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使用带有微泵和微流体比较器的压力传感技术评估血液生物物理特性

Assessment of Blood Biophysical Properties Using Pressure Sensing with Micropump and Microfluidic Comparator.

作者信息

Kang Yang Jun

机构信息

Department of Mechanical Engineering, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju 61452, Korea.

出版信息

Micromachines (Basel). 2022 Mar 13;13(3):438. doi: 10.3390/mi13030438.

DOI:10.3390/mi13030438
PMID:35334730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8949505/
Abstract

To identify the biophysical properties of blood samples consistently, macroscopic pumps have been used to maintain constant flow rates in a microfluidic comparator. In this study, the bulk-sized and expensive pump is replaced with a cheap and portable micropump. A specific reference fluid (i.e., glycerin solution [40%]) with a small volume of red blood cell (RBC) (i.e., 1% volume fraction) as fluid tracers is supplied into the microfluidic comparator. An averaged velocity () obtained with micro-particle image velocimetry is converted into the flow rate of reference fluid (Qr) (i.e., Qr = CQ × Ac × , Ac: cross-sectional area, CQ = 1.156). Two control variables of the micropump (i.e., frequency: 400 Hz and volt: 150 au) are selected to guarantee a consistent flow rate (i.e., COV < 1%). Simultaneously, the blood sample is supplied into the microfluidic channel under specific flow patterns (i.e., constant, sinusoidal, and periodic on-off fashion). By monitoring the interface in the comparator as well as Qr, three biophysical properties (i.e., viscosity, junction pressure, and pressure-induced work) are obtained using analytical expressions derived with a discrete fluidic circuit model. According to the quantitative comparison results between the present method (i.e., micropump) and the previous method (i.e., syringe pump), the micropump provides consistent results when compared with the syringe pump. Thereafter, representative biophysical properties, including the RBC aggregation, are consistently obtained for specific blood samples prepared with dextran solutions ranging from 0 to 40 mg/mL. In conclusion, the present method could be considered as an effective method for quantifying the physical properties of blood samples, where the reference fluid is supplied with a cheap and portable micropump.

摘要

为了持续识别血液样本的生物物理特性,已使用宏观泵在微流体比较器中维持恒定流速。在本研究中,体积较大且昂贵的泵被一个便宜且便携的微型泵所取代。将一种特定的参考流体(即甘油溶液[40%])与少量红细胞(RBC)(即1%体积分数)作为流体示踪剂供应到微流体比较器中。通过微粒子图像测速法获得的平均流速()被转换为参考流体的流速(Qr)(即Qr = CQ × Ac × ,Ac:横截面积,CQ = 1.156)。选择微型泵的两个控制变量(即频率:400 Hz和电压:150 au)以确保流速一致(即变异系数<1%)。同时,将血液样本以特定的流动模式(即恒定、正弦和周期性通断方式)供应到微流体通道中。通过监测比较器中的界面以及Qr,使用离散流体电路模型推导的解析表达式获得三种生物物理特性(即粘度、连接压力和压力诱导功)。根据本方法(即微型泵)与先前方法(即注射泵)之间的定量比较结果,与注射泵相比,微型泵提供了一致的结果。此后,对于用浓度范围为0至40 mg/mL的葡聚糖溶液制备的特定血液样本,始终如一地获得了包括红细胞聚集在内的代表性生物物理特性。总之,本方法可被视为一种量化血液样本物理特性的有效方法,其中参考流体由便宜且便携的微型泵供应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/527c9f27dedd/micromachines-13-00438-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/0589d56676d1/micromachines-13-00438-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/8f6c4c30a42c/micromachines-13-00438-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/fff0d064a200/micromachines-13-00438-g0A3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/c1d0d1c39794/micromachines-13-00438-g0A4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/a18fb7a16ee7/micromachines-13-00438-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/a9c73771111d/micromachines-13-00438-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/fabf6152c4db/micromachines-13-00438-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/cb2f8eec8578/micromachines-13-00438-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/f45f303deab4/micromachines-13-00438-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/527c9f27dedd/micromachines-13-00438-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/0589d56676d1/micromachines-13-00438-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/8f6c4c30a42c/micromachines-13-00438-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/fff0d064a200/micromachines-13-00438-g0A3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/c1d0d1c39794/micromachines-13-00438-g0A4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/a18fb7a16ee7/micromachines-13-00438-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/a9c73771111d/micromachines-13-00438-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/fabf6152c4db/micromachines-13-00438-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/cb2f8eec8578/micromachines-13-00438-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/f45f303deab4/micromachines-13-00438-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140a/8949505/527c9f27dedd/micromachines-13-00438-g006.jpg

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