Inglis David W, Morton Keith J, Davis John A, Zieziulewicz Thomas J, Lawrence David A, Austin Robert H, Sturm James C
Department of Physics, Macquarie University, Sydney, NSW 2109, Australia.
Lab Chip. 2008 Jun;8(6):925-31. doi: 10.1039/b800721g. Epub 2008 Apr 11.
In this work we demonstrate a new microfluidic method for the rapid assessment of platelet size and morphology in whole blood. The device continuously fractionates particles according to size by displacing them perpendicularly to the fluid flow direction in a micro-fabricated post array. Whole blood, labeled with the fluorescent, platelet specific, antibody PE-anti-CD41, was run through the device and the positions of fluorescent objects noted as they exited the array. From this, histograms of platelet size were created which show marked increases in size after exposure to thrombin or a temperature of 4 degrees C. We infer that the well known morphological changes that occur during activation are causing the observed increase in size.
在这项工作中,我们展示了一种用于快速评估全血中血小板大小和形态的新型微流控方法。该设备通过在微制造的柱阵列中垂直于流体流动方向移动颗粒,根据大小对颗粒进行连续分级。用荧光、血小板特异性抗体PE-抗-CD41标记的全血通过该设备,当荧光物体离开阵列时记录其位置。由此创建了血小板大小的直方图,结果显示在暴露于凝血酶或4摄氏度的温度后,血小板大小显著增加。我们推断,激活过程中发生的众所周知的形态变化导致了观察到的大小增加。