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Design of Cross Type of Flow Channel to Control Orientation of Cell

机译:交叉流道控制细胞定向的设计

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A cross type of flow channel has been designed to control orientation of cell by direction of flow in vitro. The flow path (4 mm width, 0.2 mm height) is made between parallel transparent plates. Flow rate of 48 cm~3/hour is controlled by a syringe pump. The wall shear rate of 500 s~(-1) is calculated by the parabolic velocity profile between the parallel plates. The direction of the flow can be changed by alternative use of the inlet and outlet port of the cross type of the channel. The flow channel is placed in a chamber, where temperature and CO_2 content are kept 310 K and 5 percent, respectively. The chamber is placed on the stage of an inverted phase contrast microscope to observe the behavior of cells adhered on the wall under a flow. After several cells adhered to the disk, the wall shear rate was applied on the cells in the medium flow for 1 hour at each direction. C2C12 (mouse myoblast cell line) was exposed to the wall shear rate with the methodology. The experimental results show that the change of the direction of myoblasts can be observed by the cross type of flow channel.
机译:已经设计了交叉类型的流动通道,以通过体外流动方向控制细胞的方向。在平行的透明板之间形成流路(宽4毫米,高0.2毫米)。流速为48 cm〜3 /小时,由注射泵控制。根据平行板之间的抛物线速度曲线计算出500 s〜(-1)的壁面剪切速率。可以通过交替使用通道的十字型入口和出口来改变流动方向。流动通道放置在一个腔室内,温度和CO_2含量分别保持在310 K和5%。将该室放置在反相显微镜的台上,以观察在流动下粘附在壁上的细胞的行为。在几个小室粘附到磁盘后,在每个方向上在介质流中对小室施加壁切速率1小时。用该方法将C2C12(小鼠成肌细胞系)暴露于壁剪切速率。实验结果表明,通过流道的交叉类型可以观察到成肌细胞方向的变化。

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