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Multiscale image-based modeling and simulation of gas flow and particle transport in the human lungs

机译:基于多尺度图像的人肺中气流和颗粒传输的建模和仿真

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摘要

Improved understanding of structure and function relationships in the human lungs in individuals and sub-populations is fundamentally important to the future of pulmonary medicine. Image-based measures of the lungs can provide sensitive indicators of localized features, however to provide a better prediction of lung response to disease, treatment and environment, it is desirable to integrate quantifiable regional features from imaging with associated value-added high-level modeling. With this objective in mind, recent advances in computational fluid dynamics (CFD) of the bronchial airways - from a single bifurcation symmetric model to a multiscale image-based subject-specific lung model - will be reviewed. The interaction of CFD models with local parenchymal tissue expansion - assessed by image registration - allows new understanding of the interplay between environment, hot spots where inhaled aerosols could accumulate, and inflammation. To bridge ventilation function with image-derived central airway structure in CFD, an airway geometrical modeling method that spans from the model ‘entrance’ to the terminal bronchioles will be introduced. Finally, the effects of turbulent flows and CFD turbulence models on aerosol transport and deposition will be discussed.CFD simulation of airflow and particle transport in the human lung has been pursued by a number of research groups, whose interest has been in studying flow physics and airways resistance, improving drug delivery, or investigating which populations are most susceptible to inhaled pollutants. The three most important factors that need to be considered in airway CFD studies are lung structure, regional lung function, and flow characteristics. Their correct treatment is important because the transport of therapeutic or pollutant particles is dependent on the characteristics of the flow by which they are transported; and the airflow in the lungs is dependent on the geometry of the airways and how ventilation is distributed to the peripheral tissue. The human airway structure spans more than 20 generations, beginning with the extra-thoracic airways (oral or nasal cavity, and through the pharynx and larynx to the trachea), then the conducting airways, the respiratory airways, and to the alveoli. The airways in individuals and sub-populations (by gender, age, ethnicity, and normal vs. diseased states) may exhibit different dimensions, branching patterns and angles, and thickness and rigidity. At the local level, one would like to capture detailed flow characteristics, e.g. local velocity profiles, shear stress, and pressure, for prediction of particle transport in an airway (lung structure) model that is specific to the geometry of an individual, to understand how inter-subject variation in airway geometry (normal or pathological) influences the transport and deposition of particles. In a systems biology – or multiscale modeling – approach, these local flow characteristics can be further integrated with epithelial cell models for the study of mechanotransduction. At the global (organ) level, one would like to match regional ventilation (lung function) that is specific to the individual, thus ensuring that the flow that transports inhaled particles is appropriately distributed throughout the lung model. Computational models that do not account for realistic distribution of ventilation are not capable of predicting realistic particle distribution or targeted drug deposition. Furthermore, the flow in the human lung can be transitional or turbulent in the upper and proximal airways, and becomes laminar in the distal airways. The flows in the laminar, transitional and turbulent regimes have different temporal and spatial scales. Therefore, modeling airway structure and predicting gas flow and particle transport at both local and global levels require image-guided multiscale modeling strategies.In this article, we will review the aforementioned three key aspects of CFD studies of the human lungs: airway structure (conducting airways), lung function (regional ventilation and boundary conditions), and flow characteristics (modeling of turbulent flow and its effect on particle transport). For modeling airway structure, we will focus on the conducting airways, and review both symmetric vs. asymmetric airway models, idealized vs. CT-based airway models, and multiscale subject-specific airway models. Imposition of physiological subject-specific boundary conditions (BCs) in CFD is essential to match regional ventilation in individuals, which is also critical in studying preferential deposition of inhaled aerosols in sub-populations, e.g. normals vs. asthmatics that may exhibit different ventilation patterns. Subject-specific regional ventilation defines flow distributions and characteristics in airway segments and bifurcations, which subsequently determines the transport and deposition of aerosols in the entire lungs. Turbulence models are needed to capture the transient and turbulent nature of the gas flow in the human lungs. Thus, the advantages and disadvantages of different turbulence models as well as their effects on particle transport will be discussed. The ultimate goal of the development is to identify sensitive structural and functional variables in sub-populations of normal and diseased lungs for potential clinical applications.
机译:更好地了解个人和亚人群在人肺中的结构和功能关系对肺医学的未来至关重要。基于图像的肺部测量可以提供局部特征的敏感指标,但是,为了更好地预测肺部对疾病,治疗和环境的反应,需要将成像中可量化的区域特征与相关的增值高级别建模相结合。考虑到这一目标,将回顾支气管气道的计算流体动力学(CFD)的最新进展-从单个分叉对称模型到基于多尺度图像的特定于受试者的肺部模型-。 CFD模型与局部实质组织扩张的相互作用(通过图像配准进行评估)使人们对环境,吸入的气溶胶可能聚集的热点和炎症之间的相互作用有了新的认识。为了在CFD中用图像衍生的中央气道结构桥接通气功能,将引入一种从“入口”模型到末梢细支气管的气道几何建模方法。最后,将讨论湍流和CFD湍流模型对气溶胶传输和沉积的影响。许多研究小组一直在进行CFD模拟人肺中气流和颗粒传输的研究,他们的兴趣一直是研究流物理学和流体力学。气道阻力,改善药物输送或调查哪些人群最容易吸入污染物。气道CFD研究中需要考虑的三个最重要因素是肺结构,区域肺功能和血流特性。它们的正确处理很重要,因为治疗性或污染物性颗粒的运输取决于它们被运输时的流动特性。肺中的气流取决于气道的几何形状以及通气如何分配到周围组织。人类的气道结构跨越了20多个世代,从胸外气道(口腔或鼻腔,通过咽部和喉部到达气管)开始,然后是传导气道,呼吸道和肺泡。个体和亚人群的气道(按性别,年龄,种族以及正常状态与患病状态)可能显示出不同的尺寸,分支模式和角度以及厚度和刚度。在本地一级,您想捕获详细的流量特性,例如局部速度剖面,切应力和压力,用于预测特定于个体几何形状的气道(肺结构)模型中的粒子传输,以了解受试者间气道几何形状(正常或病理性)的变化如何影响颗粒的运输和沉积。在系统生物学(或多尺度建模)方法中,可以将这些局部流动特性与上皮细胞模型进一步集成,以研究机械传导。在全球(器官)一级,人们希望匹配特定于个体的局部通气(肺功能),从而确保运输吸入颗粒的流量适当地分布在整个肺部模型中。不考虑实际通风分布的计算模型无法预测实际颗粒分布或目标药物沉积。此外,人肺中的气流在上呼吸道和近端气道中可能是过渡性的或湍流的,并且在远端气道中变为层流的。层流,过渡和湍流状态下的流动具有不同的时空尺度。因此,在局部和全局水平上对气道结构进行建模并预测气体流量和颗粒传输需要图像引导的多尺度建模策略。在本文中,我们将对人肺CFD研究的上述三个关键方面进行回顾:气道结构(传导气道),肺功能(区域通气和边界条件)和流动特性(湍流模型及其对颗粒传输的影响)。对于气道结构建模,我们将重点放在传导气道上,并审查对称气道模型与非对称气道模型,理想气道模型与基于CT的气道模型以及特定对象的多尺度气道模型。在CFD中施加生理对象特定的边界条件(BCs)对于匹配个体的区域通气至关重要,这对于研究吸入气雾剂在亚群(例如亚群)中的优先沉积也至关重要。正常人与哮喘患者的通气模式可能有所不同。特定对象的区域通气定义了气道段和分支中的流量分布和特征随后确定了整个肺中气溶胶的运输和沉积。需要湍流模型来捕获人肺中气流的瞬态和湍流特性。因此,将讨论不同湍流模型的优缺点及其对粒子传输的影响。开发的最终目标是确定正常和患病肺的亚群中的敏感结构和功能变量,以进行潜在的临床应用。

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