Abstract

Monitoring the electrical neural signals is an important method for understanding the neuronal mechanism. In particular, in order to perform a cell-type-specific study, it is necessary to observe the concentration of calcium ions using fluorescent indicators in addition to measuring the electrical neural signal. This paper presents a multimodal multichannel neural activity readout integrated circuit that can perform not only electrical neural recording but also fluorescence recording of neural activity for the cell-type-specific study of heterogeneous neuronal cell populations. For monitoring the calcium ions, the photodiode generates the current according to the fluorescence expressed by the reaction between the genetically encoded calcium indicators and calcium ions. The time-based fluorescence recording circuit then records the photodiode current. The electrical neural signal captured by the microelectrode is recorded through the low-noise amplifier, variable gain amplifier, and analog-to-digital converter. The proposed integrated circuit is fabricated in a 1-poly 6-metal (1P6M) 0.18-μm CMOS process. The fluorescence recording circuit achieves a recording range of 81 dB (75 pA to 860 nA) and consumes a power of 724 nW/channel. The electrical recording circuit achieves an input-referred noise of 2.7 μVrms over the bandwidth of 10 kHz, while consuming the power of 4.9 μW/channel. The functionality of the proposed circuits is verified through the in vivo and in vitro experiments. Compared to the conventional neuroscience tools, which consist of bulky off-chip components, this neural interface is implemented in a compact size to perform multimodal neural recording while consuming low power.

Highlights

  • The brain is a complex structure made up of tens of billions of neurons and tens of trillions of connections

  • To enable cell-type-specific study in a heterogeneous population of neuronal cells, we present a multimodal neural activity readout integrated circuits (ICs) with the following two features: 1) a fluorescence recording channel combined with a photodiode for monitoring the Ca2+ associated with the neural firing, 2) an electrical recording channel combined with a microelectrode array to acquire APs and local field potentials (LFPs) [16]

  • The photodiode is equipped with a filter that blocks the blue light so that the proportion of the photodiode current caused by the green fluorescence can be significantly enhanced

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Summary

INTRODUCTION

The brain is a complex structure made up of tens of billions of neurons and tens of trillions of connections. Prior works [4], [6], [9]–[11], [14] presented multimodal neural recording integrated circuits (ICs), which record neural activities in multiple modalities, but these systems still have limitations to perform the cell-type-specific study in a heterogeneous population of cells. To enable cell-type-specific study in a heterogeneous population of neuronal cells, we present a multimodal neural activity readout IC with the following two features: 1) a fluorescence recording channel combined with a photodiode for monitoring the Ca2+ associated with the neural firing, 2) an electrical recording channel combined with a microelectrode array to acquire APs and LFPs [16]. (1) Electrical recording of APs and LFPs (2) Recording of chemical neurotransmitters such as dopamine, serotonin, glutamate, etc. (3) Impedance monitoring between the cell and electrode

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