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PubMed2005

Stabilizer choice for rapid dissolving high potency itraconazole particles formed by evaporative precipitation into aqueous solution.

The objective of this study was to investigate the influence of stabilizer type on the physicochemical properties, including dissolution, of ultra-high potency powders containing itraconazole (ITZ) formed by evaporative precipitation into aqueous solution (EPAS). ITZ was dissolved in dichloromethane, which was then atomized through a heated coil at 80 degrees C into an aqueous solution over precise periods of time. Stabilizers were present in either the aqueous, organic or both phases. The dispersions were centrifuged and the supernatant was removed. Three hydrophilic stabilizers were investigated, including polysorbate 80, polyvinyl pyrrolidone and poloxamer 407. Rapid dissolving ultra-high potency of ITZ powders was successfully produced. Greater than 80% of ITZ was dissolved in 5 min compared to only 13% of ITZ bulk powders. The resulting stabilizer-coated drug particles had high drug-to-stabilizer ratios greater than 12, corresponding to potencies (wt drug/wt drug+wt surfactant) as high as 93%. An increase in dissolution rate was correlated with the amount of stabilizer adsorbed and the wettability. The combination of polysorbate 80 and poloxamer 407 present in the aqueous and organic phases, respectively, was superior in achieving high wetting and rapid dissolving ITZ powders. The ability to control the adsorption behavior of stabilizers by using synergistic combinations affords the opportunity to achieve high dissolution rates with higher potencies compared to previously reported values.

Adsorption↗
PubMed2004

A new method for measuring scouring efficiency of natural fibers based on the cellulose-binding domain-beta-glucuronidase fused protein.

Cellulose-binding domains (CBDs) are characterized by their ability to strongly bind to different forms of cellulose. This study examined the use of a recombinant CBD fused to the reporter enzyme beta-glucuronidase (CBD-GUS) to determine the extent of removal of the water-repellent waxy component of cotton fiber cuticles following hydrolytic treatment, i.e., scouring. The CBD-GUS test displayed higher sensitivity and repeatability than conventional water absorb techniques applied in the textile industry. Increases in the levels of CBD-GUS bound to the exposed cellulose correlated to increases in the fabric's hydrophilicity as a function of the severity of the scouring treatment applied, clearly indicating that the amount of bound enzyme increases proportionally with the amount of available binding sites. The binding of CBD-GUS also gave measurable and repeatable results when used on untreated or raw fabrics in comparison with conventional water drop techniques. The quantitative response of the reaction as bound enzyme activity was optimized for fully wettable fabrics. A minimal free enzyme concentration-to-swatch weight ratio of 75:1 was found to be necessary to ensure enzyme saturation (i.e., a linear response), corresponding to a free enzyme-to-bound enzyme ratio of at least 3:5.

Artificial Gene Fusion↗
PubMed2004

General method allowing the use of 100% aqueous loading conditions in reversed-phase liquid chromatography.

Reversed-phase HPLC purification of peptides, using n-alkyl modified spherical silica, has become a widely used technique within the pharmaceutical industry. One drawback of these materials is the necessity of having at least 5% organic modifier in the mobile phase, in order to avoid de-wetting of the porous stationary phase. For some preparative reversed-phase separations, it is an advantage if the feed solution can be loaded onto the column under 100% aqueous conditions. This study describes the use of post-column pressure control to avoid de-wetting of regular reversed-phase stationary phases when operated under 100% aqueous conditions. The applicability of post-column pressure control as a means of maintaining the column fully wetted is demonstrated with various buffers and with packing materials having different alkyl-chain lengths. Two peptides, insulin and oxytocin, in overloaded quantities, were loaded under 100% aqueous conditions onto a regular C8 column, and then eluted by a acetonitrile gradient following standard procedures. The retention volume and the peak shape showed that the separation was satisfactory, and proved that post-column pressure control can be used to overcome wettability problems, which are otherwise often observed for reversed-phase packing materials with high ligand density.

Chromatography, Liquid↗
PubMed2004

Advancing contact lines on chemically patterned surfaces.

We report an experimental investigation on advancing contact lines of large drops spreading on chemically patterned surfaces. The model substrates were prepared using microphotolithography allowing precise control of the position and the size of the wettability patterns. Experiments were performed exploring different surface geometries: from ordered to disordered fields of defects and from low to high surface densities. The shape of the contact line between two isolated defects was investigated as a function of the distance. Portions of the contact line on the defects and on the matrix were studied during spreading experiments and were related to the apparent contact angles measured from the final thickness of the drops. A modified Cassie equation based on the line fraction of defects is proposed.

Journal Article↗
PubMed2004

Detection of chemical alterations at internal walls of microchannel flow cells by nondestructive fluorescence depolarization.

A recent trend is the production of workable microchannel flow cells (MF cells). The nondestructive methods used to assess their reliability are based mainly on output monitoring and do not evaluate internal chemical interactions. We investigate a nondestructive method for evaluating changes in the chemical composition of the inner walls based on evaluation of the extent of alignment of a fluorescent probe in a liquid flowing within MF cells. Two MF cells were built with a 10-microm inner spacing. Their inner walls had four parallel SnO(2) strips, 2.00 mm wide, separated by 0.50-mm-wide glass strips. One cell had strips parallel to the flow and the other perpendicular. Flow-induced intermolecular alignment of rhodamine B in monoethylene glycol was scanned with 28-microm precision by fluorescence depolarization, using polarized-laser-induced fluorescence within induced flows (PLF-FI). No changes of polarization were seen when the flow was stopped. Under flowing conditions, polarization was always 4% lower in the glass region as compared to SnO(2). Glass had a higher solid-liquid interfacial tension (determined by contact angle measurements), thus being more wettable and increasing the drag, which propagates into the liquid flow, decreasing polarization. PLF-FI can thus identify regions with different chemical constitutions.

Journal Article↗
PubMed2005

Improved cellular adhesion to acetone plasma modified polystyrene surfaces.

The plasma polymerization of acetone has been used to modify polystyrene substrates for the controlled growth of human fibroblast cells. The surface modified polystyrene was studied by X-ray photoelectron spectroscopy, water contact angle and atomic force microscopy. This showed the surface oxygen levels and wettability to increase rapidly with exposure to the acetone plasma. High-resolution XPS allowed the determination of the relative amounts of surface hydroxyl, carbonyl and carboxyl groups. This showed that there was little incorporation of carboxyl groups in the deposited films. AFM measurements revealed the films to be conformal with a surface roughness equivalent to that of the underlying polystyrene substrate with film growth rates of approximately 0.5 nm min(-1). High edge-definition patterns were produced with a simple masking procedure and allowed the confinement of cells to selected areas of the substrate. These chemically patterned surfaces allowed the study of cells confined to particular regions of the substrate as a function of incubation time.

Acetone↗
PubMed2005

Surface characterization of cotton coated by a thin film of polystyrene with and without a cross-linking agent.

Thin polystyrene film coated on cotton was successfully formed by admicellar polymerization. Divinylbenzene (DVB) was used as a cross-linking agent to form networked polystyrene to improve film coverage. A wettability test and XPS analysis were used to characterize the coated surface. The optimum amount of DVB was around 1%. At this amount, the film coverage was most complete, as judged by the reduction of the O1s signal in XPS analysis.

Journal Article↗
PubMed2005

Ionic liquid ion sources: characterization of externally wetted emitters.

The feasibility of electrostatically extracting and accelerating ions from room temperature ionic liquids in a high vacuum environment is investigated using externally wetted emitters similar to those manufactured for liquid metal ion sources, made out of tungsten wire and electrochemically treated to produce a sharp tip and to increase surface wettability. The ionic liquid EMI-BF4 is used as a prototypical example. The temperature dependence on emission current suggests that liquid flow over the metallic surface is limited by viscosity. Time-of-flight spectrometry indicates that the beam is composed of EMI+ and (EMI-BF4)EMI+ ions in the positive polarity and BF4- and (EMI-BF4)BF4- ions in the negative polarity, and that these ions are emitted with energies very close to their applied potentials. Angular distribution measurements in positive and negative polarities show that ions travel near the propagation axis, diverging by not more than 18 degrees from the centerline. Thanks to the extraordinary variety of ionic liquids it should be possible to generate a correspondingly large number of bipolar nonmetallic ion beams each with unique properties and applicability in fields as diverse as ion lithography, analytical equipment and space propulsion.

Journal Article↗
PubMed2005

Unsmooth cuticles of soil animals and theoretical analysis of their hydrophobicity and anti-soil-adhesion mechanism.

Soil adhesion is a natural phenomenon, and it is harmful to terrain machines and tillage equipment that have soil as their work medium, such as automobiles, tractors, earth-moving machines, spades, hoes, and plows. Soil adhesion increases motion resistance and energy consumption, quickens damage to the soil-engaging components, and lowers work quality. The biomimetic research has provided a promising method to solve the soil adhesion problem. In this work, the cuticles of typical soil animals were observed by scanning electron microscopy (SEM) and their wettability and mechanism of antiadhesion were analyzed in theory. The results of experimental observation have shown that the cuticles of soil animals have different unsmooth appearances, such as pimple-shaped, pit-like, and undee structures. But for the cross sections of the unsmooth cuticles, their common character is undee. Theoretical analysis has indicated that the larger the ratio of the amplitude of the wave to the period of the wave, the stronger the hydrophobicity, the more easily the composite interface between the liquid and the unsmooth cuticles forms, and the function of reducing soil adhesion of the unsmooth cuticles will be better.

Journal Article↗
PubMed2005

Effect of atmospheric-pressure plasma on adhesion characteristics of polyimide film.

In this work, the effect of atmospheric-pressure plasma treatments on surface properties of polyimide film are investigated in terms of X-ray photoelectron spectroscopy (XPS), contact angles, and atomic force microscopy (AFM). The adhesion characteristics of the film are also studied in the peel strengths of polyimide/copper film. As experimental results, the polyimide surfaces treated by plasma lead to an increase of oxygen-containing functional groups or the polar component of the surface free energy, resulting in improving the adhesion characteristics of the polyimide/copper foil. Also, the roughness of the film surfaces, confirmed by AFM observation, is largely increased. These results can be explained by the fact that the atmospheric-pressure plasma treatment of polyimide surface yields several oxygen complexes in hydrophobic surfaces, which can play an important role in increasing the surface polarity, wettability, and the adhesion characteristics of the polyimide/copper system.

Journal Article↗
PubMed2005

Prediction of imbibition in unconsolidated granular materials.

A new way of modeling imbibition is proposed in this paper. It combines two elements. One is a physically consistent, dynamic criterion for the imbibition of an individual pore originally suggested by Melrose (SPEJ (November 1965) 259-271). The other is the use of a simple but physically representative model of porous media: a dense random packing of spheres that is geometrically predetermined. This approach allows truly a priori predictions of imbibition curves (saturation vs capillary pressure) for different values of contact angle, different initial conditions (e.g., different drainage endpoints), and different macroscopic sample geometries (the ratio of external to internal pores). It also provides a mechanistic basis for understanding the influence of pore-scale phenomena such as "snap-off" of nonwetting phase in the pore throats due to the coalescence of pendular rings. The simulations show that the capillary pressure curve for this unconsolidated packing is very sensitive to the wettability parameters (such as contact angle), whereas the influence of different initial conditions and snap-off is almost negligible. Predicted capillary pressure curves are compared to experimental data presented in the literature, and are consistent with them.

Journal Article↗
PubMed2005

Solvent dependence of the molecular order in ion-exchanged self-assembled dialkylammonium monolayers on mica studied with soft X-ray absorption.

Dialkyldimethylammonium films on mica prepared via ion exchange from solution have been reported to be of high quality in terms of their density and molecular orientation. Different preparation procedures are described in the literature. The molecular order and the inclination of the alkyl chains, however, are often deduced from indirect experimental evidence such as the wettability and the film thickness. In the present study we employed near edge X-ray absorption fine structure spectroscopy (NEXAFS) to determine directly the order of the molecules adsorbed from different solvents (water, methanol, water/methanol 1:1, cyclohexanol, and chloroform). It was found that films prepared from different solvents are displaying large differences in the established surface coverage and orientation. In particular, NEXAFS disclosed that the orientation of the alkyl chains can differ significantly even when similar water contact angle values are observed.

Journal Article↗
PubMed2005

Study on mono-dispersed nano-size silica by surface modification for underfill applications.

In order to improve the rheological behavior of the nanosilica composite no-flow underfill, filler surface treatment using silane coupling agents was investigated to reduce the filler-filler interaction and to achieve the mono-dispersity of the nanosilica in the underfill resin. The experimental conditions of the surface treatment were investigated in a design of experiment (DOE) in terms of the pre-treatment methods, coupling agent types, concentrations, and treatment durations. The particle dispersion after treatment was evaluated by the laser particle analyzer and the transmission electron microscopy (TEM). A mono-dispersed nanosilica solution in the polar medium was achieved using optimal experimental condition. The surface chemistry of the nanosilica was studied using Fourier transformed infrared spectroscopy (FTIR). The wettability of underfill resin and water on the silane treated glass slides was studied using a goniometer. Based on the investigations, the silane-treated nanosilica fillers were incorporated into an underfill resin to formulate a nanocomposite no-flow underfill. It was found that the proper filler treatment could significantly reduce the viscosity of the nanocomposite.

Hydrolysis↗
PubMed2005

Influence of cationic surfactant removal on the thermal stability of organoclays.

The microstructure, thermal stability, surface energy, and swelling characteristics of two kinds of commercial organoclays, before and after washing treatment with a mixture of H2O/ethanol, were investigated using X-ray diffraction (XRD), thermogravimetric analysis (TG/DTG), wettability measurement, and swelling measurement. This study demonstrates that the external-surface physically adsorbed surfactant can be removed after washing treatment, resulting in an increase in thermal stability and a decrease in surface energy of the resultant organoclays. Organoclays are difficult to be introduced into a solvent when their surface energies are lower than that of the solvent. On the other hand, the organoclay with gamma(organoclay) < gamma(solvent) is easier to be swollen and expandable by the solvent. The swelling and basal spacing measurements of the organoclays introduced into organic media indicate that the swelling factor and the interlayer swelling are two independent parameters. Both the polar character of the solvent and the swelling capacity of clay have a prominent effect on the interlayer swelling of the organoclays.

Journal Article↗
PubMed2005

Cusp at the three-fluid contact line in a cylindrical pore.

In a cylindrical pore of arbitrary wettability, we analyse the existence of a three-fluid contact line connecting the fluid-fluid interfaces between two bulk phases and the third phase contained in a cusp near the pore wall. This analysis is supported by the very similar, but simpler, analysis for a constriction between parallel plates. From the force balance at the contact line and the equations for the interface curvatures we derive expressions for the cusp height and for the capillary entry pressure related to piston-like displacement between the two bulk phases. The latter is independent of the existence of a cusp and its phase pressure. Based on some realistic assumptions, of which the most important is that a cusp grows continuously from the onset when its phase pressure is increased, we analyse under which conditions a cusp can exist, and, when it exists, what its behaviour is as a function of the cusp phase pressure. We find a simple criterion involving (two ratios of) the three interfacial tensions and two of the three contact angles, which determines whether the three-fluid contact line and, consequently, a cusp exists. The range of contact angles, as well as the size of the cusp increases, when the cusp phase is close to spreading. Not only cusps of the wetting phase can occur, but also of the intermediate-wetting phase. Numerical examples are presented to illustrate the range of behaviour of the cusps.

Journal Article↗
PubMed2006

Surfactant-mediated water transport at gelatin gel/oil interfaces.

We studied spontaneous emulsification (SE) at Water/Oil (W/O) interfaces, using several types of aqueous reservoirs immersed in dodecane plus Span80 surfactant. Above a threshold surfactant concentration C(SE), aqueous satellite droplets are formed at the W/O interface. Varying the aqueous reservoir size, from below 100 microm (droplets) to centimeters (macroscopic phases), allowed investigating SE with complementary techniques. Release (rates) and size distributions for SE droplets were measured with microscopy. For gelled aqueous phases, water expulsion due to SE was quantified. Values for C(SE) were measured and were found to be higher for aqueous phases containing gelatin and/or NaCl. We also studied water exudation during network building and syneresis in aqueous gelatin gels immersed in dodecane/Span80. Below C(SE) (i.e., in the absence of SE) this process is still responsible for significant physico-chemical changes at the W/O interface. To study these in more detail, we performed atomic force microscopy experiments (in force-distance mode) on macroscopic gels. Both changes in the local elastic response and in the wettability of the AFM tip were detected. Together they suggest the formation of "water pockets" after prolonged (gel) setting times, along with a densification of the interfacial gelatin network.

Journal Article↗
PubMed2006

Surface properties of inclusion complexes between alpha-cyclodextrin and poly(ethylene oxide).

The surface properties of the supramolecular inclusion complex (IC) obtained from the threading of alpha-cyclodextrin (alpha-CD) onto poly(ethylene oxide) (PEO) free in solution are studied. The complexes were characterized by IR, (1)H NMR spectroscopy, and thermal analysis. The variation of the interfacial tension, gamma(int), with inclusion complex (IC) concentration and temperature were determined. The results were compared with those found for PEO under the same conditions. alpha-CD does not present surface activity. To quantify the adsorption process of IC and PEO in aqueous medium, the Gibbs equation was used. The driving force for adsorption of IC at the air/aqueous interface seems to arise from an enthalpic contribution. The wettability of the alpha-CD, PEO, and IC films with two liquids was determined by static contact angle measurements. The hydrophobicity degree was estimated. IC is more hydrophobic than PEO and alpha-CD.

Macromolecular Substances↗
PubMed2006

Surface energy of talc and chlorite: Comparison between electronegativity calculation and immersion results.

The surface energies of talc and chlorite is computed using a simple model, which uses the calculation of the electrostatic energy of the crystal. It is necessary to calculate the atomic charges. We have chosen to follow Henry's model of determination of partial charges using scales of electronegativity and hardness. The results are in correct agreement with a determination of the surface energy obtained from an analysis of the heat of immersion data. Both results indicate that the surface energy of talc is lower than the surface energy of chlorite, in agreement with observed behavior of wettability. The influence of Al and Fe on this phenomenon is discussed. Surface energy of this type of solids seems to depend more strongly on the geometry of the crystal than on the type of atoms pointing out of the surface; i.e., the surface energy depends more on the physics of the system than on its chemistry.

Journal Article↗