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Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex

Implantable microelectrode arrays (MEAs) enable the recording of electrical activity of cortical neurons, allowing the development of brain-machine interfaces. However, MEAs show reduced recording capabilities under chronic conditions, prompting the development of novel MEAs that can improve long-te...

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Autores principales: Jeakle, Eleanor N., Abbott, Justin R., Usoro, Joshua O., Wu, Yupeng, Haghighi, Pegah, Radhakrishna, Rahul, Sturgill, Brandon S., Nakajima, Shido, Thai, Teresa T. D., Pancrazio, Joseph J., Cogan, Stuart F., Hernandez-Reynoso, Ana G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054633/
https://www.ncbi.nlm.nih.gov/pubmed/36985087
http://dx.doi.org/10.3390/mi14030680
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author Jeakle, Eleanor N.
Abbott, Justin R.
Usoro, Joshua O.
Wu, Yupeng
Haghighi, Pegah
Radhakrishna, Rahul
Sturgill, Brandon S.
Nakajima, Shido
Thai, Teresa T. D.
Pancrazio, Joseph J.
Cogan, Stuart F.
Hernandez-Reynoso, Ana G.
author_facet Jeakle, Eleanor N.
Abbott, Justin R.
Usoro, Joshua O.
Wu, Yupeng
Haghighi, Pegah
Radhakrishna, Rahul
Sturgill, Brandon S.
Nakajima, Shido
Thai, Teresa T. D.
Pancrazio, Joseph J.
Cogan, Stuart F.
Hernandez-Reynoso, Ana G.
author_sort Jeakle, Eleanor N.
collection PubMed
description Implantable microelectrode arrays (MEAs) enable the recording of electrical activity of cortical neurons, allowing the development of brain-machine interfaces. However, MEAs show reduced recording capabilities under chronic conditions, prompting the development of novel MEAs that can improve long-term performance. Conventional planar, silicon-based devices and ultra-thin amorphous silicon carbide (a-SiC) MEAs were implanted in the motor cortex of female Sprague–Dawley rats, and weekly anesthetized recordings were made for 16 weeks after implantation. The spectral density and bandpower between 1 and 500 Hz of recordings were compared over the implantation period for both device types. Initially, the bandpower of the a-SiC devices and standard MEAs was comparable. However, the standard MEAs showed a consistent decline in both bandpower and power spectral density throughout the 16 weeks post-implantation, whereas the a-SiC MEAs showed substantially more stable performance. These differences in bandpower and spectral density between standard and a-SiC MEAs were statistically significant from week 6 post-implantation until the end of the study at 16 weeks. These results support the use of ultra-thin a-SiC MEAs to develop chronic, reliable brain-machine interfaces.
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spelling pubmed-100546332023-03-30 Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex Jeakle, Eleanor N. Abbott, Justin R. Usoro, Joshua O. Wu, Yupeng Haghighi, Pegah Radhakrishna, Rahul Sturgill, Brandon S. Nakajima, Shido Thai, Teresa T. D. Pancrazio, Joseph J. Cogan, Stuart F. Hernandez-Reynoso, Ana G. Micromachines (Basel) Article Implantable microelectrode arrays (MEAs) enable the recording of electrical activity of cortical neurons, allowing the development of brain-machine interfaces. However, MEAs show reduced recording capabilities under chronic conditions, prompting the development of novel MEAs that can improve long-term performance. Conventional planar, silicon-based devices and ultra-thin amorphous silicon carbide (a-SiC) MEAs were implanted in the motor cortex of female Sprague–Dawley rats, and weekly anesthetized recordings were made for 16 weeks after implantation. The spectral density and bandpower between 1 and 500 Hz of recordings were compared over the implantation period for both device types. Initially, the bandpower of the a-SiC devices and standard MEAs was comparable. However, the standard MEAs showed a consistent decline in both bandpower and power spectral density throughout the 16 weeks post-implantation, whereas the a-SiC MEAs showed substantially more stable performance. These differences in bandpower and spectral density between standard and a-SiC MEAs were statistically significant from week 6 post-implantation until the end of the study at 16 weeks. These results support the use of ultra-thin a-SiC MEAs to develop chronic, reliable brain-machine interfaces. MDPI 2023-03-19 /pmc/articles/PMC10054633/ /pubmed/36985087 http://dx.doi.org/10.3390/mi14030680 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jeakle, Eleanor N.
Abbott, Justin R.
Usoro, Joshua O.
Wu, Yupeng
Haghighi, Pegah
Radhakrishna, Rahul
Sturgill, Brandon S.
Nakajima, Shido
Thai, Teresa T. D.
Pancrazio, Joseph J.
Cogan, Stuart F.
Hernandez-Reynoso, Ana G.
Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex
title Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex
title_full Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex
title_fullStr Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex
title_full_unstemmed Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex
title_short Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex
title_sort chronic stability of local field potentials using amorphous silicon carbide microelectrode arrays implanted in the rat motor cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054633/
https://www.ncbi.nlm.nih.gov/pubmed/36985087
http://dx.doi.org/10.3390/mi14030680
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