All-inkjet-printed gold microelectrode arrays for extracellular recording of action potentials

被引:37
作者
Bachmann B. [1 ,2 ]
Adly N.Y. [1 ]
Schnitker J. [1 ]
Yakushenko A. [1 ]
Rinklin P. [2 ]
Offenhäusser A. [1 ]
Wolfrum B. [1 ,2 ]
机构
[1] Peter Grünberg Institute (PGI-8, Bioelectronics), Forschungszentrum Jülich GmbH, Jülich
[2] Neuroelectronics, Munich School of Bioengineering, Department of Electrical and Computer Engineering, Technical University of Munich (TUM), BCCN Munich, Garching
来源
Flexible and Printed Electronics | 2017年 / 2卷 / 03期
关键词
Bioelectronics; Extracellular recording of action potentials supplementary material for this article is available online; Gold ink; Inkjet printing; Microelectrode array;
D O I
10.1088/2058-8585/aa7928
中图分类号
学科分类号
摘要
Inkjet printing is an attractive method for cost-effective additive manufacturing of electronic devices. Especially for applications where disposable sensor systems are of interest, it is a promising tool since it enables the production of low-cost and flexible devices. In this work, we report the fabrication of a disposable microelectrode array (MEA) using solely inkjet printing technology. The MEAs were fabricated with two different functional inks, a self-made gold ink to print conductive feedlines and electrodes and a polymer-based ink to add a dielectric layer for insulation of the feedlines. We printed different MEA designs of up to 64 electrodes with a minimum lateral spacing of 200μm and a minimum electrode diameter of ∼31 μm. As a proof-of-concept, extracellular recordings of action potentials from cardiomyocyte-like HL-1 cells were performed using the all-printed devices. Furthermore, we stimulated the cells during the recordings with noradrenaline, which led to an increase in the recorded beating frequency of the cells. The results demonstrate the feasibility of inkjet printing gold MEAs for cell-based bioelectronics. © 2017 IOP Publishing Ltd.
引用
收藏
相关论文
共 61 条
  • [1] Mack C.M., Lin B.J., Turner J.D., Johnstone A.F.M., Burgoon L.D., Shafer T.J., Burst and principal components analyses of {MEA} data for 16 chemicals describe at least three effects classes, NeuroToxicology, 40, pp. 75-85, (2014)
  • [2] Johnstone A.F.M., Gross G.W., Weiss D.G., Schroeder O.H.-U., Gramowski A., Shafer T.J., Microelectrode arrays: A physiologically based neurotoxicity testing platform for the 21st century, NeuroToxicology, 31, pp. 331-350, (2010)
  • [3] Hondebrink L., Verboven A.H.A., Drega W.S., Schmeink S., De Groot M.W.G.D.M., Van Kleef R.G.D.M., Wijnolts F.M.J., De Groot A., Meulenbelt J., Westerink R.H.S., Neurotoxicity screening of (illicit) drugs using novel methods for analysis of microelectrode array (MEA) recordings, Neuro Toxicology, 55, pp. 1-9, (2016)
  • [4] Yeung C.K., Sommerhage F., Wrobel G., Offenhausser A., Chan M., Ingebrandt S., Drug profiling using planar microelectrode arrays, Anal. Bioanal. Chem., 387, pp. 2673-2680, (2007)
  • [5] Latifi S., Et al., Natural lecithin promotes neural network complexity and activity, Sci. Rep., 6, (2016)
  • [6] Yakushenko A., Katelhon E., Wolfrum B., Parallel onchip analysis ofsingle vesicle neurotransmitter release, Anal. Chem., 85, pp. 5483-5490, (2013)
  • [7] Wang J., Trouillon R., Lin Y., Svensson M.I., Ewing A.G., Individually addressable thin-film ultramicroelectrode array for spatial measurements of single vesicle release, Anal. Chem., 85, pp. 5600-5608, (2013)
  • [8] Berdondini L., Imfeld K., Maccione A., Tedesco M., Neukom S., Koudelka-Hep M., Martinoia S., Active pixel sensor array for high spatio-temporal resolution electrophysiological recordings from single cell to large scale neuronal networks, Lab Chip, 9, pp. 2644-2651, (2009)
  • [9] Muller J., Et al., High-resolution CMOS MEA platform to study neurons at subcellular, cellular, and network levels, Lab Chip, 15, pp. 2767-2780, (2015)
  • [10] Allitt B.J., Harris A.R., Morgan S.J., Clark G.M., Paolini A.G., Thin-film microelectrode stimulation of the cochlea in rats exposed to aminoglycoside induced hearing loss, Hear. Res., 33, pp. 113-126, (2016)