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基于人体解剖学的大-中气道模型中气溶胶沉积的计算流体动力学模拟

CFD simulation of aerosol deposition in an anatomically based human large-medium airway model.

作者信息

Ma Baoshun, Lutchen Kenneth R

机构信息

Department of Biomedical Engineering, Boston University, 44 Cummington Street, Boston, MA 02215, USA.

出版信息

Ann Biomed Eng. 2009 Feb;37(2):271-85. doi: 10.1007/s10439-008-9620-y. Epub 2008 Dec 12.

Abstract

Quantitative data on aerosol deposition in the human respiratory tract are useful for understanding the causes of certain lung diseases and for designing efficient drug delivery systems via inhalation. In this study, aerosol deposition in a 3D anatomically based human large-medium airway model was simulated using computational fluid dynamics (CFD). The model extended from mouth to generation 10 and included two-thirds of the airways obtained by multi-detector row computed tomography (MDCT) imaging on normal healthy human subjects. Steady oral inhalation (15, 30, and 60 L/min) and aerosol (1-30 micrometer) deposition were computed by CFD using the realizable k-epsilon turbulence model. Based on the mean turbulence flow field, the computed extrathoracic deposition, ratio of left to right lung deposition, and deposition efficiency at each generation compared favorably with existing in vivo and in vitro experiments. The significant deposition in the large-medium airway model showed that the total tracheobronchial deposition is dominated by the large-medium airways for micrometer-sized aerosol particles. These quantitative data and the methods developed in this study provided valuable means toward subject-specific modeling of aerosol deposition in the human lung based on realistic lung geometry.

摘要

关于人体呼吸道中气溶胶沉积的定量数据,对于理解某些肺部疾病的成因以及设计高效的吸入式给药系统很有用。在本研究中,使用计算流体动力学(CFD)模拟了基于三维解剖结构的人体大中气道模型中的气溶胶沉积。该模型从口腔延伸至第10级,包括通过对正常健康人体受试者进行多排探测器计算机断层扫描(MDCT)成像获得的三分之二的气道。使用可实现的k-ε湍流模型,通过CFD计算了稳定的口腔吸入(15、30和60升/分钟)和气溶胶(1-30微米)的沉积情况。基于平均湍流流场,计算得到的胸外沉积、左右肺沉积比例以及每一级的沉积效率与现有的体内和体外实验结果相比具有优势。在大中气道模型中的显著沉积表明,对于微米级气溶胶颗粒,总气管支气管沉积主要由大中气道主导。这些定量数据以及本研究中开发的方法为基于真实肺部几何结构的人体肺部气溶胶沉积个体特异性建模提供了有价值的手段。

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