Lipid hydroperoxides in nutrition,health, and diseases

Research on lipid peroxidation in food degradation, oil and fat nutrition, and age-related diseases has gained significant international attention for the view of improvement of societal health and longevity. In order to promote basic studies on these topics, a chemiluminescence detection-high performance liquid chromatography instrument using a high-sensitivity single photon counter as a detector was developed. This instrument enabled us to selectively detect and quantify lipid hydroperoxides, a primary product of lipid peroxidation reactions, as hydroperoxide groups at the lipid class level. Furthermore, an analytical method using liquid chromatography–tandem mass spectrometry has been established to discriminate the position and stereoisomerization of hydroperoxide groups in lipid hydroperoxides. Using these two methods, the reaction mechanisms of lipid peroxidation in food and in the body have been confirmed.     

Higher harmonic atomic force microscopy: imaging of biological membranes in liquid

The contribution of higher harmonics to the movement of a dynamic force microscope cantilever interacting with a sample in liquid was investigated. The amplitude of the second harmonic has been found to be an order of magnitude higher in liquid than in air, reflecting an increased sensitivity to local variations in elasticity and interaction geometries. A theoretical model of the tip-sample interactions in liquid was introduced and shown to be consistent with experimental findings. Second harmonic amplitude images were recorded on soft biological samples yielding a lateral resolution of approximately 0.5 nm.     

Anisotropy of the turbidity of a nematic liquid crystal

The absorption coefficient of a nematic liquid present an important anisotropy. The measurement of this coefficient in three simple geometries allows the determination of the three Frank elastic constants on the same sample. We give the results obtained for MBBA at room temperature.     

Total internal reflection holographic gratings recorded in polymer-dispersed liquid crystals

We report diffraction gratings recording in polymer dispersed liquid crystals (PDLC) material with a beam suffering total internal reflection from the sample air surface. The real time diffraction efficiency kinetics as well as the polarization, voltage behavior and angular selectivity of the gratings are studied at different reconstruction geometries. An increase of three times of the diffraction efficiency in case of applied voltage is observed for one of these geometries in opposite to typical PDLC switchable gratings. Such dependence appears in most of the geometries and is connected to the specific formation of two gratings by the Stetson scheme.     

COUNTERCURRENT FLOODING IN VERTICAL-TO-INCLINED PIPES

Countercurrent flooding data have been obtained using air and water for vertical-to-downwardly inclined pipes containing elbows of varying angles. Experiments were performed with six different test sections, all having an inner diameter of 51 mm and a 1-m-tong vertical tube connected to an inclined or horizontal tube

The flooding data for 112.5° and 135° elbow angles were almost identical and showed that these geometries required the largest gas flow rates for flooding among all the geometries tested. The flooding gas velocities for the 157.5° elbow were slightly less than those of the 112.5° and 135° elbows but greater than those of the vertical pipe without any elbow and vertical-to-horizontal pipes at low to moderate liquid flow rates

In all vertical-to-inclined pipes, flooding was initiated in the inclined section at about 15 to 50 cm downstream of the elbow. Due to the countercurrent flow of gas, the liquid stream just downstream of the elbow became highly agitated and a frothy mixture was carried upstream by gas at flooding. At moderate to high liquid flow rates, the liquid was deflected off at the elbow to form a turbulent, jetlike stream that partially broke up into droplets, These droplets were, at the onset of flooding, entrained and carried over by the gas stream

Comparison of the data with the slugging correlation at low liquid flow rates and with the liquid entrainment/carryover model at high liquid flow rates suggested that these mechanisms are likely responsible for flooding in vertical-to-inclined pipes.     

Instabilities in nematic elastomers in external electric and magnetic fields

In this paper we study the macroscopic behavior of nematic side-chain liquid single crystal elastomers exposed to an external electric or magnetic field. For this purpose we use the framework of a continuum model. The geometries investigated comprise the bend and the twist geometry known from the classical Frederiks transition in low molecular weight liquid crystals. For the bend geometry we find a laterally homogeneous and a two-dimensional undulatory instability, which may compete at onset. In the case of the twist geometry three instabilities can occur at onset, two of which are two dimensional and clearly show undulations. As a major result we propose how the values of the twist coefficient K(2) and the values of the material parameters D(1) and D(2) connected to relative rotations between the director field and the polymer network can be determined from experimental observations. In addition, we explain why a twist experiment is probably the most suitable set-up in order to measure the material parameter D(1).     

Strong vortex liquid correlation from multiterminal measurements on untwinned YBa2Cu3O(7-delta) single crystals

Multiterminal transport measurements indicating a strongly correlated vortex liquid above the first order melting transition in untwinned YBa2Cu3O(7--delta) single crystals are presented. The correlation is found to be surprisingly stable for different weak variations of point disorder. We investigate the differences between intervortex and intravortex correlations in different contact geometries. The results are in agreement with the local conductivity model, with zero resistivity along straight vortex line segments.     

Comment on the validity of first-order paraxial theory for electron and ion sources with needle-type or pointed geometry

An essential feature of first-order paraxial theory is the assumption that if the potential along the axis of an axially symmetric system is known, then the potential (fields) near the axis can be obtained by a power-series expansion about points lying on axis. However, in traditional first-order theory, which commonly assumes systems with cylindrical symmetry, only terms up to second-order in the coordinate transverse to the beam axis are retained. In this letter we argue that a consequence of this restriction is that traditional first-order paraxial theory should not be applicable to electron and ion sources with pointed or needle-type geometries. In order to treat non-parallel trajectories which occur in the pointed geometries present, say, in field emission liquid metal ion sources, a modified paraxial theory is suggested which describes two-dimensional particle dynamics.This work has been supported in part by the Division of Materials Research, National Science Foundation, Grant No. DMR-81008829     

The phase behavior of mixed lipid membranes in the presence of the rippled phase

We propose a model describing liquid-solid phase coexistence in mixed lipid membranes by including explicitly the occurrence of a rippled phase. For a single component membrane, we employ a previous model in which the membrane thickness is used as an order parameter. As function of temperature, this model properly accounts for the phase behavior of the three possible membrane phases: solid, liquid and the rippled phase. Our primary aim is to explore extensions of this model to binary lipid mixtures by considering the composition dependence of important model parameters. The obtained phase diagrams show various liquid, solid and rippled phase coexistence regions, and are in quantitative agreement with the experimental ones for some specific lipid mixtures.     

Dynamic light scattering as a probe of orientational dynamics in confined liquid crystals

The eigenmodes of director orientational fluctuations in nematic liquid crystals in confined geometries were studied both theoretically and experimentally by dynamic light-scattering tehnique. The fundamental mode of the orientational fluctuations shows a crossover from bulk behavior, dominated by bulk elastic constant K, to surface dominated one, in which the relaxation rate is determined by the ratio of surface anchoring strength W and viscosity eta. The contribution of surface viscosity zeta is also significant when its characteristic length zeta/eta becomes comparable to the size of the confined system. It was measured in nematic liquid crystal in cylindrical pores of polycarbonate (Nuclepore) membranes to be of the order of 10 nm.     

Controlled cavitation in microfluidic systems

We report on cavitation in confined microscopic environments which are commonly called microfluidic or lab-on-a-chip systems. The cavitation bubble is created by focusing a pulsed laser into these structures filled with a light-absorbing liquid. At the center of a 20 microm thick and 1 mm wide channel, pancake-shaped bubbles expand and collapse radially. The bubble dynamics compares with a two-dimensional Rayleigh model and a planar flow field during the bubble collapse is measured. When the bubble is created close to a wall a liquid jet is focused towards the wall, resembling the jetting phenomenon in axisymmetry. The jet flow creates two counter-rotating vortices which stir the liquid at high velocities. For more complex geometries, e.g., triangle- and square-shaped structures, the number of liquid jets recorded correlates with the number of boundaries close to the bubble.     

A high order moving boundary treatment for compressible inviscid flows

We develop a high order numerical boundary condition for compressible inviscid flows involving complex moving geometries. It is based on finite difference methods on fixed Cartesian meshes which pose a challenge that the moving boundaries intersect the grid lines in an arbitrary fashion. Our method is an extension of the so-called inverse Lax–Wendroff procedure proposed in [17] for conservation laws in static geometries. This procedure helps us obtain normal spatial derivatives at inflow boundaries from Lagrangian time derivatives and tangential derivatives by repeated use of the Euler equations. Together with high order extrapolation at outflow boundaries, we can impose accurate values of ghost points near the boundaries by a Taylor expansion. To maintain high order accuracy in time, we need some special time matching technique at the two intermediate Runge–Kutta stages. Numerical examples in one and two dimensions show that our boundary treatment is high order accurate for problems with smooth solutions. Our method also performs well for problems involving interactions between shocks and moving rigid bodies.     

NMR of water in biological systems

Summary A simple relationship has been thought to exist between the dynamics of water in heterogeneous (liquid-solid) systems and the NMR response. This relationship is usually expressed by the Bloembergen-Purcell-Pound (BPP) equations for relaxation and the phase model. However, a requirement for the use of the BPP theory is that motions take place in an isotropic, infinite and three-dimensional space. It is shown that the mere presence of solid surfaces causes the appearance of solidlike features in the NMR response of the liquid even if its dynamics is directly affected by the surfaces. Some of these ?topological? or ?indirect? surface effects are of the same kind as the low-dimensionality effects. Their order of magnitude is estimated for simple geometries and by treating the liquid motion in a hydrodynamic approximation. Comparison with the experiment is carried on in a companion paper. To speed up publication, the authors of this paper have agreed to not receive the proofs for correction.     

Shape optimization in lipid nanotube networks

Starting from a high surface free-energy state, lipid nanotube networks are capable to self-organize into tree-like structures with particular geometrical features. In this work we analyze the process of self-organization in such networks, and report a strong similarity to the Euclidian Steiner Tree Problem (ESTP). ESTP is a well-known NP-hard optimization problem of finding a network connecting a given set of terminal points on a plane, allowing addition of auxiliary points, with the overall objective to minimize the total network length. The present study shows that aggregate lipid structures self-organize into geometries that correspond to locally optimal solutions to such problems.     

Translational order in liquid-expanded lipid monolayers functionalized with nucleosides

The monolayer behavior of a lipid containing two unsaturated alkyl chains and a nucleoside derivative as polar headgroup has been investigated by the Langmuir technique. From the surface pressure vs. molecular area isotherm, the monolayer appears as a pure liquid-expanded phase and should be then considered as a two-dimensional liquid. However, grazing incidence X-ray diffraction experiments evidence a translational order that does not exist when the lipid headgroup is a choline moiety. Since unsaturated chains are expected to induce a fluid state of the monolayer at the temperature considered, this order is likely to originate from the natural tendency nucleosides have to establish among themselves -stacking interactions between the bases. The collected X-ray data are consistent with the geometrical requirements for bases stacking. Received: 3 August 1998 / Revised: 16 September 1998 / Accepted: 21 September 1998     

Dynamics of polydisperse hard-spheres under strong confinement

We use molecular simulation to probe the connection between local structure and the unusual re-entrant dynamics observed for polydisperse hard-sphere liquids confined in thin slit pores. The local structure is characterised by calculating 2-D bond-orientational order parameters associated with square and hexatic order for particles in the layer adjacent to the confining walls. When the wall separation is commensurate with the average particle size, the particles primarily exhibit local hexatic order, whereas local square order increases in prevalence for incommensurate geometries. The relaxation time extracted from the ensemble-averaged mean-square displacement increases exponentially with the static correlation length associated with hexatic local order in strongly confined commensurate geometries, in agreement with theoretical predictions for dynamical slowing. Square order, by contrast, is not associated with a growing length scale for either commensurate or incommensurate geometries, indicating that it is strongly geometrically frustrated. Our results suggest that the influence of bond-orientational order on dynamical slowing may be altered by changing the extent of confinement.     

Membranes with rotating motors: Microvortex assemblies

We study collections of rotatory motors confined to 2-dimensional manifolds. The rotational motion induces a repulsive hydrodynamic interaction between motors leading to a non-trivial collective behavior. For high rotation speed, motors should arrange on a triangular lattice exhibiting crystalline order. At low speed, they form a disordered phase where diffusion is enhanced by velocity fluctuations. In confining geometries and under suitable boundary conditions, motor-generated flow might enhance left-right symmetry-breaking transport. All these effects should be experimentally observable for motors driven by external fields and for dipolar biological motors embedded into lipid membranes in a viscoelastic solvent.Received: 9 October 2003, Published online: 11 May 2004PACS: 87.16.-b Subcellular structure and processes - 05.40.-a Fluctuation phenomena, random processes, noise, and Brownian motion - 87.15.Kg Molecular interactions; membrane-protein interactions     

Thermodynamic approach to phase coexistence in ternary phospholipid-cholesterol mixtures

We introduce a simple and predictive model for determining the phase stability of ternary phospholipid-cholesterol mixtures. Assuming that competition between the liquid and gel order of the phospholipids is the main driving force behind lipid segregation, we derive a Gibbs free energy of mixing, based on the thermodynamic properties of the lipids main transition. A numerical approach was devised that enables the fast and efficient determination of the ternary diagrams associated with our Gibbs free energy. The computed phase coexistence diagram of DOPC/DPPC/cholesterol reproduces well-known features for this system at 10 °C, as well as its evolution with temperature.     

Slippage and nanorheology of thin liquid polymer films

Thin liquid films on surfaces are part of our everyday life; they serve, e.g.,?as coatings or lubricants. The stability of a thin layer is governed by interfacial forces, described by the effective interface potential, and has been subject of many studies in recent decades. In recent years, the dynamics of thin liquid films has come into focus since results on the reduction of the glass transition temperature raised new questions on the behavior of especially polymeric liquids in confined geometries. The new focus was fired by theoretical models that proposed significant implication of the boundary condition at the solid/liquid interface on the dynamics of dewetting and the form of a liquid front. Our study reflects these recent developments and adds new experimental data to corroborate the theoretical models. To probe the solid/liquid boundary condition experimentally, different methods are possible, each bearing advantages and disadvantages, which will be discussed. Studying liquid flow on a variety of different substrates entails a view on the direct implications of the substrate. The experimental focus of this study is the variation of the polymer chain length; the results demonstrate that inter-chain entanglements and in particular their density close to the interface, originating from non-bulk conformations, govern the liquid slip of a polymer.