Amini J A, Fallahyan F
Department of Mechanical and Medical Engineering, University of Islamic Azad, Tehran, Iran.
Biomed Sci Instrum. 1997;33:567-72.
The motion of a rigid particle suspended in two-dimensional flow through bifurcations of diverging microvessels (DMs), and converging microvessels (CMs) is dependent on multiple complex factors that include the geometry of the network, the angle of the bifurcation, the pressure gradient across the microvessel, the geometry of the cells and their radial location in the vessels. To determine how these parameters affect cell trajectories and flux into downstream branches of CMs and DMs, the motion of cells flowing into a DMs and CMs bifurcation, with a 45 degrees branch angle has been modelled, for every location by means of the finite-difference analysis (FDA). The modeling data was compared with direct experimental data from converging and diverging microvessels obtained from mesenteric microcirculation of the rat. Detailed statistical analysis showed significant correlation between the modeling data and experimental data. This model provides estimates of RBC flow along the trajectory path through bifurcations of CMs and DMs; sites which may be crucial for flow stoppage, depending on the vessel diameter and cell deformability.
悬浮在通过发散微血管(DMs)和汇聚微血管(CMs)分支的二维流中的刚性颗粒的运动取决于多个复杂因素,这些因素包括网络的几何形状、分支角度、微血管两端的压力梯度、细胞的几何形状及其在血管中的径向位置。为了确定这些参数如何影响细胞轨迹以及进入CMs和DMs下游分支的通量,借助有限差分分析(FDA)对流入具有45度分支角的DMs和CMs分支处的细胞运动进行了建模,针对每个位置进行了模拟。将建模数据与从大鼠肠系膜微循环获得的汇聚和发散微血管的直接实验数据进行了比较。详细的统计分析表明建模数据与实验数据之间存在显著相关性。该模型提供了沿通过CMs和DMs分支的轨迹路径的红细胞流动估计;根据血管直径和细胞可变形性,这些位置可能对血流停滞至关重要。