SenseBack - An implantable system for bidirectional neural interfacing

Chronic in-vivo neurophysiology experiments require highly miniaturized, remotely powered multi-channel neural interfaces which are currently lacking in power or flexibility post implantation. In this article, to resolve this problem we present the SenseBack system, a post-implantation reprogrammable wireless 32-channel bidirectional neural interfacing that can enable chronic peripheral electrophysiology experiments in freely behaving small animals. The large number of channels for a peripheral neural interface, coupled with fully implantable hardware and complete software flexibility enable complex in-vivo studies where the system can adapt to evolving study needs as they arise. In complementary ex-vivo and in-vivo preparations, we demonstrate that this system can record neural signals and perform high-voltage, bipolar stimulation on any channel. In addition, we demonstrate transcutaneous power delivery and Bluetooth 5 data communication with a PC. The SenseBack system is capable of stimulation on any channel with ±20 V of compliance and up to 315 μA of current, and highly configurable recording with per-channel adjustable gain and filtering with 8 sets of 10-bit ADCs to sample data at 20 kHz for each channel. To the best of our knowledge this is the first such implantable research platform offering this level of performance and flexibility post-implantation (including complete reprogramming even after encapsulation) for small animal electrophysiology. Here we present initial acute trials, demonstrations and progress towards a system that we expect to enable a wide range of electrophysiology experiments in freely behaving animals

A charge-metering method for voltage-mode neural stimulation

AbstractElectrical neural stimulation is the technique used to modulate neural activity by inducing an instantaneous charge imbalance. This is typically achieved by injecting a constant current and controlling the stimulation time. However, constant voltage stimulation is found to be more energy-efficient although it is challenging to control the amount of charge delivered. This paper presents a novel, fully integrated circuit for facilitating charge-metering in constant voltage stimulation. It utilises two complementary stimulation paths. Each path includes a small capacitor, a comparator and a counter. They form a mixed-signal integrator that integrates the stimulation current onto the capacitor while monitoring its voltage against a threshold using the comparator. The pulses from the comparator are used to increment the counter and reset the capacitor. Therefore, by knowing the value of the capacitor, threshold voltage and output of the counter, the quantity of charge delivered can be calculated. The system has been fabricated in 0.18μm CMOS technology, occupying a total active area of 339μm×110μm. Experimental results were taken using: (1) a resistor–capacitor EEI model and (2) platinum electrodes with ringer solution. The viability of this method in recruiting action potentials has been demonstrated using a cuff electrode with Xenopus sciatic nerve. For a 10nC target charge delivery, the results of (2) show a charge delivery error of 3.4% and a typical residual charge of 77.19pC without passive charge recycling. The total power consumption is 45μW. The performance is comparable with other publications. Therefore, the proposed stimulation method can be used as a new approach for neural stimulation

Nitric Oxide Synthase Neurons in the Preoptic Hypothalamus Are NREM and REM Sleep-Active and Lower Body Temperature.

When mice are exposed to external warmth, nitric oxide synthase (NOS1) neurons in the median and medial preoptic (MnPO/MPO) hypothalamus induce sleep and concomitant body cooling. However, how these neurons regulate baseline sleep and body temperature is unknown. Using calcium photometry, we show that NOS1 neurons in MnPO/MPO are predominantly NREM and REM active, especially at the boundary of wake to NREM transitions, and in the later parts of REM bouts, with lower activity during wakefulness. In addition to releasing nitric oxide, NOS1 neurons in MnPO/MPO can release GABA, glutamate and peptides. We expressed tetanus-toxin light-chain in MnPO/MPO NOS1 cells to reduce vesicular release of transmitters. This induced changes in sleep structure: over 24 h, mice had less NREM sleep in their dark (active) phase, and more NREM sleep in their light (sleep) phase. REM sleep episodes in the dark phase were longer, and there were fewer REM transitions between other vigilance states. REM sleep had less theta power. Mice with synaptically blocked MnPO/MPO NOS1 neurons were also warmer than control mice at the dark-light transition (ZT0), as well as during the dark phase siesta (ZT16-20), where there is usually a body temperature dip. Also, at this siesta point of cooled body temperature, mice usually have more NREM, but mice with synaptically blocked MnPO/MPO NOS1 cells showed reduced NREM sleep at this time. Overall, MnPO/MPO NOS1 neurons promote both NREM and REM sleep and contribute to chronically lowering body temperature, particularly at transitions where the mice normally enter NREM sleep

Neural Interfaces for Intracortical Recording: Requirements, Fabrication Methods, and Characteristics

Implantable neural interfaces for central nervous system research have been designed with wire, polymer, or micromachining technologies over the past 70 years. Research on biocompatible materials, ideal probe shapes, and insertion methods has resulted in building more and more capable neural interfaces. Although the trend is promising, the long-term reliability of such devices has not yet met the required criteria for chronic human application. The performance of neural interfaces in chronic settings often degrades due to foreign body response to the implant that is initiated by the surgical procedure, and related to the probe structure, and material properties used in fabricating the neural interface. In this review, we identify the key requirements for neural interfaces for intracortical recording, describe the three different types of probes—microwire, micromachined, and polymer-based probes; their materials, fabrication methods, and discuss their characteristics and related challenges

Frequency spectrum for pulses of different lengths, fitted with a Gaussian curve.

<p>In black the simulated pulse, in red the Gaussian fit. It is possible to notice that the broader spectrum is not a perfect Gaussian; this is due to the numerical dispersion being more pronounced in a source with a bigger frequency range.</p

Refractive index of a water-sucrose solution as a function of the sucrose concentration at 589.3 nm [27].

<p>In this work we are assuming that it is possible to translate the data to obtain values for different wavelengths.</p