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Multiscale bio-chemo-mechanical model of intimal hyperplasia

机译:内膜增生的多尺度生化力学模型

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We consider a computational multiscale framework of a bio-chemo-mechanical model for intimal hyperplasia. With respect to existing models, we investigate the interactions between hemodynamics, cellular dynamics and biochemistry on the development of the pathology. Within the arterial wall, we propose a mathematical model consisting of kinetic differential equations for key vascular cell types, collagen and growth factors. The luminal hemodynamics is modeled with the Navier-Stokes equations. Coupling hypothesis among time and space scales are proposed to build a tractable modeling of such a complex multifactorial and multiscale pathology. A one-dimensional numerical test-case is presented for validation by comparing the results of the framework with experiments at short and long timescales. Our model permits to capture many cellular phenomena which have a central role in the physiopathology of intimal hyperplasia. Results are quantitatively and qualitatively consistent with experimental findings at both short and long timescales.
机译:我们考虑了内膜增生的生物化学力学模型的计算多尺度框架。关于现有模型,我们研究了血流动力学、细胞动力学和生物化学对病理学发展的相互作用。在动脉壁内,我们提出了一个数学模型,该模型由关键血管细胞类型、胶原蛋白和生长因子的动力学微分方程组成。腔内血流动力学使用 Navier-Stokes 方程建模。提出了时间和空间尺度之间的耦合假设,以建立这种复杂的多因素和多尺度病理的可处理模型。通过比较框架在短时间尺度和长尺度上的实验结果,提出了一个一维数值测试用例进行验证。我们的模型允许捕获许多在内膜增生的生理病理学中起核心作用的细胞现象。结果在定量和定性上都与短期和长期的实验结果一致。

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