Thermal and Bulk Properties of Triblock Terpolymers and Modified Derivatives towards Novel Polymer Brushes.

We report the synthesis of three (3) linear triblock terpolymers, two (2) of the ABC type and one (1) of the BAC type, where A, B and C correspond to three chemically incompatible blocks such as polystyrene (PS), poly(butadiene) of exclusively (~100% vinyl-type) -1,2 microstructure (PB1,2) and poly(dimethylsiloxane) (PDMS) respectively. Living anionic polymerization enabled the synthesis of narrowly dispersed terpolymers with low average molecular weights and different composition ratios, as verified by multiple molecular characterization techniques. To evaluate their self-assembly behavior, transmission electron microscopy and small-angle X-ray scattering experiments were conducted, indicating the effect of asymmetric compositions and interactions as well as inversed segment sequence on the adopted morphologies. Furthermore, post-polymerization chemical modification reactions such as hydroboration and oxidation were carried out on the extremely low molecular weight PB1,2 in all three terpolymer samples. To justify the successful incorporation of -OH groups in the polydiene segments and the preparation of polymeric brushes, various molecular, thermal, and surface analysis measurements were carried out. The synthesis and chemical modification reactions on such triblock terpolymers are performed for the first time to the best of our knowledge and constitute a promising route to design polymers for nanotechnology applications.

Osteogenic differentiation of bone marrow mesenchymal stem cells on chitosan/gelatin scaffolds: gene expression profile and mechanical analysis.

In the present study we explore the extracellular matrix (ECM) produced by human bone marrow mesenchymal stem/stromal cells (BM-MSCs) induced to undergo osteogenic differentiation within porous chitosan/gelatin (CS:Gel) scaffolds by investigating their multiple gene expression profile and mechanical behavior. Initially, the efficiency of the BM-MSCs osteogenic differentiation within the constructs was confirmed by the significant rise in the expression of the osteogenesis associated genes DLX5, RUNX2, ALP and OSC. In line with these findings, OSC and Col1A1 protein expression was also detected in BM-MSCs on the CS:Gel scaffolds at day 14 of osteogenic differentiation. We then profiled, for the first time, the expression of 84 cell adhesion and ECM molecules using PCR arrays. The arrays, which were conducted at day 14 of osteogenic differentiation, demonstrated that 49 genes including collagens, integrins, laminins, ECM proteases, catenins, thrombospondins, ECM protease inhibitors and cell-cell adhesion molecules were differentially expressed in BM-MSCs seeded on scaffolds compared to tissue culture polystyrene control. Moreover, we performed dynamic mechanical analysis of the cell-loaded scaffolds on days 0, 7 and 14 to investigate the correlation between the biological results and the mechanical behavior of the constructs. Our data demonstrate a significant increase in the stiffness of the constructs with storage modulus values of 2 MPa on day 7, compared to 0.5 MPa on day 0, following a drop of the stiffness at 0.8 MPa on day 14, that may be attributed to the significant increase of specific ECM protease gene expression such as MMP1, MMP9, MMP11 and MMP16 at this time period.

Development and Characterization of High Performance Shape Memory Alloy Coatings for Structural Aerospace Applications.

This paper presents an innovative approach, which enables control of the mechanical properties of metallic components by external stimuli to improve the mechanical behavior of aluminum structures in aeronautical applications. The approach is based on the exploitation of the shape memory effect of novel Shape Memory Alloy (SMA) coatings deposited on metallic structural components, for the purpose of relaxing the stress of underlying structures by simple heating at field-feasible temperatures, therefore enhancing their structural integrity and increasing their stiffness and rigidity while allowing them to withstand expected loading conditions safely. Numerical analysis provided an insight in the expected response of the SMA coating and of the SMA-coated element, while the dependence of alloy composition and heat treatment on the experienced shape memory effect were investigated experimentally. A two-phase process is proposed for deposition of the SMA coating in an order that induces beneficial stress relaxation to the underlying structure through the shape memory effect.

Secondhand smoke exposure within semi-open air cafes and tobacco specific 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) concentrations among nonsmoking employees.

OBJECTIVES: Secondhand smoke (SHS) is a defined occupational hazard. The association though between SHS exposure in semi-open air venues and tobacco specific carcinogen uptake is an area of debate. MATERIAL AND METHODS: A cross sectional survey of 49 semi-open air cafes in Athens, Greece was performed during the summer of 2008, prior to the adoption of the national smoke free legislation. All venues had at least 1 entire wall open to allow for free air exchange. Indoor concentrations of particulate matter smaller than 2.5 microns (PM2.5) attributable to SHS were assessed during a work shift, while 1 non-smoking employee responsible for indoor and outdoor table service from each venue provided a post work shift urine sample for analysis of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL). RESULTS: Post work shift NNAL concentrations were correlated with work shift PM2.5 concentrations attributable to SHS (r = 0.376, p = 0.0076). Urinary NNAL concentrations among employees increased by 9.5%, per 10 µg/m(3) increase in PM2.5 concentrations attributable to SHS after controlling for the time of day and day of week. CONCLUSIONS: These results indicate that the commonly proposed practice of maintaining open sliding walls as a means of free air exchange does not lead to the elimination of employee exposure to tobacco specific carcinogens attributable to workplace SHS.

Routine application of a novel MLPA-based first-line screening test uncovers clinically relevant copy number aberrations in haematological malignancies undetectable by conventional cytogenetics.

OBJECTIVE: The presence of numerical and/or structural chromosomal abnormalities is a frequent finding in clonal hematopoietic malignant disease, typically diagnosed through routine karyotyping and/or fluorescent in situ hybridization (FISH) analysis. Recently, the application of array comparative genomic hybridization (aCGH) has uncovered many new cryptic genomic copy number imbalances, most of which are now recognized as clinically useful markers of haematological malignancies. In view of the limitations of both FISH and aCGH techniques, in terms of their routine application as a first line screening test, we designed a new multiple ligation-dependent probe amplification (MLPA) probemix for use in addition to classic karyotype analysis. METHODS: A novel MLPA probemix was developed to interrogate copy number changes involving chromosomal regions: 2p23-24 (MYCN, ALK), 5q32-34 (MIR145A, EBF1, MIR146A), 6q21-27, 7p12.2 (IKZF1), 7q21-36, 8q24.21 (MYC), 9p24 (JAK2 V617F point mutation), 9p21.3 (CDKN2A/2B), 9p13.2 (PAX5), 10q23 (PTEN), 11q22.3 (ATM), 12p13.2 (ETV6), 13q14 (RB1, MIR15A, DLEU2, DLEU1), 17p13.1 (TP53), and 21q22.1 (RUNX1/AML1) and was applied to DNA extracted from 313 consecutive bone marrow patient samples, referred for routine karyotype analysis. RESULTS: More than half of the samples originated from newly investigated patients. We discovered clinically relevant genomic aberrations, involving a total of 24 patients (8%) all with a normal karyotype, which would have remained undiagnosed. DISCUSSION: Our data clearly indicate that routine application of this MLPA screening panel, as an adjunct to karyotype analysis, provides a sensitive, robust, rapid and low-cost approach for uncovering clinically important genomic abnormalities, which would have otherwise remained undetected.

Synthesis and study of physical properties of dental light-cured nanocomposites using different amounts of a urethane dimethacrylate trialkoxysilane coupling agent.

OBJECTIVE: The purpose of this work was the study of the effect of the amount of a urethane dimethacrylate silane (UDMS) coupling agent on physical properties of dental light-cured resin nanocomposites based on Bis-GMA/TEGDMA (50/50 wt/wt) matrix and Aerosil OX50 as filler. METHODS: Silica nanoparticles (Aerosil OX 50) used as filler were silanized with 5 different amounts of UDMS 1.0, 2.5, 5.0, 7.5 and 10 wt% relative to silica. The silanizated silica nanoparticles were identified by FT-IR spectroscopy and thermogravimetric analysis (TGA). Then the silanized nanoparticles (60 wt%) were mixed with a Bis-GMA/TEGDMA (50/50 wt/wt) matrix. Degree of conversion of light cured composites was determined by FT-IR analysis. The static flexural strength and flexural modulus were measured using a three-point bending set up. The dynamic thermomechanical properties were determined by DMA analyzer. Measurements were taken in samples stored, immediately after curing, in water at 37°C for 24 h. Sorption, solubility and volumetric change were determined after storage of composites in water or ethanol/water of 75 vol% for 30 days. Thermogravimetric analysis of composites was performed in nitrogen atmosphere from 50 to 800°C. RESULTS: Almost all of used amount of silane remained chemically bounded on the surface of silica particles, forming a layer around them, which have dense accumulation of methacrylate groups. No significant statistic difference was found to exist between the degree of conversion values of composites with different silane contents. The composite with the lowest amount of UDMS (1.0 wt%) showed the lower flexural strength value, the higher static and dynamic elastic modulus values and the higher sorbed liquid value and solubility. SIGNIFICANCE: The optimum concentration of UDMS seems to be that of 2.5 wt%. Higher concentrations of UDMS did not improve the properties of composites.

Sorption of water, ethanol or ethanol/water solutions by light-cured dental dimethacrylate resins.

OBJECTIVES: This work is concerned with the study of the sorption and desorption process of water, ethanol or ethanol/water solution 50% (v/v) or 75% (v/v) by the dental resins prepared by light curing of Bis-GMA, Bis-EMA, UDMA, TEGDMA or D3MA. METHODS: A thin resin disc is placed in a bath of time to obtain the sorption curve m(t)=f(t). Then the liquid is desorbed until a constant mass for the disc is reached and the desorption curve is recorded. These experimental curves help in the determination of the sorbed/desorbed liquid amount at equilibrium, the percentage of the extracted mass of unreacted monomer known as "solubility", and the sorption/desorption diffusion coefficient which expresses correspondingly the rate of the liquid sorption/desorption. RESULTS: The highest liquid uptake by dental resins was 13.3wt% ethanol for Bis-GMA-resin, 12.0wt% ethanol for UDMA-resin, 10.10wt% ethanol/water solution for TEGDMA-resin, 7.34wt% ethanol for D(3)MA-resin and 6.61wt% ethanol for Bis-EMA-resin. The diffusion coefficient for all resins was higher in water than in ethanol/water solution or ethanol. Bis-GMA-resin showed the highest diffusion coefficient (11.01 × 10⁻8cm² s⁻¹) followed by Bis-EMA-resin (7.43 × 10⁻8 cm² s⁻¹), UDMA-resin (6.88 × 10⁻8cm² s⁻¹), D(3)MA-resin (6.22 × 10⁻8 cm² s⁻¹) and finally by TEGDMA-resin (1.52 ×10⁻8 cm² s⁻¹). SIGNIFICANCE: All studied dental resins, except TEGDMA-resin, absorbed higher amount of pure ethanol than water or ethanol water solution. TEGDMA-resin absorbed higher amount of ethanol/water solution (50/50 or 75/25 (v/v)) than water or ethanol. For all studied dental resins the diffusion coefficient was higher in water than in ethanol/water solution or ethanol.

Synthesis and study of properties of dental resin composites with different nanosilica particles size.

OBJECTIVES: The aim of this work was the synthesis of light-cured resin nanocomposites using nanosilica particles with different particle size and the study of some physical-mechanical properties of the composites. METHODS: Various types of silica nanoparticles (Aerosil) with average particle size of 40, 20, 16, 14, and 7 nm, used as filler were silanized with the silane 3-methacryloxypropyl-trimethoxysilane (MPS). The total amount of silane used was kept constant at 10 wt% relative to the filler weight to ensure the complete silanization of nanoparticles. The silanizated silica nanoparticles were identified by FT-IR spectroscopy and thermogravimetric analysis (TGA). Then the silanized nanoparticles (55 wt%) were mixed with a photoactivated Bis-GMA/TEGDMA (50/50 wt/wt) matrix. Degree of conversion of composites was determined by FT-IR analysis. The static flexural strength and flexural modulus were measured using a three-point bending set up. The dynamic thermomechanical properties were determined by dynamic mechanical analyzer (DMA). Sorption, solubility and volumetric change were determined after storage of composites in water or ethanol/water solution 75 vol% for 30 days. The TGA for composites was performed in nitrogen atmosphere from 30 to 700 °C. RESULTS: As the average silica particle size decreases, the percentage amount of MPS attached on the silica surface increases. However, the number of MPS molecules attached on the silica surface area of 1 nm(2) is independent of filler particle size. As the average filler particles size decreases a progressive increase in the degree of conversion of composites and an increase in the amount of sorbed water is observed. SIGNIFICANCE: The prepared composites containing different amount of silica filler, with different particle size, but with the same amount of silanized silica and organic matrix showed similar flexural strength and flexural modulus, except composite with the lowest filler particle size, which showed lower flexural modulus.

Physical properties of current dental nanohybrid and nanofill light-cured resin composites.

OBJECTIVES: The purpose of this work was the detailed study of sorption characteristics of water or artificial saliva, the determination of flexural strength and the flexural modulus, and the study of the thermal stability of some current commercial dental light-cured nanocomposites containing nano-sized filler particles. METHODS: Three nanohydrid dental composites (Tetric EvoCeram (TEC), Grandio (GR) and Protofill-nano (PR)) and two nanofill composites (Filtek Supreme Body (FSB) and the Filtek Supreme Translucent (FST)) were used in this work. The volumetric shrinkage due to polymerization was first determined. Also the sorption, solubility and volumetric increase were measured after storage of composites in water or artificial saliva for 30 days. The flexural strength and flexural modulus were measured using a three-point bending set-up according to the ISO-4049 specification, after immersion of samples in water or artificial saliva for 1 day or 30 days. Thermal analysis technique TGA method was used to investigate the thermal stability of composites. RESULTS: GR and TEC composites showed statistically no difference in volumetric shrinkage (%) which is lower than the other composites, which follow the order PR

The relationship between venue indoor air quality and urinary cotinine levels among semiopen-air café employees: what factors determine the level of exposure?

BACKGROUND: Exposure to second-hand smoke (SHS) is increasingly recognized as an occupational hazard to workers in the service industry. In areas of the world with moderate climates, open windows and doors are assumed to provide a work environment with only marginally increased exposures to SHS. METHODS: We measured indoor fine particulate matter (PM2.5) in 50 semiopen air venues in Greece during the summer. Cotinine levels from a nonsmoking employee of each of these venues were measured from a postshift urine sample. RESULTS: In these semiopen-air venues, the mean level of indoor PM 2.5 levels were 113.5 ± 72.3 µg/m(3). The mean postshift urinary cotinine levels of nonworking workers in these venues was 15 ng/mL. PM2.5 levels were strongly correlated with urinary cotinine concentrations (Spearman's r = 0.914). Linear regression analyses indicated that when taking into account the time of the measurement, the day of the week, for each 1 cigarette/100 m(3) the indoor PM2.5 concentrations increased by 26.6 µg/m(3) [95% confidence interval (CI): 7.6-45.7 µg/m(3), p = 0.007) and urinary cotinine levels of nonsmoking workers increased by 5.0 ng/mL (95% CI: 0.4 to 9.6, p = 0.034). CONCLUSIONS: In a sample of bars and restaurants with windows and doors open, indoor PM2.5 concentrations were elevated and increased proportionately to the density of smoking. Cotinine levels of nonsmoking employees increased with indoor PM2.5 concentrations, and also with the density of smoking. Open windows and doors do not protect workers from exposure to second-hand smoke.

Physical properties of a hybrid and a nanohybrid dental light-cured resin composite.

This work was aimed at the study of some physical properties of two current light-cured dental resin composites, Rok (hybrid) and Ice (nanohydrid). As filler they both contain strontium aluminosilicate particles, however, with different size distribution, 40 nm-2.5 mum for Rok and 10 nm-1 mum for Ice. The resin matrix of Rok consists of UDMA, that of Ice of UDMA, Bis-EMA and TEGDMA. Degree of conversion was determined by FT-IR analysis. The flexural strength and modulus were measured using a three-point bending set-up according to the ISO-4049 specification. Sorption, solubility and volumetric change were measured after storage of composites in water or ethanol/water (75 vol%) for 1 day, 7 or 30 days. Thermogravimetric analysis was performed in air and nitrogen atmosphere from 30 to 700 degrees C. Surface roughness and morphology of the composites was studied by atomic force microscopy (AFM). The degree of conversion was found to be 56.9% for Rok and 61.0% for Ice. The flexural strength of Rok does not significantly differ from that of Ice, while the flexural modulus of Rok is higher than that of Ice. The flexural strengths of Rok and Ice did not show any significant change after immersion in water or ethanol solution for 30 days. The flexural modulus of Rok and Ice did not show any significant change either after immersion in water for 30 days, while it decreased significantly, even after 1 day immersion, in ethanol solution. Ice sorbed a higher amount of water and ethanol solution than Rok and showed a higher volume increase. Thermogravimetric analysis showed that Rok contains about 80 wt% inorganic filler and Ice about 75 wt%.

Dynamic mechanical analysis of a hybrid and a nanohybrid light-cured dental resin composite.

This work was aimed at the study of the viscoelastic properties of two current light-cured dental resin composites, Rok (hybrid) and Ice (nanohybrid), by dynamic mechanical analysis, under the influence of variable temperatures and frequencies 1 h after curing or after storage at 37 degrees C either in air or distilled water for 1, 7 or 30 days. They both contain about the same amount of filler, which is strontium aluminosilicate particles, but they have different size distribution, 40 nm-2.5 microm for Rok and 10 nm-1 microm for Ice. The resin matrix of Rok consists of UDMA, while that of Ice consists of UDMA, Bis-EMA and TEGDMA. During dynamic testing elastic modulus (E'), viscous modulus (E'') and loss tangent (tan delta) were determined over a temperature range from 25 to 185 degrees C at a frequency of 0.1, 1.0 or 10.0 Hz. The elastic modulus (8.40 +/- 0.61 GPa) and tan delta (0.114) of Rok at 37 degrees C and 1 Hz was slightly higher than that of Ice (E' = 7.58 +/- 0.50 GPa and tan delta = 0.110) which, however, were not statistically different (P < or = 0.05). Both the light-cured composites showed two T(g) values, at 58 and 121 degrees C for Rok and at 63 and 117.0 degrees C for Ice. The first T(g) has an apparent value, since inside the glass transition region an additional curing reaction occurred of the unreacted C=C methacrylate groups; the second T(g) is due to the new material formed during the DMA scan. During the storage of composites in air or water also an additional curing reaction took place. The nanohybrid Ice showed a slight lower elastic modulus and tan delta than the hybrid Rok at 25-50 degrees C, which, however, were not statistically different (P < or = 0.05).

Effect of the amount of 3-methacyloxypropyltrimethoxysilane coupling agent on physical properties of dental resin nanocomposites.

OBJECTIVES: The purpose of this study was to evaluate the effect of the amount of 3-methacryloxypropyl-trimethoxysilane (gamma-MPS) coupling agent on some physical-mechanical properties of an experimental resin composite for understanding the optimum amount of silanization. METHODS: Silica nanoparticles (Aerosil OX 50) used as filler were silanized with 5 different amounts of gamma-MPS 1.0, 2.5, 5.0, 7.5 and 10 wt% relative to silica. The silanizated silica nanoparticles were identified by FT-IR spectroscopy and thermogravimetric analysis (TGA). Then the silanized nanoparticles (60 wt%) were mixed with a Bis-GMA/TEGDMA (50/50 wt/wt) matrix. Degree of conversion of light cured composites was determined by FT-IR analysis. The static flexural strength and flexural modulus were measured using a three-point bending set up. The dynamic thermomechanical properties were determined by DMA analyzer. Sorption, solubility and volumetric change were determined after storage of composites in water or ethanol/water solution. Thermogravimetric analysis was performed in air and in nitrogen atmosphere from 50 to 800 degrees C. RESULTS: At lower silane amounts used (1.0, 2.5 wt%) the silane molecules must have a parallel orientation relative to the silica surface. At higher silane amounts (>2.5 wt%) silane molecules form a layer around the filler particles which now have to occupy a random, parallel and perpendicularly orientation relative to the silica surface. No significant statistic difference was found to exist between the flexural strength and flexural modulus values of composites with different silane contents. Dynamic elastic modulus E' showed a maximum value for the composite contained 5 wt% silane. The composites with the higher amounts of silane showed the lower values for the tandelta at the T(g) revealing that these composites have better interfacial adhesion between filler and matrix. SIGNIFICANCE: The amount of silane used for the silanization of silica particles affect the orientation of the silane molecules relative to the silica surface. This seems to affect the dynamic mechanical properties of composites.

Effect of the structure of silane coupling agent on sorption characteristics of solvents by dental resin-nanocomposites.

OBJECTIVE: This work was aimed at the study of sorption characteristics of water or ethanol/water solution (75vol%/25vol%) by dental nanocomposites consisting of a Bis-GMA/TEGDMA (50/50, wt/wt) matrix and silica nanoparticles (Aerosil OX50) as filler, silanized with various silanes. The silanes used were 3-[(1,3(2)-dimethacryloyloxypropyl)-2(3)-oxycarbonylamido]propyltriethoxysilane, which is a urethane dimethacrylate silane (UDMS), 3-methacryloxypropyltrimethoxysilane (MPS), octyltrimethoxysilane (OTMS), blends UDMS/OTMS (50/50, wt/wt) or blends MPS/OTMS (50/50, wt/wt). METHODS: The composite specimens (15mm diameterx1mm height) were immersed in water or ethanol/water solution at 37+/-1 degrees C for 30 days. At fixed time intervals they were removed, weighed and returned to the liquid for the study of sorption kinetics. Then desorption kinetics was studied by heating the samples in a drying oven maintained at 37 degrees C. The sorbed or desorbed liquid at equilibrium, diffusion coefficients, solubility, and volume increase after sorption were calculated. The sorption/desorption cycle was repeated for a second time. RESULTS: The silane structure used for the silanization of nanosilica was found to affect the sorption behavior of water or ethanol/water solution (37 degrees C) by the composites. The composite containing the UDMS with the hydrophilic urethane group showed the highest amount of sorbed water. The composite with the OTMS, which does not contain a methacrylate moiety and cannot react with the dimethacrylate monomers showed the highest solubility both in water and ethanol/water. In all composites the amount of sorbed ethanol/water solution is much higher than that of water. OTMS-composite sorbed the highest amount of ethanol/water and the MPS-composite with the 3-methacryloxypropyltrimethoxysilane the lowest. SIGNIFICANCE: The silane structure used for the silanization of nanosilica has an effect on the solvent sorption and solubility of composites.

Volumetric dimensional changes of dental light-cured dimethacrylate resins after sorption of water or ethanol.

OBJECTIVES: This study evaluated the influence of water and ethanol sorption on the volumetric dimensional changes of resins prepared by light curing of Bis-GMA, Bis-EMA, UDMA, TEGDMA or D(3)MA. METHODS: The resin specimens (15mm diameterx1mm height) were immersed in water or ethanol 37+/-1 degrees C for 30 days. Volumetric changes of specimens were obtained via accurate mass measurements using Archimedes principle. The specimens were reconditioned by dry storage in an oven at 37+/-1 degrees C until constant mass was obtained and then immersed in water or ethanol for 30 days. The volumetric changes of specimens were determined and compared to those obtained from the first sorption. RESULTS: Resins showed similar volume increase during the first and second sorptions of water or ethanol. The volume increase due to water absorption is in the following order: poly-TEGDMA>poly-Bis-GMA>poly-UDMA>poly-Bis-EMA>poly-D(3)MA. On the contrary, the order in ethanol is poly-Bis-GMA>poly-UDMA>poly-TEGDMA>poly-Bis-EMA approximately poly-D(3)MA. The volume increase was found to depend linearly on the amount of water or ethanol absorbed. SIGNIFICANCE: In the choice of monomers for preparation of composite resin matrix the volume increase in the resin after immersion in water or ethanol must be taken into account. Resins of Bis-EMA and D(3)MA showed the lowest values.

Dynamic thermomechanical properties and sorption characteristics of two commercial light cured dental resin composites.

OBJECTIVES: The first objective of this work is the study by DMTA of viscoelastic properties (E', E'', tandelta, Tg) of two current dental resin composites Tetric EvoCeram (nanohybrid) and Heliomolar (microfilled) in dry condition and in water for up to 30 days. The second objective is to determine the sorption characteristics of these composites in water and ethanol/water solution 75vol.%. METHODS: For DMTA the bar-shaped specimens divided into five groups of three samples each. The first group consisted of dry samples measured 1h after curing. The second and third group consisted of samples, which had been heated in air at 80+/-1 degrees C for 1 day or had been stored in distilled water at 80+/-1 degrees C for 1 day. The fourth and fifth group consisted of samples, which had been stored in distilled water at 37+/-1 degrees C for periods 1 and 7 days correspondingly. Also specimen discs (15mm in diameter and 1mm in thickness) were immersed in water or a 75vol.% ethanol/water solution at 37+/-1 degrees C. At fixed time intervals they were removed, blotted dry to remove excess liquid, weighted and returned to the liquid. This process continued for 30 days. RESULTS: The viscoelastic properties (E', E'', tandelta, Tg) of the two composites treated under different conditions were recorded and compared. Also the mass uptake, diffusion coefficient, solubility and volumetric changes for immersion of composites in water and ethanol/water solution 75vol.% at 37+/-1 degrees C were determined. SIGNIFICANCE: Tetric EvoCeram a nanohybrid composite with similar about resin matrix with Heliomolar which is a microfilled showed better dynamic thermomechanical properties and sorption characteristics than Heliomolar.

Sorption kinetics of ethanol/water solution by dimethacrylate-based dental resins and resin composites.

In the present investigation the sorption-desorption kinetics of 75 vol % ethanol/water solution by dimethacrylate-based dental resins and resin composites was studied in detail. The resins examined were made by light-curing of bisphenol A glycol dimethacrylate (Bis-GMA), triethylene glycol dimethacrylate (TEGDMA), urethane dimethacrylate (UDMA), bisphenol A ethoxylated dimethacrylate (Bis-EMA), and mixtures of these monomers. The resin composites were prepared from two commercial light-cured restorative materials (Z100 MP and Filtek Z250), the resin matrix of which is based on copolymers of the above-mentioned monomers. Ethanol/water sorption/desorption was examined in both equilibrium and dynamic conditions in two adjacent sorption-desorption cycles. For all the materials studied, it was found that the amount of ethanol/water sorbed or desorbed was always larger than the corresponding one reported in literature in case of water immersion. It was also observed that the chemical structure of the monomers used for the preparation of the resins directly affects the amount of solvent sorbed or desorbed, as well as sorption kinetics, while desorption rate was nearly unaffected. In the case of composites studied, it seems that the sorption/desorption process is not influenced much by the presence of filler. Furthermore, diffusion coefficients calculated for the resins were larger than those of the composites and were always higher during desorption than during sorption. Finally, an interesting finding concerning the rate of ethanol/water sorption was that all resins and composites followed Fickian diffusion kinetics during almost the whole sorption curve; however, during desorption the experimental data were overestimated by the theoretical model. Instead, it was found that a dual diffusion-relaxation model was able to accurately predict experimental data during the whole desorption curve. Kinetic relaxation parameters, together with diffusion coefficients, are reported for all resins and composites.

Aging studies of light cured dimethacrylate-based dental resins and a resin composite in water or ethanol/water.

OBJECTIVE: To study the aging of neat resins, prepared from bis-GMA, UDMA, D(3)MA or a mixture of bis-GMA/UDMA/D(3)MA (65/20/15 w/w/w), in water or 75% (v/v) ethanol/water 37 degrees C. Also the study of aging of Heliomolar RO, which is a radiopaque, microfilled, light cured composite, the resin matrix of which is the copolymer of bis-GMA/UDMA/D(3)MA (65/20/15 w/w/w). METHODS: Samples of neat resins and Heliomolar RO prepared by light curing were immersed in water or 75% (v/v) ethanol/water 37 degrees C, for 1, 7 or 30 days. Then the flexural and tensile strength were determined. The fractured surface of samples after the flexural tests was observed by scanning electron microscopy. RESULTS: Bis-GMA and copolymer resin did not showed any significant change in mechanical properties after immersion in water or 75% (v/v) ethanol/water 37 degrees C, for 30 days. On the contrary UDMA, D(3)MA and the composite Heliomolar RO showed a significant decrease. SIGNIFICANCE: The results obtained showed that the effect of aging in water or ethanol/water solution on mechanical properties of a light cured dimethacrylate resin depends on the chemical structure of resin. In the case of resin composite this effect depends on the filler-matrix bond strength.

Water sorption characteristics of light-cured dental resins and composites based on Bis-EMA/PCDMA.

The water uptake characteristics of resins and composites based on an ethoxylated bisphenol A glycol dimethacrylate (Bis-EMA) and a polycarbonate dimethacrylate (PCDMA) were studied in detail. Polydimethacrylate resins were prepared by photopolymerization of the neat monomers and mixtures of them with various weight ratios, using the camphoroquinone/N,N-dimethylaminoethyl methacrylate system as initiator, while the composites were prepared from the light-curing of commercial samples (Sculpt-It and Alert). Water sorption/desorption was examined both in equilibrium and dynamic conditions in two adjacent sorption-desorption cycles. The equilibrium water uptake from all resins was very small with a trend to increase as the amount of PCDMA was increased. The inverse effect was observed in the solubility values. The composites studied exhibited also very low water uptake values in comparison to other composite materials reported in the literature. It was also observed that the equilibrium uptake decreased with increasing filler loading. Slightly larger equilibrium water uptake and much smaller solubility values were obtained during the second sorption-desorption cycle in comparison to the first one. Concerning the sorption rate data, it was observed that the resin materials followed Fickian diffusion during almost the whole sorption or desorption curve, while the composites showed this behavior until only M(t)/M( infinity ) congruent with 0.5. The diffusion coefficients calculated for the resins were larger than those of the composites and always higher during desorption compared to sorption. The values of the diffusion coefficients for both resins and composites were in the same order of magnitude with the values of the corresponding materials reported in the literature.