TY - JOUR
T1 - Immersed finite element method and its applications to biological systems
AU - Liu, Wing Kam
AU - Liu, Yaling
AU - Farrell, David
AU - Zhang, Lucy
AU - Wang, X. Sheldon
AU - Fukui, Yoshio
AU - Patankar, Neelesh
AU - Zhang, Yongjie
AU - Bajaj, Chandrajit
AU - Lee, Junghoon
AU - Hong, Juhee
AU - Chen, Xinyu
AU - Hsu, Huayi
N1 - Funding Information:
The support of this research by the National Science Foundation (NSF), the National Aeronautics and Space Administration (NASA), the NSF Summer Institute on Nano Mechanics and Materials, and NSF IGERT is gratefully acknowledged.
PY - 2006/2/15
Y1 - 2006/2/15
N2 - This paper summarizes the newly developed immersed finite element method (IFEM) and its applications to the modeling of biological systems. This work was inspired by the pioneering work of Professor T.J.R. Hughes in solving fluid-structure interaction problems. In IFEM, a Lagrangian solid mesh moves on top of a background Eulerian fluid mesh which spans the entire computational domain. Hence, mesh generation is greatly simplified. Moreover, both fluid and solid domains are modeled with the finite element method and the continuity between the fluid and solid sub-domains is enforced via the interpolation of the velocities and the distribution of the forces with the reproducing Kernel particle method (RKPM) delta function. The proposed method is used to study the fluid-structure interaction problems encountered in human cardiovascular systems. Currently, the heart modeling is being constructed and the deployment process of an angioplasty stent has been simulated. Some preliminary results on monocyte and platelet deposition are presented. Blood rheology, in particular, the shear-rate dependent de-aggregation of red blood cell (RBC) clusters and the transport of deformable cells, are modeled. Furthermore, IFEM is combined with electrokinetics to study the mechanisms of nano/bio filament assembly for the understanding of cell motility.
AB - This paper summarizes the newly developed immersed finite element method (IFEM) and its applications to the modeling of biological systems. This work was inspired by the pioneering work of Professor T.J.R. Hughes in solving fluid-structure interaction problems. In IFEM, a Lagrangian solid mesh moves on top of a background Eulerian fluid mesh which spans the entire computational domain. Hence, mesh generation is greatly simplified. Moreover, both fluid and solid domains are modeled with the finite element method and the continuity between the fluid and solid sub-domains is enforced via the interpolation of the velocities and the distribution of the forces with the reproducing Kernel particle method (RKPM) delta function. The proposed method is used to study the fluid-structure interaction problems encountered in human cardiovascular systems. Currently, the heart modeling is being constructed and the deployment process of an angioplasty stent has been simulated. Some preliminary results on monocyte and platelet deposition are presented. Blood rheology, in particular, the shear-rate dependent de-aggregation of red blood cell (RBC) clusters and the transport of deformable cells, are modeled. Furthermore, IFEM is combined with electrokinetics to study the mechanisms of nano/bio filament assembly for the understanding of cell motility.
KW - Aggregation
KW - Cardiovascular system
KW - Cell motility
KW - Cytoskeletal dynamics
KW - Fluid-structure interaction
KW - Immersed finite element method
KW - Micro-circulation
KW - Nano-electro-mechanical-sensors
KW - Red blood cell
KW - Reproducing Kernel particle method
KW - Surgical corrective procedures
KW - Thrombosis
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U2 - 10.1016/j.cma.2005.05.049
DO - 10.1016/j.cma.2005.05.049
M3 - Article
C2 - 20200602
AN - SCOPUS:30944434458
SN - 0045-7825
VL - 195
SP - 1722
EP - 1749
JO - Computer Methods in Applied Mechanics and Engineering
JF - Computer Methods in Applied Mechanics and Engineering
IS - 13-16
ER -