Fluid–structure interaction modeling of compliant aortic valves using the lattice Boltzmann CFD and FEM methods

IF 3 3区 医学 Q2 BIOPHYSICS
Adi Morany, Karin Lavon, Ricardo Gomez Bardon, Brandon Kovarovic, Ashraf Hamdan, Danny Bluestein, Rami Haj-Ali
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引用次数: 2

Abstract

The lattice Boltzmann method (LBM) has been increasingly used as a stand-alone CFD solver in various biomechanical applications. This study proposes a new fluid–structure interaction (FSI) co-modeling framework for the hemodynamic-structural analysis of compliant aortic valves. Toward that goal, two commercial software packages are integrated using the lattice Boltzmann (LBM) and finite element (FE) methods. The suitability of the LBM-FE hemodynamic FSI is examined in modeling healthy tricuspid and bicuspid aortic valves (TAV and BAV), respectively. In addition, a multi-scale structural approach that has been employed explicitly recognizes the heterogeneous leaflet tissues and differentiates between the collagen fiber network (CFN) embedded within the elastin matrix of the leaflets. The CFN multi-scale tissue model is inspired by monitoring the distribution of the collagen in 15 porcine leaflets. Different simulations have been examined, and structural stresses and resulting hemodynamics are analyzed. We found that LBM-FE FSI approach can produce good predictions for the flow and structural behaviors of TAV and BAV and correlates well with those reported in the literature. The multi-scale heterogeneous CFN tissue structural model enhances our understanding of the mechanical roles of the CFN and the elastin matrix behaviors. The importance of LBM-FE FSI also emerges in its ability to resolve local hemodynamic and structural behaviors. In particular, the diastolic fluctuating velocity phenomenon near the leaflets is explicitly predicted, providing vital information on the flow transient nature. The full closure of the contacting leaflets in BAV is also demonstrated. Accordingly, good structural kinematics and deformations are captured for the entire cardiac cycle.

Abstract Image

基于点阵Boltzmann CFD和FEM方法的柔性主动脉瓣流固耦合建模
晶格玻尔兹曼方法(LBM)已越来越多地作为一种独立的CFD求解器应用于各种生物力学应用。本研究提出了一种新的流固耦合(FSI)协同建模框架,用于柔性主动脉瓣血流动力学-结构分析。为了实现这一目标,使用晶格玻尔兹曼(LBM)和有限元(FE)方法集成了两个商业软件包。LBM-FE血流动力学FSI分别用于健康三尖瓣和二尖瓣主动脉瓣(TAV和BAV)的建模。此外,已经采用的多尺度结构方法明确识别异质小叶组织,并区分嵌入在小叶弹性蛋白基质中的胶原纤维网络(CFN)。CFN多尺度组织模型的灵感来自于监测15只猪小叶中胶原蛋白的分布。研究了不同的模拟,并分析了结构应力和由此产生的血流动力学。我们发现LBM-FE FSI方法可以很好地预测TAV和BAV的流动和结构行为,并且与文献报道的结果有很好的相关性。多尺度非均质CFN组织结构模型增强了我们对CFN力学作用和弹性蛋白基质行为的理解。LBM-FE FSI的重要性还体现在其解决局部血流动力学和结构行为的能力上。特别是,在小叶附近的舒张波动速度现象被明确地预测,提供了关于流动瞬态性质的重要信息。还演示了BAV中接触传单的完全闭合。因此,良好的结构运动学和变形捕获整个心脏周期。
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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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