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At least 307 records · Page 17Linked to original sources
PubMed1991

Characterization of the interface in the plasma-sprayed HA coating/Ti-6Al-4V implant system.

The successful use of plasma-sprayed hydroxyapatite (HA) coatings on Ti-alloy implants for implant-to-bone fixation requires strong adherence of the ceramic coating to the underlying metal substrate. In this study, the metal-ceramic interface was evaluated using mechanical, chemical, and structural characterization methods. Evaluations of an HA-coated Ti-6Al-4V implant system using a modified short bar technique for interfacial fracture toughness determination revealed relatively low fracture toughness values. Additionally, conventional tensile bond strength testing indicated much lower values than previously reported. Using high resolution electron spectroscopic imaging, evidence of chemical bonding was revealed at the plasma-sprayed HA/Ti-6Al-4V interface, though bonding was primarily due to mechanical interlock at the interface. This study illustrates the benefits of, and the need for, a multilevel approach to evaluate and improve these plasma-sprayed ceramic-metal substrate interfaces.

Alloys↗
PubMed2005

Effect of poly(ethylene oxide) on the release behaviors of poly(epsilon-caprolactone) microcapsules containing erythromycin.

The biodegradable poly(epsilon-caprolactone) (PCL)/poly(ethylene oxide) (PEO) microcapsules and the analyzing of form and features for the manufacturing conditions were investigated in a prospective drug delivery systems (DDS) through drug release. The effects of emulsifier, emulsifier concentration, and stirring rate on the diameter and form of the microcapsules were examined using image analyzer (IA) and scanning electron microscope (SEM). The role of interfacial adhesion between PCL/PEO and drug was determined by contact angle measurements, and the drug release rate of the microcapsules was characterized by UV-vis spectroscopy. As a result, the microcapsules were made in spherical forms with a mean particle size of 170 nm approximately 68 microm. And the work of adhesion between water and PCL/PEO was increased with increasing the PEO content, which is due to higher hydrophilicity of PEO. The drug release rate of the microcapsules was significantly increased as the PEO content increased, which could be attributed to the increasing of the hydrophilic groups or the degree of adhesion at the interfaces.

Adhesiveness↗
PubMed2005

On the Lagrangian/Eulerian modeling of dispersed droplet inertia: internal circulation transition.

This article addresses a limitation of Lagrangian methods for droplet tracking, when approaching the transition point of internal circulation within droplets. Laminar multiphase flow with dispersed droplets in a co-flowing airstream is considered. Analytical and numerical formulations of droplet motion are developed based on a Lagrangian finite difference method of droplet tracking. Cases of both high and low relative Reynolds numbers are formulated. The role of interfacial drag in cross-phase momentum exchange increases at higher relative Reynolds numbers. A new transition criterion is developed to characterize conditions leading to shear-driven non-uniformities of velocity within a droplet. This criterion entails a momentum Biot number, in analogy with the Biot number criterion for conjugate heat transfer problems involving conduction and convection. At sufficiently high momentum Biot numbers, appreciable changes of velocity within a droplet imply that Lagrangian methods become unsuitable and transition to Eulerian volume averaging is needed. Predicted results of Lagrangian modeling of droplet motion in a co-flowing airstream are presented and discussed.

Journal Article↗
PubMed2004

Quantitative measurements of dielectric spectra with microdielectric fringe-effect sensors.

The parallel-plate method is a gold standard for measuring dielectric properties of materials. However, it requires sampling of the material under testing (MUT), which makes it less suitable for real time, dynamic, and in situ measurements. The alternative to the parallel-plate method is to use the microdielectric fringe-effect (FE) sensors, which can be placed inside the process or laboratory equipment to provide rapid, on-line, and noninvasive characterization of the dielectric properties. An additional potential advantage of the FE measurements is the ability to obtain spatially localized and interfacial measurements, which may be important in some applications. Unfortunately, interpretation of the FE sensor measurements is difficult because of the spatial nonuniformity of the electrical excitation field created by the FE sensor and the extraneous contributions from the sensor substrate and unknown stray elements. The objective of this study is to summarize the theoretical basis of the dielectric measurements using planar interdigitated sensors and to use it in the development of a new method for obtaining quantitative measurements with FE sensors. As the first step, the basic correlation between the impedance measurements obtained with the FE sensor and the dielectric properties of the MUT is elucidated. The theoretical results are then used to analyze the contribution of the sensor substrate and unknown stray components to the overall measurements. A novel calibration method to eliminate extraneous contributions is then proposed. The application example demonstrates the application of the developed method to the measurement of the dielectric permittivities of a polydispersed cis-polyisoprene samples. The results are compared with those obtained using the parallel-plate measurements and show excellent agreement. Experimental comparison with the alternative calibration methods is also performed, indicating significant improvement in accuracy of dielectric measurements over a broad range of frequencies.

Journal Article↗
PubMed2005

Stability of a viscoelastic falling film with surfactant subjected to an interfacial shear.

The long-wavelength stability is analyzed for a surfactant-laden, viscoelastic liquid flowing down an inclined plane when the liquid undergoes additional interfacial shear. The upper convected Maxwell model is employed for describing the elastic nature of the fluid. The system stability is characterized by the interface and the surfactant modes. The interface mode involves both elastic and Marangoni effects that modulate the stability with applied shears and gravity-driven flow. The surfactant mode is only determined by the shear-induced Marangoni effects. A phase diagram is established to identify the dominant mode and the overall features of instability. It reveals that the system is susceptible to instability, except in a stable window when the applied shear opposes the gravity-driven flow.

Journal Article↗
PubMed2003

Effect of bleaching on fracture toughness of composite-dentin bonds.

PURPOSE: The effect of carbamide peroxide concentration and length of exposure on fracture toughness (KIC) of existing composite-dentin interfaces was assessed using the notchless triangular prism (NTP) specimen KIC test. MATERIALS AND METHODS: Freshly extracted human molars and premolars were wet ground on 600-grit SiC to obtain 4 x 4 x 4 x 4 mm triangular prisms, exposing buccal or lingual dentin. Dentin surfaces were bonded using a resin composite (Z-250, 3M) and SingleBond dentin bonding system (3M) to obtain 180 8-mm-long dentin-composite NTP specimens. The bonding system was applied using the "wet-bonding" technique. The bonded specimens were randomly assigned to 20 groups. The effect of exposure to three control solutions (tap water, Carbopol, and Carbopol-urea) and to four concentrations (11%, 13%, 16%, 21%) of carbamide peroxide (Perfecta, Premier) was assessed. Testing was conducted after 1, 2, and 3 weeks representing a cumulative exposure of 14, 42, and 70 h. The maximum force recorded before fracture was used to calculate KIC. The data were statistically analysed using two-factor ANOVA followed by one-way ANOVA and Bonferroni multiple means comparisons. Selected fractured surfaces were characterized using SEM. RESULTS: Data analysis revealed that cumulative exposure to bleaching agent for 70 h significantly (p < 0.01) decreased the interfacial KIC, regardless of concentration. For the 16% and 21% concentrations, a significant reduction was observed after 42 h. CONCLUSION: The results suggest that bleaching could adversely affect the interfacial fracture toughness of dentin-resin composite adhesive interfaces.

Acrylic Resins↗
PubMed1995

Lipid structural reorganization induced by the pancreatic lipase cofactor, procolipase.

Pancreatic colipase and its precursor, procolipase, facilitate interfacial lipid hydrolysis catalyzed by pancreatic lipase. To better understand how procolipase functions, its interactions with mixed-lipid monolayers at the argon-buffer interface have been characterized. The lipid mixtures consisted of 1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine and either 1,3-dioleoylglycerol, a model lipase substrate, or 13,16-cis,cis-docosadienoic acid, a model lipase product. Analysis of the lipid composition dependence of procolipase-induced surface pressure increases shows thermodynamically that procolipase interacts strongly and preferentially with the lipase substrate or product. This finding was confirmed by fluorescence measurements of procolipase interaction with pyrene lipid analogs. Analysis of the quantity of procolipase adsorbed to the lipid monolayers shows that interfacial packing obeys a simple, geometric model. The partial molecular areas obtained for procolipase (708 A2) and the phosphatidylcholine (70 A2) agree with their known cross-sectional areas. However, the areas for the fatty acid (14 A2) and diacylglycerol (18 A2) are less than half the expected values, indicating the formation of substrate multilayers. Overall, the results indicate a previously unrecognized role for procolipase, recruiting substrate laterally to its vicinity and, hence, to pancreatic lipase with which procolipase forms a 1:1 interfacial complex. Accompanying this preferential interaction of procolipase with lipase substrates is their rearrangement normal to the interface. These previously unrecognized properties of this lipase cofactor should have relevance for the regulation of other lipases, like lipoprotein lipase, which are regulated by cofactor proteins.

Adsorption↗
PubMed2005

Fluorescence probing of interior, interfacial, and exterior regions in solution aggregates of poly(ethylene oxide)- poly(propylene oxide)-poly(ethylene oxide) triblock copolymers.

Fluorescence spectroscopy is used to probe local environments within regions of different polarity and hydrophobicity in aqueous aggregates of PEO(109)-PPO(41)-PEO(109) triblock copolymers. These copolymer aggregates have well characterized microphases in aqueous solution. Concentrations and temperatures for our studies are chosen such that the copolymers are in unimer, micellar, or micellar hydrogel forms. The observed fluorescence spectra and lifetimes from solutions individually labeled with each of the three coumarin probes report on the changes in the local polarity of the core, exterior, interfacial, and corona regions of these copolymer aggregates. This multiple fluorescence probe methodology will be straightforward to apply in general to problems in polymer and biopolymer aggregates, especially those that display strong hydrophobic effects.

Coumarins↗
PubMed1985

Transport of potassium ions across planar lipid membranes by the antibiotic, grisorixin: I. The equilibrium state and self-diffusion K+ fluxes.

42K+ tracer flux and steady-state conductance measurements were carried out with bilayer lipid membranes containing grisorixin, a carboxylic polyether antibiotic. When the membranes are placed between two bulk aqueous solutions of identical composition, the exchange or self-diffusion transmembrane flux of potassium is measured by a method which allows the characterization of the bilayer K+ permeability at the equilibrium state. The K+ self-diffusion flux increases with the pH in the range pH 6 to pH 9 and reaches a constant value for values above 9. This can be directly related to the increase of the surface concentration of the 1:1 complex formed by K+ and the deprotonated polyether at both bilayer membrane interfaces. The transport model initially proposed by Pressman and co-workers (Proc. Natl. Acad. Sci. USA 58:1949-1956, 1967) is again taken into consideration in the quantitative analysis of the flux data. The transmembrane transport of K+ results from the translocation of its neutral complex with grisorixin and the association-dissociation of the antibiotic with either potassium or protons taking place at both interfacial space layers while the turnover of the mobile carrier is accomplished under asymmetrical conditions by a translocation process of the acidic grisorixin. Using the data of some previous studies for mixed ionophore-lipid monolayers at the air/water interface and the present results for the self-diffusion flux measurements, it was possible to propose an evaluation of the more important parameters characterizing the transport; namely, the total surface concentration of grisorixin, the interfacial pK and the translocation rate constant of its potassium neutral complex.(ABSTRACT TRUNCATED AT 250 WORDS)

Anti-Bacterial Agents↗
PubMed1999

Nucleation at surfaces: the importance of interfacial energy.

The nucleation and growth of stone-forming minerals on the surfaces of other crystalline phases, cellular material, and immobilized macromolecules must be important in the formation of stones in the urinary tract. The nucleation and growth of calcium oxalate monohydrate (COM) crystals were studied using the constant composition kinetics technique, in solution supersaturated with respect to COM (sigmaCOM = 1.44). The solid phases during the reaction were examined by x-ray diffraction, scanning electron microscopy, and diffuse reflectance Fourier transform infrared spectroscopy. Human serum albumin was found to nucleate COM crystals when immobilized on hydroxyapatite (HAP) surfaces. The induction period for nucleation of COM on HAP surfaces preadsorbed with albumin significantly decreased to about 65 min from about 230 min for pure HAP particles. The initial growth rate of COM on pure HAP particles, Rm approximately/= 0.56 X 10(-7) mol/min per m2, was slower than that for HAP surfaces preadsorbed with albumin, 2.14 x 10(-7) mol/min per m2. The surface properties were characterized using contact angle measurements by sessile drop and thin layer wicking. The thermodynamic results suggested that surfaces with high Lewis base parameter values (gamma-) and low interfacial tension with water (gammaSL) are more effective in the nucleation and growth of crystal phases.

Calcium Oxalate↗
PubMed1993

Hydroxyapatite-coated strain gauges for long-term in vivo bone strain measurements.

The aim of this study was to examine the bonding process between hydroxyapatite-coated strain gauges and bone in order to continue development of a long term in vivo strain measurement device. Two types of commercially available hydroxyapatite (HA) particles were applied to the sensing surface of uniaxial strain gauges using a polysulfone solution as an adhesive. Characterization by scanning electron microscopy and x-ray diffraction (XRD) was used to determine materials property differences between the two powders. Interfacial strengths between the HA coatings and the strain gauges were tested and found comparable to interfacial strength obtained by a plasma sprayed HA coating on the surface of a titanium implant. Gauges were surgically placed on the periosteal surface of greyhound femora. Three groups of dogs were implanted with gauges for periods of 3, 6, and 12 weeks using cyanoacrylate, resorbable sutures, and cable ties to initially hold the gauge against the surface of the bone. Following euthanasia, the femora of the dogs were explanted and subjected to cantilever loading. Response of the implanted HA-coated gauges were compared to a control set that had been freshly glued onto the contralateral femur. Full response, that is, 100% of the strain measurement with respect to the control, was obtained after 12 weeks in vivo. Attachment of HA-coated gauges with circumferential suture showed bonding, while HA-coated gauges attached with cyanoacrylate did not bond to bone. After mechanical testing, femora were embedded in polymethylmethacrylate, cut, ground, and polished. Sections were stained using mineralized bone stain (MIBS) and optical microscopy was performed using transmitted and fluorescent light to allow analysis of remodeling occurring in the region of the strain gauges. Bone formation occurred at the HA surface of sutured gauges, and a fibrous tissue layer developed between the bone and HA coating when the tissue adhesive was used to initially bond the gauge. Fluorescence microscopy indicated an increase in the number of areas of bone remodeling adjacent to the gauge but a normal rate of remodeling of 0.93 +/- 0.07 mum/day was observed. No gross bone remodeling due to strain gauge placement was observed. Backscattered electron imaging (BSE) indicated new bone apposition at all time periods.

Animals↗
PubMed2006

Formation and structural anomaly of the metastable phases in an immiscible Ag-Mo system studied by ion beam mixing and molecular dynamics simulation.

For the equilibrium immiscible Ag-Mo system characterized by a large positive heat of formation, the nanosized Ag-Mo multilayered samples are designed and prepared to include sufficient interfacial free energy to elevate their initial energetic states to be higher than that of either the amorphous phase or solid solution and then subject to 200 keV xenon ion irradiation. The results show that a uniform amorphous alloy can be obtained within a composition range, at least, from 25 to 88 atom % of Mo. Interestingly, in the intermediate stage of ion irradiation, a bcc phase, an amorphous phase, and an order (bcc)-disorder coexisting state appear simultaneously in the Ag12Mo88 multilayered sample and extend over the entire bright field image with unanimously homogeneous composition. In thermodynamic modeling, a Gibbs free energy diagram of the Ag-Mo system is constructed, based on Miedema's model, and suggests that within a narrow composition regime of 85-90 atom % of Mo, the energy difference between the bcc and the amorphous phases is extremely small, which is probably the very reason for the order-disorder coexisting state to appear. In atomistic modeling, an ab initio derived Ag-Mo potential is applied to perform molecular dynamics simulations. The simulations not only determine an intrinsic glass-forming ability/range (GFA/GFR) of the Ag-Mo system to be from 10 to 88 atom % of Mo but also reveal the possibility of the formation/appearance of a crystalline and amorphous mixture in a narrow composition regime of 88-92 atom % of Mo. Apparently, the theoretical results are in excellent agreement and/or compatible with the experimental observations in ion beam mixing.

Journal Article↗
PubMed1999

Transmission electron microscopy of interfaces in structural ceramic composites

Ceramic composites based either on a particulate, fibre or a lamellar architecture are potentially useful as damage-tolerant high-temperature engineering materials. The ability of the interfaces in such systems to deflect cracks is vital to the damage tolerance of these materials. Transmission electron microscopy techniques enable the chemical and physical characterization of these interfaces, providing information on interlayer thicknesses, chemical species, local bonding and the microstructural features which give rise to the interfacial properties, thereby enabling a full understanding not only of composites after processing, but also after exposure to aggressive environments such as air at high temperature. Examples of the application of transmission electron microscopy to all three composite architectures are described.

Journal Article↗
PubMed1982

Conformational analysis of the calcium--A23187 complex at a lipid--water interface.

A possible conformation of the complex formed by one calcium ion and two molecules of the ionophore A23187 at a simulated lipid--water interface was predicted by a variant method for conformational analysis. This method takes into account, in addition to the Van der Waals energy, electrostatic interaction, and torsional potential, the alteration of electrostatic forces attributable to changes in dielectric constant at the interface and the transfer energy for each part of the complex as it moves through the lipid-water interface. The most probable conformer was characterized by a two-fold axial symmetry that was maintained during transition to the hydrophobic bulk conformation. Minor changes in the interfacial structure were sufficient to achieve the configuration characteristic of the hydrophobic bulk phase.

Anti-Bacterial Agents↗
PubMed1994

Current progress in crystallographic studies of new lipases from filamentous fungi.

Lipases from filamentous fungi have been studied extensively over many years. They exhibit properties attractive for industrial applications, e.g. in laundry detergents, tanning and paper industries and stereospecific organic synthesis. Enzymes from the fungi Rhizomucor miehei and Geotrichum candidum have been among the first neutral lipases to be characterized structurally by X-ray diffraction methods. In this paper we report a preliminary account of crystallographic studies of three other fungal lipases homologous to that from R. miehei and obtained from Humicola lanuginosa, Penicillium camembertii and Rhizopus delemar. These newly characterized structures have important implications for our understanding of structure-function relationships in lipases in general and the molecular basis of interfacial activation.

Amino Acid Sequence↗
PubMed1986

Biocompatibility: bioengineering aspects.

Bioengineers have contributed to biocompatibility research. Many materials have been designed, synthesized, and characterized by use of various analytical instruments. The blood compatibility of materials has been studied by focusing on the blood-material interfacial reactions. Although much information has been accumulated regarding such local reactions, understanding of biocompatibility is still limited. A more global approach to study is needed. A new approach to understanding biocompatibility is proposed and discussed. Three points are stressed: interaction within body's defense system and its effect on blood-material reactions; induction of a systemic reaction by a local reaction, which then affects the blood-material interaction; the time sequence of such interactions between local and systemic reactions. To establish a logical approach to study biocompatibility is most important at this moment for the future progress in biocompatibility research.

Biocompatible Materials↗
PubMed2002

Hole nucleation in thin diblock copolymer films.

This paper reports an experimental study of a homogeneous nucleation process in the direct space, using an atomic-force microscope. Nucleated patterns are holes in a thin diblock copolymer film. The formation of nuclei from the metastable majority phase is followed either by the dissolution or by the growth of the hole. It is also preceded by the unexpected presence of a bump at the free surface. From the study of the nucleus surface topography at different stages of the evolution, we infer a description of the nucleation mechanism at a molecular level. It involves the existence of ordered metastable states characterized by the presence of compressed internal layers, the formation of pores in the center of the film, and the existence of interfacial flows across these pores. The presence of compressed internal layers was directly demonstrated using Neutron Reflectivity experiments, Our scheme is also consistent with all existing experimental data. After hole nucleation, we identify two distinct growth regimes: the first one is individual and the second one is interactive.

Journal Article↗
PubMed2006

Enhanced electrorheological activity of mesoporous Cr-doped TiO2 from activated pore wall and high surface area.

To enhance electrorheological (ER) activity by improving interfacial polarization, we prepared a new mesoporous Cr-doped TiO2 ER material by a copolymer-templated sol-gel method. The material was characterized by differential scanning calorimeter and thermogravimetric (DSC-TG) analysis, Fourier transform infrared (FT-IR), X-ray powder diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption, and X-ray photoelectron spectroscopy (XPS) techniques. The ER activity was studied by the rheological curve and yield stress under an electric field. The results showed that the mesoporous Cr-doped TiO2 ER material possessed a high surface area over 200 m2/g and a crystalline anatase pore wall doped by different valent Cr ions. The ER activity of mesoporous Cr-doped TiO2 was higher than that of nonporous Cr-doped TiO2. The yield stress and ER efficiency of the mesoporous Cr-doped TiO2 ER suspension was 3 times as high as that of the nonporous Cr-doped TiO2 ER suspension, 7 times as high as that of the mesoporous undoped TiO2 ER suspension, and 20 times as high as that of the nonporous pure TiO2 ER suspension. Furthermore, the ER activity of mesoporous Cr-doped TiO2 showed a dependence on surface area, and the high porosity or surface area samples showed higher ER activity. The dielectric spectra analysis showed that the mesoporous Cr-doped TiO2 ER suspension possessed a significantly larger interfacial polarizability compared with the nonporous Cr-doped TiO2 ER suspension, and the regular change of polarizability with surface area or porosity was in accordance with the change of ER activity with surface area or porosity. The improvement of dielectric properties or polarization could well explain the enhancement of the ER activity of mesoporous Cr-doped TiO2.

Journal Article↗