Kang Yang Jun
Department of Mechanical Engineering, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju 61452, Korea.
Micromachines (Basel). 2020 Feb 20;11(2):215. doi: 10.3390/mi11020215.
To quantify the variation of red blood cells (RBCs) or plasma proteins in blood samples effectively, it is necessary to measure blood viscosity and erythrocyte sedimentation rate (ESR) simultaneously. Conventional microfluidic measurement methods require two syringe pumps to control flow rates of both fluids. In this study, instead of two syringe pumps, two air-compressed syringes (ACSs) are newly adopted for delivering blood samples and reference fluid into a T-shaped microfluidic channel. Under fluid delivery with two ACS, the flow rate of each fluid is not specified over time. To obtain velocity fields of reference fluid consistently, RBCs suspended in 40% glycerin solution (hematocrit = 7%) as the reference fluid is newly selected for avoiding RBCs sedimentation in ACS. A calibration curve is obtained by evaluating the relationship between averaged velocity obtained with micro-particle image velocimetry (μPIV) and flow rate of a syringe pump with respect to blood samples and reference fluid. By installing the ACSs horizontally, ESR is obtained by monitoring the image intensity of the blood sample. The averaged velocities of the blood sample and reference fluid (<>, <>) and the interfacial location in both fluids () are obtained with μPIV and digital image processing, respectively. Blood viscosity is then measured by using a parallel co-flowing method with a correction factor. The ESR is quantified as two indices (, ) from image intensity of blood sample (<>) over time. As a demonstration, the proposed method is employed to quantify contributions of hematocrit ( = 30%, 40%, and 50%), base solution (1× phosphate-buffered saline [PBS], plasma, and dextran solution), and hardened RBCs to blood viscosity and ESR, respectively. Experimental Results of the present method were comparable with those of the previous method. In conclusion, the proposed method has the ability to measure blood viscosity and ESR consistently, under fluid delivery of two ACSs.
为了有效量化血液样本中红细胞(RBCs)或血浆蛋白的变化,有必要同时测量血液粘度和红细胞沉降率(ESR)。传统的微流体测量方法需要两个注射泵来控制两种流体的流速。在本研究中,新采用了两个空气压缩注射器(ACSs)来代替两个注射泵,将血液样本和参考流体输送到T形微流体通道中。在使用两个ACS进行流体输送时,每种流体的流速随时间并不确定。为了持续获得参考流体的速度场,新选择悬浮在40%甘油溶液(血细胞比容 = 7%)中的RBCs作为参考流体,以避免RBCs在ACS中沉降。通过评估用微粒子图像测速仪(μPIV)获得的平均速度与注射泵相对于血液样本和参考流体的流速之间的关系,得到校准曲线。通过水平安装ACSs,通过监测血液样本的图像强度来获得ESR。血液样本和参考流体的平均速度(<>,<>)以及两种流体中的界面位置()分别通过μPIV和数字图像处理获得。然后使用具有校正因子的平行共流方法测量血液粘度。ESR从血液样本(<>)随时间的图像强度量化为两个指标(,)。作为一个演示,所提出的方法被用于分别量化血细胞比容( = 30%、40%和50%)、基础溶液(1×磷酸盐缓冲盐水[PBS]、血浆和葡聚糖溶液)以及硬化RBCs对血液粘度和ESR的贡献。本方法的实验结果与先前方法的结果相当。总之,所提出的方法有能力在两个ACSs进行流体输送的情况下持续测量血液粘度和ESR。