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Microfluidic-Based Biosensor for Blood Viscosity and Erythrocyte Sedimentation Rate Using Disposable Fluid Delivery System

机译:基于微流体的生物传感器通过使用一次性输液系统实现血液粘度和红细胞沉降速率

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摘要

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.
机译:为了有效地量化血液样本中的红细胞(RBC)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)。常规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。在这项研究中,代替两个注射泵,新采用了两个空气压缩注射器(ACS)将血液样本和参考液输送到T形微流体通道中。在使用两个ACS进行流体输送的情况下,没有随时间指定每种流体的流速。为了始终如一地获得参考液的速度场,重新选择了悬浮在40%甘油溶液(血细胞比容= 7%)中的RBC作为参考液,以避免RBC在ACS中沉淀。通过评估使用微粒图像测速(μPIV)获得的平均速度与注射泵相对于血样和参考液的流速之间的关系来获得校准曲线。通过水平安装ACS,可以通过监视血液样本的图像强度来获得ESR。分别通过μPIV和数字图像处理获得了血液样本和参考液的平均速度(<>,<>)以及两种液体中的界面位置()。然后通过使用平行共流方法和校正因子来测量血液粘度。 ESR随时间从血样(<>)的图像强度量化为两个指标()。为了证明这一点,所提出的方法用于量化血细胞比容(= 30%,40%和50%),基本溶液(1x磷酸盐缓冲盐水[PBS],血浆和右旋糖酐溶液)和硬化的RBC的贡献。血液粘度和ESR。本方法的实验结果与以前的方法相当。总之,在两种ACS输液的情况下,该方法能够始终如一地测量血液粘度和ESR。

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