Literature DB >> 25446286

Numerical simulation of red blood cell distributions in three-dimensional microvascular bifurcations.

Toru Hyakutake1, Shinya Nagai2.   

Abstract

We constructed three-dimensional microvascular bifurcation models using a parent vessel of diameter 10μm and investigated the flow behavior of the red blood cells (RBCs) through bifurcations. We considered symmetric and asymmetric model types. Two cases of equal daughter vessel diameter were employed for the asymmetric models, where the first was 10μm, which is the same as the parent vessel and the second was 7.94μm, which satisfies Murray's law. Simulated blood flow was computed using the lattice Boltzmann method in conjunction with the immersed boundary method for incorporating fluid-membrane interactions between the flow field and deformable RBCs. First, we investigated the flow behavior of a single RBC through microvascular bifurcations. In the case of the symmetric bifurcation, the turning point of the fractional plasma flow wherein the RBC flow changed from one daughter vessel to the other was 0.50. This turning point was however different for asymmetric bifurcations. Additionally, we varied the initial offset of RBCs from the centerline of the parent vessel. The simulation results indicated that the RBCs preferentially flow through the branch of a larger flow ratio. Next, we investigated the distribution characteristics of multiple RBCs. Simulations indicated that the results of the symmetric model were similar to those predicted by a previously published empirical model. On the other hand, results of asymmetric models deviated from those of the symmetric and empirical models. These results suggest that the distribution of RBCs varies according to the bifurcation angle and daughter vessel diameter in a microvascular bifurcation of the size considered.
Copyright © 2014 Elsevier Inc. All rights reserved.

Keywords:  Immersed boundary method; Lattice Boltzmann method; Microvascular bifurcation; Numerical simulation; Red blood cell

Mesh:

Year:  2014        PMID: 25446286     DOI: 10.1016/j.mvr.2014.10.001

Source DB:  PubMed          Journal:  Microvasc Res        ISSN: 0026-2862            Impact factor:   3.514


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