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Computational simulation methodologies for mechanobiological modelling: a cell-centred approach to neointima development in stents

机译:机械生物学建模的计算仿真方法:支架新内膜发展的细胞中心方法

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摘要

The design of medical devices could be very much improved if robust tools were available for computational simulation of tissue response to the presence of the implant. Such tools require algorithms to simulate the response of tissues to mechanical and chemical stimuli. Available methodologies include those based on the principle of mechanical homeostasis, those which use continuum models to simulate biological constituents, and the cell-centred approach, which models cells as autonomous agents. In the latter approach, cell behaviour is governed by rules based on the state of the local environment around the cell; and informed by experiment. Tissue growth and differentiation requires simulating many of these cells together. In this paper, the methodology and applications of cell-centred techniques—with particular application to mechanobiology—are reviewed, and a cell-centred model of tissue formation in the lumen of an artery in response to the deployment of a stent is presented. The method is capable of capturing some of the most important aspects of restenosis, including nonlinear lesion growth with time. The approach taken in this paper provides a framework for simulating restenosis; the next step will be to couple it with more patient-specific geometries and quantitative parameter data.
机译:如果健壮的工具可用于组织对植入物存在的组织响应的计算仿真,则医疗设备的设计可能会大大改善。这样的工具需要算法来模拟组织对机械和化学刺激的响应。可用的方法包括基于机械动态平衡原理的方法,使用连续体模型来模拟生物成分的方法以及以细胞为中心的方法,该方法将细胞建模为自主因子。在后一种方法中,单元行为由基于单元周围局部环境状态的规则控制;并根据实验得知组织的生长和分化需要一起模拟许多这些细胞。在本文中,对以细胞为中心的技术的方法论和应用(尤其是在机械生物学中的应用)进行了综述,并提出了一种以动脉为中心的腔体组织响应支架展开的组织形成的细胞中心模型。该方法能够捕获再狭窄的一些最重要方面,包括随时间的非线性病变增长。本文采用的方法为模拟再狭窄提供了一个框架。下一步是将其与更多特定于患者的几何形状和定量参数数据结合起来。

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