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首页> 外文期刊>Biomechanics and modeling in mechanobiology >Invariant formulation for dispersed transverse ssotropy in aortic heart valves: An efficient means for modeling fiber splay
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Invariant formulation for dispersed transverse ssotropy in aortic heart valves: An efficient means for modeling fiber splay

机译:用于主动脉瓣离散性横向各向异性的不变公式:模拟纤维张开的有效方法

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摘要

Most soft tissues possess an oriented architecture of collagen fiber bundles, conferring both anisotropy and nonlinearity to their elastic behavior. Transverse isotropy has often been assumed for a subset of these tissues that have a single macroscopically-identifiable preferred fiber direction. Micro-structural studies, however, suggest that, in some tissues, collagen fibers are approximately normally distributed about a mean preferred fiber direction. Structural constitutive equations that account for this dispersion of fibers have been shown to capture the mechanical complexity of these tissues quite well, Such descriptions, however, are computationally cumbersome for two-dimensional (2D) fiber distributions, let alone for fully three-dimensional (3D) fiber populations. In this paper, we develop a new constitutive law for such tissues, based on a novel invariant theory for dispersed transverse isotropy. The invariant theory is derived from a novel closed-form 'splay invariant' that can easily handle 3D fiber populations, and that only requires a single parameter in the 2D case. The model fits biaxial data for aortic valve tissue as accurately as the standard structural model. Modification of the fiber stress-strain law requires no reformulation of the constitutive tangent matrix, making the model flexible for different types of soft tissues. Most importantly, the model is computationally expedient in a finite-element analysis, demonstrated by modeling a bioprosthetic heart valve.
机译:大多数软组织都具有胶原纤维束的定向结构,从而赋予其弹性行为各向异性和非线性。对于这些组织的子集,通常具有横向各向同性,这些子集具有单个宏观可识别的首选纤维方向。然而,微观结构研究表明,在某些组织中,胶原纤维大约平均分布在平均首选纤维方向上。业已证明,解释这种纤维分散的结构本构方程很好地捕获了这些组织的机械复杂性。但是,这种描述对于二维(2D)纤维分布在计算上很麻烦,更不用说对三维纤维进行分布了( 3D)纤维数量​​。在本文中,我们基于一种新的不变的离散横观各向同性理论,为此类组织开发了一种新的本构定律。不变性理论源于一种新颖的闭合形式的“张开不变性”,它可以轻松处理3D纤维群,在2D情况下仅需要一个参数。该模型与标准结构模型一样准确地拟合了主动脉瓣组织的双轴数据。修改纤维应力-应变定律不需要重新构造本征切线矩阵,从而使模型对于不同类型的软组织具有灵活性。最重要的是,该模型在有限元分析中具有计算上的优势,通过对生物人工心脏瓣膜进行建模可以证明这一点。

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