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Development of ultra-low volume, multi-bio fluid, cortisol sensing platform
The development of a non-faradaic electrochemical sensor for screening across multiple bio-fluids that demonstrate the expression of cortisol using a gold microelectrode-based sensor is reported in this paper. Room temperature ionic liquid (RTIL), BMIM[BF(4)] was used as the buffer to modulate the e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233171/ https://www.ncbi.nlm.nih.gov/pubmed/30425312 http://dx.doi.org/10.1038/s41598-018-35199-5 |
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author | Upasham, Sayali Tanak, Ambalika Jagannath, Badrinath Prasad, Shalini |
author_facet | Upasham, Sayali Tanak, Ambalika Jagannath, Badrinath Prasad, Shalini |
author_sort | Upasham, Sayali |
collection | PubMed |
description | The development of a non-faradaic electrochemical sensor for screening across multiple bio-fluids that demonstrate the expression of cortisol using a gold microelectrode-based sensor is reported in this paper. Room temperature ionic liquid (RTIL), BMIM[BF(4)] was used as the buffer to modulate the electrical double layer (EDL) to enhance the electrochemical signal response of the sensor. The sensor design and the surface chemistry was optimized using COMSOL Multiphysics software simulations and FTIR respectively. The sensor was designed so that it uses ultra-low volumes between 3–5 µL of bio-fluid for detection. Cortisol detection was achieved in the physiologically relevant ranges when tested in serum, blood, sweat, and, saliva using non-faradaic Electrochemical Impedance Spectroscopy (EIS) and performance parameters of the sensor were determined. Sensor’s response was tested against the only commercially available salivary cortisol point-of-care kit using regression analysis. Cross-reactive studies using prednisone indicated that the sensor is specific for cortisol. The sensor displayed a correlation value i.e. R(2) > 0.95 between the signal response and the concentration of cortisol present in the system. Dynamic range of the sensor was across the physiologically relevant range of cortisol i.e. 50–200 ng/ml for serum/blood, 1–40 ng/ml for saliva, and 10–150 ng/ml for sweat. Limit of detection for serum and sweat was 10 ng/ml and 1 ng/ml for saliva. |
format | Online Article Text |
id | pubmed-6233171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62331712018-11-28 Development of ultra-low volume, multi-bio fluid, cortisol sensing platform Upasham, Sayali Tanak, Ambalika Jagannath, Badrinath Prasad, Shalini Sci Rep Article The development of a non-faradaic electrochemical sensor for screening across multiple bio-fluids that demonstrate the expression of cortisol using a gold microelectrode-based sensor is reported in this paper. Room temperature ionic liquid (RTIL), BMIM[BF(4)] was used as the buffer to modulate the electrical double layer (EDL) to enhance the electrochemical signal response of the sensor. The sensor design and the surface chemistry was optimized using COMSOL Multiphysics software simulations and FTIR respectively. The sensor was designed so that it uses ultra-low volumes between 3–5 µL of bio-fluid for detection. Cortisol detection was achieved in the physiologically relevant ranges when tested in serum, blood, sweat, and, saliva using non-faradaic Electrochemical Impedance Spectroscopy (EIS) and performance parameters of the sensor were determined. Sensor’s response was tested against the only commercially available salivary cortisol point-of-care kit using regression analysis. Cross-reactive studies using prednisone indicated that the sensor is specific for cortisol. The sensor displayed a correlation value i.e. R(2) > 0.95 between the signal response and the concentration of cortisol present in the system. Dynamic range of the sensor was across the physiologically relevant range of cortisol i.e. 50–200 ng/ml for serum/blood, 1–40 ng/ml for saliva, and 10–150 ng/ml for sweat. Limit of detection for serum and sweat was 10 ng/ml and 1 ng/ml for saliva. Nature Publishing Group UK 2018-11-13 /pmc/articles/PMC6233171/ /pubmed/30425312 http://dx.doi.org/10.1038/s41598-018-35199-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Upasham, Sayali Tanak, Ambalika Jagannath, Badrinath Prasad, Shalini Development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
title | Development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
title_full | Development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
title_fullStr | Development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
title_full_unstemmed | Development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
title_short | Development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
title_sort | development of ultra-low volume, multi-bio fluid, cortisol sensing platform |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233171/ https://www.ncbi.nlm.nih.gov/pubmed/30425312 http://dx.doi.org/10.1038/s41598-018-35199-5 |
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