bisphenol-A Glycidyl Dimethacrylate Research Articles

Novel dental adhesive with triple benefits of calcium phosphate recharge, protein-repellent and antibacterial functions

ObjectiveA new adhesive containing nanoparticles of amorphous calcium phosphate (NACP) with calcium (Ca) and phosphate (P) ion rechargeability was recently developed; however, it was not antibacterial. The objectives of this study were to: (1) develop a novel adhesive with triple benefits of Ca and P ion recharge, protein-repellent and antibacterial functions via dimethylaminohexadecyl methacrylate (DMAHDM) and 2-methacryloyloxyethyl phosphorylcholine (MPC); and (2) investigate dentin bond strength, protein adsorption, Ca and P ion concentration, microcosm biofilm response and pH properties. MethodsMPC, DMAHDM and NACP were mixed into a resin consisting of ethoxylated bisphenol A dimethacrylate (EBPADMA), pyromellitic glycerol dimethacrylate (PMGDM), 2-hydroxyethyl methacrylate (HEMA) and bisphenol A glycidyl dimethacrylate (BisGMA). Protein adsorption was measured using a micro bicinchoninic acid method. A human saliva microcosm biofilm model was tested on resins. Colony-forming units (CFU), live/dead assay, metabolic activity, Ca and P ion concentration and biofilm culture medium pH were determined. ResultsThe adhesive with 5% MPC+5% DMAHDM+30% NACP inhibited biofilm growth, reducing biofilm CFU by 4 log, compared to control (p<0.05). Dentin shear bond strengths were similar (p>0.1). Biofilm medium became a Ca and P ion reservoir having ion concentration increasing with NACP filler level. The adhesive with 5% MPC+5% DMAHDM+30% NACP maintained a safe pH>6, while commercial adhesive had a cariogenic pH of 4. SignificanceThe new adhesive with triple benefits of Ca and P ion recharge, protein-repellent and antibacterial functions substantially reduced biofilm growth, reducing biofilm CFU by 4 orders of magnitude, and yielding a much higher pH than commercial adhesive. This novel adhesive is promising to protect tooth structures from biofilm acids. The method of using NACP, MPC and DMAHDM is promising for application to other dental materials to combat caries.

Polymer-based material containing calcium phosphate particles functionalized with a dimethacrylate monomer for use in restorative dentistry.

Dicalcium phosphate dihydrate particles functionalized with triethyleneglycol dimethacrylate were synthesized and added to a photocurable mixture of bisphenol-A glycidyl dimethacrylate and triethyleneglycol dimethacrylate with the purpose of developing a resin composite capable of releasing calcium and phosphate ions to foster dental remineralization. Particle functionalization would minimize the deleterious effect of adding low cohesive strength nano-structured particles with no chemical interaction with the organic matrix on the material's mechanical properties. The results showed that calcium release over 28 days was not impaired by particle functionalization. A statistically significant 32% increase in strength was recorded with the use of functionalized dicalcium phosphate dihydrate in comparison to the material containing non-functionalized particles. However, the strength of the unfilled resin was not matched by the composite with functionalized particles. Elastic modulus increased with particle incorporation, regardless of functionalization. Degree of conversion and optical properties (total transmittance and color change/ΔE) of the resin-based materials were not affected by the addition of dicalcium phosphate dihydrate particles (functionalized or not).

Rechargeable calcium phosphate orthodontic cement with sustained ion release and re-release.

White spot lesions (WSL) due to enamel demineralization are major complications for orthodontic treatments. Calcium phosphate (CaP) dental resins with Ca and P ion releases are promising for remineralization. However, previous Ca and P releases lasted for only weeks. Experimental orthodontic cements were developed using pyromellitic glycerol dimethacrylate (PMGDM) and ethoxylated bisphenol A dimethacrylate (EBPADMA) at mass ratio of 1:1 (PE); and PE plus 10% of 2-hydroxyethyl methacrylate (HEMA) and 5% of bisphenol A glycidyl dimethacrylate (BisGMA) (PEHB). Particles of amorphous calcium phosphate (ACP) were incorporated into PE and PEHB at 40% filler level. Specimens were tested for bracket-enamel shear bond strength, water sorption, CaP release, and ion recharge and re-release. PEHB+40ACP had higher bracket-enamel bond strength and ion release and rechargeability than PE+40ACP. ACP incorporation into the novel orthodontic cement did not adversely affect the bracket-enamel bond strength. Ion release and re-release from the novel ACP orthodontic cement indicated favorable release and re-release patterns. The recharged orthodontic cement could release CaP ions continuously for four weeks without further recharge. Novel rechargeable orthodontic cement containing ACP was developed with a high bracket-enamel bond strength and the ability to be repeatedly recharged to maintain long-term high levels of CaP ion releases.

Bioactive glass surface for fiber reinforced composite implants via surface etching by Excimer laser

Biostable fiber-reinforced composites (FRC) prepared from bisphenol-A-glycidyldimethacrylate (BisGMA)-based thermosets reinforced with E-glass fibers are promising alternatives to metallic implants due to the excellent fatigue resistance and the mechanical properties matching those of bone. Bioactive glass (BG) granules can be incorporated within the polymer matrix to improve the osteointegration of the FRC implants. However, the creation of a viable surface layer using BG granules is technically challenging. In this study, we investigated the potential of Excimer laser ablation to achieve the selective removal of the matrix to expose the surface of BG granules. A UV–vis spectroscopic study was carried out to investigate the differences in the penetration of light in the thermoset matrix and BG. Thereafter, optimal Excimer laser ablation parameters were established. The formation of a calcium phosphate (CaP) layer on the surface of the laser-ablated specimens was verified in simulated body fluid (SBF). In addition, the proliferation of MG63 cells on the surfaces of the laser-ablated specimens was investigated. For the laser-ablated specimens, the pattern of proliferation of MG63 cells was comparable to that in the positive control group (Ti6Al4V). We concluded that Excimer laser ablation has potential for the creation of a bioactive surface on FRC-implants.

Comparative evaluation of marginal leakage of provisional crowns cemented with different temporary luting cements: In vitro study.

Background or Statement of Problem:As, the longevity of provisional restorations is related to, a perfect adaptation and a strong, long-term union between restoration and teeth structures, therefore, evaluation of marginal leakage of provisional restorative materials luted with cements using the standardized procedures is essential.Aims and Objectives:To compare the marginal leakage of the provisional crowns fabricated from Autopolymerizing acrylic resin crowns and bisphenol A-glycidyl dimethacrylate (BIS-GMA) resin crowns. To compare the marginal leakage of the provisional crowns fabricated from autopolymerizing acrylic resin crowns and BIS-GMA resin crowns cemented with different temporary luting cements. To compare the marginal leakage of the provisional crowns fabricated from autopolymerizing acrylic resin (SC-10) crowns cemented with different temporary luting cements. To compare the marginal leakage of the provisional crowns fabricated from BIS-GMA resin crowns (Protemp 4) cemented with different temporary luting cements.Methodology:Freshly extracted 60 maxillary premolars of approximately similar dimensions were mounted in dental plaster. Tooth reduction with shoulder margin was planned to use a customized handpiece-holding jig. Provisional crowns were prepared using the wax pattern fabricated from computer aided designing/computer aided manufacturing milling machine following the tooth preparation. Sixty provisional crowns were made, thirty each of SC-10 and Protemp 4 and were then cemented with three different luting cements. Specimens were thermocycled, submerged in a 2% methylene blue solution, then sectioned and observed under a stereomicroscope for the evaluation of marginal microleakage. A five-level scale was used to score dye penetration in the tooth/cement interface and the results of this study was analyzed using the Chi-square test, Mann–Whitney U-test, Kruskal–Wallis H-test and the results were statistically significant P < 0.05 the power of study - 80%.Results:Marginal leakage was significant in both provisional crowns cemented with three different luting cements along the axial walls of teeth (P < 0.05) confidence interval - 95%.Conclusion:The temporary cements with eugenol showed more microleakage than those without eugenol. SC-10 crowns showed more microleakage compared to Protemp 4 crowns. SC-10 crowns cemented with Kalzinol showed maximum microleakage and Protemp 4 crowns cemented with HY bond showed least microleakage.

Microleakage of Glass Ionomer-based Provisional Cement in CAD/CAM-Fabricated Interim Crowns: An in vitro Study.

The aim of this study was to compare in vitro the marginal microleakage of glass ionomer-based provisional cement with resin-based provisional cement and zinc oxide non-eugenol (ZONE) provisional cement in computer-aided design and computer-aided manufacturing (CAD/CAM)-fabricated interim restorations. Fifteen intact human premolars were prepared in a standardized manner for complete coverage of crown restorations. Interim crowns for the prepared teeth were then fabricated using CAD/CAM, and the specimens were randomized into three groups of provisional cementing agents (n = 5 each): Glass ionomer-based provisional cement (GC Fuji TEMP LT™), bisphenol-A-glycidyldimethacrylate (Bis-GMA)/ triethylene glycol dimethacrylate (TEGDMA) resin-based cement (UltraTemp® REZ), and ZONE cement (TempBond NE). After 24 hours of storage in distilled water at 37°C, the specimens were thermocycled and then stored again for 24 hours in distilled water at room temperature. Next, the specimens were placed in freshly prepared 2% aqueous methylene blue dye for 24 hours and then embedded in autopolymerizing acrylic resin blocks and sectioned in buccolingual and mesiodistal directions to assess dye penetration using a stereomicroscope. The results were statistically analyzed using a nonparametric Kruskal-Wallis test. Dunn's post hoc test with a Bonferroni correction test was used to compute multiple pairwise comparisons that identified differences among groups; the level of significance was set at p < 0.05. All groups exhibited marginal microleakage; the Bis-GMA/TEGDMA resin-based provisional cement demonstrated the lowest microleakage scores, which were statistically different from those of the glass ionomer-based provisional cement and the ZONE cement. The provisional cementing agents exhibited different sealing abilities. The Bis-GMA/TEGDMA resin-based provisional cement exhibited the most effective favorable sealing properties against dye penetration compared with the glass ionomer-based provisional cement and conventional ZONE cement. Newly introduced glass ionomer-based provisional cement proved to be inferior to resin-based provisional cement as far as marginal microleakage is concerned.

Novel rechargeable calcium phosphate dental nanocomposite

ObjectivesCalcium phosphate (CaP) composites with Ca and P ion release can remineralize tooth lesions and inhibit caries. But the ion release lasts only a few months. The objectives of this study were to develop rechargeable CaP dental composite for the first time, and investigate the Ca and P recharge and re-release of composites with nanoparticles of amorphous calcium phosphate (NACP) to achieve long-term inhibition of caries. MethodsThree NACP nanocomposites were fabricated with resin matrix of: (1) bisphenol A glycidyl dimethacrylate (BisGMA) and triethylene glycol dimethacrylate (TEGDMA) at 1:1 mass ratio (referred to as BT group); (2) pyromellitic glycerol dimethacrylate (PMGDM) and ethoxylated bisphenol A dimethacrylate (EBPADMA) at 1:1 ratio (PE group); (3) BisGMA, TEGDMA, and Bis[2-(methacryloyloxy)ethyl] phosphate (BisMEP) at 2:1:1 ratio (BTM group). Each resin was filled with 20% NACP and 50% glass particles, and the composite was photo-cured. Specimens were tested for flexural strength and elastic modulus, Ca and P ion release, and Ca and P ion recharge and re-release. ResultsNACP nanocomposites had strengths 3-fold of, and elastic moduli similar to, commercial resin-modified glass ionomer controls. CaP ion recharge capability was the greatest for PE group, followed by BTM group, with BT group being the lowest (p<0.05). For each recharge cycle, CaP re-release reached similarly high levels, showing that CaP re-release did not decrease with more recharge cycles. After six recharge/re-release cycles, NACP nanocomposites without further recharge had continuous CaP ion release for 42 d. SignificanceNovel rechargeable CaP composites achieved long-term and sustained Ca and P ion release. Rechargeable NACP nanocomposite is promising for caries-inhibiting restorations, and the Ca and P ion recharge and re-release method has wide applicability to dental composites, adhesives, cements and sealants to achieve long-term caries-inhibition.

BisGMA/EPDM/amine functionalised MWCNTs based nanocomposites

Purpose– This paper aims to focus on the development and study properties of bisphenol-A glycidyldimethacrylate (BisGMA) and ethylene–propylene–diene monomer (EPDM) blend-based nanocomposites containing amine-functionalised multi-walled carbon nanotubes (MWCNT-NH2) as a compatibiliser.Design/methodology/approach– First, BisGMA was synthesised from epoxy and methacrylic acid followed by the amine functionalisation of MWCNTs. A novel two-roll milling technique was then conducted to prepare nanocomposite specimens with MWCNT-NH2 as compatibiliser. Effect of MWCNT-NH2 content on the mechanical, thermal, electrical, corrosive and water absorption properties of the nanocomposites was investigated and results have been reported.Findings– The results of the present work reveal that MWCNT-NH2 acts as a potential compatibiliser and nanofiller in BisGMA/EPDM blend-based nanocomposites. The authors report here that the nanocomposites exhibit improved mechanical, thermal and electrical properties with increased addition of MWCNT-NH2. Moreover, desirable results are obtained at 5 phr of nanofiller loading beyond which the properties deteriorate due to particle agglomeration. The nanocomposites display negligible corrosion and water absorption characteristics. Thus, the above fabricated nanocomposites with optimum compatibiliser content can serve as low-cost structural, thermal and electrical materials which can also be utilised in corrosive and moist environments.Research limitations/implications– The present investigation has come up with the successful and cost-effective fabrication of BisGMA/EPDM blend-based nanocomposites with optimum nanofiller/compatibiliser (MWCNT-NH2) content that can be used for a wide range of structural, thermal and electrical projects, as it is corrosion and moisture resistant. It is also the most durable from the mechanical point of view.Originality/value– The above nanocomposites have never been designed before.

Rechargeable dental adhesive with calcium phosphate nanoparticles for long-term ion release

ObjectivesThe tooth-resin bond is the weak link of restoration, with secondary caries as a main reason for failure. Calcium phosphate-containing resins are promising for remineralization; however, calcium (Ca) and phosphate (P) ion releases last only a couple of months. The objectives of this study were to develop the first rechargeable CaP bonding agent and investigate the key factors that determine CaP ion recharge and re-release. MethodsNanoparticles of amorphous calcium phosphate (NACP) were synthesized. Pyromellitic glycerol dimethacrylate (PMGDM), ethoxylated bisphenol-A dimethacrylate (EBPADMA), 2-hydroxyethyl methacrylate (HEMA), and bisphenol-A glycidyl dimethacrylate (BisGMA) were used to synthesize three adhesives (denoted PE, PEH and PEHB). NACP were mixed into adhesive at 0–30% by mass. Dentin shear bond strengths were measured. Adhesive specimens were tested for Ca and P initial ion release. Then the ion-exhausted specimens were immersed in Ca and P solution to recharge the specimens, and the recharged specimens were then used to measure ion re-release for 7 days as one cycle. Then these specimens were again recharged and the re-release was measured for 7 days as the second cycle. Three recharge/re-release cycles were tested. ResultsPEHB had the highest dentin bond strength (p<0.05). Increasing NACP content from 0 to 30% did not affect dentin bond strength (p>0.1), but increased CaP release and re-release (p<0.05). PEHB-NACP had the greatest recharge/re-release, and PE-NACP had the least (p<0.05). Ion release remained high and did not decrease with increasing the number of recharge/re-release cycles (p>0.1). After the third cycle, specimens without further recharge had continuous CaP ion release for 2–3 weeks. SignificanceRechargeable CaP bonding agents were developed for the first time to provide long-term Ca and P ions to promote remineralization and reduce caries. Incorporation of NACP into adhesive had no negative effect on dentin bond strength. Increasing NACP filler level increased the ion recharge and re-release capability. The new CaP recharge method and PMGDM-EBPADMA-NACP composition may have wide application in adhesives, composites and cements, to combat caries and remineralize lesions.

2-hydroxyethyl Acrylate Grafted Jute Fiber/ Treated Coir Pith/Vinyl ester Hybrid Composites

The present work demonstrates the fabrication and properties study of Vinyl ester i.e. Bisphenol-A glycidyldimethacrylate (BisGMA) composites hybridized with 2-hydroxyethyl acrylate (HEA-10% w/w) grafted jute fiber and aqueous NaOH (5% w/w) treated coir pith used in various proportions and to characterize thereof. The mechanical and dynamic mechanical properties were measured in dependence of treated & untreated fiber as well as filler content. Composite with HEA grafted jute fiber and coir pith (15 wt%) exhibited maximum improvement in the above mentioned properties. Thermogravimetric analysis indicated the thermal stability of composites due to effective hybridization. The corrosive and water ingress properties of the composites were found to be negligible contributing to longer durability of the panels in moist and corrosive conditions.

BisGMA-polyvinylpyrrolidone blend based nanocomposites reinforced with chitosan grafted f-multiwalled carbon nanotubes

In this work, initially a non-destroyable surface grafting of acid functionalized multiwalled carbon nanotubes (f-MWCNTs) with biopolymer chitosan (CS) was carried out using glutaraldehyde as a cross-linking agent via the controlled covalent deposition method which was characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Then, BisGMA (bisphenol-A glycidyldimethacrylate)-polyvinylpyrrolidone (PVP) blend was prepared (50:50wt%) by a simple sonication method. The CS grafted f-MWCNTs (CS/f-MWCNTs) were finally dispersed in BisGMA-PVP blend (BGP50) system in different compositions i.e. 0, 2, 5 and 7wt% and pressed into molds for the fabrication of reinforced nanocomposites which were characterized by SEM. Nanocomposites reinforced with 2wt% raw MWCNTs and acid f-MWCNTs were also fabricated and their properties were studied in detail. The results of comparative study report lower values of the investigated properties in nanocomposites with 2wt% raw and f-MWCNTs than the one with 2wt% CS/f-MWCNTs proving it to be a better reinforcing nanofiller. Further, the mechanical behavior of the nanocomposites with various CS/f-MWCNTs content showed a dramatic increase in Young’s Modulus, tensile strength, impact strength and hardness along with improved dynamic mechanical, thermal and electrical properties at 5wt% content of CS/f-MWCNTs. The addition of CS/f-MWCNTs also resulted in reduced corrosion and swelling properties. Thus, the fabricated nanocomposites with optimum nanofiller content could serve as low cost and light weight structural, thermal and electrical materials compatible in various corrosive and solvent based environments.

Mapping camphorquinone consumption, conversion and mechanical properties in methacrylates with systematically varied CQ/amine compositions

ObjectivesTo evaluate conversion, bulk mechanical properties and camphorquinone (CQ) consumption in methacrylate resins, comprising a range of overall initiator concentrations and CQ/amine ratios. MethodsBisGMA (Bisphenol-A glycidyl dimethacrylate), TEGDMA (triethyleneglycol dimethacrylate) and UDMA (urethane dimethacrylate) were mixed at a 1:1:1 molar ratio. CQ was used as the visible light photosensitizer, in combination with EDMAB (Ethyl p-dimethylamino benzoate), at 3:1, 2:1, 1:1, 1:2 and 1:3 weight ratios, at 0.5, 1.0, 1.5, 2.0 and 3.0wt% overall initiator concentration. Butylhydroxytoluene was added at 0.05wt% as an inhibitor. Unfilled resins were photoactivated with a dental light source (VIP Jr, Bisco) for 60s at 600mW/cm2. Flexural strength/modulus were assessed in 2×1×10mmbars, tested in three-point bending. Degree of conversion was assessed at the bottom of the same specimens using FT-RAMAN. CQ consumption was measured using a UV–vis spectrometer. Data were analyzed with two-way ANOVA/Tukey test (α=5%). ResultsLower conversion and inferior mechanical properties were observed with lower overall initiator concentrations and higher amine/CQ ratios. The lowest overall initiator concentration (0.5%) presented the statistically lowest conversion/properties results, except for the 1:3 amine/CQ ratio. For overall concentrations equal or greater to 1.5%, the amine/CQ ratio did not influence conversion or mechanical properties. CQ consumption was less efficient for the highest overall initiator concentrations and lower amine/CQ ratios. Clinical relevanceAbove 1.5wt% overall initiator concentration, the conversion and general mechanical properties were independent of the initiator concentration. Therefore, there seems to be no benefit to increasing the initiator concentration above that level. At higher camphorquinone concentrations, light transmission and photosensitizer consumption becomes impaired, which could lead to decreased depth of cure and yellowing of the restoration.

BisGMA/jute fibre/fly ash hybrid composites

Purpose – This paper aims to prepare BisGMA (bisphenol-A glycidyldimethacrylate)/jute fibre/fly ash hybrid composites with improved mechanical and corrosive properties. Design/methodology/approach – BisGMA prepolymer was first synthesised using diglycidyl ether of bisphenol-A and methacrylic acid. Then 2-hydroxy ethylacrylate-treated jute fibre and sodium hydroxide-treated fly ash were incorporated in the fabrication of composites using dicumyl peroxide, cobalt naphthenate and N,N-dimethyl aniline as catalyst, accelerator and promoter, respectively. The composition of BisGMA, jute fibre and fly ash was kept constant, whereas treated and untreated jute fibre and fly ash were used alternatively. Findings – Treatment of both jute and fly ash leads to improved mechanical properties of composites. However, treated fabric plays a dominant role compared to treated fly ash as filler. Among all the composites, the one having both treated jute fibre and treated fly ash is the most suitable composite for structural applications. Research limitations/implications – The present investigation has come up with a hybrid composite that can be used for a wide range of applications like low-cost housing and structural projects, structural laminates, etc., as it is both corrosion- and moisture-resistant. It is also the most durable from the mechanical point of view. There is also a scope of using other fillers instead of fly ash to study the changes brought about in the mechanical properties. Originality/value – The above composites have never been fabricated before.

BisGMA-induced cytotoxicity and genotoxicity in macrophages are attenuated by wogonin via reduction of intrinsic caspase pathway activation.

Bisphenol-A-glycidyldimethacrylate (BisGMA) is a frequently used monomer in dental restorative resins. However, BisGMA could leach from dental restorative resins after polymerization leading to inflammation in the peripheral environment. Wogonin, a natural flavone derivative, has several benefits, such as antioxidative, anti-inflammatory and neuroprotective properties. Pretreatment of macrophage RAW264.7 cells with wogonin inhibited cytotoxicity which is induced by BisGMA in a concentration-dependent manner. BisGMA induced apoptotic responses, such as redistribution of phosphatidylserine from the internal to the external membrane and DNA fragmentation, were decreased by wogonin in a concentration-dependent manner. In addition, BisGMA-induced genotoxicity, which detected by cytokinesis-blocked micronucleus and single-cell gel electrophoresis assays, were inhibited by wogonin in a concentration-dependent manner. Furthermore, wogonin suppressed BisGMA-induced activation of intrinsic caspase pathways, such as caspases-3 and -8. Parallel trends were observed in inhibition of caspase-3 and -8 activities, apoptosis, and genotoxicity. These results indicate wogonin suppressed the BisGMA-induced apoptosis and genotoxicity mainly via intrinsic caspase pathway in macrophages.

Influence of intermediate resin on the bond strength of light-curing composite resin to polymer substrate

Objectives. The aim of this study was to examine the effect of intermediate resin (IMR) of different monomer compositions and viscosities on the shear bond strength between polymer substrate and light-curing composite. Methods. The substrate used in the study was an autopolymerizing polymethyl methacrylate (PMMA) based polymer. The substrate was treated with the IMR for 3 min before application of light polymerizable particulate filler composite resin. The monomers of the IMR were either bisphenol-A-glycidyl dimethacrylate (BisGMA) and triethyleneglycol dimethacrylate (TEGDMA) or BisGMA and methyl methacrylate (MMA). The shear bond strength of the IMR treated substrate to the particulate filler composite was evaluated after storing the specimens dry and after thermocycling the specimens in water. Light microscope examination was accomplished to determine the swelled layer of the substrate. Results. Significant differences were found between the shear bond strength values of the IMRs (p < 0.001). The bond strengths were generally higher in the BisGMA-MMA groups than in the BisGMA-TEGDMA groups. Two-way ANOVA revealed significant effects of type of IMR (p < 0.001) and thermocycling (p = 0.017) on the shear bond strength. No interaction was found between these variables (p > 0.05). Conclusions. The results suggest that the monomer composition and ratio of the IMRs used in the study influence the shear bond strength of the polymer substrate to the new resin.

Cell toxicity of methacrylate monomers—The role of glutathione adduct formation

Polymer-based dental restorative materials are designed to polymerize in situ. However, the conversion of methacrylate monomer to polymer is never complete, and leakage of the monomer occurs. It has been shown that these monomers are toxic in vitro; hence concerns regarding exposure of patients and dental personnel have been raised. Different monomer methacrylates are thought to cause toxicity through similar mechanisms, and the sequestration of cellular glutathione (GSH) may be a key event. In this study we examined the commonly used monomer methacrylates, 2-hydroxyethylmethacrylate (HEMA), triethylenglycol-dimethacrylate (TEGDMA), bisphenol-A-glycidyl-dimethacrylate (BisGMA), glycerol-dimethacrylate (GDMA) and methyl-methacrylate (MMA). The study aimed to establish monomers' ability to complex with GSH, and relate this to cellular toxicity endpoints. Except for BisGMA, all the monomer methacrylates decreased the GSH levels both in cells and in a cell-free system. The spontaneous formation of methacrylate-GSH adducts were observed for all methacrylate monomers except BisGMA. However, we were not able to correlate GSH depletion and toxic response measured as SDH activity and changes in cell growth pattern. Together, the current study indicates mechanisms other than GSH-binding to be involved in the toxicity of methacrylate monomers.

The Effect of Inhibitor Concentrations on the Chemical and Mechanical Properties of Bis-GMA-Based Resin Dental Composites

Bis-GMA (Bisphenol A glycidyl methacrylate) based resin composites in dentistry require UV induced light polymerization to be used as restorative materials. This polymerization induces shrinkage stresses on command light polymerization, which can be clinically significant. To resolve this issue inhibitors such as Bisphenol-A-glycidyl dimethacrylate (BHT) have been introduced as an alternative method to try to decrease this polymerization shrinkage. However increases in inhibitor concentration whilst reducing polymerization shrinkage might induce an effect on the mechanical properties of the resin composite. In addition, the oral cavity is a fluid environment and can induce changes in the resin composite. The aim of this study was to try to determine if an increase in inhibitor concentration had an effect on the flexural strength and elastic modulus of resin composites after short and medium term aging immersion. These assessments were accomplished by looking at Flexural Strength and Elastic Modulus after short and medium term aging immersion. An experimental composite was prepared using a blend of Bisphenol A glycidyl dimethacrylate (Bis-GMA): Urethane Dimethacrylate (UDMA): Triethylene glycol dimethacrylate (TEGDMA) (1:1:1 weight ratio) with 70 wt% silanized glass fillers. Four group concentrations of BHT were tested mechanically using flexural strength and elastic modulus. Based on this laboratory study, changes in BHT concentrations can induce and maintain high strength in resin composites.

Observation of oxygen inhibited layer of organic dental resin by confocal Raman-microscopy

AbstractThis study investigated degrees of conversion of oxygen inhibited layer (OIL) of organic dental resins for restoration using Confocal-Raman spectroscopy. The aim was to determine which laser is adapted to determine the degrees of conversion of OIL and to measure variations of thickness and degrees of conversion in OIL with respect to monomers proportions. Bis-GMA (bis-phenol A glycidyl dimethacrylate) and TEGDMA (triethylene glycol dimethacrylate) based resins with various ratio of an equimolecular mixture of camphorquinone/EDMAB (ethyl (4-dimethyl amino) benzoate) were studied with different lasers by confocal- Raman spectroscopy. Results show that this technique is adapted for the non destructive measurement of OIL. The Thickness of OIL is not correlated with the proportions of Bis-GMA and TEGDMA in the resin and was close to 3-4μm. Thickness of OIL is very thin without inorganic fillers (3 or 4 μm). Inorganic fillers might be responsible of greater OIL in composite resins.

Synergistic interaction caused to human gingival fibroblasts from dental monomers

ObjectivesThe toxicity of monomers like bisphenol-A-glycidyldimethacrylate (BisGMA) and urethane-dimethacrylate (UDMA) to cells is well studied. In these studies solubilizers, which have a toxic potential, are used to dissolve the basic monomers in the aqueous medium. In these experiments it is not possible to confidently exclude a synergistic effect of basic monomers and solubilizers in cells. Moreover, less is known about the synergistic interaction between basic- and comonomers (triethyleneglycoldimethacrylate (TEGDMA); 2-hydroxyethylmethacrylate (HEMA)) in cells. We dissolved the basic monomers in the comonomers and incubated human gingival fibroblasts (HGFs) with these binary mixtures in different concentrations. MethodsProliferating HGFs monolayers were cultured in the absence or presence of mixtures of BisGMA/TEGDMA, BisGMA/HEMA, UDMA/TEGDMA and UDMA/HEMA. Twenty-four hours later XTT was added and the formazan formation was quantified. EC50 values were obtained at half-maximum-effect concentrations from fitted curves. ResultsEC50 values were (mmol/l; mean±sem; n=5): 0.01 BisGMA/0.48 TEGDMA; 0.04 BisGMA/4.99 HEMA; 0.04 UDMA/1.60 TEGDMA and 0.02 UDMA/2.26 HEMA.All tested mixtures induced a dose-dependent loss of viability in HGFs after 24h. SignificanceThe EC50 values of binary mixtures were significantly (p<0.05) lower compared to the EC50 values of the pure substances indicating a synergistic interaction of the mixtures on the HGFs. The widely used (co)monomers BisGMA and TEGDMA have the lowest EC50 values. The highest decrease of EC50 values, compared with the pure substances, were found in the mixture UDMA/HEMA. Worst case calculations show that the EC50 values from binary mixtures are at least 6 fold lower compared with known amounts of elutable (co)monomers from polymerized composites.

Changes in soft tissues around immediate full‐arch rehabilitations: a prospective study

Nowadays, aesthetic appearance is receiving more and more attention from clinicians and patients. Therefore, it is of paramount importance for the surgeon to maintain or to improve the quality and the stability of the soft tissue-implant interface. The scientific literature supports the idea that the immediate placement and provisionalization of endosseus implants and abutments can indeed offer additional clinical control over the peri-implant tissue architecture. On this basis, this prospective study aims to evaluate the changes in soft tissues around immediately loaded dental implants in full-arch rehabilitations, over a period of 3 months. Fifteen subjects were treated for immediate full-arch rehabilitations. Following implant placement, provisional rehabilitations made of bisphenol-A-glycidyldimethacrylate (BIS-GMA) and resin were placed. All records were made using a periodontal probe. The facial soft-tissue level was measured evaluating the distance between the soft-tissue margin and the incisal edge of the crown. Moreover, papilla levels were measured at the mesial and distal sites from a reference line connecting the occlusal edge of the crowns. The average value at the mesial site was -0.035 mm (±1, median 0 mm), while at the midfacial site, it was 0 mm (±0.76, median 0 mm) and at the distal site, -0.05 mm (±0.92, median 0 mm). The plaque score index showed a reduction during the follow-up period. Our data indicate that no differences at the midfacial point were detectable over the observation period. This is in agreement with several studies; it is plausible that these results are linked to a correct position of the implant in the alveolar socket. Moreover, comparing our results with what has been reported by other authors, it is surprising that while other studies highlight that papilla loss at the mesial and distal aspect is an expected consequence of immediate implant restorations, our data do not show any changes. The explanation of these results remains unclear. Further studies are needed to support our data and to clarify what mechanisms are involved in the maintenance of soft tissue.