A 1024-Channel CMOS Microelectrode Array With 26,400 Electrodes for Recording and Stimulation of Electrogenic Cells In Vitro

Marco Ballini(Imec the Netherlands), Jan Müller(ETH Zurich), Paolo Livi(ETH Zurich), Yihui Chen(ETH Zurich), Urs Frey(ETH Zurich), Alexander Stettler(ETH Zurich), Amir Shadmani(ETH Zurich), Vijay Viswam(ETH Zurich), Ian L. Jones(ETH Zurich), David Jäckel(ETH Zurich), Miloš Radivojević(ETH Zurich), Marta Lewandowska(ETH Zurich), Wei Gong(ETH Zurich), Michele Fiscella(ETH Zurich), Douglas J. Bakkum(ETH Zurich), F J de Heer(ETH Zurich), Andreas Hierlemann(ETH Zurich)
IEEE Journal of Solid-State Circuits
October 14, 2014
Cited by 246Open Access
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Abstract

To advance our understanding of the functioning of neuronal ensembles, systems are needed to enable simultaneous recording from a large number of individual neurons at high spatiotemporal resolution and good signal-to-noise ratio. Moreover, stimulation capability is highly desirable for investigating, for example, plasticity and learning processes. Here, we present a microelectrode array (MEA) system on a single CMOS die for in vitro recording and stimulation. The system incorporates 26,400 platinum electrodes, fabricated by in-house post-processing, over a large sensing area (3.85 2.10 mm ) with sub-cellular spatial resolution (pitch of 17.5 μm). Owing to an area and power efficient implementation, we were able to integrate 1024 readout channels on chip to record extracellular signals from a user-specified selection of electrodes. These channels feature noise values of 2.4 μV in the action-potential band (300 Hz-10 kHz) and 5.4 μV in the local-field-potential band (1 Hz-300 Hz), and provide programmable gain (up to 78 dB) to accommodate various biological preparations. Amplified and filtered signals are digitized by 10 bit parallel single-slope ADCs at 20 kSamples/s. The system also includes 32 stimulation units, which can elicit neural spikes through either current or voltage pulses. The chip consumes only 75 mW in total, which obviates the need of active cooling even for sensitive cell cultures.


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