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GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells

Emergent trends in the device development for neural prosthetics have focused on establishing stimulus localization, improving longevity through immune compatibility, reducing energy re-quirements, and embedding active control in the devices. Ultrasound stimulation can single-handedly address severa...

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Autores principales: Balasubramanian, Priya S., Singh, Ankur, Xu, Chris, Lal, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033194/
https://www.ncbi.nlm.nih.gov/pubmed/32080204
http://dx.doi.org/10.1038/s41598-020-58133-0
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author Balasubramanian, Priya S.
Singh, Ankur
Xu, Chris
Lal, Amit
author_facet Balasubramanian, Priya S.
Singh, Ankur
Xu, Chris
Lal, Amit
author_sort Balasubramanian, Priya S.
collection PubMed
description Emergent trends in the device development for neural prosthetics have focused on establishing stimulus localization, improving longevity through immune compatibility, reducing energy re-quirements, and embedding active control in the devices. Ultrasound stimulation can single-handedly address several of these challenges. Ultrasonic stimulus of neurons has been studied extensively from 100 kHz to 10 MHz, with high penetration but less localization. In this paper, a chip-scale device consisting of piezoelectric Aluminum Nitride ultrasonic transducers was engineered to deliver gigahertz (GHz) ultrasonic stimulus to the human neural cells. These devices provide a path towards complementary metal oxide semiconductor (CMOS) integration towards fully controllable neural devices. At GHz frequencies, ultrasonic wavelengths in water are a few microns and have an absorption depth of 10–20 µm. This confinement of energy can be used to control stimulation volume within a single neuron. This paper is the first proof-of-concept study to demonstrate that GHz ultrasound can stimulate neurons in vitro. By utilizing optical calcium imaging, which records calcium ion flux indicating occurrence of an action potential, this paper demonstrates that an application of a nontoxic dosage of GHz ultrasonic waves [Formula: see text] caused an average normalized fluorescence intensity recordings >1.40 for the calcium transients. Electrical effects due to chip-scale ultrasound delivery was discounted as the sole mechanism in stimulation, with effects tested at α = 0.01 statistical significance amongst all intensities and con-trol groups. Ionic transients recorded optically were confirmed to be mediated by ion channels and experimental data suggests an insignificant thermal contributions to stimulation, with a predicted increase of 0.03 (o)C for [Formula: see text] This paper paves the experimental framework to further explore chip-scale axon and neuron specific neural stimulation, with future applications in neural prosthetics, chip scale neural engineering, and extensions to different tissue and cell types.
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spelling pubmed-70331942020-02-28 GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells Balasubramanian, Priya S. Singh, Ankur Xu, Chris Lal, Amit Sci Rep Article Emergent trends in the device development for neural prosthetics have focused on establishing stimulus localization, improving longevity through immune compatibility, reducing energy re-quirements, and embedding active control in the devices. Ultrasound stimulation can single-handedly address several of these challenges. Ultrasonic stimulus of neurons has been studied extensively from 100 kHz to 10 MHz, with high penetration but less localization. In this paper, a chip-scale device consisting of piezoelectric Aluminum Nitride ultrasonic transducers was engineered to deliver gigahertz (GHz) ultrasonic stimulus to the human neural cells. These devices provide a path towards complementary metal oxide semiconductor (CMOS) integration towards fully controllable neural devices. At GHz frequencies, ultrasonic wavelengths in water are a few microns and have an absorption depth of 10–20 µm. This confinement of energy can be used to control stimulation volume within a single neuron. This paper is the first proof-of-concept study to demonstrate that GHz ultrasound can stimulate neurons in vitro. By utilizing optical calcium imaging, which records calcium ion flux indicating occurrence of an action potential, this paper demonstrates that an application of a nontoxic dosage of GHz ultrasonic waves [Formula: see text] caused an average normalized fluorescence intensity recordings >1.40 for the calcium transients. Electrical effects due to chip-scale ultrasound delivery was discounted as the sole mechanism in stimulation, with effects tested at α = 0.01 statistical significance amongst all intensities and con-trol groups. Ionic transients recorded optically were confirmed to be mediated by ion channels and experimental data suggests an insignificant thermal contributions to stimulation, with a predicted increase of 0.03 (o)C for [Formula: see text] This paper paves the experimental framework to further explore chip-scale axon and neuron specific neural stimulation, with future applications in neural prosthetics, chip scale neural engineering, and extensions to different tissue and cell types. Nature Publishing Group UK 2020-02-20 /pmc/articles/PMC7033194/ /pubmed/32080204 http://dx.doi.org/10.1038/s41598-020-58133-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Balasubramanian, Priya S.
Singh, Ankur
Xu, Chris
Lal, Amit
GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
title GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
title_full GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
title_fullStr GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
title_full_unstemmed GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
title_short GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells
title_sort ghz ultrasonic chip-scale device induces ion channel stimulation in human neural cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033194/
https://www.ncbi.nlm.nih.gov/pubmed/32080204
http://dx.doi.org/10.1038/s41598-020-58133-0
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