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Particle deposition in replica healthy and emphysematous alveolar models using computational fluid dynamics.

机译:使用计算流体动力学在健康和气肿性肺泡模型中进行颗粒沉积。

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摘要

Particle deposition in the pulmonary region of the lung has gained increasing interest in the past years. Of particular interest are nano-sized particles, because they have the potential of crossing the blood-gas barrier and into the capillaries. Many factors contribute to how and where particles deposit, such as lung morphology, breathing conditions, fluid flow characteristics, and alveolar wall movement. These many factors make simulating particle deposition in the alveoli difficult. The experimental in vivo studies have commonly used micron sized particles and there is a lack of data for smaller sized particles. Due to these many factors, deposition in the pulmonary region is not well understood. Furthermore, little attention has been paid to the emphysematous lungs, which have characteristics quite different than the healthy lung.;In this work, healthy and emphysematous replica acinus models were created from human lung casts using a 3D reconstruction software package. The models were used for simulating the particle deposition due to diffusion using Fine Particle Model (FPM). The FPM program was validated against an analytical solution using a straight tube, before moving on to predict the deposition in the alveolar models. Two particle sizes, 1 and 3 nm, were used to understand and compare pure diffusion in the lung using concentration contours. Results showed the particle deposition rate (particles/s) to be higher in the emphysemic. However, deposition rate per area (particles/m2s) was found to be higher in the healthy model. The deposition efficiency (% of particles that deposit) of the healthy model was greater than the emphysemic model, consistent with literature. Results were found to be lower than experimental in vivo measurements and whole lung model of local alveolar deposition (particles deposited in alveoli/particles entering alveoli) in comparison to our results in the pulmonary region, showing the importance of including axial diffusion effects. More work must be done experimentally and numerically before an understanding of deposition of particles of this size can be determined.
机译:近年来,在肺的肺区域中的颗粒沉积越来越引起人们的关注。特别令人感兴趣的是纳米级颗粒,因为它们具有穿越血气屏障进入毛细血管的潜力。许多因素影响颗粒沉积的方式和位置,例如肺的形态,呼吸条件,流体流动特性和肺泡壁运动。这些因素使模拟在肺泡中的颗粒沉积变得困难。体内实验性研究已经普遍使用了微米级的颗粒,并且缺乏较小尺寸颗粒的数据。由于这些因素,人们对肺部区域的沉积还没有很好的了解。此外,对气肿性肺的关注很少,其特征与健康肺完全不同。在这项工作中,使用3D重建软件包从人的肺部铸型创建了健康和气肿性腺泡复制模型。该模型用于使用“细颗粒模型”(FPM)模拟由于扩散导致的颗粒沉积。在继续预测肺泡模型中的沉积之前,已使用直管针对分析解决方案对FPM程序进行了验证。使用浓度等高线使用两种粒径(1和3 nm)来了解和比较肺中的纯扩散。结果表明,在肺气肿中,颗粒沉积速率(颗粒/秒)更高。但是,在健康模型中发现每单位面积的沉积速率(颗粒/ m2s)更高。健康文献的沉积效率(沉积颗粒的百分比)大于肺气肿模型,与文献一致。与我们在肺区域的结果相比,发现结果低于体内实验性测量结果和局部肺泡沉积的整个肺部模型(在肺泡中沉积的颗粒/进入肺泡的颗粒),显示出包括轴向扩散作用的重要性。在确定对这种尺寸颗粒的沉积的认识之前,必须在实验和数值上做更多的工作。

著录项

  • 作者

    Harding, Edward M., Jr.;

  • 作者单位

    Rochester Institute of Technology.;

  • 授予单位 Rochester Institute of Technology.;
  • 学科 Engineering Biomedical.
  • 学位 M.S.
  • 年度 2010
  • 页码 145 p.
  • 总页数 145
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 公共建筑;
  • 关键词

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