Integrated 16-Channel Neural Recording Circuit with SPI Interface
and Error Correction Code in 130Nm CMOS Technology
Andreas Bahr, Lait Abu Saleh, Dietmar Schroeder and Wolfgang Krautschneider
Institute of Nano and Medical Electronics, Hamburg University of Technology, Eißendorfer Str. 38, Hamburg, Germany
Keywords: Biomedical Signal Acquisition, Neural Recording, Integrated Circuit, Mixed-signal Integrated Circuit, Error
Correction Code, 130nm CMOS Technology, SPI Interface.
Abstract: In the research of neural diseases like epilepsy and schizophrenia genetic mouse models play a very
important role. Dysfunctions during early brain development might cause these diseases. The analysis of the
brain signals is the key to understand this process and develop treatments. To enable the acquisition of brain
signals from neonatal mice, an integrated circuit for neural recording is presented. It is minimized for low
area consumption and can be placed in a miniaturized system on the head of the mouse. It is intended to
acquire the local field and action potentials from the brain. 16 analog input channels are implemented. The
biomedical signals are amplified with analog pre-amplifiers. Two parallel structures of 8:1 multiplexer,
post-amplifier and ADC are implemented to digitize the signals. The post-amplifier has programmable gain
and high driving capability. The ADC is implemented as a 10 bit SAR ADC. Digital SPI interfacing is used
to reduce the number of transmission lines. Reed Solomon Error Correction Coding has been implemented
to enable error correction. The mixed-signal integrated circuit has been successfully implemented in a 130
nm CMOS technology. It is optimized for low area consumption; the channel density is approximately 10
channels/mm
2
.
1 INTRODUCTION
In the development of treatments for diseases like
epilepsy, schizophrenia or autism spectrum disorders
(ASD), the neural recording of the signals from the
brain from neonatal mice plays a key role. The
development of the brain and its neural networks is a
complex process in which neurons are born, migrate
and establish synaptic connections (Ben-Ari et al.,
1997). The neurodevelopmental hypothesis suggests
that neurological diseases can arise from
dysfunctions during early brain development (Lewis
and Levitt, 2002). Genetic mouse disease models are
used to investigate this hypothesis and to
development treatments against this diseases. The
brain signals of the mice are recorded and analysed
at neural level. Of special interest are neonatal mice,
since the diseases develop in this period. Neonatal
mice are very small and have a body weight of only
3-5 g.
For the neural recording, microelectrodes are
inserted into the cortex of mice. The microelectrodes
are connected to the integrated circuit. The
integrated circuit amplifies and digitizes the signals.
The system of microelectrodes and integrated circuit
will be placed on the head of the mouse. This system
is connected to the recording system with wires. Due
to the small size of the neonatal mice, the size of the
integrated circuit has to be minimized. To reduce the
constraints in the behaviour, the wiring has to be
reduced as much as possible.
Every analog transmission is a potential source
of noise and distortion to a signal. As soon as the
signal is digitized, theoretically it can be transferred
without any errors. Because of this it is of high
importance to digitize the signals as close to the
brain of the mouse as possible. In this context the
presented integrated circuit provides the best
possible solution. It can be placed on a miniaturized
system directly next to the electrode.
The presented integrated circuit is optimized for
the signal acquisition of extracellular action
potentials (AP) and local field potentials (LFP). The
LFP are typically measured in the range up to 300
Hz, AP in the range up to 10 kHz. The amplitude
range is up to several millivolts for LFP and
hundreds of micro volts for AP.