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连续体微血流动力学的反向流变学建模。

Continuum microhaemodynamics modelling using inverse rheology.

机构信息

Department of Bioengineering, Imperial College London, London, UK.

Department of Mechanical Engineering, University College London, London, UK.

出版信息

Biomech Model Mechanobiol. 2022 Feb;21(1):335-361. doi: 10.1007/s10237-021-01537-2. Epub 2021 Dec 14.

DOI:10.1007/s10237-021-01537-2
PMID:34907491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8807439/
Abstract

Modelling blood flow in microvascular networks is challenging due to the complex nature of haemorheology. Zero- and one-dimensional approaches cannot reproduce local haemodynamics, and models that consider individual red blood cells (RBCs) are prohibitively computationally expensive. Continuum approaches could provide an efficient solution, but dependence on a large parameter space and scarcity of experimental data for validation has limited their application. We describe a method to assimilate experimental RBC velocity and concentration data into a continuum numerical modelling framework. Imaging data of RBCs were acquired in a sequentially bifurcating microchannel for various flow conditions. RBC concentration distributions were evaluated and mapped into computational fluid dynamics simulations with rheology prescribed by the Quemada model. Predicted velocities were compared to particle image velocimetry data. A subset of cases was used for parameter optimisation, and the resulting model was applied to a wider data set to evaluate model efficacy. The pre-optimised model reduced errors in predicted velocity by 60% compared to assuming a Newtonian fluid, and optimisation further reduced errors by 40%. Asymmetry of RBC velocity and concentration profiles was demonstrated to play a critical role. Excluding asymmetry in the RBC concentration doubled the error, but excluding spatial distributions of shear rate had little effect. This study demonstrates that a continuum model with optimised rheological parameters can reproduce measured velocity if RBC concentration distributions are known a priori. Developing this approach for RBC transport with more network configurations has the potential to provide an efficient approach for modelling network-scale haemodynamics.

摘要

由于血液流变学的复杂性,对微血管网络中的血流进行建模具有挑战性。零维和一维方法无法再现局部血液动力学,而考虑单个红细胞 (RBC) 的模型计算成本过高。连续体方法可以提供有效的解决方案,但对大型参数空间的依赖以及验证的实验数据稀缺限制了它们的应用。我们描述了一种将实验 RBC 速度和浓度数据同化到连续体数值建模框架中的方法。在各种流动条件下,在顺序分支微通道中获取 RBC 的成像数据。评估 RBC 浓度分布,并将其映射到具有 Quemada 模型规定的流变学的计算流体动力学模拟中。预测速度与粒子图像测速数据进行比较。使用案例的子集进行参数优化,然后将得到的模型应用于更广泛的数据集以评估模型效果。与假设牛顿流体相比,预优化模型将预测速度的误差降低了 60%,而优化进一步将误差降低了 40%。证明 RBC 速度和浓度分布的不对称性起着关键作用。如果预先知道 RBC 浓度分布,则不考虑 RBC 浓度的不对称性会将误差增加一倍,但不考虑剪切率的空间分布几乎没有影响。本研究表明,如果预先知道 RBC 浓度分布,则具有优化流变学参数的连续体模型可以再现测量速度。为具有更多网络配置的 RBC 运输开发这种方法有可能为网络规模血液动力学建模提供一种有效的方法。