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Measuring Electrical And Mechanical Properties Of Red Blood Cells With Double Optical Tweezers

机译:用双光镊测量红细胞的电气和机械性能

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Red blood cell (RBC) aggregation in the blood stream is prevented by the zeta potential created by its negatively charged membrane. There are techniques, however, to decrease the zeta potential and allow cell agglutination, which are the basis of most of antigen-antibody tests used in immunohematology. We propose the use of optical tweezers to measure membrane viscosity, adhesion, zeta potential, and the double layer thickness of charges (DLT) formed around the cell in an electrolytic solution. For the membrane viscosity experiment, we trap a bead attached to RBCs and measure the force to slide one RBC over the other as a function of the velocity. Adhesion is quantified by displacing two RBCs apart until disagglutination. The DLT is measured using the force on the bead attached to a single RBC in response to an applied voltage. The zeta potential is obtained by measuring the terminal velocity after releasing the RBC from the trap at the last applied voltage. We believe that the methodology proposed here can provide information about agglutination, help to improve the tests usually performed in transfusion services, and be applied for zeta potential measurements in other samples.
机译:血流中的红细胞(RBC)聚集可通过其带负电荷的膜产生的zeta电位来阻止。但是,有一些技术可以降低zeta电位并允许细胞凝集,这是免疫血液学中大多数抗原抗体测试的基础。我们建议使用光镊来测量膜的粘度,粘附力,ζ电位和在电解液中围绕电池形成的电荷双层厚度(DLT)。对于膜粘度实验,我们捕获了附着在RBC上的珠子,并测量了一个RBC在另一RBC上滑动的力与速度的关系。通过将两个RBC分开直到粘连来量化粘附力。响应施加的电压,使用附着在单个RBC上的小珠上的力来测量DLT。通过在最后施加电压将RBC从阱释放后,通过测量终端速度获得zeta电位。我们相信,这里提出的方法可以提供有关凝集的信息,有助于改进通常在输血服务中执行的测试,并可以用于其他样品中的ζ电位测量。

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