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Novel Design of a Layered Electrochemical Dopamine Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified Gold Electrode
[Image: see text] Change in the level of dopamine (DA) concentration in the human body causes critical diseases such as schizophrenia and Parkinson’s disease. Therefore, the determination of DA concentration and monitoring its level in human body fluids is of great importance. An electrochemical sen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6843716/ https://www.ncbi.nlm.nih.gov/pubmed/31720498 http://dx.doi.org/10.1021/acsomega.9b01222 |
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author | Atta, Nada F. Galal, Ahmed El-Said, Dalia M. |
author_facet | Atta, Nada F. Galal, Ahmed El-Said, Dalia M. |
author_sort | Atta, Nada F. |
collection | PubMed |
description | [Image: see text] Change in the level of dopamine (DA) concentration in the human body causes critical diseases such as schizophrenia and Parkinson’s disease. Therefore, the determination of DA concentration and monitoring its level in human body fluids is of great importance. An electrochemical sensor based on modification of the gold electrode surface with Nafion (NF), β-cyclodextrin (CD), and gold nanoparticles (AuNPs) was fabricated for the determination of DA in biological fluids. Combined impact of all the modifiers enhances the catalytic activity of the sensor. Gold nanoparticles increase the surface area of the sensor and enhance the electron transfer rate. CD plays a main role in enhancing the accumulation of protonated DA and forming stable complexes via electrostatic interactions and hydrogen bond formation. In addition, extra preconcentration of positively charged DA is achieved through ionic selectivity of NF. High electrocatalytic activity was achieved using the modified sensor for determination of DA in real urine samples in a wide concentration range, 0.05–280 μM with a low detection limit of 0.6 nM in the small linear dynamic range, 0.05–20 μM. Furthermore, common overlapped oxidation peaks of DA in presence of biologically interfering compounds at the gold electrode were resolved by using the modified sensor. Excellent recovery results were obtained using the proposed method for determination of DA in real urine samples. |
format | Online Article Text |
id | pubmed-6843716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-68437162019-11-12 Novel Design of a Layered Electrochemical Dopamine Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified Gold Electrode Atta, Nada F. Galal, Ahmed El-Said, Dalia M. ACS Omega [Image: see text] Change in the level of dopamine (DA) concentration in the human body causes critical diseases such as schizophrenia and Parkinson’s disease. Therefore, the determination of DA concentration and monitoring its level in human body fluids is of great importance. An electrochemical sensor based on modification of the gold electrode surface with Nafion (NF), β-cyclodextrin (CD), and gold nanoparticles (AuNPs) was fabricated for the determination of DA in biological fluids. Combined impact of all the modifiers enhances the catalytic activity of the sensor. Gold nanoparticles increase the surface area of the sensor and enhance the electron transfer rate. CD plays a main role in enhancing the accumulation of protonated DA and forming stable complexes via electrostatic interactions and hydrogen bond formation. In addition, extra preconcentration of positively charged DA is achieved through ionic selectivity of NF. High electrocatalytic activity was achieved using the modified sensor for determination of DA in real urine samples in a wide concentration range, 0.05–280 μM with a low detection limit of 0.6 nM in the small linear dynamic range, 0.05–20 μM. Furthermore, common overlapped oxidation peaks of DA in presence of biologically interfering compounds at the gold electrode were resolved by using the modified sensor. Excellent recovery results were obtained using the proposed method for determination of DA in real urine samples. American Chemical Society 2019-10-24 /pmc/articles/PMC6843716/ /pubmed/31720498 http://dx.doi.org/10.1021/acsomega.9b01222 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Atta, Nada F. Galal, Ahmed El-Said, Dalia M. Novel Design of a Layered Electrochemical Dopamine Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified Gold Electrode |
title | Novel Design of a Layered Electrochemical Dopamine
Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified
Gold Electrode |
title_full | Novel Design of a Layered Electrochemical Dopamine
Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified
Gold Electrode |
title_fullStr | Novel Design of a Layered Electrochemical Dopamine
Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified
Gold Electrode |
title_full_unstemmed | Novel Design of a Layered Electrochemical Dopamine
Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified
Gold Electrode |
title_short | Novel Design of a Layered Electrochemical Dopamine
Sensor in Real Samples Based on Gold Nanoparticles/β-Cyclodextrin/Nafion-Modified
Gold Electrode |
title_sort | novel design of a layered electrochemical dopamine
sensor in real samples based on gold nanoparticles/β-cyclodextrin/nafion-modified
gold electrode |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6843716/ https://www.ncbi.nlm.nih.gov/pubmed/31720498 http://dx.doi.org/10.1021/acsomega.9b01222 |
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