Water sorption of CH3- and CF3-Bis-GMA based resins with additives

Objectives

To evaluate the effect of additives on the water sorption characteristics of Bis-GMA based copolymers and composites containing TEGDMA, CH₃Bis-GMA or CF₃Bis-GMA.

Material and methods

Fifteen experimental copolymers and corresponding composites were prepared combining Bis-GMA and TEGDMA, CH₃Bis-GMA or CF₃Bis-GMA, with aldehyde or diketone (24 and 32 mol%) totaling 30 groups. For composites, barium aluminosilicate glass and pyrogenic silica was added to comonomer mixtures. Photopolymerization was effected by 0.2 wt% each of camphorquinone and N,N-dimethyl-p-toluidine. Specimen densities in dry and water saturated conditions were obtained by Archimedes'' method. Water sorption and desorption were evaluated in a desorption-sorption-desorption cycle. Water uptake (%WU), water desorption (%WD), equilibrium solubility (ES; µg/mm³), swelling (f) and volume increase (%V) were calculated using appropriate equations.

Results

All resins with additives had increased %WU and ES. TEGDMA-containing systems presented higher %WU, %WD, ES, f and %V values, followed by resins based on CH₃Bis-GMA and CF₃Bis-GMA.

Conclusions

Aldehyde and diketone led to increases in the water sorption characteristics of experimental resins.     

牙科纳米氧化铝复合树脂的制备与性能研究

目的 制备一种新型的光固化纳米氧化铝复合树脂,探讨其用于口腔临床的可行性。方法 以双酚A双甲基丙烯酸缩水甘油酯(Bis-GMA)为树脂基质,甲基丙烯酸羟乙酯(HEMA)为活性稀释剂,添加纳米氧化铝填料对树脂基质进行增强增韧改性,制备一种新型牙科纳米氧化铝复合树脂,并表征其固化程度、弯曲强度、硬度、断面形貌、耐磨性、吸水性与水溶解性。结果 添加纳米氧化铝能提高复合树脂材料的刚性和硬度,当添加量达到3wt%时,复合树脂的力学性能、吸水和溶解性能均为最优。结论 复合树脂中加入一定比例的纳米氧化铝可达到增韧和耐磨的效果,该研究为开发新型牙科复合树脂提供了理论和实验基础。     

Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical,solubilized telopeptide and proteomic assays

Objectives

We investigated the biostability of dentin organic matrices treated with epigallocatechin gallate (EGCG) in comparison to chlorhexidine (CHX), both extracted from functionalized copolymers.

Preparation of low shrinkage stress Bis-GMA free dental resin composites with a synthesized urethane dimethacrylate monomer

A new urethane dimethacrylate TMA was synthesized through a typical urethane reaction. TMA was used to replace 1,6-bis(methacryloxy-2-ethoxycarbonyl- amino)-2,4,4- trimethylhexane (UDMA) in UDMA based composite partially or totally to prepare TMA containing composites. Critical properties of TMA containing composites were investigated. 2,2-bis[4(2-hydroxy-3-methacryloy- propyloy)phenyl]propane (Bis-GMA) based and UDMA based composites were used as references. FT-IR and ¹H-NMR confirmed the structure of TMA. All of experimental dental resin composites had the similar double bond conversion (p?>?0.05). With a certain amount of TMA, TMA containing composites could have lower volumetric shrinkage (p?<?0.05) and shrinkage stress (p?<?0.05) than control groups. Water sorption, solubility, flexural strength and modulus of TMA containing composites were not worse than those of control groups. All of TMA containing composites and UDMA based composite had the same fracture toughness (p?>?0.05), which was higher than that of Bis-GMA based composite (p?<?0.05). TMA has potential as Bis-GMA substitute to prepare Bis-GMA free dental resin composites with low shrinkage stress.     

Network structures of Bis-GMA/TEGDMA resins differ in DC, shrinkage-strain, hardness and optical properties as a function of reducing agent

Objectives

To evaluate the influence of different tertiary amines on degree of conversion (DC), shrinkage-strain, shrinkage-strain rate, Knoop microhardness, and color and transmittance stabilities of experimental resins containing BisGMA/TEGDMA (3:1 wt), 0.25 wt% camphorquinone, 1 wt% amine (DMAEMA, CEMA, DMPT, DEPT or DABE). Different light-curing protocols were also evaluated.

Methods

DC was evaluated with FTIR-ATR and shrinkage-strain with the bonded-disk method. Shrinkage-strain-rate data were obtained from numerical differentiation of shrinkage-strain data with respect to time. Color stability and transmittance were evaluated after different periods of artificial aging, according to ISO 7491:2000. Results were evaluated with ANOVA, Tukey, and Dunnett's T3 tests (α = 0.05).

Results

Studied properties were influenced by amines. DC and shrinkage-strain were maximum at the sequence: CQ < DEPT < DMPT ≤ CEMA ≈ DABE < DMAEMA. Both DC and shrinkage were also influenced by the curing protocol, with positive correlations between DC and shrinkage-strain and DC and shrinkage-strain rate. Materials generally decreased in L* and increased in b*. The strong exception was the resin containing DMAEMA that did not show dark and yellow shifts. Color varied in the sequence: DMAEMA < DEPT < DMPT < CEMA < DABE. Transmittance varied in the sequence: DEPT ≈ DABE < DABE ≈ DMPT ≈ CEMA < DMPT ≈ CEMA ≈ DMAEMA, being more evident at the wavelength of 400 nm. No correlations between DC and optical properties were observed.

Significance

The resin containing DMAEMA showed higher DC, shrinkage-strain, shrinkage-strain rate, and microhardness, in addition to better optical properties.     

Cytotoxicity of bisphenol A glycidyl methacrylate on cytochrome P450-producing cells

Of the cytochrome P450 (CYP) family of carcinogen-activating enzymes, CYP3A is the major form found in human livers. The purpose of this study was to investigate the cytotoxic effects of dental resin monomers after being metabolized by CYP3A4 and CYP3A7, using a colony formation assay and a neutral red assay. Specimen wells were plated with transfected cells derived from the Chinese hamster lung at 100 cells well(-1). The experimental group consisted of CYP-producing 3A4-10 and 3A7-40 cells, while the control group consisted of non-CYP-producing CR-119 cells. Bisphenol A (BPA) and bisphenol A glycidyl methacrylate (Bis-GMA) and a positive control (Aflatoxine Bl) were added separately to each well and cultured for 7 days. After cultivation, the number of the colonies was counted and IC50 values were determined. The data were statistically analysed by a Student's t-test. The resultant of IC50 values indicated that the monomers were not metabolically activated by CYP3A4 or CYP3A7 as compared with the control (P < 0.05). We also confirmed that these monomers act neither as activators nor as inhibitors of CYP3A4 and CYP3A7.     

The Bond Strength of an Adhesive Resin Luting Cement to a Variety of Surface Treatments of a High-Palladium Copper Alloy

Purpose This study evaluated the tensile bond strength of a bisphenol glycidyl methacrylate (Bis-GMA) resin luting cement with four different surface treatments of a high Pd-Cu alloy. Materials and Methods For each surface treatment type (tin-plated, porcelain furnace oxide, air-abraded, and finished-only), 15 opposing half-dumbbell-shaped samples were cast and prepared in new Pd?Cu alloy. Samples were luted with a Bis-GMA resin luting cement at a film thickness of 80 μm using a custom alignment apparatus. Samples were stored in distilled water at 37°C for 24 hours, thermocycled for 1,000 cycles, and then stored for 30 days in distilled water at 37°C. Samples were then subjected to fracture in tension at a loading rate of 0.5 cm/min with the bond strengths calculated in megapascals (MPa). The fractured surfaces were examined using stereomicroscopy and scanning electron microscopy at various magnifications ranging from 5.5x to 500x to determine the type of bond failure (adhesive, cohesive, or mixed). Results Tensile bond strengths (mean ± SD MPa) were: tin-plated, 30 ± 15.7; porcelain furnace oxide, 23 ± 8.6; air-abraded, 8 ± 8.1; and finished-only, 4 ± 4.5. Statistical analysis of the tensile bond values using an ANCOVA and Tukey's multiple comparison test at a significance level of 0.05 indicated that there was no difference between the tin-plated and the furnace oxide groups, as well as between the air-abraded and the furnace oxide groups. However, there was significant difference between the tin-plated, the air-abraded, and the finished-only groups. The observed bond failures were predominantly mixed and cohesive in nature with only one adhesive failure. Conclusions There was no significant difference in the tensile bond strengths between the tin-plated group or the porcelain furnace oxide surface group. This suggests that the less-technique-sensitive porcelain furnace oxide surface treatment offers an alternative for achieving high metal-resin bonds to a high Pd?Cu alloy.     

The influence of "C-factor" and light activation technique on polymerization contraction forces of resin composite

Objectives

This study evaluated the influence of the cavity configuration factor ("C-Factor") and light activation technique on polymerization contraction forces of a Bis-GMA-based composite resin (Charisma, Heraeus Kulzer).

Material and Methods

Three different pairs of steel moving bases were connected to a universal testing machine (emic DL 500): groups A and B - 2x2 mm (CF=0.33), groups C and D - 3x2 mm (CF=0.66), groups e and F - 6x2 mm (CF=1.5). After adjustment of the height between the pair of bases so that the resin had a volume of 12 mm³ in all groups, the material was inserted and polymerized by two different methods: pulse delay (100 mW/cm² for 5 s, 40 s interval, 600 mW/cm² for 20 s) and continuous pulse (600 mW/cm² for 20 s). Each configuration was light cured with both techniques. Tensions generated during polymerization were recorded by 120 s. The values were expressed in curves (Force(N) x Time(s)) and averages compared by statistical analysis (ANOVA and Tukey''s test, p<0.05).

Results:

For the 2x2 and 3x2 bases, with a reduced C-Factor, significant differences were found between the light curing methods. For 6x2 base, with high C-Factor, the light curing method did not influence the contraction forces of the composite resin.

Conclusions

Pulse delay technique can determine less stress on tooth/restoration interface of adhesive restorations only when a reduced C-Factor is present.     

Degree of conversion and monomer elution of CQ/amine and TPO adhesives

Objective

To evaluate the effect of photo-initiator on the degree of conversion (DC) and elution of Bis-GMA and HEMA for 8 one-step adhesive formulations.

Methods

We used Scotchbond Universal (‘SBU-CQ/amine_4.0’, 3M ESPE), containing about 2 wt% camphorquinone (CQ) and 2 wt% ethyl-4-dimethylamino benzoate (EDMAB), an experimental ‘SBU-TPO_2.1’ version, containing 2.1 wt% diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO), and 6 experimental LUB adhesives (Kuraray Noritake), namely ‘LUB-CQ/amine_0.7’, ‘LUB-CQ/amine_1.4’, ‘LUB-CQ/amine_4.0’, ‘LUB-TPO_0.35’, ‘LUB-TPO_0.7’ and ‘LUB-TPO_2.0’, respectively containing 0.35 wt% CQ and 0.35 wt% EDMAB, 0.7 wt% CQ and 0.7 wt% EDMAB, 2.0 wt% CQ and 2.0 wt% EDMAB, 0.35 wt% TPO, 0.7 wt% TPO, and 2.0 wt% TPO. DC was measured using micro-Raman spectroscopy. Additional specimens were immersed in ethanol for 24 h to determine the elution of Bis-GMA and HEMA using HPLC.

Results

DC of the respective SBU and LUB adhesives was alike at high photo-initiator concentration. At low concentration, TPO was significantly more efficient than CQ/amine (LUB adhesives only). A statistically significant positive photo-initiator concentration effect on DC was noted for both CQ/amine and TPO (LUB adhesives only). A statistically significant inverse photo-initiator concentration effect on HEMA elution was noted for both the CQ/amine- and TPO-containing LUB adhesives. A significantly strong correlation was found between DC and Bis-GMA elution (R² = 0.744, p = 0.026), and between DC and HEMA elution (R² = 0.913, p = 0.002) for the LUB adhesives.

Significance

The photo-initiator kind and concentration affect DC and the Bis-GMA/HEMA elution. TPO can be used as an alternative photo-initiator for CQ/amine.     

Dental restorative composite materials: A review

BackgroundThis review article discusses the effect of reinforcements in the parent dental restorative materials that results in enhanced performance in real-time situations.HighlightThe review article includes the details of the properties of different reinforced dental composite materials such as mechanical strength, thermal properties, physical/chemical properties, tribological performance.ConclusionIt revealed that nanofiller particles enhance the properties of various dental composite materials. The hybrid dental composites also contribute significantly in increasing the mechanical and tribological properties. A silane-treated filler improved the dental composite bonding strength.