Fontes Adriana, Fernandes Heloise P, de Thomaz André A, Barbosa Luiz C, Barjas-Castro Maria L, Cesar Carlos L
Universidade Federal de Pernambuco, Cidade Universitária, Departamento de Biofísica e Radiobiologia, Av. Professor Moraes Rego, 50670-901, Recife-PE, Brasil.
J Biomed Opt. 2008 Jan-Feb;13(1):014001. doi: 10.1117/1.2870108.
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.
血流中的红细胞(RBC)聚集可通过其带负电荷的膜所产生的ζ电位来防止。然而,存在一些技术可降低ζ电位并使细胞凝集,这是免疫血液学中大多数抗原 - 抗体检测的基础。我们建议使用光镊来测量膜粘度、粘附力、ζ电位以及在电解液中细胞周围形成的电荷双层厚度(DLT)。对于膜粘度实验,我们捕获附着在红细胞上的珠子,并测量一个红细胞相对于另一个红细胞滑动时的力与速度的函数关系。通过将两个红细胞分开直至解凝集来量化粘附力。DLT是通过测量附着在单个红细胞上的珠子在施加电压时所受的力来测量的。ζ电位是通过在最后施加的电压下将红细胞从捕获中释放后测量其终端速度而获得的。我们相信,这里提出的方法可以提供有关凝集的信息,有助于改进输血服务中通常进行的检测,并应用于其他样品的ζ电位测量。