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On-chip testing of a carbon-based platform for electro-adsorption of glutamate

It is known that excessive concentrations of glutamate in the brain can cause neurotoxicity. A common approach to neutralizing this phenomenon is the use of suppressant drugs. However, excessive dependence on suppressant drugs could potentially lead to adversarial side effects, such as drug addictio...

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Autores principales: Whulanza, Y., Arafat, Y.B., Rahman, S.F., Utomo, M.S., Kassegne, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133582/
https://www.ncbi.nlm.nih.gov/pubmed/35647339
http://dx.doi.org/10.1016/j.heliyon.2022.e09445
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author Whulanza, Y.
Arafat, Y.B.
Rahman, S.F.
Utomo, M.S.
Kassegne, S.
author_facet Whulanza, Y.
Arafat, Y.B.
Rahman, S.F.
Utomo, M.S.
Kassegne, S.
author_sort Whulanza, Y.
collection PubMed
description It is known that excessive concentrations of glutamate in the brain can cause neurotoxicity. A common approach to neutralizing this phenomenon is the use of suppressant drugs. However, excessive dependence on suppressant drugs could potentially lead to adversarial side effects, such as drug addiction. Here, we propose an alternative approach to this problem by controlling excessive amounts of glutamate ions through carbon-based, neural implant–mediated uptake. In this study, we introduce a microfluidic system that enables us to emulate the uptake of glutamate into the carbon matrix. The uptake is controlled using electrical pulses to incorporate glutamate ions into the carbon matrix through electro-adsorption. The effect of electric potential on glutamate ion uptake to control the amount of glutamate released into the microfluidic system was observed. The glutamate concentration was measured using a Ultra Violet-Visible spectrophotometer. The current setup demonstrated that a low pulsatile electric potential (0.5–1.5 V) was able to effectively govern the uptake of glutamate ions. The stimulated carbon matrix was able to decrease glutamate concentration by up to 40%. Furthermore, our study shows that these “entrapped” glutamate molecules can be effectively released upon electrical stimulation, thereby reversing the carbon electrical charge through a process called reverse uptake. A release model was used to study the profile of glutamate release from the carbon matrix at a potential of 0–1.5 V. This study showed that a burst release of glutamate was evident at an applied voltage higher than 0.5 V. Ultimately, the MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) test for cytotoxicity indicated a cell viability of more than 80% for the carbon matrix. This test demonstrates that the carbon matrix can support the proliferation of cells and has a nontoxic composition; thus, it could be accepted as a candidate material for use as neural implants.
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spelling pubmed-91335822022-05-27 On-chip testing of a carbon-based platform for electro-adsorption of glutamate Whulanza, Y. Arafat, Y.B. Rahman, S.F. Utomo, M.S. Kassegne, S. Heliyon Research Article It is known that excessive concentrations of glutamate in the brain can cause neurotoxicity. A common approach to neutralizing this phenomenon is the use of suppressant drugs. However, excessive dependence on suppressant drugs could potentially lead to adversarial side effects, such as drug addiction. Here, we propose an alternative approach to this problem by controlling excessive amounts of glutamate ions through carbon-based, neural implant–mediated uptake. In this study, we introduce a microfluidic system that enables us to emulate the uptake of glutamate into the carbon matrix. The uptake is controlled using electrical pulses to incorporate glutamate ions into the carbon matrix through electro-adsorption. The effect of electric potential on glutamate ion uptake to control the amount of glutamate released into the microfluidic system was observed. The glutamate concentration was measured using a Ultra Violet-Visible spectrophotometer. The current setup demonstrated that a low pulsatile electric potential (0.5–1.5 V) was able to effectively govern the uptake of glutamate ions. The stimulated carbon matrix was able to decrease glutamate concentration by up to 40%. Furthermore, our study shows that these “entrapped” glutamate molecules can be effectively released upon electrical stimulation, thereby reversing the carbon electrical charge through a process called reverse uptake. A release model was used to study the profile of glutamate release from the carbon matrix at a potential of 0–1.5 V. This study showed that a burst release of glutamate was evident at an applied voltage higher than 0.5 V. Ultimately, the MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) test for cytotoxicity indicated a cell viability of more than 80% for the carbon matrix. This test demonstrates that the carbon matrix can support the proliferation of cells and has a nontoxic composition; thus, it could be accepted as a candidate material for use as neural implants. Elsevier 2022-05-16 /pmc/articles/PMC9133582/ /pubmed/35647339 http://dx.doi.org/10.1016/j.heliyon.2022.e09445 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Whulanza, Y.
Arafat, Y.B.
Rahman, S.F.
Utomo, M.S.
Kassegne, S.
On-chip testing of a carbon-based platform for electro-adsorption of glutamate
title On-chip testing of a carbon-based platform for electro-adsorption of glutamate
title_full On-chip testing of a carbon-based platform for electro-adsorption of glutamate
title_fullStr On-chip testing of a carbon-based platform for electro-adsorption of glutamate
title_full_unstemmed On-chip testing of a carbon-based platform for electro-adsorption of glutamate
title_short On-chip testing of a carbon-based platform for electro-adsorption of glutamate
title_sort on-chip testing of a carbon-based platform for electro-adsorption of glutamate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133582/
https://www.ncbi.nlm.nih.gov/pubmed/35647339
http://dx.doi.org/10.1016/j.heliyon.2022.e09445
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