Search Results (35)

Dental composites are commonly used for the restoration of hard tooth tissues, but their low fracture toughness may limit their lifespan. In this study, the effect of liquid rubber modification on the mechanical properties and fracture mechanisms of two types of dental composites, flow and classic, was evaluated. The study used experimental composites containing a mixture of dimethacrylate resins: BisGMA (20% by weight), BisEMA (30% by weight), UDMA (30% by weight), and TEGDMA (20% by weight). Composites were reinforced with Al-Ba-B-Si glass, Ba-Al-B-F-Si glass with particle sizes of 0.7 and 2 μm respectively, as well as pyrogenic silica (20 nm). The inorganic phase was introduced in an amount of 50% vol. for flow material and 80% vol. for classic composite. As a modifier, Hypro 2000X168LC VTB liquid rubber (Huntsman International LLC, USA) was used in an amount of 5% by weight relative to the matrix. The flexural strength, Young’s modulus, and fracture toughness were evaluated. Numerical FEM analysis allowed for the evaluation of stress distribution in the filling area. The results confirmed that the modification of composites with liquid rubber contributes to an increase in fracture toughness. For the flow-type material, the fracture toughness increased from 1.04 to 1.13 MPa·m^1/2. At the same time, a decrease in flexural strength from 71.90 MPa to 61.48 MPa and in Young’s modulus from 2.98 GPa to 2.53 GPa. In the case of the classical composite, the modification with liquid rubber also improved the resistance to fracture, increasing it from 1.97 to 2.18 MPa·m^1/2 while the flexural strength decreased from 102.30 MPa to 90.96 MPa, and the modulus dropped from 7.33 GPa to 6.16 GPa. FEA analysis confirmed that modified composites exhibit a more favorable stress distribution with lower tensile stress levels (approximately 20 MPa in contrast to 25 MPa for the classic composite). Mechanisms of fracture and strengthening were also identified. The main fracture mechanism was intermolecular cracking with crack deflections. Modification with liquid rubber resulted in the formation of elastic bridges and plastic shear zones at the front of the crack. Full article

This study aimed to assess how different resin matrix formulations affect the fatigue resistance of resin dental composites. Model dental composites were formulated using six distinct monomer mixtures: two Bis-GMA (bisphenol A-glycidyl methacrylate):TEGDMA (triethylene glycol dimethacrylate) (60:40 and 80:20 mole%), two UDMA (urethane dimethacrylate):TEGDMA (60:40 and 80:20 mole%), one Bis-GMA:UDMA:TEGDMA (35:35:30 mole%), and one Fit852:UDMA:TEGDMA (35:35:30 mole%). Cyclic fatigue resistance (CFR) of the resin composites was measured in a biaxial test mode using staircase analysis. Additional evaluations included biaxial flexural strength (BFS), degree of conversion (DC), water sorption (WS), and viscoelastic properties of the unfilled resins, such as the storage modulus (E′), loss modulus (E″), tan δ (E″/E′), and stiffness (k′). Data were subjected to one-way ANOVA with Tukey post hoc analyses. Pearson correlation and stepwise regression analyses were conducted to examine the relationships among variables. The UT6040 model composite exhibited the highest CFR (82.61 ± 8.83 MPa), significantly outperforming other formulations. Tan δ of the resin matrix showed the strongest correlation with CFR (r = 0.974), and was also shown to be the most influential predictor for the CFR of the particulate composites. The composition of the resin matrix has a significant impact on the CFR of dental composites. Among the properties evaluated, the viscoelastic parameter tan δ emerged as a strong and reliable predictor of CFR, emphasizing the importance of targeting viscoelastic behavior in the design of dental composite formulations. Full article

Background: This study aimed to assess the impact of methacrylate-functionalized polyhedral oligomeric silsesquioxanes dispersed in nanosilica (MA/Ns-POSS) on the mechanical properties of light-curable dental resins and composites. The primary goal was to evaluate how different concentrations of MA/Ns-POSS (0.5–20 wt.%) affect the hardness, flexural strength, modulus, diametral tensile strength, polymerization shrinkage stress, and degree of conversion of these materials. Methods: A mixture of Bis-GMA, UDMA, TEGDMA, HEMA, and camphorquinone, with a tertiary amine as the photoinitiator, was used to create resin and composite samples, incorporating 45 wt.% silanized silica for the composites. Hardness (Vickers method, HV), flexural strength (FS), and flexural modulus (E_f) were assessed using three-point bending tests, while diametral tensile strength (DTS) polymerization shrinkage stresses (PSS), and degree of conversion (DC) analysis were analyzed for the composites. Results: The results showed that resins with 10 wt.% MA/Ns-POSS exhibited the highest E_f and FS values. Composite hardness peaked at 20 wt.% MA/Ns-POSS, while DTS increased up to 2.5 wt.% MA/Ns-POSS but declined at higher concentrations. PSS values decreased with increasing MA/Ns-POSS concentration, with the lowest values recorded at 15–20 wt.%. DC analysis also showed substantial improvement for 15–20 wt.% Conclusion: Incorporating MA/Ns-POSS improves the mechanical properties of both resins and composites, with 20 wt.% showing the best results. Further studies are needed to explore the influence of higher additive concentrations. Full article

A method to prepare free-standing, few-micron-thick films from a dental photopolymer resin, namely UDMA-TEGDMA in a 3:1 weight ratio, doped with gold nanorods, is presented. The method is based on a sandwich structure consisting of a 4 μm thick PVA sacrificial layer, the Au-nanorod/UDMA-TEGDMA nanocomposite layer, and glycerol, all spin-coated sequentially onto a glass slide. Glycerol serves as a cover layer to shut out oxygen during photopolymerization, while the water-soluble PVA enables the subsequent detachment of the nanocomposite film by simple immersion into a liquid bath. Layer thicknesses were controlled by profilometry, while the presence of homogeneously dispersed gold nanorods was confirmed by optical spectroscopy and dark-field optical microscopy. A total of five similar spin-coating scenarios were tested, out of which two approaches produced positive results, with final nanocomposite layer thicknesses in the 2.5–4 μm range, which is smaller than the usual thickness of the oxygen inhibition layer (OIL) commonly present in these types of resins. Optimization of these technological processes and parameters to control film thickness and consistency is discussed in detail. Full article

Resin-based composites are common and widely used materials in dentistry in direct and indirect applications. Their mechanical properties depend on the composition and homogeneity of the resulting structure. This study aims to optimize the mixing process to obtain the most homogeneous mixture possible, which will allow for the better mechanical properties of the composite. A mixture of bis-GMA/UDMA/HEMA/TEGDMA monomers forming a polymer matrix was filled with silanized silica (45 wt%) using different mixing methods. This study analyzed five manufacturing methods—hand mixing (agate mortar), mixing in a centrifugal Hauschild SpeedMixer, and the hybrid method—combined with the abovementioned methods. The effect of the mixing method on the Vickers hardness (HV), flexural strength (FS), compressive strength (CS), and diametral tensile strength (DTS) of the produced composites was investigated, and the stresses generated during composite polymerization were determined. Mechanically prepared composites have the highest flexural strength and hardness. The lowest shrinkage stress was achieved by the composite, which was prepared partially manually. The results showed that the mixing method affects the morphology of the filler and, hence, the strength properties of the resulting material. Full article

To create an orthodontic bracket material combining the favourable properties of ceramic and polymer while minimising their limitations, graded porous ceramic scaffolds were created using unidirectional gelation-freeze casting, following which the pores were infiltrated with polymer. Two processing parameters were investigated: (1) sedimentation times of 0, 8, and 24 h, with ceramic solid loading of 20 vol.% and 2.5 wt.% gelatine concentration, and (2) ceramic solid loadings of 15, 20, and 25 vol.% with a fixed 2.5 wt.% gelatine concentration and an 8 h sedimentation time. The graded ceramic structures demonstrated porosity gradients ranging from 9.86 to 63.84 vol.%, except those with 25 vol.% ceramic solid loading at 8 h sedimentation. The Al₂O₃-UDMA/TEGDMA composites had compressive strengths of 60.25 to 120.92 MPa, modulus of elasticity of 19.84 to 35.29 GPa, and fracture toughness of 0.78 to 1.78 MPa·m^1/2. The values observed were between those of dense ceramic and pure polymer. Statistical analysis was conducted using Excel^® 2019 (Microsoft^®, Washington, DC, USA). Means, standard deviations, and 95% confidence intervals (CI) were calculated at a significance level of α = 0.05, alongside polynomial regression to evaluate relationships between variables. Composites with 20 vol.% ceramic solid loading at 8 h sedimentation displayed promising potential for further clinical validation. Full article

This study was conducted to evaluate the material properties of polymer-infiltrated zinc oxide networks (PICN) and the effect of using a phosphate monomer-containing primer applied before polymer infiltration. A total of 148 ZnO-network (zinc oxide) specimens were produced: n = 74 were treated with a primer before polymer infiltration and light curing, while the remaining specimens were untreated. Each group was divided into two subgroups (n = 37) based on the infiltrating polymer: UDMA (aliphatic urethane-dimethacrylates)-TEGDMA (triethylene glycol-dimethacrylate) or BisGMA (bisphenol A-glycidyl-methacrylate)-TEGDMA. Additionally, n = 7 specimens of each polymer type were prepared for comparison. Then, biaxial flexural strength was measured before and after 150 days of water storage at 37 °C, including 37,500 thermal cycles (5 °C to 55 °C). The Vickers hardness, surface roughness, and water absorption at 37 °C were also tested. The initial biaxial flexural strength was reduced in the ZnO network specimens compared to in the pure polymers. Primer application improved the flexural strength, though the strength of BisGMA-TEGDMA significantly decreased after water storage. The ZnO network increased hardness, and the polymer-infiltrated networks showed higher roughness post-grinding and absorbed less water than the pure polymer groups. The ZnO networks did not improve the flexural strength over that of the pure polymers. However, the primer’s positive impact and the network’s long-term stability suggest potential if the network structure can be modified to contain thicker, more stable branches. Full article

Dental caries are treated using dental composite restorative materials (DCRM). However, commercial DCRMs lack antibacterial activity. This research aimed to analyze the in vitro antibacterial activity of a series of copolymers consisting of a urethane–dimethacrylate monomer (UDMA), bisphenol A glycerolate dimethacrylate (Bis-GMA), triethylene glycol dimethacrylate (TEGDMA) and urethane–dimethacrylate monomer with two quaternary ammonium groups and a 1,3-bis(1-isocyanate-1-methylethyl)benzene core (QAn+TMXDI, where n = 8, 10, or 12 is the number of carbon atoms in the N-alkyl substituent). QAn+TMXDI contents in copolymers were 20 and 40 wt.%. The results of the Staphylococcus aureus and Escherichia coli adhesion test demonstrated that the logCFU/mL decreased as the length of the N-alkyl chain decreased and QAn+TMXDI content increased. The copolymers of QA8+TMXDI 40 wt.%, Bis-GMA 40 wt.%, and TEGDMA 20 wt.% showed the highest antibacterial activity, with a logCFU/mL of 2.39 for S. aureus and no viable E. coli cells. Full article

Repairing or reconstructing significant bone defects is typically challenging. In the present study, two composite cements were used as scaffolds in a sub-critical femoral defect in rats. A control group and two experimental batches were used to compare the outcomes. This research aimed to investigate the osteogenic potential and toxicological tolerance of the bioproducts through histopathology and computed tomography imaging analysis at 14, 28, 56, and 90 days post-implantation. The biomaterials used in the investigation consisted of a 65% bioactive salinized inorganic filler and a 25% weight organic matrix. The organic part of the biomaterial was composed of Bis-GMA (bisphenol A-glycidyl methacrylate), UDMA (urethane dimethacrylate), HEMA (2-Hydroxyethyl methacrylate), and TEGDMA (triethylene glycol dimethacrylate), while the inorganic filler was composed of silica, barium glass, hydroxyapatite, and fluor aluminosilicate glass. The first findings of this research are encouraging, revealing that there is a slight difference between the groups treated with biomaterials, but it might be an effective approach for managing bone abnormalities. Material C1 exhibited a faster bone defect healing time compared to material C2, where bone fractures occurred in some individuals. It is unclear if the fractures were caused by the presence of the biomaterial C2 or whether additional variables were to blame. By the end of the research, the mice appeared to tolerate the biomaterials without exhibiting any inflammatory or rejection responses. Full article

Recent developments in biomaterials have resulted in the creation of cement composites with potential wound treatment properties, even though they are currently mainly employed for bone regeneration. Their ability to improve skin restoration after surgery is worth noting. The main purpose of this research is to evaluate the ability of composite cement to promote wound healing in a rat experimental model. Full-thickness 5 mm skin defects were created, and the biomaterials were applied as wound dressings. The hybrid light-cured cement composites possess an organic matrix (Bis-GMA, TEGDMA, UDMA, and HEMA) and an inorganic phase (bioglasses, silica, and hydroxyapatite). The organic phase also contains γ-methacryloxypropyl-trimethoxysilane, which is produced by distributing bioactive silanized inorganic filler particles. The repair of the defect is assessed using a selection of macroscopic and microscopic protocols, including wound closure rate, histopathological analysis, cytotoxicity, and biocompatibility. Both composites exerted a favorable influence on cells, although the C1 product demonstrated a more extensive healing mechanism. Histological examination of the kidney and liver tissues revealed no evidence of toxicity. There were no notable negative outcomes in the treated groups, demonstrating the biocompatibility and efficacy of these bioproducts. By day 15, the skin of both groups had healed completely. This research introduces a pioneering strategy by utilizing composite cements, traditionally used in dentistry, in the context of skin wound healing. Full article

This study aims to develop multi-functional bio-safe dental resin composites with capabilities for mineralization, high in vitro biocompatibility, and anti-biofilm properties. To address this issue, experimental resin composites consisting of UDMA/TEGDMA-based dental resins and low quantities (1.9, 3.8, and 7.7 vol%) of 45S5 bioactive glass (BAG) particles were developed. To evaluate cellular responses of resin composites, MC3T3-E1 cells were (1) exposed to the original composites extracts, (2) cultured directly on the freshly cured resin composites, or (3) cultured on preconditioned composites that have been soaked in deionized water (DI water), a cell culture medium (MEM), or a simple HEPES-containing artificial remineralization promotion (SHARP) solution for 14 days. Cell adhesion, cell viability, and cell differentiation were, respectively, assessed. In addition, the anti-biofilm properties of BAG-loaded resin composites regarding bacterial viability, biofilm thickness, and biofilm morphology, were assessed for the first time. In vitro biological results demonstrated that cell metabolic activity and ALP expression were significantly diminished when subjected to composite extracts or direct contact with the resin composites containing BAG fillers. However, after the preconditioning treatments in MEM and SHARP solutions, the biomimetic calcium phosphate minerals on 7.7 vol% BAG-loaded composites revealed unimpaired or even better cellular processes, including cell adhesion, cell proliferation, and early cell differentiation. Furthermore, resin composites with 1.9, 3.8, and 7.7 vol% BAG could not only reduce cell viability in S. mutans biofilm on the composite surface but also reduce the biofilm thickness and bacterial aggregations. This phenomenon was more evident in BAG7.7 due to the high ionic osmotic pressure and alkaline microenvironment caused by BAG dissolution. This study concludes that multi-functional bio-safe resin composites with mineralization and anti-biofilm properties can be achieved by adding low quantities of BAG into the resin system, which offers promising abilities to mineralize as well as prevent caries without sacrificing biological activity. Full article

The objective of this study was to detail the monomer composition of resin-based dental materials sold in the market in 2023 and to evaluate the proportion of bisphenol A (BPA)-derivatives in relation to their applications. A search on manufacturers’ websites was performed to reference resin-based dental materials currently on the European market (including the European Union (EU) and United Kingdom (UK). Their monomer composition was determined using material-safety data sheets and was completed by a search on the PubMed database. Among the 543 material compositions exploitable, 382 (70.3%) contained BPA derivatives. Among them, 56.2% contained BisGMA and 28% BisEMA, the most frequently reported. A total of 59 monomers, of which six were BPA derivatives, were found. In total, 309 materials (56.9%) contained UDMA and 292 (53.8%) TEGDMA. Less than one third of materials identified contained no BPA derivatives. These proportions vary a lot depending on their applications, with materials dedicated to the dental care of young populations containing the highest proportions of BPA-derivative monomers. The long-term effects on human health of the different monomers identified including BPA-derivative monomers is a source of concern. For children and pregnant or lactating women arises the question of whether to take a precautionary principle and avoid the use of resin-based dental materials likely to release BPA by opting for alternative materials. Full article

In this study, two novel quaternary ammonium urethane-dimethacrylates (QAUDMAs) were designed for potential use as comonomers in antibacterial dental composite restorative materials. QAUDMAs were synthesized via the reaction of 1,3-bis(1-isocyanato-1-methylethyl)benzene with 2-(methacryloyloxy)ethyl-2-decylhydroxyethylmethylammonium bromide (QA10+TMXDI) and 2-(methacryloyloxy)ethyl-2-dodecylhydroxyethylmethylammonium bromide (QA12+TMXDI). Their compositions with common dental dimethacrylates comprising QAUDMA 20 wt.%, urethane-dimethacrylate monomer (UDMA) 20 wt.%, bisphenol A glycerolate dimethacrylate (Bis-GMA) 40 wt.%, and triethylene glycol dimethacrylate (TEGDMA) 20 wt.%, were photocured. The achieved copolymers were characterized for their physicochemical and mechanical properties, including their degree of conversion (DC), glass transition temperature (T_g), polymerization shrinkage (S), water contact angle (WCA), flexural modulus (E), flexural strength (FS), hardness (HB), water sorption (WS), and water leachability (WL). The antibacterial activity of the copolymers was characterized by the minimum bactericidal concentration (MBC) and minimum inhibitory concentration (MIC) against Staphylococcus aureus and Escherichia coli. The achieved results were compared to the properties of a typical dental copolymer comprising UDMA 40 wt.%, Bis-GMA 40 wt.%, and TEGDMA 20 wt.%. The introduction of QAUDMAs did not deteriorate physicochemical and mechanical properties. The WS and WL increased; however, they were still satisfactory. The copolymer comprising QA10+TMXDI showed a higher antibacterial effect than that comprising QA12+TMXDI and that of the reference copolymer. Full article

A low ratio of polymerization is a major problem in resin-based composites. In this paper, the plasmonic effect of gold-covered silica nanoparticles on the physicochemical and mechanical properties of bisphenol A diglycidyl dimethacrylate (Bis-GMA), triethylene glycol dimethacrylate (TEGDMA) and urethane dimethacrylate (UDMA) green light-photopolymerizable dental resin was investigated at an intensity of 1.4 mW/cm² for 40 s. Transmission electron microscopy (TEM) showed silica of about 350 nm covered with 12–15 nm gold nanoparticles (Au NPs) at 100% nominal coverage. Five different concentrations of bare and patchy silica particles were used; in the latter composite, the calculated Au wt% were 0.0052 wt%, 0.0104 wt%, 0.0208 wt%, 0.04160 wt%, and 0.0823 wt%. The plasmon peak of patchy silica-filled nanocomposite overlapped with the absorption of Irgacure 784 photoinitiator and green LED light emission peak. The effect of plasmon-enhanced polymerization achieved with green light illumination was analyzed using diametral tensile strength (DTS), differential scanning calorimetry (DSC), surface plasmon resonance imaging (SPRi), and degree of conversion (DC) based on Raman spectroscopy. The values of the Au NP with 0.0208 wt% was found to be maximum in all the measured data. Based on our result, it can be concluded that the application of patchy silica particles in dental resin can improve the polymerization ratio and the mechanical parameters of the composite. Full article

Background and Objectives: The objective of this study was (1) to measure the amount of monomers released into the saliva depending on the time elapsed after the hardening of the composite and on the type of monomer used; and (2) with the prolongation of the light-curing procedure, to publish information on whether it would be possible to influence the level of leached monomers. Materials and Methods: HPLC technique was used to monitor the levels of the unpolymerized monomers Bis-GMA, Bis/EMA, TEGDMA, and UDMA from the four commonly used composite materials, released into the saliva of a volunteer with intact dentition. The levels were monitored in 3 time periods during 24 h after composite hardening. From every composite material, 4 samples were formed and cured with an LED lamp for 10 s, 20 s, 40 s, and 60 s. After the light curing, the same polishing procedure was used and the samples were leached in blank saliva samples. Results: We observed that every monitored composite material eluted monomers into the saliva after its application. The amount of monomers depended on the time elapsed after the curing of the composite and on the type of composite used. A 40 s LED curing procedure can reduce the amount of leached monomers in comparison with the standard 20 s procedure, especially for monomers of higher molecular weight. Conclusions: Our study confirmed the hypothesis that the release of monomers gradually decreases with increasing time after the hardening of the composite filling. Full article