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Synthesis, Follow-Up, and Characterization of Polydopamine-like Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations
[Image: see text] The understanding of oxidized species derived from the neurotransmitter dopamine (DA) is a relevant topic for both the medical field (Parkinson’s disease) as well as for the field of materials science where the formation process of polydopamine (PDA) films is an active area of rese...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330902/ https://www.ncbi.nlm.nih.gov/pubmed/32637775 http://dx.doi.org/10.1021/acsomega.0c00676 |
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author | Jaramillo, Andrés M. Barrera-Gutiérrez, Ricardo Cortés, María T. |
author_facet | Jaramillo, Andrés M. Barrera-Gutiérrez, Ricardo Cortés, María T. |
author_sort | Jaramillo, Andrés M. |
collection | PubMed |
description | [Image: see text] The understanding of oxidized species derived from the neurotransmitter dopamine (DA) is a relevant topic for both the medical field (Parkinson’s disease) as well as for the field of materials science where the formation process of polydopamine (PDA) films is an active area of research. Polymers that interact strongly with almost all surfaces but have a low electrical conductivity have been obtained by the chemical oxidation of DA. Since electrical conductivity is a desired property for several applications, deposition alternatives such as electrochemical PDA synthesis have been proposed, but the results are still insufficient. In this context, we propose a new PDA chemical–electrochemical deposition process on glassy carbon electrodes. The chemical oxidation step that converts dopamine into dopamine-o-quinone previous to the electrochemical deposition was crucial to decrease the precursor concentration to the micromolar range. The PDA-like films synthesized by this method had high adhesion and low charge-transfer resistance, which was evidenced by impedance measurements and the successful electrodeposition of a polypyrrole coating on top of a PDA-like film. In addition, we observed that anodization of GC surfaces increases sensitivity toward six electroactive couples derived from DA oxidation in the pH regimes studied. These results show the complexity of the intermediates formed during the electrochemical polymerization of PDA. |
format | Online Article Text |
id | pubmed-7330902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73309022020-07-06 Synthesis, Follow-Up, and Characterization of Polydopamine-like Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations Jaramillo, Andrés M. Barrera-Gutiérrez, Ricardo Cortés, María T. ACS Omega [Image: see text] The understanding of oxidized species derived from the neurotransmitter dopamine (DA) is a relevant topic for both the medical field (Parkinson’s disease) as well as for the field of materials science where the formation process of polydopamine (PDA) films is an active area of research. Polymers that interact strongly with almost all surfaces but have a low electrical conductivity have been obtained by the chemical oxidation of DA. Since electrical conductivity is a desired property for several applications, deposition alternatives such as electrochemical PDA synthesis have been proposed, but the results are still insufficient. In this context, we propose a new PDA chemical–electrochemical deposition process on glassy carbon electrodes. The chemical oxidation step that converts dopamine into dopamine-o-quinone previous to the electrochemical deposition was crucial to decrease the precursor concentration to the micromolar range. The PDA-like films synthesized by this method had high adhesion and low charge-transfer resistance, which was evidenced by impedance measurements and the successful electrodeposition of a polypyrrole coating on top of a PDA-like film. In addition, we observed that anodization of GC surfaces increases sensitivity toward six electroactive couples derived from DA oxidation in the pH regimes studied. These results show the complexity of the intermediates formed during the electrochemical polymerization of PDA. American Chemical Society 2020-06-19 /pmc/articles/PMC7330902/ /pubmed/32637775 http://dx.doi.org/10.1021/acsomega.0c00676 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Jaramillo, Andrés M. Barrera-Gutiérrez, Ricardo Cortés, María T. Synthesis, Follow-Up, and Characterization of Polydopamine-like Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations |
title | Synthesis, Follow-Up, and Characterization of Polydopamine-like
Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations |
title_full | Synthesis, Follow-Up, and Characterization of Polydopamine-like
Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations |
title_fullStr | Synthesis, Follow-Up, and Characterization of Polydopamine-like
Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations |
title_full_unstemmed | Synthesis, Follow-Up, and Characterization of Polydopamine-like
Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations |
title_short | Synthesis, Follow-Up, and Characterization of Polydopamine-like
Coatings Departing from Micromolar Dopamine-o-Quinone Precursor Concentrations |
title_sort | synthesis, follow-up, and characterization of polydopamine-like
coatings departing from micromolar dopamine-o-quinone precursor concentrations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330902/ https://www.ncbi.nlm.nih.gov/pubmed/32637775 http://dx.doi.org/10.1021/acsomega.0c00676 |
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