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Real-Time Monitoring of Platelet Activation Using Quartz Thickness-Shear Mode Resonator Sensors

机译:使用石英厚度-剪切模式谐振器传感器实时监测血小板活化

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In this study, quartz thickness-shear mode (TSM) resonator sensors were adopted to monitor the process of platelet activation. Resting platelets adhering to fibrinogen-coated electrodes were activated by different concentrations of thrombin (1, 10, and 100 U/mL), and the corresponding electrical admittance spectra of TSM resonators during this process were recorded. Based on a bilayer-loading transmission line model of TSM resonators, the complex shear modulus (G' + jG '') and the average thickness (h(PL)) of the platelet monolayer at a series of time points were obtained. Decrease in thrombin concentration from 100 to 1 U/mL shifted all peaks and plateaus in G', G '', and h(PL) to higher time points, which could be attributed to the partial activation of platelets by low concentrations of thrombin. The peak value of h(PL) was acquired when platelets presented their typical spherical shape as the first transformation in activation process. The G' peak appeared 10 similar to 20 min after h(PL) peak, when some filopods were observed along the periphery of platelets but without obvious cell spreading. As platelet spreading began and continued, G', G '', and h(PL). decreased, leading to a steady rise of resonance frequency shift of TSM resonator sensors. The results show high reliability and stability of TSM resonator sensors in monitoring the process of platelet activation, revealing an effective method to measure platelet activities in real-time under multiple experimental conditions. The G', G '', and h(PL) values could provide useful quantitative measures on platelet structure variations in activation process, indicating potential of TSM resonators in characterization of cells during their transformation.
机译:在这项研究中,采用石英厚度剪切模式(TSM)谐振器传感器来监测血小板活化过程。粘附到纤维蛋白原涂层电极上的静息血小板被不同浓度的凝血酶(1、10和100 U / mL)激活,并记录了该过程中TSM谐振器的相应电导率谱。基于TSM谐振器的双层加载传输线模型,获得了血小板单层在一系列时间点的复数剪切模量(G'+ jG'')和平均厚度(h(PL))。凝血酶浓度从100 U / mL降低到G',G''和h(PL)的所有峰和平台都移至更高的时间点,这可能归因于低浓度的凝血酶对血小板的部分活化。当血小板呈现其典型的球形形状作为活化过程中的第一个转变时,获得了h(PL)的峰值。当在血小板外围观察到一些丝虫但没有明显的细胞扩散时,G'峰在h(PL)峰之后的20分钟出现了大约10分钟。随着血小板的扩散开始并继续,G',G''和h(PL)。减小,导致TSM谐振器传感器的谐振频率偏移稳定上升。结果表明,TSM谐振器传感器在监测血小板活化过程中具有很高的可靠性和稳定性,从而揭示了一种在多种实验条件下实时测量血小板活性的有效方法。 G',G''和h(PL)值可以提供激活过程中血小板结构变化的有用定量方法,表明TSM共振器在转化过程中表征细胞的潜力。

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