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On the effects of membrane viscosity on transient red blood cell dynamics

TLDR
In this paper, the authors studied the time-dependent response of an erythrocyte membrane to external mechanical loads via ab-initio, mesoscale numerical simulations, with a primary focus on the detailed characterisation of the RBC relaxation time following the arrest of the external mechanical load.
Abstract
Computational Fluid Dynamics (CFD) is currently used to design and improve the hydraulic properties of biomedical devices, wherein the large scale blood circulation needs to be simulated by accounting for the mechanical response of red blood cells (RBCs) at mesoscales. In many practical instances, biomedical devices work on time-scales comparable to the intrinsic relaxation time of RBCs: thus, a systematic understanding of the time-dependent response of erythrocyte membranes is crucial for the effective design of such devices. So far, this information has been deduced from experimental data, which do not necessarily adapt to the the broad variety of the fluid dynamic conditions that can be encountered in practice. This work explores the novel possibility of studying the time-dependent response of an erythrocyte membrane to external mechanical loads via ab-initio, mesoscale numerical simulations, with a primary focus on the detailed characterisation of the RBC relaxation time $t_c$ following the arrest of the external mechanical load. The adopted mesoscale model exploits a hybrid Immersed Boundary-Lattice Boltzmann Method (IB-LBM), coupled with the Standard Linear Solid model (SLS) to account for the RBC membrane viscosity. We underscore the key importance of the 2D membrane viscosity $\mu_{m}$ to correctly reproduce the relaxation time of the RBC membrane. A detailed assessment of the dependencies on the typology and strength of the applied mechanical loads is also provided. Overall, our findings open interesting future perspectives for the study of the non-linear response of RBCs immersed in time-dependent strain fields.

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Journal ArticleDOI

Computational interfacial rheology

TL;DR: In this paper, the authors present a review of different approaches to measure interfacial rheological properties, and a discussion of advanced numerical implementations for deforming interfaces, and conclude with an outlook for this relatively young and exciting field.
Journal ArticleDOI

A Lattice Boltzmann dynamic-Immersed Boundary scheme for the transport of deformable inertial capsules in low-Re flows

TL;DR: A dynamic-Immersed–Boundary method combined with a BGK-Lattice–Boltzmann technique is developed and critically discussed, widely validated against well known benchmark data for rigid and deformable objects.
Journal ArticleDOI

Impact of the membrane viscosity on the tank-treading behavior of red blood cells

TL;DR: In this paper, the authors compared the impact of the internal fluid viscosity and the membrane viscosities on an isolated tank-treading red blood cell and found that both decrease the tank treading frequency, with moderate changes in the deformation and inclination of the red blood cells.
Journal ArticleDOI

Lattice Boltzmann simulations on the tumbling to tank-treading transition: effects of membrane viscosity

TL;DR: It is found that, at fixed viscosity ratios λ, larger values of μm lead to an increased range of values of capillary number at which the TB-TT transition occurs; moreover, increasing λ or increasing μm results in a qualitatively but not quantitatively similar behaviour.
Journal ArticleDOI

Red blood cell shape transitions and dynamics in time-dependent capillary flows

- 01 Jan 2022 - 
TL;DR: In this article , the authors explore the dynamics and shape transitions of RBCs on the cellular scale under confined and unsteady flow conditions using a combination of microfluidic experiments and numerical simulations.
References
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Journal ArticleDOI

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Journal ArticleDOI

Discrete lattice effects on the forcing term in the lattice Boltzmann method

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Connections between single-cell biomechanics and human disease states: gastrointestinal cancer and malaria

TL;DR: Comparing and contrast chemomechanical pathways whereby intracellular structural rearrangements lead to global changes in mechanical deformability of the cell, and examining the biochemical conditions mediating increases or decreases in modulus, and their implications for disease progression are compared.
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