Coupled macroscopic and microscopic scale modeling of fibrillar tissues and tissue equivalents

被引:50
作者
Agoram, B [1 ]
Barocas, VH
机构
[1] Univ Colorado, Dept Chem Engn, Boulder, CO 80309 USA
[2] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
来源
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME | 2001年 / 123卷 / 04期
关键词
D O I
10.1115/1.1385843
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Collagen mechanics are crucial to the function and dysfunction of many. tissues, including blood vessels and articular cartilage, and bioartificial tissues. Previous attempts to develop computer simulations of collagenous tissue based on macroscopic property descriptions have often been limited in application by, the simplicity of the model; simulations based on microscopic descriptions, in contrast, have numerical limitations imposed by, the size of the mathematical problem. We present a method that combines the tractability of the macroscopic approach with the flexibility of the microstructural approach. The macroscopic domain is divided into finite elements (as in standard FEM). Each element contains a microscopic scale network. Instead of a stress constitutive equation; the macroscopic problem is distributed over the microscopic scale network, and solved in each element to satisfy, the weak formulation of Cauchy's stress continuity equation over the macroscopic domain. The combined method scales by, order 1.1 us the overall number of degrees of freedom is increased, allowing it to handle larger problems than a direct microstructural approach. Model predictions agree qualitatively with tensile tests on isotropic and aligned reconstituted type I collagen gels.
引用
收藏
页码:362 / 369
页数:8
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