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A structure-based constitutive model of arterial tissue considering individual natural configurations of elastin and collagen

机译:考虑ELASTIN和胶原蛋白个体自然配置的动脉组织基于结构的组成模型

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The study proposes a novel theoretical-experimental approach for structure-based constitutive modeling of the passive mechanical properties of arterial tissue. The major novelty is accounting for the existence of individual natural configurations of elastin and collagen and their mechanical interaction in terms of the constituents' individual prestretches in the tissue natural state. The structure-based modeling of collagen allows accounting for effects of change in constituents' prestretch in terms of the change in feasible microstructural parameters, such as range of collagen recruitment stretch, mode of collagen mass fraction intensity function, and fiber directions. The results from an illustrative example for a porcine renal artery show that the model is robust and can adequately describe pressure-radius response and the stress-stretch relationship. The predictive capability of the model is tested in simulations of an isolated change in collagen prestretch and of elastin degradation in an artery kept at constant length. We expect this model to advance understanding about arterial rheology and serve as a useful tool for interpreting experimental data and solving boundary value problems relevant to vascular physiology at normal and pathological states.
机译:该研究提出了一种新颖的基于结构的基于结构的结构性实验方法,其动脉组织的被动力学性能的基于结构基础建模。主要的新奇是核算Elastin和胶原的个体自然配置以及组织自然状态中的成分单个粒度的机械相互作用。胶原蛋白的基于结构的建模允许在可行的微观结构参数的变化方面占组成粒子变化的影响,例如胶原蛋白招生拉伸的范围,胶原质量分数强度函数和纤维方向的变化。来自猪肾动脉的说明性示例的结果表明,该模型是稳健的并且可以充分描述压力 - 半径响应和应力拉伸关系。模型的预测能力在胶原蛋白普拉斯特的分离变化和在恒定长度保持恒定的动脉中的弹性蛋白降解的模拟中进行了测试。我们预计该模型将推进关于动脉流变学的理解,并用作解释与正常和病理状态下与血管生理学相关的实验数据和解决与血管生理相关的边界值问题的有用工具。

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