COMPUTATIONAL STUDY OF GEOMETRIC EFFECTS OF BOTTOM WALL MICROGROOVES ON CELL DOCKING INSIDE MICROFLUIDIC DEVICES

S. Ahandoust, M. Saadatmand
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Abstract

Single cell and regularly cells docking inside the microstructure of microfluidic systems are advantageous in different analyses of single cells exposed to equal drug concentration and mechanical stimulus. In this study, we investigated bottom wall microgrooves with semicircular and rectangular geometries with different sizes which are suitable for single cell docking along the length of the microgroove in x direction and numerous cells docking regularly in one line inside the microgroove in a 3D microchannel. We used computational fluid dynamics to analyze the fluid recirculation area inside different microgrooves. The height of recirculation area in the bottom of microgroove can affect the cell attachment, and also materials delivery to attached cells, so the height of recirculation area has to be optimum amount. In addition, we analyzed the fluid drag force on cell movement toward the microgroove. This parameter was proportional to the fluid velocities in x and y directions changing in different microgrooves geometries. In different microgrooves geometries the fluid velocity in y direction does not change. If the fluid velocity in x direction decreases inside the microgroove, the cell movement time inside the microgroove will increase, and also the drag force in y direction can push the cells toward the bottom due to the lower drag force in x direction. The percentages of negative shear stress and average shear stress on the adhered cell surface were also calculated. The lower average shear stress, and negative shear stress around 50% on the cell surface are against cell detachment from the substrate. The results indicated that at the constant fluid inlet velocity and microchannel height, microgroove geometry and ratio of cell size to the microgroove size play pivotal roles in the cell initial adhesion to the substrate as well as the cell detachment.
微流控装置内底壁微槽对细胞对接几何效应的计算研究
单细胞和规则细胞在微流控系统的微观结构内对接,有利于对暴露于相同药物浓度和机械刺激下的单细胞进行不同的分析。在本研究中,我们研究了三维微通道中具有不同尺寸的半圆形和矩形几何形状的底壁微槽,这些微槽适合单细胞沿微槽长度在x方向上对接,也适合多个细胞在微槽内沿一条线有规则地对接。采用计算流体力学方法对不同微槽内的流体再循环面积进行了分析。微槽底部再循环区域的高度会影响到细胞的附着,也会影响到附着细胞的物料输送,所以再循环区域的高度必须是最优的。此外,我们还分析了流体阻力对细胞向微槽移动的影响。该参数与不同微槽几何形状下x、y方向的流体速度成正比。在不同几何形状的微槽中,流体在y方向上的速度不变。如果微槽内x方向的流体速度减小,则细胞在微槽内的运动时间会增加,并且由于x方向的阻力较小,y方向的阻力会将细胞推向底部。并计算了粘附细胞表面的负剪应力和平均剪应力的百分比。细胞表面较低的平均剪应力和约50%的负剪应力都不利于细胞脱离基质。结果表明,在流体进口速度和微通道高度恒定的情况下,微槽几何形状和微槽尺寸与微槽尺寸之比对细胞与基质的初始粘附和脱离起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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