light Bond in the 1-day sample against S. mutans (p < 0.05). No statistically significant differences were found among the other groups (p > 0.05). Conclusion: Blugloo had the most potent antibacterial activity against S. salivarious.     

Inactivation of Bacillus cereus and Salmonella enterica serovar typhimurium by Aqueous Ozone: Modeling and UV-Vis Spectroscopic Analysis

Antibacterial efficacy of aqueous ozone (O₃) against B. cereus vegetative cells and S. typhimurium by was studied by using GInaFiT tool and results were validated using UV-Vis spectroscopy. Ozone gas was generated using a domestic ozone generator. Buffer solutions containing known amounts (≈10⁸–10⁹ cfu/mL) of bacterial pathogens were treated with aqueous ozone (200 mg/hr or 0.1 mg/l) for 16 min with sampling at 0-, 0.5-, 1-, 2-, 4-, 8- and 16-min intervals. A reduction of 4.6 log of B. cereus and 7.7 log cycle reduction of S. typhimurium was obtained in 16 min. Biphasic shoulder and double Weibull models were good fit for the experimental inactivation kinetics data. Principal Component Analysis showed discrete grouping based on the time of treatment. The highest correct classification results for SIMCA were achieved for both B. cereus and S. typhimurium after 1 and 8 min of treatment, respectively. In partial least squares regression analysis, maximum R² values for calibration and validation were found to be 0.84, 0.80 for B. cereus and 0.90, 0.89 for S. typhimurium, respectively.     

A highly efficient method for concentrating DNA from river water by combined coagulation and foam separation

ABSTRACT

Both Escherichia coli and Enterococci were collected in foam within 7 min from 500 mL of bacteria-spiked water by coagulation and foam separation using ferric chloride and milk casein. These bacterial DNA isolated in the 100 µL of extract from the foam more than 87.5% recovery using the DNeasy PowerWater® Kit. To test this method with water from three natural rivers, 0.67–2.70 µg of DNA were concentrated in 100 µL of extract from 1,000 mL of river water. When the DNA extract was subjected to 16S rRNA gene sequencing analysis, information on the bacterial flora could be obtained.     

Evaluation of the effects of different remineralizing agents on Streptococcus mutans biofilm adhesion

The aim of the study was to compare the effects of different remineralization methods that are well established in clinical and daily use on S. mutans biofilm adhesion. In this study 72 human third molars were used. From each tooth two pieces of 4?mm x 7?mm enamel blocks were acquired. The samples were divided into 6 groups in which include 10 samples per time period (24h and 48?h) and for each remineralization method; control, flouride, ozone, CPP-ACP, arginine, novamin. After remineralization procedures, enamel surfaces were covered with saliva. 10⁵ CFU/mL of active S. mutans culture were inoculated onto the samples. S. mutans colonies were counted with Plate Count Agar (PCA) decimal dilution method. Micromorphologic effects of different remineralization methods were observed by Scanning Electron Microscopy (SEM). The most S. mutans biofilm formation for both time periods was observed in the control group whereas the less biofilm adhesion was showed in the arginine group. There were no statistically significant differences among remineralization agents (p?>?0.05). In the control group there was statistical difference between 24?h and 48?h (p?<?0.005) but in the other study groups there were no significant difference between the time periods (p?>?0.05). Remineralization agents did not significant differ on S. mutans biofilm adhesion.     

The Effect of Surface Treatments on Tensile Bond Strength between a Silicone Soft Liner and a Heat-Cured Denture Base Resin

This study evaluated tensile bond strength of a denture soft lining material to a poly (methylmethacrylate) (PMMA) denture base resin subjected to different surface treatment modalities and thermocycling. The materials tested were a silicone-based liner, Molloplast B®, and a heat-cured denture base resin, Meliodent^TM. The denture soft lining material was packed against cured PMMA base resin, which was smoothed; sandblasted with 250-μm Al₂O₃ particles; or lased with a KTP laser; or against uncured PMMA dough (n = 10). In each group, five specimens were thermocycled in a water bath (5–55°C; 3000 cycles) before testing, whereas the other five were directly tested after 24 h. A tensile test was performed using a universal testing machine. Data showed that different treatment modalities of resin surfaces affected adhesion between these two materials and the highest bond values were recorded for cured/smoothed samples under each condition tested. Thermocycling of specimens had no significant reducing effect on measured bond strength values.     

Effects of O3, O3/H2O2 and Coagulation on Natural Organic Matter and Arsenic Removal from Typical Northern Serbia Source Water

The objectives of this study were to investigate the effects of ozone and the O₃/H₂O₂ process on FeCl₃ coagulation efficiency for the removal of the high content of natural organic matter (NOM) and arsenic (As) from groundwater (DOC = 9.27 ± 0.92 mg/L; 51.7 ± 16.4 µg As/L). Arsenic and NOM removal mechanisms during coagulation/flocculation are well investigated. However, data concerning arsenic removal in the presence of NOM, which is the subject of this article, are still insufficient. Laboratory and pilot plant test results have shown that the competition of NOM and As for adsorption sites on the coagulant surface have great influence on coagulation/flocculation efficiency for their removal. With both oxidation pre-treatments, arsenic content after the coagulation process was less than 2.0 µg/L in treated water. Application of ozone has a lower influence on coagulation efficacy in terms of DOC reduction, compared to the O₃/H₂O₂ process with the same ozone dose.     

Energy Conversion and Temperature Dependence in Ozone Generator Using Pulsed Discharge in Oxygen

A detailed reaction kinetic model consisting of 10 species and 63 reactions is developed to investigate the energy conversion and temperature dependence in an ozone generator using oxygen pulsed discharge. The energy conversion ratios of total electric energy converted into reaction heat, heat carried by gas and heat loss to ambient, namely η_reaction, η_gas and η_loss, are obtained for the first time. The ratio of reaction heat η_reaction decreases substantially with increasing specific energy and inlet gas temperature, which represents how much energy is utilized effectively to synthesize ozone. Correspondingly, η_loss and η_gas increase gradually. η_reaction declines from 55.4% to 27.7% at inlet gas temperature of 298 K when specific energy changes from 0.06 J/cm³ to 0.78 J/cm³. The detailed reaction pathway including the degree of transformation among species for ozone formation is also obtained via kinetics simulation. Meanwhile, sensitivity analysis and rate-of-production analysis for the four most important species O₃, O, O(1D) and O₂(b¹∑) obtained from the reaction pathway are executed to understand quantitatively the temperature dependence of sensitivity coefficient and production rate for each individual reaction. The production rate of ozone via the most important ozone generation reaction O+O₂+O₂ = > O₃+O₂ increases linearly with the increase of gas temperature, as well as the destruction rates of ozone via the most important ozone decomposition reactions O₃+O₃ = > O₂+O₂+O₂ and O₃ + O = > O₂(b¹∑)+O₂.     

Inter-comparison of low-cost sensors for measuring the mass concentration of occupational aerosols

Low-cost sensors are effective for measuring the mass concentration of ambient aerosols and second-hand smoke in homes, but their use at concentrations relevant to occupational settings has not been demonstrated. We measured the concentrations of four aerosols (salt, Arizona road dust, welding fume, and diesel exhaust) with three types of low-cost sensors (a DC1700 from Dylos and two commodity sensors from Sharp), an aerosol photometer, and reference instruments at concentrations up to 6500 µg/m³. Raw output was used to assess sensor precision and develop equations to compute mass concentrations. EPA and NIOSH protocols were used to assess the mass concentrations estimated with low-cost sensors compared to reference instruments. The detection efficiency of the DC1700 ranged from 0.04% at 0.1 µm to 108% at 5 µm, as expected, although misclassification of fine and coarse particles was observed. The raw output of the DC1700 had higher precision (lower coefficient of variation, CV = 7.4%) than that of the two sharp devices (CV = 25% and 17%), a finding attributed to differences in manufacturer calibration. Aerosol type strongly influenced sensor response, indicating the need for on-site calibration to convert sensor output to mass concentration. Once calibrated, however, the mass concentration estimated with low-cost sensors was highly correlated with that of reference instruments (R²= 0.99). These results suggest that the DC1700 and Sharp sensors are useful in estimating aerosol mass concentration for aerosols at concentrations relevant to the workplace.

© 2016 American Association for Aerosol Research     

Influence of accelerated ageing on methacrylate‐based denture resins heterogeneity as viewed by ESR‐spin‐probe method

The electron‐spin‐resonance (ESR) spin‐probe method, was used to study the heterogeneity of denture resins based on poly(methyl methacrylate). Results for three resins processed by microwave energy, conventional curing and cold curing (depending on the curing procedure and exposed to ageing in various environmental conditions) were compared. All three cured resins were stored over the same time (1200 h) in distilled water at ambient temperature and in artificial saliva at 348 K. The temperature‐dependent ESR spectra of a spin probe dispersed in the denture resins are analyzed in terms of line‐shapes and line‐widths. The appearance of two spectral components was taken as an indication of resin heterogeneity. The results reveal that the cold‐cured resin has a lower local density in comparison with microwave and conventionally cured resin. The amount of residual monomer also contributes to the local motion of polymer segments. The change of denture resins exposed to ageing is influenced both by the structure of the original resin and the ageing conditions. Restricted motion of a spin probe incorporated into the acrylic resins exposed to accelerated ageing suggests additional crosslinking of polymer chains. The differences are observed for all the investigated resins, but the highest change is observed with the cold‐cured resin. The ESR results are accompanied by T_g and T_m measurements. Copyright © 2005 Society of Chemical Industry     

Thermodynamic and Kinetic Study of Adsorption of R,S‐α‐Tetralol Enantiomers on the Chiral Adsorbent CHIRALPAK AD

Abstract

Experimental results for the separation of S,R‐α‐Tetralol enantiomers obtained on preparative columns packed with particle size 20 µm of chiral adsorbent CHIRALPAK AD are presented. The total porosity was measured by using the non‐retained compound 1,3,5‐Tri‐tert‐butylbenzene and was 0.61. The permeability of the bed packed with CHIRALPAK AD was calculated as 4.4×10^?13 m². The efficiency of columns was characterized by the height equivalent to a theoretical plate (HETP) and a linear dependency has been found over tested flow rates. The HETP of S‐α‐Tetralol and R‐α‐Tetralol calculated at the flow rate 5.0 cm³/min were 320 µm and 340 µm, respectively. Thermodynamic adsorption parameters enthalpy, ΔH and entropy, ΔS, have been calculated from van't Hoff plot. Equilibrium and kinetics of adsorption of single enantiomers and racemic mixture of α‐Tetralol on CHIRALPAK AD were evaluated as well. The parameters for multicomponent isotherm linear‐Langmuir model are presented. The breakthrough curves of α‐Tetralol enantiomers are simulated with a mathematical model that accounts for axial dispersion and linear driving force for the intraparticle mass transfer.