Bis-GMA Research Articles

Synthesis and characterization of graphene oxide-zirconia (GO-ZrO2) and hydroxyapatite-zirconia (HA-ZrO2) nano-fillers for resin-based composites for load-bearing applications

ObjectivesThe study aims to synthesize two different types of nano-fillers based on zirconia (ZrO2), which was functionalized with graphene oxide (GO-ZrO2), and hydroxyapatite (HA-ZrO2), and to implement them in an experimental methacrylate matrix containing new dimethacrylic oligomers. MethodsNano-particles were synthesized via a modified Hummer’s method and a sol-gel route. Bisphenol A-glycidyl methacrylate oligomers (Bis-GMA336[0–1]) were synthesized from an epoxy resin that reacted with methacrylic acid in the presence of a basic catalyst. Traditional dental glass-fillers (Barium oxide/BaO and Barium fluoride/BaF2) were synthesized to create an experimental resin-based composite (RBC) used as reference. Filler morphology was evaluated via Transmission Electron Microscopy. RBCs were characterised by real-time Fourier transform infrared spectroscopy (degree of cure/DC, polymerisation kinetics), real-time spectrometry (light transmittance), 3-point bending test (flexural strength and modulus, Weibull parameters), and depth-sensing indentation test (plastic and elastic deformation parameters). ResultsThe synthesized nanohybrid fillers proved good dispersing performance. Mechanical properties and materials’ reliability are within or above the mean values reported in the literature for RBCs. Addition of HA-ZrO2-fillers resulted in a decrease light transmission, DC and mechanical properties. Except for the HA-ZrO2 RBC, materials showed a high resistance to softening in solvent. ConclusionsThe synthesis of GO-ZrO2 and HA-ZrO2 nanohybrid particles and their implementation in experimental RBCs has proven successful. Adjustments of the light transmission through suitable co-fillers in addition to GO-ZrO2 as well as adjustments of the amount of HA-ZrO2 are necessary to enable reduced curing time (<20 s). Clinical significanceThe addition of nanofillers with tailor-made properties can help improving the performance of modern restoratives.

Risk assessment of predicted serum concentrations of bisphenol A in children and adults following treatment with dental composite restoratives, dental sealants, or orthodontic adhesives using physiologically based pharmacokinetic modeling

Bisphenol A (BPA) is a chemical used to manufacture bisphenol A glycidyl methacrylate (BisGMA). BisGMA has been used for decades in dental composite restoratives, sealants, and adhesives. Based on published studies, exposure to low concentrations of BPA are possible from dental and orthodontic devices. The serum BPA concentrations arising from such devices and oral doses were predicted using a PBPK model in children and adult females based on 1) published extraction data for cured and uncured 3M ESPE Filtek Supreme Ultra Flowable, 3M ESPE Filtek Bulk Fill Restorative, and 3M ESPE Clinpro Sealant and 2) published 20% ethanol/water and water rinsate data following orthodontic application with 3M ESPE Transbond MIP Primer and 3M ESPE Transbond XT Adhesive. Predicted oral exposure to BPA arising from these dental and orthodontic devices is low (median <10 ng/treatment) and predicted serum BPA concentrations were also low (<10−4 nM). Even the maximum predicted exposure in this study (533.2 ng/treatment) yields a margin of exposure of 7.5 relative to the EFSA t-TDI (4 μg/kg-day) and is only 2.8% of the daily BPA exposure for the US population in a 58-kg woman (15,660 ng/day). Therefore, the exposure to BPA arising from the 3M ESPE dental and orthodontic devices evaluated in this study is negligible relative to daily BPA exposure in the general population and these potential BPA sources do not constitute a risk to patients.

Enhanced mechanical properties are possible with urethane dimethacrylate-based experimental restorative dental composite

This laboratory study aimed to replace the traditional bisphenol A-glycidyl methacrylate (bisGMA) resin system with a urethane dimethacrylate (UDMA)-based resin system to enhance the physicomechanical properties of dental restorative composite (DRC). We evaluated surface roughness, porosity %, nanohardness, elastic modulus, and compressive strength (CS) in the control group (the bisGMA-resin system) and two experimental groups (UDMA-based resin systems with 20 wt.% SiO2 or Al2O3, each 30 μm in size spherical fillers). Cylindrically shaped samples 4 mm in diameter and 6 mm in height were fabricated using light curing (n = 10). One-way analysis of variance method was used to statistically analyze the results (p ≤ 0.05). The data suggest that both UDMA-based resin systems showed increased surface roughness (Ra) and porosity % in the sample fabrication compared with the control. However, the nanohardness in both SiO2-based UDMA composite (0.20 ± 0.09 GPa) and Al2O3-based UDMA composite (0.22 ± 0.07 GPa) was not significantly higher compared with the control (0.19 ± 0.05 GPa). Likewise, while improved CS values were observed in both SiO2-based UDMA composite (15.5 ± 1.9 MPa) and Al2O3-based UDMA composite (16.2 ± 0.7 MPa) compared to the control (14.5 ± 4.5 MPa), this increase was not statistically significant. The newly developed UDMA-based resin formulation with Al2O3 micro-filler showed promising physicomechanical properties and may be appropriate for use as DRC.

Hybrid Dental Composites Biomechanical Properties

In the last two decades, both general and oral health status became more important for individuals, being associated to their quality of life, social provenance and income. Society�s evolution is associated to high expectations regarding edentulous and decays treatment. Metal filling such as gaudent or amalgam have been replaced by aesthetic materials, to achieve similarity to the patient�s genuine biological tissue. Along with the aesthetic demand, dental materials have to fulfill biocompatibility and mechanical properties proximate to healthy soft either hard tissues. Composite materials have the advantages of accomplishing biological and mechanical demands and to be accessible financially, compared to ceramics. Composites are classified according to the main monomer, filling, particles� dimension, addition of external molecules, this entirety having a direct influence on materials� properties. The objective of this prospective interventional in vitro study was to evaluate biomechanical properties of four different hybrid composites: Premise direct™ - Premise indirect™ (Kerr, Orange, California, USA), Gradia� Direct (GC, Alsip, Illinois, USA) and Ceramage� (SHOFU Dental, Ratinger, Germany). Vickers microhardness, compressive strenght, direct tensile strenght, water absorption and solubility were assessed. The results showed that microfilled hybrid composites UDMA (urethane dimethacrylate)-based monomer had the highest evaluations regarding Vickers microhardness, compressive strenght and tensile strenght, whereas water absorption was the highest for nanofilled hybrid Bis-GMA (bisphenol A-glycidyl methacrylate)/TEGDMA (triethylene glycol dimethacrylate), and solubility for microfilled hybrid UDMA based monomer.

Niobium silicate particles as bioactive fillers for composite resins

ObjectivesThis study aimed to evaluate the influence of niobium silicate (SiNb) particles in the physicomechanical and biological properties of an experimental composite resin. MethodsThe SiNb particles were incorporated (50 wt%) into a polymeric matrix formulated with 70 wt% Bisphenol A-Glycidyl Methacrylate and 30 wt% Triethylene Glycol Dimethacrylate to formulate an experimental composite resin. A control group was formulated with barium silicate glass (SiBa) as filler for the same polymeric matrix. The composite resins were tested for their refractive index, polymerization kinetics, flexural strength, radiopacity, softening in solvent, pH, cytotoxicity and mineral deposition. ResultsThe SiBa group presented refractive index results between 1.50 and 1.52 and the SiNb between 1.43−1.45. No statistically significant difference in the degree of conversion, flexural strength, and softening in solvent was observed between different groups. Radiopacity was lower for SiNb, while the addition of these particles increased cell viability. The pH was increased for all groups after immersion. The mineral deposition analysis resulted in increased deposition above specimens after the immersion in SBF. SignificanceNiobium silicate particles may be used as an alternative inorganic filler to achieve an adequate balance between physical-chemical and biological properties for the development of bioactive composite resins.

Immediate Hypersensitivity Reaction to Composite Restorations

Restorative materials used in dentistry are constantly exposed to salivary components like enzymes that have a high impact on the degradation of these materials and subsequent leaching of some of their constituents which may be harmful to the oral tissues in some patients. Released triethyleneglycolmethacrylate, bisphenol A-glycidyl methacrylate (Bis-GMA), diurethanedimethacrylate (UDMA) and formaldehyde have been detected from incompletely polymerized composite and are implicated in occurrence of various adverse reactions. We present a case of a 60 year old female who had composite restorations done. She later presented with complaints of several episodes of intermittent gingival and cheek swellings of sudden onset adjacent to the restored teeth. The filling was taken off and patient was placed on anti-allergy medications with a close follow-up. This presentation highlights the occurrence of a typical allergy to composite material in our centre. It serves to educate dental practitioners about the awareness of such adverse reactions to dental resin materials and the need to be prompt in management of the condition.&#x0D;

Niobium silicate particles promote in vitro mineral deposition on dental adhesive resins

ObjectiveThis study aims to analyze the addition of niobium silicate particles to dental adhesive resins and evaluate its physicomechanical and biological properties. Methods: The SiNb particles were produced by the sol-gel route and presented a mean particle size of 2.1 μm and a specific surface area of 616,96m2/g. An experimental adhesive resin was formulated with 66 wt% Bisphenol A-Glycidyl Methacrylate and 33 wt% Hydroxyethyl methacrylate with diphenyl(2,4,6-trimethyl benzoyl)phosphine oxide as the photoinitiator. The SiNb particles were incorporated into the adhesive resins in 1 wt% (SiNb1%) and 2 wt% (SiNb2%) concentration. A control group (SiNb0%) without the addition of particles was used. The developed adhesives were evaluated by their polymerization kinetics, refractive index, softening in solvent, cytotoxicity, mineral deposition, ultimate tensile strength, and micro shear bond strength. ResultsThe refractive index range was increased by the addition of niobium silicate particles. No statistically significant difference was found between groups in the degree of conversion,.softening in solvent analysis, cytotoxicity and ultimate tensile strength. The deposition of minerals increased after immersion of specimens in SBF after 14 days on the SiNb2%. The SiNb2% group showed high micro shear bond strength values, reaching 33.87 MPa. Conclusion: In the present study, the addition of 2 wt% of niobium silicate into dental adhesive resins promoted the mineral deposition with increased bond strength without affecting other material properties. Clinical significance: Bioactive fillers must maintain the physical-chemical properties of dental adhesives, guaranteeing their clinical performance. Niobium silicate particles could promote the remineralization of dentin hard tissues without compromising the physico-mechanical properties on these materials.

Bulk Fill Composites Have Similar Performance to Conventional Dental Composites

The aim of the study was to perform comprehensive characterization of two commonly used bulk fill composite materials (SDR Flow (SDR) and Filtek™ Bulk Fill Flowable Restorative (FBF) and one conventional composite material (Tetric EvoCeram; TEC). Eleven parameters were examined: flexural strength (FS), flexural modulus (FM), degree of conversion, depth of cure, polymerisation shrinkage (PS), filler particle morphology, filler mass fraction, Vickers hardness, surface roughness following simulated toothbrush abrasion, monomer elution, and cytotoxic reaction of human gingival fibroblasts, osteoblasts, and cancer cells. The degree of conversion and depth of cure were the highest for SDR, followed by FBF and TEC, but there was no difference in PS between them. FS was higher for bulk fill materials, while their FM and hardness were lower than those of TEC. Surface roughness decreased in the order TEC→SDR→FBF. Bisphenol A-glycidyl methacrylate (BisGMA) and urethane dimethacrylate were found in TEC and FBF eluates, while SDR released BisGMA and triethylene glycol dimethacrylate. Conditioned media accumulated for 24 h from FBF and TEC were cytotoxic to primary human osteoblasts. Compared to the conventional composite, the tested bulk fill materials performed equally or better in most of the tests, except for their hardness, elastic modulus, and biocompatibility with osteoblasts.

A Prospective Cohort Study of Bisphenol A Exposure from Dental Treatment

Laboratory studies show that bisphenol A (BPA) leaches from bisphenol A-glycidyl methacrylate (bisGMA)-based dental materials. We aimed to quantify the extent to which children are exposed to BPA from dental treatment with bisGMA materials, by amount of treatment and type of sedation. We hypothesized that posttreatment urinary BPA (uBPA) concentrations would be higher among patients with more surfaces treated with bisGMA-based materials and among patients receiving general anesthesia compared with pretreatment concentrations. We conducted a prospective cohort study in 211 children, 4 to 12 y old, who had no prior resin-based dental treatment. We measured uBPA concentrations twice before treatment and at 2 d and 1, 4, and 16 wk posttreatment. We abstracted treatment data (surfaces treated) from the chart. We generated descriptive statistics and compared pre- and posttreatment uBPA concentrations using generalized estimating equations. Participants were 51% female, 46% non-White, and 74% publicly insured. The median age was 6 y. The mean number of tooth surfaces exposed to BisGMA materials (composites/sealants) was 7.5 (SD 5.3). Overall, uBPA concentrations were 86% higher (95% confidence interval [CI] 42% to 143%, P < 0.001) at 2 d posttreatment compared with pretreatment concentrations. The uBPA concentrations 2 d posttreatment versus pretreatment tended to be higher (112%, 95% CI 53% to 194%) among those receiving treatment on >4 surfaces than those receiving treatment on ≤4 surfaces (50%, 95% CI −2% to 130%). Two days after treatment, uBPA was significantly higher than pretreatment concentrations in children receiving nitrous oxide but not in those receiving general anesthesia. Among all findings, uBPA concentrations returned to baseline by 4 wk. Children experience short-term increases in BPA from dental treatment. The impact of relatively high, short-term BPA exposure on child health is unknown. Given the widespread use of BisGMA-based dental materials and that chronic low-dose BPA exposure may adversely affect child health, strategies that minimize BPA exposure could potentially improve child health.

Alternative monomer for BisGMA-free resin composites formulations

ObjectiveWater sorption, high volumetric shrinkage, polymerization stress, and potential estrogenic effects triggered by leached compounds are some of the major concerns related to BisGMA-TEGDMA co-monomer systems used in dental composites. These deficiencies call for the development of alternative organic matrices in order to maximize the clinical lifespan of resin composite dental restorations. This study proposes BisGMA-free systems based on the combination of UDMA and a newly synthesized diurethane dimethacrylate, and evaluates key mechanical and physical properties of the resulting materials. Methods2EMATE-BDI (2-hydroxy-1-ethyl methacrylate) was synthesized by the reaction between 2-hydroxy-1-ethyl methacrylate with a difunctional isocyanate (1.3-bis (1- isocyanato-1-methylethylbenzene) – BDI). The compound was copolymerized with UDMA (urethane dimethacrylate) at 40 and 60wt%. UDMA copolymerizations with 40 and 60wt% TEGDMA (triethylene glycol dimethacrylate) were tested as controls, as well as a formulation based in BisGMA (bisphenol A-glycidyl methacrylate)-TEGDMA 60:40% (BT). The organic matrices were made polymerizable by the addition of DMPA (2.2-dimethoxyphenoxy acetophenone) and DPI-PF6 (diphenyliodonium hexafluorophosphate) at 0.2 and 0.4wt%, respectively. Formulations were tested as composite with the addition of 70wt% inorganic content consisting of barium borosilicate glass (0.7μm) and fumed silica mixed in 95 and 5wt%, respectively. All photocuring procedures were carried out by a mercury arc lamp filtered to 320–500nm at 800mW/cm2. The experimental resin composites were tested for kinetics of polymerization and polymerization stress in real time. Flexural strength, elastic modulus, water sorption, and solubility were assessed according to ISO 4049. Biofilm formation was analyzed after 24h by luciferase assay. Data were statistically analyzed by one-way ANOVA and Tukey's test (α≤0.05). ResultsIn general, the addition of 2EMATE-BDI into the formulations decreased the maximum rate of polymerization (RPMAX), the degree of conversion at RPMAX (DC at RPMAX), and the final degree of conversion (final DC). However, these reductions did not compromise mechanical properties, which were comparable to the BT controls, especially after 7-day water incubation. The incorporation of 60wt% 2EMATE-BDI reduced water sorption of the composite. 2EMATE-BDI containing formulations showed reduction in polymerization stress of 30% and 50% in comparison to BT control and TEGDMA copolymerizations, respectively. Biofilm formation was similar among the tested groups. SignificanceThe use of the newly synthesized diurethane dimethacrylate as co-monomer in dental resin composite formulations seems to be a promising option to develop polymers with low-shrinkage and potentially decreased water degradation.

Investigation of the physical, mechanical and thermal properties of nano and microsized particulate-filled dental composite material

Objective The purpose of this study was to fabricate bisphenol-a glycidyl methacrylate /tri-ethylene glycol dimethacrylate (TEGDMA)-based nano and micro-sized-filled dental composite and to study the effect of varying silane-treated nano hydroxyapatite on physical, mechanical and thermal properties. Methods The dental resin matrix was fabricated by bisphenol-a glycidyl (53 wt.%), TEGDMA (46 wt.%), camphorquinone (0.3 wt.%) and 2-(dimethylamino) ethyl methacrylate (0.7 wt.%). Silane-treated nano hydroxyapatite (nHA) filler content was varied from 0 to 8 wt.%, while zinc oxide (microsized) remains constant with 20 wt.%. A light curing unit was employed for polymerization of the resinous dental mixture. Results The result revealed that infrared spectra of untreated and treated nHA filler particles were confirmed by Fourier transform infrared spectroscopy. The dental composite filled with 6 wt.% nHA (DHZ6) exhibited maximum compressive strength (249 MPa) and Vickers hardness (49 Hv), while dental composite filled with 8 wt.% nHA (DHZ8) showed minimum depth of cure (5.12 mm), degree of conversion (54%) and polymerization shrinkage (1.12%). Significance Silane treatment of nano hydroxyapatite has a significant role in physical, mechanical, and thermal properties. Bonding strength of coupling agent has been seen between organic and inorganic materials.

Fluorinated Montmorillonite and 3YSZ as the Inorganic Fillers in Fluoride-Releasing and Rechargeable Dental Composition Resin

Dental caries (tooth decay) is the most frequent oral disease in humans. Filling cavities with a dental restorative material is the most common treatment, and glass ionomer cements are the main fluoride ion release restorative materials. The goal of this study was to develop a restorative compound with superior fluoride ion release and recharge abilities. Previously developed fluorinated bentolite and hydrophobized 3YSZ were used as two different inorganic fillers mixed in a bisphenol A-glycidyl methacrylate (Bis-GMA) matrix. XRD, FTIR, and TGA were used to determine the hydrophobic modification of these two inorganic fillers. In mechanical tests, including diameter tensile strength, flexural strength, and wear resistance, the developed composite resin was significantly superior to the commercial control. A WST-1 assay was used to confirm that the material displayed good biocompatibility. Furthermore, the simulation of the oral environment confirmed that the composite resin had good fluoride ion release and reloading abilities. Thus, the composite resin developed in this study may reduce secondary caries and provide a new choice for future clinical treatments.

Quantum Dots of Tantalum Oxide with an Imidazolium Ionic Liquid as Antibacterial Agent for Adhesive Resin.

To synthesize tantalum oxide quantum dots (Ta2O5QDs) using an imidazolium ionic liquid as a precursor and evaluate the effect of its addition to an experimental adhesive resin on the degree of conversion (DC) and antibacterial activity. Ta2O5QDs was synthesized from the hydrolysis of an imidazolium ionic liquid (1-n-decyl-3-methylimidazolium hexachlorotantalate [DMI.TaCl6]) and evaluated by transmission electron microscopy (TEM). The adhesive was formulated with 66.7 wt% bisphenol A-glycidyl methacrylate (bis-GMA), 33.3 wt% 2-hydroxyethyl methacrylate (HEMA) with a photoinitiator/co-initiator system. In one group, Ta2O5QDS was added to the adhesive at 1 wt% Ta2O5QDs) and one group remained without Ta2O5QDS as control (CTRL). The adhesives were evaluated for DC by Fourier Transform Infrared spectroscopy. Direct contact inhibition assay was used to evaluate the antibacterial activity of the experimental adhesive resins against biofilm formation and planktonic bacteria. Ta2O5QDs had a particle size distribution of 1.52 ± 0.73 nm. DC was 50.91 ± 4.94% for CTRL and 55.4 ± 4.58% for Ta2O5QDs (p = 0.310). Ta2O5QDs showed less Streptococcus mutans biofilm formation on adhesive surfaces (p = 0.013). There was no statistically significant difference in terms of antibacterial activity against planktonic bacteria (p = 0.079). Non-agglomerated Ta2O5QDs synthesized from an imidazolium ionic liquid provided antibacterial activity to the experimental adhesive resin against biofilm formation of Streptococcus mutans.

Effect of layer thickness on the elution of monomers from two high viscosity bulk-fill composites: A high-performance liquid chromatography analysis.

Aim:The aim is to evaluate the effect of different layer thickness on the amount of elution of monomers from two high viscosity bulk-fill composites after 24 h and 1 month storage in ethanol using high-performance liquid chromatography (HPLC) analysis.Materials and Methods:Forty-eight samples prepared from two high viscosity bulk-fill composite resins; Tetric EvoCeram Bulk Fill and x-tra fil were divided into three groups (n = 8) based on their layer thickness, i.e., Group 1 (2 mm), Group 2 (4 mm), and Group 3 (6 mm) and were then subdivided based on their storage period. The analysis of the eluates was performed using HPLC unit. Statistical analysis was performed using One-way ANOVA, independent sample t-test, and paired “t” test at a significance level of 0.05 (P < 0.05).Results:Increase in layer thickness resulted in increased amount of bisphenol A-glycidyl methacrylate (Bis-GMA) and urethane dimethacrylate (UDMA) elution for both composites, i.e., Group 3 > Group 2 > Group 1 and there was statistically significant difference among all the groups. Tetric EvoCeram Bulk Fill showed a statistically significant increase in amount of Bis-GMA and UDMA elution for all groups compared to x-tra fil. Furthermore, increase in storage period resulted in statistically significant increase in amount of Bis-GMA and UDMA elution for both composites, i.e., Group 1B > Group 1A, Group 2B > Group 2A, and Group 3B > Group 3A. The mean value of UDMA elution was higher when compared to that of Bis-GMA elution for both composites and there was statistically significant difference for all groups.Conclusion:Within the limitations of this in vitro study, it was concluded that increase in layer thickness resulted in increased amount of Bis-GMA and UDMA elution for both Tetric EvoCeram Bulk Fill and x-tra fil.

Diametral Tensile Strength and Reflectance Evaluation of Dental Composite Prototype Using Modified Dental Composite Procedures

Dental composite is used to restore disease or fracture tooth structure and modify tooth shape as well as color in order to enhance the aesthetic properties. This restoration should possess sufficient strength and translucency at the same time. Diametral tensile strength and reflectance of dental composite were related to the selection of three main components; filler, coupling agent and resin matrix. Quarsi-experimental. This study was a follow-up study whereby the filler silica-zirconia-alumina system were synthesized by sol-gel technique with precursors composition ratio 70:20:10. The surface of subsequent filler were modified by 3-mercaptoppropyltrimethoxysilane (MPTMS) and aminopropyltrimethoxysilane (APTES) then becoming group A and B respectively. In order to prepared the dental composite, acetone was used to reduce the viscosity of Bisphenol A Glycidyl Methacrylate (BisGMA) thus enable introducing more content of filler into resin matrix. Phase of crystalline and particle morphology were identified by X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) consecutively. Universal Testing Machine (Lloyd) with crosshead speed 1mm/min was used to evaluate diametral tensile strength between two samples group. Dental composite contain filler-MPTMS coated were continuing tested to measure the reflectance values. Disc of each samples were prepared (n=3) with different thickness (1.5 mm and 3 mm) and same diameter (20 mm). Both diametral tensile strength and reflectance evaluation data were analysis by t-test unpaired. The result showed no statistically significant differences in diametral tensile strength between group A (47,6548 MPa) and B (41,4265 MPa). Reflectance evaluation also exhibited no statistically significant differences in dental composite contain filler-coated MPTMS with different thickness. Dental composite prototype based on diametral tensile strength and reflectance evaluation were potential to be used as alternative dental restoration.

Niobium containing bioactive glasses as remineralizing filler for adhesive resins

ObjectiveThe aim of this study was to incorporate sol–gel-derived bioactive glass as filler into experimental adhesive resins and evaluate the influence of glass composition on the physicochemical and biological properties of the developed adhesives. Materials and methodsSol–gel particles were produced with or without the addition of niobium (BAGNb or BAG, respectively). The produced particles were incorporated (2wt%) into experimental adhesive resins formulated with 66wt% bisphenol A-glycidyl methacrylate and 33wt% hydroxyethyl methacrylate. Ethyl dimethyl-4-aminobenzoate and camphorquinone were used as photoinitiator system. Two experimental groups were produced: ABAGNb and ABAG. The adhesive without particles was used as control (ACG). The materials were tested for their degree of conversion, softening in solvent, and cytotoxicity. The mineral deposition was analyzed by Raman spectroscopy. Flexural strength and immediate and 1-year microtensile bond strength were evaluated. ResultsNo statistical difference was found in degree of conversion. ABAGNb showed reduced softening and higher mineral deposition than ACG and ABAG after 28 days. ABAG and ABAGNb resulted in higher cell viability and lower flexural strength when compared to ACG. After 1-year, ABAGNb and ABAG presented statistically significant lower μTBS values. SignificanceSol–gel-derived bioactive glasses promoted increased mineral deposition and cell viability for experimental adhesives with increased phosphate content and longitudinal μTBS values for the ABAGNb group. These results suggest the potential of the studied particles to be applied as bioactive fillers for dental adhesives. Reductions in longitudinal μTBS and flexural strength, however, were observed for both glasses compositions and must be considered.

Development of Bis-GMA-free biopolymer to avoid estrogenicity

ObjectiveAlthough bisphenol A-glycidyl methacrylate (Bis-GMA)-based dental materials are widely used in dentistry, Estrogenicity from released bisphenol A remains a concern due to possibility of adversely affecting the growth of children and homeostasis of adults. Here, a new family of isosorbide-derived biomonomers were synthesized and experimentally utilized as a matrix of dental sealants to provide physico-mechanical and biological properties comparable to those of a conventional Bis-GMA-based material but without the the potential estrogenicity. MethodsAfter synthesis of isosorbide-derived biomonomers (ISDB) by light polymerization, an experimental dental sealant with different silica filler concentrations (0–15wt%) was characterized and compared to a commercially available Bis-GMA-based sealant. Cytotoxicity and estrogenicity assays were conducted with human oral keratinocytes and estrogen-sensitive MCF-7 cells, respectively. ResultsISDB-based dental sealants exhibited typical initially smooth surfaces with depth of cure, Vickers hardness, compressive strength/modulus, water resorption/solubility, and flowability comparable to those of the commercial sealant and met the ISO standard for dental sealants and polymer-based restorative materials. Indirect cytotoxicity tests using an extract showed comparable viability among experimental ISDB-based materials and a commercial Bis-GMA-incorporated control. DNA synthesis in MCF-7 cells (a marker of estrogenicity) and the release of bisphenol A under enzymatic incubation were not detected in ISDB-based materials. SignificanceIn conclusion, the comparable physico-mechanical properties of ISDB-based materials with their cytocompatibility and lack of estrogenicity suggest the potential usefulness of ISDBs as a newly developed and safe biomaterial.

Degree of conversion of experimental resin composites containing bioactive glass 45S5: the effect of post-cure heating

Resin composites containing reinforcing inert glass fillers combined with bioactive glass (BG) can aid in the prevention of secondary caries, which is a major cause of failure of contemporary composite restorations. A series of previous studies on experimental resin composites filled with BG 45S5 has demonstrated that methacrylate resin polymerization can be impaired by the addition of unsilanized BG, leading to lower degrees of conversion (DC). In order to distinguish whether the polymerization inhibition is caused by a direct (temperature-independent) effect of BG or an indirect (temperature-dependent) effect of restricted mobility of reactive species, this study used Raman spectroscopy to evaluate the DC values of experimental composites post-cured at 37 °C and 150 °C. The potential of BG to adversely affect DC was highly dependent on the resin system. The highest DC reduction was observed in the resin system based on ethoxylated bisphenol A dimethacrylate (Bis-EMA), followed by bisphenol A glycidyl methacrylate (Bis-GMA). In contrast, the DC for urethane dimethacrylate (UDMA) was not compromised by BG. Increasing the mobility of reactive species by heating at 150 °C showed limited potential for increasing the DC in the Bis-EMA and Bis-GMA resin systems, indicating a direct inhibitory effect of BG on polymerization.

Effect of diphenyliodonium hexafluorphosphate in the yellowing and properties of experimental resin cements

Aim: The yellowing effect is undesirable and can occur in the dental restoration margins when light-cured resin cements containing camphorquinone as photoinitiator is used. This study aimed to evaluate the effect of diphenyliodonium hexafluorphosphate (DPI) in photoinitiator systems that contained different concentrations of camphorquinone (CQ) and dimethylamino ethyl benzoate (EDAB) on resin cements. Methods: A base (1:1) of bisphenol A diglycidyl methacrylate (BisGMA) and triethylene glycol dimethacrylate (TEGDMA) was obtained, and 60wt% of glass fillers was added. Eight formulations were obtained: RC1 (0.5mol% CQ / 1mol% EDAB), RC2 (0.5mol% CQ / 2mol% EDAB), RC3 (1mol% CQ / 1mol% EDAB), RC4 (1mol% CQ / 2mol% EDAB), and RC5 to RC8, which contained the same bases plus 0.5mol% DPI. Experimental resin cements were evaluated by the degree of conversion (DC), L*a*b* color analysis, water sorption (WS) and solubility (S), flexural strength, and Elastic Modulus. The data were analyzed by three-way ANOVA, Tukey’s and Mann-Whitney tests (α = 0.05). Results: The combination of DPI and 0.5mol% CQ increased DC in RC6 and L* in RC5 without increasing the WS and a* b* values. CQ at 1mol% showed higher values of b* and lower values of a*, except for RC3. Groups with 2mol% EDAB showed higher DC. Conclusion: The addition of DPI reduces CQ, generating a decreased yellowing effect, while maintaining adequate properties in the resin cements, especially with 2mol% EDAB.

Synthesis of antibacterial dimethacrylate derived from niacin and its application in preparing antibacterial dental resin system

In this research, a bio-based monomer 1,3-bis(methacryloyloxy)propyl-carbonyl- hexylpyridinium bromide (QANMA) that derived from niacin was synthesized and incorporated into Bisphenol A glycidyl methacrylate (Bis-GMA)/triethylene glycol dimethacrylate (TEGDMA) (50 wt/50 wt) with a series of mass fraction as antibacterial agent. The double bond conversion (DC), volumetric shrinkage (VS), mechanical properties, water sorption (WS) and solubility (SL) were investigated among groups with different QANMA concentrations. Antibacterial activity against S. mutans were conducted by bacteria colony counting and bacteria LIVE/DEAD staining. The results showed that QANMA had no influence on DC of dental resin (p > 0.05), but would lead to lower volumetric shrinkage (p < 0.05). Only dental resin with 10 wt% and 20 wt% of QANMA showed obviously antibacterial activity. Mechanical properties, WS and SL of dental resin could be impaired by incorporation QANMA, flexural strength and modulus were decreased with the increasing of QANMA concentration (p < 0.05), while WS and SL were increased with the increasing of QANMA concentration (p < 0.05). Dental resin with 10 wt% of QANMA seemed to be the optimal resin system in this research, for it showed significant antibacterial activity and its flexural strength was still met the requirement of ISO standard. This work suggested that bio-based monomer QANMA could be used as antibacterial agent in dental materials, but further optimization experiment and biocompatibility evaluation should be taken in future.