On-chip microelectrode array and in situ transient calibration for measurement of transient concentration gradients near surfaces of 2D cell cultures

被引:9
作者
Sridharan, Siddarth V. [1 ,2 ]
Rivera, Jose F. [1 ,2 ]
Nolan, James K. [2 ,3 ]
Alam, Muhammad A. [1 ,2 ]
Rickus, Jenna L. [3 ]
Janes, David B. [1 ,2 ]
机构
[1] Purdue Univ, Elect & Comp Engn, W Lafayette, IN 47907 USA
[2] Purdue Univ, Birck Nanotechnol Ctr, W Lafayette, IN 47907 USA
[3] Purdue Univ, Agr & Biol Engn, W Lafayette, IN 47907 USA
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2018年 / 260卷
基金
美国国家科学基金会;
关键词
Microelectrode array; Amperometric sensing; Hydrogen peroxide; Concentration gradient; Concentration transients; 2D cell culture; Human astrocytes; Cellular gradients; Biosensors; Platinum electrodes; SCANNING ELECTROCHEMICAL MICROSCOPY; HYDROGEN-PEROXIDE; REAL-TIME; CONCENTRATION PROFILES; SPATIAL-RESOLUTION; CHROMAFFIN CELLS; RELEASE; GLUCOSE; H2O2; EXOCYTOSIS;
D O I
10.1016/j.snb.2017.12.194
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Amperometric microelectrode arrays (MEAs) interrogate the concentration at multiple positions simultaneously and with sufficient sampling rates, thus being able to capture fast transient gradients. However, sensitivity variability issues in amperometric MEAs degrade the reliability of the measurements, particularly at the small concentration scales found in physiological studies. This paper describes the development of on-chip platinum amperometric MEAs and in situ transient calibration for reliable measurement of physiological transient concentration gradients. The designed MEA geometry facilitates positioning near a 2D cell culture setup, and the proposed in situ transient calibration minimizes the effects of sensitivity variability, thus allowing for calculation of gradients based on concentration differences between closely spaced electrodes. The effectiveness of the MEA and the in situ transient calibration was evaluated by measuring controllably-generated gradients, and then calculating the difference between experimental and simulated data using normalized time analysis. Gradients generated by periodic uptake intervals as fast as 150 ms followed by recovery intervals of 60 s were measured over a spatial range of 70 tim, with spatial resolution of 35 mu m, and sampling time and measurement time of 10 ms. Transient gradients of hydrogen peroxide were also measured above the surface of a 2D cell culture of human astrocytes, thus demonstrating the approach in actual physiological measurements. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:519 / 528
页数:10
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