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Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements

Implantable devices to measure neurochemical or electrical activity from the brain are mainstays of neuroscience research and have become increasingly utilized as enabling components of clinical therapies. In order to increase the number of recording channels on these devices while minimizing the im...

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Autores principales: Nicolai, Evan N., Michelson, Nicholas J., Settell, Megan L., Hara, Seth A., Trevathan, James K., Asp, Anders J., Stocking, Kaylene C., Lujan, J. Luis, Kozai, Takashi D.Y., Ludwig, Kip A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215211/
https://www.ncbi.nlm.nih.gov/pubmed/30424427
http://dx.doi.org/10.3390/mi9100494
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author Nicolai, Evan N.
Michelson, Nicholas J.
Settell, Megan L.
Hara, Seth A.
Trevathan, James K.
Asp, Anders J.
Stocking, Kaylene C.
Lujan, J. Luis
Kozai, Takashi D.Y.
Ludwig, Kip A.
author_facet Nicolai, Evan N.
Michelson, Nicholas J.
Settell, Megan L.
Hara, Seth A.
Trevathan, James K.
Asp, Anders J.
Stocking, Kaylene C.
Lujan, J. Luis
Kozai, Takashi D.Y.
Ludwig, Kip A.
author_sort Nicolai, Evan N.
collection PubMed
description Implantable devices to measure neurochemical or electrical activity from the brain are mainstays of neuroscience research and have become increasingly utilized as enabling components of clinical therapies. In order to increase the number of recording channels on these devices while minimizing the immune response, flexible electrodes under 10 µm in diameter have been proposed as ideal next-generation neural interfaces. However, the representation of motion artifact during neurochemical or electrophysiological recordings using ultra-small, flexible electrodes remains unexplored. In this short communication, we characterize motion artifact generated by the movement of 7 µm diameter carbon fiber electrodes during electrophysiological recordings and fast-scan cyclic voltammetry (FSCV) measurements of electroactive neurochemicals. Through in vitro and in vivo experiments, we demonstrate that artifact induced by motion can be problematic to distinguish from the characteristic signals associated with recorded action potentials or neurochemical measurements. These results underscore that new electrode materials and recording paradigms can alter the representation of common sources of artifact in vivo and therefore must be carefully characterized.
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spelling pubmed-62152112018-11-06 Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements Nicolai, Evan N. Michelson, Nicholas J. Settell, Megan L. Hara, Seth A. Trevathan, James K. Asp, Anders J. Stocking, Kaylene C. Lujan, J. Luis Kozai, Takashi D.Y. Ludwig, Kip A. Micromachines (Basel) Communication Implantable devices to measure neurochemical or electrical activity from the brain are mainstays of neuroscience research and have become increasingly utilized as enabling components of clinical therapies. In order to increase the number of recording channels on these devices while minimizing the immune response, flexible electrodes under 10 µm in diameter have been proposed as ideal next-generation neural interfaces. However, the representation of motion artifact during neurochemical or electrophysiological recordings using ultra-small, flexible electrodes remains unexplored. In this short communication, we characterize motion artifact generated by the movement of 7 µm diameter carbon fiber electrodes during electrophysiological recordings and fast-scan cyclic voltammetry (FSCV) measurements of electroactive neurochemicals. Through in vitro and in vivo experiments, we demonstrate that artifact induced by motion can be problematic to distinguish from the characteristic signals associated with recorded action potentials or neurochemical measurements. These results underscore that new electrode materials and recording paradigms can alter the representation of common sources of artifact in vivo and therefore must be carefully characterized. MDPI 2018-09-27 /pmc/articles/PMC6215211/ /pubmed/30424427 http://dx.doi.org/10.3390/mi9100494 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Nicolai, Evan N.
Michelson, Nicholas J.
Settell, Megan L.
Hara, Seth A.
Trevathan, James K.
Asp, Anders J.
Stocking, Kaylene C.
Lujan, J. Luis
Kozai, Takashi D.Y.
Ludwig, Kip A.
Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements
title Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements
title_full Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements
title_fullStr Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements
title_full_unstemmed Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements
title_short Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements
title_sort design choices for next-generation neurotechnology can impact motion artifact in electrophysiological and fast-scan cyclic voltammetry measurements
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215211/
https://www.ncbi.nlm.nih.gov/pubmed/30424427
http://dx.doi.org/10.3390/mi9100494
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