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Coupling of Navier–Stokes equations with protein molecular dynamics and its application to hemodynamics
Author(s) -
Liu Yaling,
Zhang Lucy,
Wang Xiaodong,
Liu Wing Kam
Publication year - 2004
Publication title -
international journal for numerical methods in fluids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 112
eISSN - 1097-0363
pISSN - 0271-2091
DOI - 10.1002/fld.798
Subject(s) - viscoelasticity , rheology , mechanics , finite element method , red blood cell , eulerian path , rigidity (electromagnetism) , shear (geology) , coupling (piping) , lagrangian , classical mechanics , biophysics , chemistry , physics , materials science , mathematics , mathematical analysis , thermodynamics , biology , biochemistry , quantum mechanics , composite material , metallurgy
The red blood cell (RBC) aggregation plays an important role in many physiological phenomena, in particular the atherosclerosis and thrombotic processes. In this research, we introduce a new modelling technique that couples Navier–Stokes equations with protein molecular dynamics to investigate the behaviours of RBC aggregates and their effects on the blood rheology. In essence, the Lagrangian solid mesh, which represents the immersed deformable cells, is set to move on top of a background Eulerian mesh. The effects of cell–cell interaction (adhesive/repulsive) and hydrodynamic forces on RBC aggregates are studied by introducing equivalent protein molecular potentials into the immersed finite element method. The aggregation of red blood cells in quiescent fluids is simulated. The de‐aggregation of a RBC cluster at different shear rates is also investigated to provide an explanation of the shear‐rate‐dependence of the blood viscoelastic properties. Finally, the influences of cell–cell interaction, RBC rigidity, and vessel geometry are addressed in a series of test cases with deformable cells (normal and sickle RBCs) passing through micro‐ and capillary vessels. Copyright © 2004 John Wiley & Sons, Ltd.