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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Label-free monitoring of cell-based assays: Combining impedance analysis with SPR for multiparametric cell profiling
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Label-free monitoring of cell-based assays: Combining impedance analysis with SPR for multiparametric cell profiling

机译:对基于细胞的测定进行无标记监测:将阻抗分析与SPR结合使用以进行多参数细胞分析

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摘要

Label-free approaches to monitor cell-based assays provide an unprecedented, time-resolved and non-invasive view on the response of mammalian cells to chemical, biological or physical stimuli. The most widespread techniques are impedance analysis and optical sensing using evanescent waves like SPR. This study describes the combination of both in one experimental setup so that a given cell population can be monitored simultaneously for electrical and optical changes. The device is based on commercial SPR chips that are processed by photolithography to provide electrodes for impedance analysis and gold spots for surface plasmon excitation on the same substrate. Simultaneous recordings do not interfere with each other but provide independent, time-resolved information on cell shape changes (impedance) and dynamic mass redistribution (SPR) as they occur during exposure of the cells to drugs or toxins or along their normal life cycle. This study provides proof-of-concept experiments of the dual biosensor platform in two experimental settings: signals are recorded and analyzed (i) during cell attachment, spreading and differentiation of initially suspended cells and (ii) during the exposure of the mature cells to an actin cytoskeleton disrupting drug. Impedance and SPR recordings provide complementary information that can be used to trace and assign intracellular mechanisms of action.
机译:监测基于细胞的测定的无标记方法提供了关于哺乳动物细胞对化学,生物或物理刺激反应的前所未有的,时间分辨的和非侵入性的观点。最普遍的技术是使用impedance逝波(例如SPR)进行阻抗分析和光学传感。这项研究描述了在一个实验装置中两者的结合,以便可以同时监视给定的细胞群的电和光变化。该设备基于商业SPR芯片,通过光刻技术对其进行处理,以在同一基板上提供用于阻抗分析的电极和用于表面等离子体激元激发的金点。同步记录不会互相干扰,但是会在细胞暴露于药物或毒素期间或沿其正常生命周期发生时,提供有关细胞形状变化(阻抗)和动态质量重新分布(SPR)的独立的时间分辨信息。这项研究在以下两个实验环境中提供了双生物传感器平台的概念验证实验:记录和分析信号(i)在细胞附着,初始悬浮细胞的扩散和分化过程中以及(ii)成熟细胞暴露于信号期间肌动蛋白细胞骨架破坏药物。阻抗和SPR记录可提供补充信息,可用于跟踪和分配细胞内作用机制。

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