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PubMed2005

Surface induced hydrogen-bonded macrocluster formation of methanol on silica surfaces.

Recently, we have succeeded in identifying the structure of the adsorption layer of ethanol on a silica surface in cyclohexane to be a hydrogen-bonded linear aggregate (polymer), which we call a surface molecular macrocluster. In this work, we studied the effect of the miscibility of liquids on the formation of the surface molecular macroclusters for confirming that this is a surface induced phenomenon. We investigated the interaction and the structure of methanol adsorbed on a silica surface in methanol-cyclohexane binary liquids by a combination of colloidal probe atomic force microscopy, adsorption excess isotherm measurement, and FTIR spectroscopy using the attenuated total reflection (ATR) mode, and compared the results with those of the ethanol-cyclohexane and 1-propanol-cyclohexane binary liquids. The former system is immiscible at methanol concentrations of ca. 8-90 mol %, and the latter two are miscible at any composition. At 0.03 mol % methanol, which is far from the critical concentration for the phase separation, the contact of the methanol macrocluster layers formed on the silica surface brought about the attraction from a distance of 42 +/- 5 nm which was similar to that observed in ethanol-cyclohexane. At a methanol concentration of 9.0 mol %, above bulk phase separation, completely different force profiles were observed. These results demonstrated that the molecular macrocluster formation was different from the wetting induced by the bulk.

Journal Article↗

PubMed1980

Phase equilibria for highly unsymmetrical plasmas and electrolytes.

The conclusion of classical Debye-Hückel theory that a phase separation may occur in highly unsymmetrical plasmas or electrolytes is shown to be false and to arise from a serious error in the treatment of the interaction of pairs of the most highly charged ions. After an approximate correction for this error, no phase separation is predicted. Specific application to iron in the solar plasmas is discussed.

Journal Article↗

PubMed2004

Finite-difference lattice Boltzmann model with flux limiters for liquid-vapor systems.

In this paper we apply a finite difference lattice Boltzmann model to study the phase separation in a two-dimensional liquid-vapor system. Spurious numerical effects in macroscopic equations are discussed and an appropriate numerical scheme involving flux limiter techniques is proposed to minimize them and guarantee a better numerical stability at very low viscosity. The phase separation kinetics is investigated and we find evidence of two different growth regimes depending on the value of the fluid viscosity as well as on the liquid-vapor ratio.

Journal Article↗

PubMed1990

Stability of famotidine in a 3-in-1 total nutrient admixture.

The stability of famotidine in a 3-in-1 total nutrient admixture stored at room temperature (24 degrees C) was evaluated over 24 hours. Famotidine injection was diluted to a theoretical concentration of 20 mg/L in a total nutrient admixture containing 5% amino acid injection, 25% dextrose injection, and 2.25% intravenous fat emulsion. Admixtures were prepared in 2-L ethylene-vinyl acetate bags using conventional techniques and stored at room temperature. At 0, 4, 8, 12, and 24 hours, the admixtures were visually inspected for color change, creaming, or phase separation, and samples were obtained for assay with a stability-indicating method of HPLC, using samples obtained at time zero as controls. Two-way analysis of variance was used for data evaluation. There was no evidence of color change, creaming, or phase separation before quantitative analysis was performed, nor was there significant change in observed famotidine concentration over 24 hours. Based upon our data, famotidine intravenous solution 20 mg/L in the solution tested is stable at room temperature for 24 hours.

Chromatography, High Pressure Liquid↗

PubMed2004

Biocompatibility and biostability of a series of poly(carbonate)urethanes.

In this work, we synthesized several MDI-based poly(carbonate)urethanes (PCU) by using four different soft segments, including two aliphatic macrodiols (poly(hexyl, ethyl)carbonate diols, MW 2017 and 865, respectively) and two aromatic macrodiols (MW approximately 2000 and 1000, respectively), in different molar ratios to MDI. We demonstrate that these polymers exhibited various degree of micro-phase separation that further influenced their surface protein adsorption, platelet activation as well as cellular attachment and growth. Polyurethanes based on poly(hexyl, ethyl)carbonate diol with MW 2017 in a molar ratio MDI/macrodiol/chain extender of either 3/2/1 or 4/3/1 resulted in greater micro-phase separation as well as superior biocompatibility and biostability.

Adsorption↗

PubMed2006

Domain memory of mixed polymer brushes.

The nano-phase-separation in mixed polymer brushes consisting of polystyrene and poly(methyl methacrylate) (PS-PMMA) chains attached to a silicon surface is studied. The topographies of the mixed brushes are examined after they have been exposed to solvents which induce or erase nano-phase-separation. It is discussed whether the brush locally forms the same pattern every time the transition from the smooth and featureless to the nanopatterned state occurs ("domain memory") or if the local assembly of the domains emerges in a different arrangement after each cycle of topography switching. A memory measure parameter is introduced, which characterizes quantitatively the domain memory effect in the nanopattern. It is shown that at constant grafting density but with increasing molecular weight of the brush chains the memory measure parameter decreases. In contrast to this, brushes with constant molecular weight, but differing in grafting density, all have a similar domain memory. We discuss a possible origin of the domain memory effect in the mixed brush systems studied and point out its impact on the motion of nanoparticles adsorbed on top of such systems.

Journal Article↗

PubMed2000

Instabilities of concentration stripe patterns in ferrocolloids

Equations describing the kinetics of the phase separation in ferrocolloids in a Hele-Shaw cell under the action of a rotating magnetic field are proposed. Numerical simulation on the basis of a pseudospectral technique demonstrates that upon the action of a rotating field on a magnetic colloid which undergoes the phase separation a periodical system of stripes parallel to the plane of a rotating magnetic field stripes is created. The period of a structure found numerically satisfactorily corresponds to the one calculated on the basis of the energy minimum. Thus, the undulation instability leading to the formation of chevron structures takes place if the tangential component of a rotating magnetic field is eliminated, whereas the normal component is increased at the same time. If during the development of the undulation deformations of a concentration pattern the magnetic Bond number is large enough the secondary instabilities may occur leading to the fingering of stripes to bring about merging and break-up of stripes. It is shown that an increase in the magnetic Bond number leads to the onset of the instability at the boundaries between the regions with homogeneous orientation of stripes as well as to formation of the characteristic hairpin patterns.

Journal Article↗

PubMed1984

Lamellar-to-hexagonalII phase transitions in the plasma membrane of isolated protoplasts after freeze-induced dehydration.

In protoplasts isolated from nonacclimated rye leaves (Secale cereale L. cultivar Puma), cooling to -- 10 degrees C at a rate of 1 degrees C/min results in extensive freeze-induced dehydration (osmotic contraction), and injury is manifested as the loss of osmotic responsiveness during warming. Under these conditions, several changes were observed in the freeze-fracture morphology of the plasma membrane. These included (i) lateral phase separations in the plasma membrane, (ii) aparticulate lamellae lying next to the plasma membrane, and (iii) regions of the plasma membrane and associated lamellae in various stages of lamellar-to-hexagonalII transition. These morphological changes also were observed after equilibration in 5.37 osmolal sorbitol at 0 degrees C, which produced a similar extent of dehydration as did freezing to -- 10 degrees C. In contrast, only small areas of lateral phase separation in the plasma membrane, with no observable aparticulate lamellae or hexagonalII configurations, were observed in protoplasts supercooled to -- 10 degrees C. Therefore, freeze-induced lamellar-to-hexagonalII phase transitions in the plasma membrane are a consequence of dehydration rather than subzero temperature per se. When suspensions of protoplasts isolated from cold-acclimated leaves were frozen to -- 10 degrees C, no injury was incurred, and hexagonalII phase transitions were not observed. No hexagonalII phase was observed even at -- 35 degrees C, though acclimated protoplasts are injured at this temperature.

Cell Membrane↗

PubMed2003

An automated matrix-assisted laser desorption/ionization quadrupole Fourier transform ion cyclotron resonance mass spectrometer for "bottom-up" proteomics.

Here we describe a new quadrupole Fourier transform ion cyclotron resonance hybrid mass spectrometer equipped with an intermediate-pressure MALDI ion source and demonstrate its suitability for "bottom-up" proteomics. The integration of a high-speed MALDI sample stage, a quadrupole analyzer, and a FT-ICR mass spectrometer together with a novel software user interface allows this instrument to perform high-throughput proteomics experiments. A set of linearly encoded stages allows sub-second positioning of any location on a microtiter-sized target with up to 1536 samples with micrometer precision in the source focus of the ion optics. Such precise control enables internal calibration for high mass accuracy MS and MS/MS spectra using separate calibrant and analyte regions on the target plate, avoiding ion suppression effects that would result from the spiking of calibrants into the sample. An elongated open cylindrical analyzer cell with trap plates allows trapping of ions from 1000 to 5000 m/z without notable mass discrimination. The instrument is highly sensitive, detecting less than 50 amol of angiotensin II and neurotensin in a microLC MALDI MS run under standard experimental conditions. The automated tandem MS of a reversed-phase separated bovine serum albumin digest demonstrated a successful identification for 27 peptides covering 45% of the sequence. An automated tandem MS experiment of a reversed-phase separated yeast cytosolic protein digest resulted in 226 identified peptides corresponding to 111 different proteins from 799 MS/MS attempts. The benefits of accurate mass measurements for data validation for such experiments are discussed.

Calibration↗

PubMed2003

Local density approach for modeling fluids with density-dependent interactions.

In a recent paper [Phys. Rev. Lett. 86, 2038 (2001)] a simple fluid with a particular density-dependent pair potential was shown to exhibit, together with the vapor-liquid transition, a liquid-liquid phase separation and it was evidenced that, in order to adequately define the correct boundaries of stability, a simulation procedure based on the use of local densities had to be devised. It was found that for certain thermodynamic states the potential drives the system toward a phase separation that is otherwise frustrated by the change in the interactions induced by density fluctuations. Therefore, when integral equations or global density simulations are used, the critical points estimated from the thermodynamics are not associated with divergent correlations and vice versa. Here, we will explore in depth this fluid and introduce a detailed account of the proposed local density simulation technique. The results presented bear general significance for density-dependent potentials, like those of liquid metals or charge-stabilized colloids.

Journal Article↗

PubMed2006

Anomalously slow domain growth in fluid membranes with asymmetric transbilayer lipid distribution.

The effect of asymmetry in the transbilayer lipid distribution on the dynamics of phase separation in fluid vesicles is investigated numerically. This asymmetry is shown to set a spontaneous curvature for the domains that alter the morphology and dynamics considerably. For moderate tension, the domains are capped and the spontaneous curvature leads to anomalously slow dynamics, as compared to the case of symmetric bilayers. In contrast, in the limiting cases of high and low tensions, the dynamics proceeds toward full phase separation.

Anisotropy↗

PubMed2005

Interaction of surfactants with thickeners used in waterborne paints: a rheological study.

Studies of the phase diagram and linear viscoelasticity of aqueous solutions of hydrophobically modified hydroxyethyl cellulose (HMHEC), a thickener used in water-based paints, and SDS reveal that SDS-HMHEC mixed micelles are formed that increase the number of hydrophobic junctions and enhance interpolymer association up to an [SDS]/[HMHEC] ratio. This fact produces a strong increase of viscoelasticity or a phase separation, depending on the [HMHEC]. At higher ratios the excess of micelles with predominant SDS isolates hydrophobes and disrupts the micellar network. Then, viscoelastic functions decrease and HMHEC behaves as a nonassociative polymer. TTAB and Brij30 also interact with HMHEC, but in a different way. No phase separation is observed with these surfactants. TTAB forms mixed micelles and new junction points in the same way as SDS. However, this surfactant does not stabilize the micelles as SDS does, presumably due to the different interaction between the OH from the cellulose and the charged groups. Results seem to indicate that Brij30 enters into the hydrophobic aggregates of HMHEC and stabilizes them, increasing relaxation time, but it does not form new junction points, since it forms quite big micelles.

Journal Article↗

PubMed2000

Tandem-cartridge solid-phase extraction followed by GC/MS analysis for measuring partition coefficients of association of polycyclic aromatic hydrocarbons to humic acid.

A tandem-cartridge solid-phase extraction system combining reversed-phase separation and dynamic ion exchange followed by GC/MS analysis was studied for measuring partition coefficients (Kdoc) of association of polycyclic aromatic hydrocarbons (PAHs) to humic acid. Time course batch experiments revealed that the association of PAHs to humic acid included a slow stage with equilibrium time of 5-7 days. The disequlibrium and retention of the PAH-humic acid associate during reversed-phase separation lead to systematic negative error for the measured partition coefficients; more accurate results were achieved with a three-cartridge tandem system in which the negative error was assessed and corrected via the PAH analytes measured on the second reversed-phase cartridge. The potential and advantages of use of C18 disk cartridges instead of conventional C18 cartridges to set up the tandem system for measuring the partition coefficients were also studied. With the tandem-cartridge system, the measured partition coefficients did not change with most experimental conditions, but a trend of decreasing partition coefficients with humic acid concentration was observed, implying possible nonlinear association of the PAHs and humic acid.

Environmental Pollutants↗

PubMed2004

Lateral and vertical nanophase separation in Langmuir-Blodgett films of phospholipids and semifluorinated alkanes.

It has recently been found that monodisperse surface micelles (hemimicelles) were formed in Langmuir monolayers of the semifluorinated alkane C8F17C16H33 (F8H16) after transfer onto silicon wafers. Grazing incidence X-ray diffraction studies have demonstrated that compression of mixed Langmuir monolayers made from combinations of dipalmitoyl phosphatidylethanolamine (DPPE) and diblock F8H16 in various molar ratios resulted in the complete expulsion of the diblock molecule at high surface pressure. F8H16 then formed a second layer on top of a DPPE-only monolayer, demonstrating a novel type of reversible, pressure-induced, vertical phase separation. Using atomic force microscopy and X-ray reflectivity, we show now that mixed DPPE/F8H16 (1:1.3) Langmuir-Blodgett films transferred onto silicon wafers below 10 mN m(-1) are laterally phase separated and consist of domains of F8H16 surface micelles in coexistence with a monolayer of DPPE. The density of the network of F8H16 surface micelles increases when the surface pressure of transfer increases. Around 10 mN m(-1), the F8H16 surface micelles start to glide on the DPPE monolayer, progressively overlying it, until total coverage is achieved.

Hydrocarbons, Fluorinated↗

PubMed1997

Stability of Dilute Colloidal Silica Suspensions in the Vicinity of the Binodal Curve of the System 2-Butoxyethanol/Water

In the temperature-composition diagram of the system 2-butoxyethanol (abbreviated C4E1)/water, SiO2 [mass fraction of SiO2, y(SiO2) approximately 0.01; volume fraction phi(SiO2) approximately 10(-3)] there exists a flocculation temperature-composition curve running below the binodal curve for x > xc (x, mole fraction of C4E1; xc = 0.0598). The concentration of the colloidal particles is low enough to consider them an "impurity." In the region of the phase diagram bound by the binodal and the flocculation curve the suspension of the colloidal SiO2 particles is unstable and the particles flocculate reversibly. The difference between the temperature of phase separation and the flocculation temperature increases with increasing values of x - xc up to a maximum value of x (xmax). For x > xmax the suspensions are unstable at all temperatures studied. For x < xc the suspension of the SiO2 particles is stable up to the temperature of phase separation of the C4E1/water mixture. The flocculation curve is assumed to reflect the influence of local concentration fluctuations with long range correlations on the stability of the SiO2 suspensions. For x > xc these concentration fluctuations are water rich and interact with the hydrophilic surface of the colloidal SiO2 particles by forming an adsorption layer. This layer is assumed to modify the interparticle potential energy-distance curve and to trigger flocculation. For x < xc the concentration fluctuations are C4E1 rich and no adsorption layer is formed at the hydrophilic surface of the colloidal particles. Copyright 1997Academic Press

Journal Article↗

PubMed1983

Forskolin and ethanol both perturb the structure of liver plasma membranes and activate adenylate cyclase activity.

Both forskolin and ethanol elicit the activation of basal and ligand-stimulated adenylate cyclase activities in rat liver plasma membranes. Ethanol is most potent at activating the fluoride- and glucagon-stimulated activities whilst having little effect on basal activity. In contrast forskolin exerts its greatest effect on basal activity. Over the concentration range that ethanol activates adenylate cyclase, it also increases bilayer fluidity as indicated by a decrease in the values of the order parameters for an incorporated fatty acid spin probe. At high concentrations forskolin does increase bilayer fluidity. However, it only begins to do so at concentrations above those where forskolin has already exerted its maximal effect in activating adenylate cyclase. Forskolin can still activate, albeit to a reduced extent, detergent-solubilized adenylate cyclase whereas ethanol cannot. Forskolin elicits a pronounced rise in hepatocyte intracellular cyclic AMP concentrations, whereas ethanol does not. Both forskolin and ethanol reduce the temperature of onset of the lipid phase separation occurring in rat liver plasma membranes. This is detected in Arrhenius plots of both glucagon-stimulated adenylate cyclase activity and order parameters of an incorporated fatty acid spin probe, where we find that forskolin is particularly potent in decreasing the temperature at which this lipid phase separation occurs. Our results are consistent with the notion that forskolin exerts its effect on adenylate cyclase primarily by a direct action on the catalytic unit of the enzyme. However, as forskolin is a potent perturber of the organisation of the lipid bilayer it is possible that this could modulate its effect on adenylate cyclase and might be expected to affect the activity of other membrane enzymes.

Adenylyl Cyclases↗

PubMed2005

Relevance of lipid polar headgroups on boron-mediated changes in membrane physical properties.

Using liposomes composed of either brain phosphatidylcholine (PC), or binary mixtures of PC and phosphatidylserine (PS), galactolipids (GL), phosphatidylinositol (PI), cardiolipin (CL), phosphatidic acid (PA), or phosphatidylethanolamine (PE), we investigated the effects of graded amounts of boric acid (B, 0.5-1000 microM) on the following membrane physical properties: (a) surface potential, (b) lipid rearrangement through lateral phase separation, (c) fluidity, and (d) hydration. Incubation of the different populations of vesicles with B was associated with a small, but statistically significant, increase in membrane surface potential in PC, PC:PS, PC:GL, PC:PI, PC:PA, and PC:PE liposomes. B-induced lipid lateral rearrangement through lateral phase separation in PC, PC:PA, and PC:PE liposomes; but had no effects on PC:PS, PC:GL, and PC:PI liposomes. In PC liposomes B affected membrane fluidity at the water-lipid interface without affecting the hydrophobic core of the bilayer. In all the other binary liposomes studied, B increased membrane fluidity in both, the hydrophobic portion of the membrane and in the anionic domains. The above was associated with a decrease in the fluidity of the cationic domains. B (10-1000 microM) decreased membrane hydration regardless the composition of the liposomes. The obtained results demonstrate the ability of B to interact with membranes, and induce changes in membrane physical properties. Importantly, the extent of B-membrane interactions and the consequent effects were dependent on the nature of the lipid molecule; as such, B had greater affinity with lipids containing polyhydroxylated moieties such as GL and PI. These differential interactions may result in different B-induced modulations of membrane-associated processes in cells.

Boron↗

PubMed2001

Comparison of the effects of clozapine, chlorpromazine, and haloperidol on membrane lateral heterogeneity.

The interactions of three neuroleptic drugs, clozapine (CLZ), chlorpromazine (CPZ), and haloperidol (HPD) with phospholipids were compared using DSC and Langmuir balance. Main emphasis was on the drug-induced effects on the lateral organization of lipid mixtures of the saturated zwitterionic 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and the unsaturated acidic phosphatidylserine, brainPS. In multilamellar vesicles (MLV) phase separation was observed by DSC at X(PS)> or =0.05. All three drugs bound to these MLVs, abolishing the pretransition at X(drug)> or =0.03. The main transition temperature (T(m)) decreased almost linearly with increasing contents of the drugs, CLZ having the smallest effect. In distinction from the other two drugs, CLZ abolished the phase separation evident in the endotherms for DPPC/brainPS (X(PS)=0.05) MLVs. Compression isotherms of DPPC/brainPS/drug (X(PS)=X(drug)=0.05) monolayers revealed the neuroleptics to increase the average area/molecule, CLZ being the most effective. Penetration into brainPS monolayers showed strong interactions between the three drugs and this acidic phospholipid (in decreasing order CPZ>HPD>CLZ). Hydrophobic interactions demonstrated using neutral eggPC monolayers decreased in a different order, CLZ>CPZ>HPD. Fluorescence microscopy revealed domain morphology of DPPC/brainPS monolayers to be modulated by these drugs, increasing the gel-fluid domain boundary length in the phase coexistence region. To conclude, our data support the view that membrane-partitioning drugs could exert part of their effects by changing the lateral organization and thus also the functions of biomembranes.

Antipsychotic Agents↗