Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “GLASSES”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 721 records · Page 40Linked to original sources

Relationship between 3T3 cell spreading and the strength of adhesion on glass and silane surfaces.

Cell detachment by laminar shear stresses was used to characterize cellular interactions with hydrophilic glass and hydrophobic silane. In this study, we examined whether smaller, rounder cells were preferentially detached by laminar flow, and whether cell detachment occurred by dissociation of adhesion proteins and their membrane receptors or rupture of the membrane. Shear-induced detachment from glass and silane were similar after 0.5 h static attachment to the surfaces, even though 3T3 cells had a greater projected area on silane. No particular cell size was preferentially detached by fluid shear stresses. After 2 h attachment and spreading, 3T3 cells were more easily detached from the silane surface even though the cells were more spread than on glass. On glass, smaller cells were preferentially detached below 30 dyne/cm2, increasing the mean projected area of the population. Above 30 dyne/cm2, larger cells also detached from the surface. Cell detachment from the silane surfaces did not show any size preference. The strength of adhesion and projected areas on both surfaces increased significantly when the surfaces were preincubated with fibronectin. Simple geometric models of spreading cells were used to estimate the forces exerted on cells. The hydrodynamic forces exerted on spreading cells were similar, but the bond density needed to resist detachment declined as the projected area increased. Analysis of Dil-C18(3) membrane fragments indicated that cell detachment by membrane rupture was a significant mechanism of cell detachment from glass for shear stresses above 40 dyne/cm2, but was unimportant for cell detachment from the silane surfaces. The results indicate that differences in the strength of 3T3 cell adhesion were probably due to differences in bond strength and the numbers of receptor-ligand bonds formed on the two surfaces and, on glass, cell detachment due to membrane failure at higher shear stresses.

3T3 Cells↗

Polymethylmethacrylate composites: disturbed bone formation at the surface of bioactive glass and hydroxyapatite.

The effects of polymethylmethacrylate on bone formation were studied alone and as composites in combination with hydroxyapatite and bioactive glass in the rabbit subchondral femur. Radiographs, histology, computer assisted histomorphometry, scanning electron microscopy and energy dispersive X-ray analysis were used for evaluation. A total of 60 cones were implanted for 3, 6 and 12 weeks. The composite cones consisted of granules of bioactive glass (S56.5P4) or hydroxyapatite embedded in polymethylmethacrylate. Pure polymethylmethacrylate cones served as controls. At the interface of the cones, bone contact was observed only when bioactive glass or hydroxyapatite was present at the cone surface. Fibrous tissue was always found at the polymethylmethacrylate-tissue interface. The osteoconductive bone formation at the surface of bioactive glass and hydroxyapatite was disturbed by polymethylmethacrylate. It seemed to resist bone formation at the interface of both bioactive glass and hydroxyapatite. However, bioactive glass was better able to withstand the detrimental effect of polymethylmethacrylate than hydroxyapatite.

Animals↗

Grafting of ethylene glycol-butadiene block copolymers onto dimethyl-dichlorosilane-coated glass by gamma-irradiation.

Amphipathic ethylene glycol-butadiene block copolymers (PEG-PB) with different chain lengths of poly(ethylene glycol) (PEG) were synthesized by reacting poly(ethylene glycol methyl ether) (m-PEG, mol. wt = 350, 550, 750, 2000 and 5000) with telechelic polybutadiene (PB). The PEG-PB copolymers formed were covalently grafted to dimethyldichlorosilane-coated glass (DDS-glass) by gamma-irradiation. The PEG-grafted surface was characterized by measuring advancing and receding contact angles, fibrinogen adsorption, the number of adherent platelets and the area of spread platelets. The grafting efficiency was measured indirectly from the ability of the surface to prevent platelet adhesion. The total dose of gamma-irradiation necessary for grafting of PEG-PB onto DDS-glass in aqueous solutions was less than 0.24 Mrad at atmospheric pressure and ambient temperature. For successful grafting, the surface-adsorbed copolymers should be gamma-irradiated in the presence of water. gamma-Irradiation in the dried state did not result in copolymer grafting. The adsorption of copolymers for 30 min before exposure to gamma-irradiation was enough for effective grafting. The grafting was equally effective whether or not DDS-glass was exposed to the air-copolymer solution interface when the DDS-glass was introduced into the copolymer solution. The copolymers were able to prevent platelet adhesion only when they were adsorbed onto DDS-glass at certain bulk concentrations. Too low or too high copolymer concentrations in the adsorption solution resulted in a surface where platelets could adhere and activate. The range of copolymer concentration which prevented platelet adhesion was larger as the PEG chain length of the grafted copolymers became longer. Our data indicate that platelet-resistant surfaces can be made by grafting PEG-PB onto chemically inert surfaces by a simple gamma-irradiation process.

Adsorption↗

Sintering effects in a glass reinforced hydroxyapatite.

Glass was incorporated into hydroxyapatite (HA) to act as a sintering aid in order to improve the mechanical properties. The glass was added at 2 and 4 wt% and the powders compacted uniaxially. The compacts were sintered at a variety of temperatures (1200, 1250, 1300 and 1350 degrees C) and the effects of the glass addition and the firing temperature were studied to determine their effects on the sintering process. It was found that the glass promoted some phase changes, related to the amount of glass added to the composite. At 1200 and 1250 degrees C, some beta-tricalcium phosphate (TCP) was found with the residual being HA. However, at 1300 and 1350 degrees C, both beta- and alpha-TCP were formed. The 4 wt% addition, as expected, promoted higher levels of secondary phases in the composite. The flexural bend strength (FBS) showed high values and also significant differences dependent on the amount of glass added. A 2 wt% addition gave a gradual increase in FBS with temperature. With a 4 wt% addition there was an increase in FBS, but above 1300 degrees C there was a rapid decrease. These effects were mirrored in the linear shrinkage. Both the linear shrinkage and the FBS results were attributed to both the phase changes occurring and also change in grain size with increasing firing temperature.

Chemical Phenomena↗

Microleakage in restorations with glass ionomer liners after thermocycling.

The purpose of this study was to compare microleakage around two types of restorations lined with polyalkenoate (glass ionomer) cements after thermocycling. Preparations were made in 48 molars to a diameter and depth of 2.0 mm. Half of the preparations were lined with glass ionomer, and the remainder were not lined. Dental amalgam or glass ionomer restorative material was placed and the amalgams were left unburnished and unpolished. Selected restorations were thermocycled 625 times between 4 degrees C and 50 degrees C. Teeth were immersed in 0.5 per cent methylene blue solution, sectioned and visually scored for microleakage at X 100 magnification. Data analysis indicated significant differences in microleakage because of: thermocycling (chi 2 = 103.38, d.f. = 19,2P less than 0.0004); presence of glass ionomer liners (chi 2 = 53.28, d.f. = 19,2P less than 0.0001); and type of restorative material (chi 2 = 103.44,d.f. = 19,2P less than 0.0004). The use of a glass ionomer liner significantly reduced microleakage in both amalgam and glass ionomer restorations when subjected to thermocycling.

Chi-Square Distribution↗

Marginal breakdown of fired ceramic inlays cemented with glass polyalkenoate (ionomer) cement or resin composite.

The marginal breakdown of fired porcelain inlays in vivo, luted with either a dual-cured resin composite or a glass polyalkenoate(ionomer) cement, was evaluated by scanning electron microscopy. Immediately following polishing (baseline) and after 1 year, replica impressions were made of the occlusal and proximal margins of two inlays, one cemented with the resin composite and the other with the glass ionomer cement, in each of 12 patients. At baseline the best marginal adaptation was observed along the proximal margins of the composite luted inlays, while occlusally glass ionomer luted inlays showed better marginal qualities than the composite luted inlays. At 1 year the composite luted inlays showed significantly better marginal adaptation than the glass ionomer luted ones at all interfaces. The greatest breakdown was observed occlusally, especially in the glass ionomer luted inlays. Gap sizes varied proximally between 83 and 100 microns and occlusally between 107 and 143 microns. Severe ditching was observed occlusally in the glass ionomer luted inlays. The overall marginal quality was significantly better for the inlays luted with the resin composite both at baseline and after 1 year.

Analysis of Variance↗

An in vitro evaluation of bond strength of three glass ionomer cements.

The purpose of this study was to determine the bond strength of three commercially available glass ionomer cements when used to bond mesh-backed medium twin (0.130 inch) brackets to enamel surface. Three different enamel surface conditions, which included use of pumice, pumice and polyacrylic acid, and pumice followed by acidulated phosphate fluoride, were also tested to determine their effect on the bond strength. In addition, bond strength of one composite resin was compared with those of glass ionomer cements. The teeth were bonded with all the materials according to manufacturers' instructions. Each specimen was embedded in Super-Die with the bonded facial surface exposed. A surveyor was used to align the teeth in the stone uniformly for all specimens. A special bracket holder was used to hold the brackets precisely under the wings during debonding. An Instron universal testing machine was used to measure the force required for bond failure. To stimulate oral conditions, the direction of pull was so designed that it included an element of torsional stress along with tensile force. The findings indicate that a large variation existed between the bond strengths of all materials tested. The bond strength of glass ionomer cements was significantly less than that composite resin. However, the bond strength of at least one glass ionomer cement appears to be adequate for clinical use. The different surface preparation before bonding did not significantly affect the bond strengths of glass ionomer cements. Further investigation is required to test the bond strengths of glass ionomer cements clinically.

Acidulated Phosphate Fluoride↗

The influence of crystallised Fe3O4 on the magnetic properties of coprecipitation-derived ferrimagnetic glass-ceramics.

Ferrimagnetic glass-ceramics are potential candidates for magnetic induction hyperthermia, which is one form of inducing deep-regional hyperthermia, by using a magnetic field. The aim of this work was to analyse the influence of the amount of crystallised magnetite on the magnetic properties of glass-ceramic samples. Thus, two different ferrimagnetic glass-ceramics with the composition of the system Na(2)O-CaO-SiO(2)-P(2)O(5)-FeO-Fe(2)O(3) were prepared by melting at 1500 degrees C for 30 min of the coprecipitation-derived starting products. The X-ray diffraction patterns show the presence of nanometric magnetite crystals in a glassy matrix after cooling from melting temperature. The estimated amount of crystallised magnetite varies between 20 and 45 wt.%, as a function of the chemical composition. The morphology of the crystals was studied by scanning electron micrography and transmission electron micrography. Glass transition temperature and thermal stability were investigated by differential thermal analysis. Magnetic hysteresis cycles were analysed using a vibrating sample magnetometer with a maximum applied field of 17 kOe, at room temperature, in quasi-static conditions. Calorimetric measurements were carried out using a magnetic induction furnace. The power losses estimated from calorimetric measurements under a magnetic field of 40 kA/m and 440 kHz are 65 W/g for the glass-ceramic with lower iron oxides content and 25 W/g for the glass-ceramic with higher iron oxide content.

Biocompatible Materials↗

Rabbit pilot study on the resorbability of three-dimensional bioactive glass fibre scaffolds.

Bioactive glass composed of Na2O-K2O-MgO-CaO-B2O3-P2O5-SiO2 is used in this study to manufacture three-dimensional glass fibre scaffolds for a synthetic bone filler material for the treatment of bone defects. The glass is characterized by a large working range, which is the temperature interval at which forming of glass can take place. A preliminary in vivo study on New Zealand skeletally mature rabbit's tibia is reported here. Bone defects were prepared in the medial surfaces of the diaphyses of the tibia. For the first time melt derived three-dimensional bioactive glass fibre constructs were used to fill the cavities. The different implants investigated here were a scaffold with a porosity of 45-50%, scaffold with a porosity of 55-60% and morsels with a porosity of 55-60%. The implanted bone substitutes were dissected after 6 months and evaluated by histological and synchrotron radiation micro tomography analysis. PerioGlas and empty defects were used as positive and negative controls, respectively. The result was that the surgically created tibial defects were healed and new bone formation was found in the medullary cavities. Despite the intrinsic limitations of a pilot study, the preliminary results indicate that in 6 months the glass fibre scaffolds are completely resorbed and that the osteoconductive properties of the filling material are strictly correlated with the structural and morphological characteristics of the bone substitute.

Animals↗

New macroporous calcium phosphate glass ceramic for guided bone regeneration.

This work describes a method to obtain macroporous resorbable glass and glass ceramic scaffolds with controlled biodegradability for tissue engineering applications. The constructs consisted of glass and glass ceramics in the system P(2)O(5)-CaO-Na(2)O-TiO(2) and they were prepared by foaming a slurry of glass particles by addition of a H(2)O(2) solution, and subsequent sintering of the porous structures obtained. Different thermal treatments were applied to control the degree of devitrification of the glass. The resultant materials showed a porosity percentage between 40% and 55% with a wide variety of pores ranging from 20 to 500 microm in diameter as determined by SEM and Image Analysis. The resulting constructs were predominantly formed by a vitreous phase, although small amounts of calcium metaphosphate and pyrophosphates were detected by X-ray diffraction and Raman spectroscopy after the sintering process. The biological response was also evaluated by means of the MTT test, the material showed a non-cytotoxic effect.

Absorbable Implants↗

Early and long-term wear of 'fast-set' conventional glass-ionomer cements.

OBJECTIVE: Fast setting high viscous glass-ionomer cements have been introduced to reach the set state sooner and to improve early mechanical properties. The aim of this study was to investigate whether 'fast-set' cements have improved the early three-body wear. METHOD: The three-body wear of four glass-ionomer cements was measured after 1, 4, 7, 30, 90, and 365 days. The chemical composition of the cements was determined with EDAX. The particle size of the powders was determined with a Mastersizer 2000. RESULTS: The three-body wear of Fuji IX Fast was only slightly less than that of 'regular-set' Fuji IX, but Ketac Molar Quick showed a higher wear compared to the regular-set Ketac Molar. The wear rate of all four glass-ionomer cements decreased over a period of 1 year and could be described by second order reaction kinetics and depended on polyalkenoic acid content, chemical composition, and the size of the glass particles. SIGNIFICANCE: Based on the results of this laboratory study on long-term wear, the glass-ionomer cements investigated may compete with composites, but the early wear characteristics should be further improved. Furthermore, a better understanding of the wear and reaction behavior of glass-ionomer cements is obtained.

Electron Probe Microanalysis↗

Effect of water storage on the impact strength of three glass fiber-reinforced composites.

OBJECTIVES: The effect of water sorption on the impact strengths of two pre-impregnated fiber-reinforced composites (FRCs) and one impregnated FRC were studied. All FRCs were available clinically. METHODS: Eight 1.0 mm x 2.0 mm x 25.0mm bar-shaped specimens of each material were prepared according to manufacturers' instructions. The impact strength of each specimen was tested (adoption from ISO 179-1 Plastics-Determination of Charpy impact properties) after the specimens were immersed in 23.0+/-1 degrees C distilled water for seven, 60 and 180 days. The data were analyzed using the Weibull method. Scanning electron micrographs were taken to examine the mode of failure. RESULTS: Weibull analysis of the B10 strength of the FRCs showed that the difference in impact strength for each FRC due to the duration of water immersion was not significant (P>0.05). The impact strength of pre-impregnated E-glass FRC (Vectris) (75 kJ/m(2)) was not significantly different from the pre-impregnated S-glass FRC (FiberKor) (66 kJ/m(2)) (P>0.05). The impregnated FRC possessed impact strength (42 kJ/m(2)) that was not significantly different from the pre-impregnated S-glass FRC but was significantly lower than the pre-impregnated E-glass FRC. x100 SEMs of the three types of FRC specimens revealed fiber failure to be the predominant mode of failure. SIGNIFICANCE: Water immersion up to 180 days duration did not significantly affect the impact strength of three FRCs. The impact strength of the impregnated FRC was not significantly different from the pre-impregnated S-glass FRC but was significantly lower than the pre-impregnated E-glass FRC.

Composite Resins↗

Arsenic release from glass containers by action of intravenous nutrition formulation constituents.

Pharmacopoeias prescribe tests to determine the levels of arsenic in raw materials and glass containers. In this study, glass ampoules for injectables containing individually the main components of intravenous nutrition formulations were submitted to the hydrolytic resistance test by heating at 121 degrees C for 30 min. As(V) and As(III) levels in these solutions after heating were determined by hydride generation atomic absorption spectrometry. The arsenic content of substances used in these formulations was previously determined, as well as the arsenic content of the glass containers. The results showed that raw substances as well as glass containers contain arsenic. Moreover, arsenic is released during the heating (hydrolytic resistance test). However, the amount released and the arsenic species present in solution depend on the solution composition. While As(V) was the predominant specie in glass, solutions containing reducing substances such as glucose and vitamins had As(III) in higher concentration. Therefore, arsenic is released from glass containers during the heating for sterilization, and reacts with formulation constituents depending on their reducing properties.

Arsenic↗

A hypothesis of the disc-sphere transformation of the erythrocytes between glass surfaces and of related observations.

Erythrocytes suspended at a low hematocrit in a non-buffered isotonic saline change from biconcave discs to spheres between glass surfaces of a slide and of a coverslip with the echinocyte as an intermediate. A pH increase is a major factor responsible for this disc-sphere transformation or glass effect. It is also observed between surfaces made of various polymers and of mica provided that the distance between them is controlled (0.1 mm). The glass effect is antagonized by serum, plasma, serum albumin, ammonium salts and CO2. It is not observed above a 1-2% hematocrit, but is enhanced by gamma-globulins. The sites of reappearance of the spicules are the same and the order of their disappearance is the inverse of the order of their reappearance during the repetitive cycle of the disc-sphere transformation and reversal when a small glass rod is alternatively approached near a site on the erythrocyte surface and withdrawn. A mechanism of erythrocyte shape control has been previously hypothesized in which Band 3 (AE1), the anion exchange protein, plays a central role. Specifically, decrease and increase of the ratio of its outward-facing conformation (Band 3o) and inward-facing conformation (Band 3i) contract and relax the membrane skeleton, promoting the echinocytosis and stomatocytosis, respectively. The Band 3o/Band 3i equilibrium ratio is determined by the Donnan equilibrium ratio of Cl-, HCO3- and H+ (r=Cl(i)-/Cl(o)-=HCO3i-/HCO3o-=Ho+/Hi+), increasing with it. The mechanism could explain by a change of the Donnan ratio the above observations with the assumptions that polymers are permeable to CO2 and that an unstirred layer slows the propagation of the change occurring at the site of approach of the glass rod to peripheral sites. The presence of HCO3- in serum or plasma may be the basis for the absence of the glass effect in these fluids.

Aluminum Silicates↗

Optical absorption and photoluminescence properties of Er3+ doped mixed alkali borate glasses.

An investigations of the optical absorption and fluorescence spectra of 0.2 mol% Er2O3 in mixed alkali borate glasses of the type 67.8B2O3 x xLi2O(32-x)Na2O, 67.8B2O3 x xLi2O(32-x)K2O and 67.8B2O3 x xNa2O(32-x)K2O (where x = 8, 12, 16, 20 and 24) are presented. The glasses were obtained by quenching melts consisting of H3BO3, Li2CO3, Na2CO3, K2CO3 and Er2O3 (950-1100 degrees C, 1.5-2 h) between two brass plates. Spectroscopic parameters like Racah (E1, E2 and E3), spin-orbit (xi(4f)) and configuration interaction (alpha) parameters are deduced as function of x. Using Judd-Ofelt theory, Judd-Ofelt intensity parameters (omega2, omega4 and omega6) are obtained. Radiative and non-radiative transition rates (A(T) and W(MPR)), radiative lifetimes (tauR), branching ratios (beta) and integrated absorption cross-sections (sigma) have been computed for certain excited states of Er3+ in these mixed alkali borate glasses. Emission spectra have been studied for all the three Er3+ doped mixed alkali borate glasses. The present paper throws light on the trends observed in the intensity parameters, radiative lifetimes, branching ratios and emission cross-sections as a function of x in these borate glasses, keeping in view the effect of mixed alkalies in borate glasses.

Absorption↗

Raman study of TiO2 role in SiO2-Al2O3-MgO-TiO2-ZnO glass crystallization.

Tough glass-ceramic material of special mechanical properties with nanosize crystal phases formed by appropriately controlled crystallization was studied by Raman spectroscopy. It was obtained by TiO2 activated crystallization of Mg-aluminosilicate glass of SiO2-Al2O3-MgO-TiO2-ZnO composition. Crystallization was preceded by a change in the TiO2 structural position and state, which is manifested by a changed color of glass from yellow into blue shortly before the glass transformation (Tg) temperature. Raman spectroscopy was applied to explain the mechanism of this process and to establish the role of TiO2 in the early stage of glass crystallization that precedes a complete crystal phase formation. The starting glasses were found in almost complete disorder, since all bands were weak, broad and dominated by a Bose band at about 90 cm-1. After the sample annealing all bands turned out better resolved and the Bose band practically disappeared, both confirming the amorphous structure reorganization process. A multiplet observed in the vicinity of 150 cm-1 we assigned to the anatase and other titania structures that can be considered prime centers of crystallization. Finally, in the closest neighborhood of the Rayleigh line the low frequency mode characterizing nanoparticles was observed. According to this band theory, the mean size of initial titania crystallites is about 10nm for all samples, but the size distribution varies within factor two among them.

Aluminum Oxide↗

Optical characterization of Eu3+ and Tb3+ ions doped zinc lead borate glasses.

This paper reports on the spectral analysis of Eu3+ or Tb3+ ions (0.5 mol%) doped heavy metal oxide (HMO) based zinc lead borate glasses from the measurement of their absorption, emission spectra and also different physical properties. From the XRD, DSC profiles, the glass nature and glass thermal properties have been studied. The measured emission spectrum of Eu3+ glass has revealed five transitions (5D0-->7F0, 7F1, 7F2, 7F3 and 7F4) at 578, 591, 613, 654 and 702 nm, respectively, with lambdaexci=392 nm (7F0-->5L6). In the case of Tb3+:ZLB glass, four emission transitions such as (5D4-->7F6, 7F5, 7F4 and 7F3) that are located at 489, 542, 585 and 622 nm, respectively, have been measured with lambdaexci=374 nm. For all these emission bands decay curves have been plotted to evaluate their lifetimes and the emission processes that arise in the glasses have been explained in terms of energy level schemes.

Borates↗

Mixed trehalose/sucrose glasses used for protein incorporation as studied by infrared and optical spectroscopy.

Evaporation of water from a 1/1 mixture of trehalose and sucrose gives rise to optically clear glasses that are transparent in the UV and visible ranges and do not crystallize when they are prepared at ambient temperatures. Two proteins, liver alcohol dehydrogenase and parvalbumin, and the tryptophan derivative N-acetyl-tryptophanamide were incorporated into the glasses. Infrared spectroscopy of the amide I band reveals that the proteins retain secondary structure in the glass over a temperature range of 20-300K. The amide II band of the protein and the HOH bending band of residual water in the glass shift with temperature changes, consistent with increased H-bonding strength as temperature is lowered. Phosphorescence of tryptophan can be seen from the proteins at room temperature, which shows the immobilization of the protein by the glass and the curbing of oxygen diffusion. It is suggested that using mixed sugars to form glasses is a way to immobilize proteins over a wide temperature range without distortions from solvent crystals.

Alcohol Dehydrogenase↗