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1.
Nat Biomed Eng ; 4(2): 207-222, 2020 02.
Article in English | MEDLINE | ID: mdl-32076132

ABSTRACT

Clinically approved neural stimulators are limited by battery requirements, as well as by their large size compared with the stimulation targets. Here, we describe a wireless, leadless and battery-free implantable neural stimulator that is 1.7 mm3 and that incorporates a piezoceramic transducer, an energy-storage capacitor and an integrated circuit. An ultrasonic link and a hand-held external transceiver provide the stimulator with power and bidirectional communication. The stimulation protocols were wirelessly encoded on the fly, reducing power consumption and on-chip memory, and enabling protocol complexity with a high temporal resolution and low-latency feedback. Uplink data indicating whether stimulation occurs are encoded by the stimulator through backscatter modulation and are demodulated at the external transceiver. When embedded in ex vivo porcine tissue, the integrated circuit efficiently harvested ultrasonic power, decoded downlink data for the stimulation parameters and generated current-controlled stimulation pulses. When cuff-mounted and acutely implanted onto the sciatic nerve of anaesthetized rats, the device conferred repeatable stimulation across a range of physiological responses. The miniaturized neural stimulator may facilitate closed-loop neurostimulation for therapeutic interventions.


Subject(s)
Implantable Neurostimulators , Wireless Technology , Animals , Electric Power Supplies , Equipment Design , Rats , Sciatic Nerve/physiology , Signal Processing, Computer-Assisted , Ultrasonics
2.
Neuron ; 97(6): 1356-1368.e4, 2018 03 21.
Article in English | MEDLINE | ID: mdl-29503189

ABSTRACT

Animals acquire behaviors through instrumental conditioning. Brain-machine interfaces have used instrumental conditioning to reinforce patterns of neural activity directly, especially in frontal and motor cortices, which are a rich source of signals for voluntary action. However, evidence suggests that activity in primary sensory cortices may also reflect internally driven processes, instead of purely encoding antecedent stimuli. Here, we show that rats and mice can learn to produce arbitrary patterns of neural activity in their primary visual cortex to control an auditory cursor and obtain reward. Furthermore, learning was prevented when neurons in the dorsomedial striatum (DMS), which receives input from visual cortex, were optogenetically inhibited, but not during inhibition of nearby neurons in the dorsolateral striatum. After learning, DMS inhibition did not affect production of the rewarded patterns. These data demonstrate that cortico-basal ganglia circuits play a general role in learning to produce cortical activity that leads to desirable outcomes.


Subject(s)
Basal Ganglia/physiology , Brain-Computer Interfaces , Nerve Net/physiology , Visual Cortex/physiology , Volition/physiology , Animals , Male , Mice , Mice, Inbred C57BL , Rats , Rats, Long-Evans
3.
Curr Opin Neurobiol ; 50: 64-71, 2018 06.
Article in English | MEDLINE | ID: mdl-29331738

ABSTRACT

The neural dust platform uses ultrasonic power and communication to enable a scalable, wireless, and batteryless system for interfacing with the nervous system. Ultrasound offers several advantages over alternative wireless approaches, including a safe method for powering and communicating with sub mm-sized devices implanted deep in tissue. Early studies demonstrated that neural dust motes could wirelessly transmit high-fidelity electrophysiological data in vivo, and that theoretically, this system could be miniaturized well below the mm-scale. Future developments are focused on further minimization of the platform, better encapsulation methods as a path towards truly chronic neural interfaces, improved delivery mechanisms, stimulation capabilities, and finally refinements to enable deployment of neural dust in the central nervous system.


Subject(s)
Brain-Computer Interfaces , Neurons/physiology , User-Computer Interface , Wireless Technology , Animals , Humans , Neural Prostheses , Ultrasonics
4.
Neuron ; 91(3): 529-39, 2016 Aug 03.
Article in English | MEDLINE | ID: mdl-27497221

ABSTRACT

The emerging field of bioelectronic medicine seeks methods for deciphering and modulating electrophysiological activity in the body to attain therapeutic effects at target organs. Current approaches to interfacing with peripheral nerves and muscles rely heavily on wires, creating problems for chronic use, while emerging wireless approaches lack the size scalability necessary to interrogate small-diameter nerves. Furthermore, conventional electrode-based technologies lack the capability to record from nerves with high spatial resolution or to record independently from many discrete sites within a nerve bundle. Here, we demonstrate neural dust, a wireless and scalable ultrasonic backscatter system for powering and communicating with implanted bioelectronics. We show that ultrasound is effective at delivering power to mm-scale devices in tissue; likewise, passive, battery-less communication using backscatter enables high-fidelity transmission of electromyogram (EMG) and electroneurogram (ENG) signals from anesthetized rats. These results highlight the potential for an ultrasound-based neural interface system for advancing future bioelectronics-based therapies.


Subject(s)
Electromyography/instrumentation , Electrophysiology/instrumentation , Peripheral Nervous System/physiology , Ultrasonic Waves , Wireless Technology/instrumentation , Animals , Prostheses and Implants , Rats , Remote Sensing Technology/methods
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