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1.
Philos Trans A Math Phys Eng Sci ; 379(2208): 20200399, 2021 Oct 18.
Article in English | MEDLINE | ID: mdl-34455838

ABSTRACT

The ordering of particles in the drying process of a colloidal suspension is crucial in determining the properties of the resulting film. For example, microscopic inhomogeneities can lead to the formation of cracks and defects that can deteriorate the quality of the film considerably. This type of problem is inherently multiscale and here we study it numerically, using our recently developed method for the simulation of soft polymeric capsules in multicomponent fluids. We focus on the effect of the particle softness on the film microstructure during the drying phase and how it relates to the formation of defects. We quantify the order of the particles by measuring both the Voronoi entropy and the isotropic order parameter. Surprisingly, both observables exhibit a non-monotonic behaviour when the softness of the particles is increased. We further investigate the correlation between the interparticle interaction and the change in the microstructure during the evaporation phase. We observe that the rigid particles form chain-like structures that tend to scatter into small clusters when the particle softness is increased. This article is part of the theme issue 'Progress in mesoscale methods for fluid dynamics simulation'.

2.
Phys Rev E ; 97(1-1): 012404, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29448354

ABSTRACT

Widely regarded as an interesting model system for studying flow properties of blood, vesicles are closed membranes of phospholipids that mimic the cytoplasmic membranes of red blood cells. In this study we analyze the rheology of a suspension of vesicles in a confined geometry: the suspension, bound by two planar rigid walls on each side, is subject to a shear flow. Flow properties are then analyzed as a function of shear rate γ[over ̇], the concentration of the suspension ϕ, and the viscosity contrast λ=η_{in}/η_{out}, where η_{in} and η_{out} are the fluid viscosities of the inner and outer fluids, respectively. We find that the apparent (or effective viscosity) of the suspension exhibits both shear thinning (decreasing viscosity with shear rate) or shear thickening (increasing viscosity with shear rate) in the same concentration range. The shear thinning or thickening behaviors appear as subtle phenomena, dependant on viscosity contrast λ. We provide physical arguments on the origins of these behaviors.


Subject(s)
Lipid Bilayers , Models, Biological , Suspensions , Animals , Capillaries/physiology , Computer Simulation , Erythrocytes/physiology , Hemodynamics , Lipid Bilayers/chemistry , Lipid Bilayers/metabolism , Phospholipids/chemistry , Rheology , Stress, Mechanical , Viscosity
3.
Sci Rep ; 4: 4348, 2014 Mar 11.
Article in English | MEDLINE | ID: mdl-24614613

ABSTRACT

The supply of oxygen and nutrients and the disposal of metabolic waste in the organs depend strongly on how blood, especially red blood cells, flow through the microvascular network. Macromolecular plasma proteins such as fibrinogen cause red blood cells to form large aggregates, called rouleaux, which are usually assumed to be disaggregated in the circulation due to the shear forces present in bulk flow. This leads to the assumption that rouleaux formation is only relevant in the venule network and in arterioles at low shear rates or stasis. Thanks to an excellent agreement between combined experimental and numerical approaches, we show that despite the large shear rates present in microcapillaries, the presence of either fibrinogen or the synthetic polymer dextran leads to an enhanced formation of robust clusters of red blood cells, even at haematocrits as low as 1%. Robust aggregates are shown to exist in microcapillaries even for fibrinogen concentrations within the healthy physiological range. These persistent aggregates should strongly affect cell distribution and blood perfusion in the microvasculature, with putative implications for blood disorders even within apparently asymptomatic subjects.


Subject(s)
Dextrans/pharmacology , Erythrocyte Aggregation/drug effects , Erythrocytes/drug effects , Fibrinogen/pharmacology , Microvessels/physiology , Adult , Animals , Dose-Response Relationship, Drug , Erythrocytes/cytology , Fluorescein-5-isothiocyanate/analogs & derivatives , Fluorescent Dyes , Hematocrit , Humans , Mice , Microfluidics , Microvessels/ultrastructure , Molecular Imaging , Oxygen/metabolism , Video Recording
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