Liu Wing Kam, Liu Yaling, Farrell David, Zhang Lucy, Wang X Sheldon, Fukui Yoshio, Patankar Neelesh, Zhang Yongjie, Bajaj Chandrajit, Lee Junghoon, Hong Juhee, Chen Xinyu, Hsu Huayi
Department of Mechanical Engineering, 2145 Sheridan Road, Northwestern University, Evanston, IL 60208, United States.
Comput Methods Appl Mech Eng. 2006 Feb 15;195(13-16):1722-1749. doi: 10.1016/j.cma.2005.05.049.
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 subdomains 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.
本文总结了新开发的浸入式有限元方法(IFEM)及其在生物系统建模中的应用。这项工作受到了T.J.R.休斯教授在解决流固相互作用问题方面的开创性工作的启发。在IFEM中,拉格朗日固体网格在跨越整个计算域的背景欧拉流体网格上移动。因此,网格生成大大简化。此外,流体和固体域均采用有限元方法建模,流体和固体子域之间的连续性通过用再生核粒子方法(RKPM)δ函数对速度进行插值和对力进行分布来实现。所提出的方法用于研究人体心血管系统中遇到的流固相互作用问题。目前,正在构建心脏模型,并模拟了血管成形术支架的展开过程。给出了关于单核细胞和血小板沉积的一些初步结果。对血液流变学,特别是红细胞(RBC)簇的剪切速率依赖性解聚和可变形细胞的运输进行了建模。此外,IFEM与电动学相结合,以研究纳米/生物细丝组装的机制,从而理解细胞运动。