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Direct simulations of cells motions and deformations in flow.

机译:直接模拟细胞运动和流动变形。

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摘要

Direct numerical simulations (DNS) are used to study the motions and deformations of blood cells, especially leukocytes, in pressure driven flows in parallel plate channels with both smooth and uneven walls under adhesion force between the leukocytes and the channel wall.Leukocytes are represented by two composite fluid models. The first model is the compound-drop model in which the cytoplasm and the nucleus are modeled as fluids, and the second one is the drop-rigid-particle model in which the cytoplasm is modeled as a fluid and the nucleus as a rigid particle. The adhesion force is computed using two adhesion force models. In the first model, the adhesion force is given by a potential, and in the second model it is given by Dembo's kinetic adhesion model. The numerical code is based on the finite element method and the level-set technique is used to track the cell membrane position.In the absence of the adhesion force, in a pressure driven flow the leukocyte moves away from the wall to an equilibrium location. In presence of the adhesion force, provided it is located within the range of the force, the leukocyte is attracted to the layer of endothelial cells and it flattens under the action of hydrodynamic forces. It is found that for the normal parameter values and flow rates the adhesive force given by the kinetic model is too small to capture the leukocyte. The time at which all bonds are broken and the leukocyte moves away from the wall increases when the capillary number is increased, and decreases with increasing Reynolds number. The former suggests that the adhesion tendency of a leukocyte increases as its cortical tension is reduced. The distance traveled by a leukocyte before all bonds are broken increases with the Reynolds and capillary numbers. The rolling velocity of the leukocyte near an uneven wall varies in the sense that it appears to slip when its lower surface is in the gap between the spheres and stick when it comes close to the spheres' surfaces, which is in qualitative agreement with the experimental data.
机译:直接数值模拟(DNS)用于研究在白细胞与通道壁之间的粘附力作用下,具有光滑壁和不平坦壁的平行平板通道中压力驱动的血细胞的运动和变形,特别是白细胞。两个复合流体模型。第一个模型是化合物-液滴模型,其中将细胞质和细胞核建模为流体,第二个模型是滴-刚性颗粒模型,其中,将细胞质建模为流体,细胞核建模为刚性颗粒。使用两个粘附力模型计算粘附力。在第一个模型中,粘附力由电势给出,而在第二个模型中,粘附力由Dembo的动力学粘附模型给出。数值代码基于有限元方法,水平设置技术用于跟踪细胞膜位置。在没有粘附力的情况下,在压力驱动的血流中,白细胞从壁移动到平衡位置。在存在粘附力的情况下,只要其位于该力的范围内,白细胞就被吸引到内皮细胞层,并且在流体动力的作用下变平。发现对于正常参数值和流速,动力学模型给出的粘附力太小而不能捕获白细胞。当毛细管数增加时,所有键断裂且白细胞从壁移开的时间增加,并且随着雷诺数增加而减少。前者表明白细胞的粘附趋势随着其皮层张力的降低而增加。白血球在所有键断裂之前所经过的距离随着雷诺数和毛细管数的增加而增加。白细胞在不平坦壁附近的滚动速度在某种意义上有所变化,即白细胞的下表面在球体之间的间隙中似乎会滑动,而当其接近球体表面时会粘着,这与实验的定性一致数据。

著录项

  • 作者

    Jin, Quan.;

  • 作者单位

    New Jersey Institute of Technology.;

  • 授予单位 New Jersey Institute of Technology.;
  • 学科 Engineering Mechanical.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 98 p.
  • 总页数 98
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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