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Increasing operating frequency band of cytometric biosensor for single cell impedance characterization

机译:增加细胞计数生物传感器的工作频带以用于单细胞阻抗表征

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This paper proposes to optimize the operating frequency band of a lab on a chip, based on bio-impedance spectroscopy for single cell. Bio-impedance allows to characterize low cells concentration or single cell by providing an electrical signature. Thus, it is necessary to perform impedance measurements up to several tens of mega-Hertz in order to extract the internal cell signature. In the case of a single cell, characterization is performed in a very small volume down to 1 pL. In the same time measured impedances increase up to hundreds of kilo-ohms. At frequencies above mega-Hertz, parasitic effects such as coupling capacitances could prevail over sample impedance and completely short-circuit it. To optimize the pass band, a complete model of a cytometric device was developed including coupling capacitances as a function of chosen materials. Simulation results prove the ability to increase the high frequency simply by optimizing track geometries and placement. This is done without any change of the sensing structure (microelectrodes design and microchannel). This assumption was obtained by measuring and comparing parasitic effects of our first sensors and the new optimized ones. Decrease of coupling capacitance by a factor higher than 10 was obtained allowing to perform characterizations in a wide frequency band.
机译:本文提出了基于单细胞生物阻抗光谱技术来优化芯片实验室的工作频段。生物阻抗允许通过提供电信号来表征低细胞浓度或单细胞。因此,有必要进行高达几十兆赫兹的阻抗测量,以提取内部细胞特征。在单个电池的情况下,特征分析可在很小的体积(低至1 pL)中进行。同时,测得的阻抗增加到数百千欧姆。在兆赫以上的频率上,诸如耦合电容之类的寄生效应可能会超过采样阻抗,并使采样阻抗完全短路。为了优化通带,开发了完整的细胞计数设备模型,其中包括耦合电容随所选材料的变化。仿真结果证明了仅通过优化轨道几何形状和位置即可增加高频的能力。无需更改感应结构(微电极设计和微通道)即可完成此操作。这个假设是通过测量和比较我们的第一个传感器和新优化的传感器的寄生效应得出的。耦合电容减小了10倍以上,从而可以在宽频带内进行表征。

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