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Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay

The efficiency of the diagnostic platforms utilizing ELISA technique or immunoassays depends highly on incubation times of the recognition elements or signaling molecules and volume of the patient samples. In conventional immunoassays, long incubation times and excess amounts of the recognition and...

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Autores principales: Yasun, Emir, Trusty, Travis, Abolhosn, Rania W., Clarke, Nigel J., Mezić, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934526/
https://www.ncbi.nlm.nih.gov/pubmed/31882622
http://dx.doi.org/10.1038/s41598-019-56205-4
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author Yasun, Emir
Trusty, Travis
Abolhosn, Rania W.
Clarke, Nigel J.
Mezić, Igor
author_facet Yasun, Emir
Trusty, Travis
Abolhosn, Rania W.
Clarke, Nigel J.
Mezić, Igor
author_sort Yasun, Emir
collection PubMed
description The efficiency of the diagnostic platforms utilizing ELISA technique or immunoassays depends highly on incubation times of the recognition elements or signaling molecules and volume of the patient samples. In conventional immunoassays, long incubation times and excess amounts of the recognition and signaling molecules are used. The technology proposed here uses electrokinetic mixing of the reagents involved in a sandwich immunoassay based diagnostic assay in electrode-enabled microwell plates in such a way that the incubation times and volumes can be reduced substantially. The integration of the electrodes at the bottom of the conventional microwell plates ensures that the motions of the liquid flows in the wells can be controlled through the application of high frequency AC current along these electrodes. The strategy to generate chaotic mixing by modification of standard multiwell plates, enables its use in high throughput screening, in contrast to microfluidic channel-based technologies that are difficult to incorporate into conventional plates. An immunoassay for detection of glycated hemoglobin (HbA1c) that can reveal a patient’s average level of blood sugar from the past 2–3 months instead of just measuring the current levels and thereby constitutes a reliable diabetes monitoring platform was chosen as a pilot assay for technology demonstration. The overall incubation time for the assay was reduced by approximately a factor of five when electrokinetic mixing was employed. Furthermore, when the quantity of the reagents was reduced by half, almost no distinguishable signals could be obtained with conventional immunoassay, while electrokinetic mixing still facilitated acquisition of signals while varying concentration of the glycated hemoglobin. There was also a substantial difference in the signal intensities especially for the low concentrations of the HbA1c obtained from electrokinetic mixing assisted and conventional immunoassay when the quantity of the reagents and incubation times were kept constant, which is also an indication of the increase in bioassay efficiency. The electrokinetic mixing technique has the potential to improve the efficiency of immunoassay based diagnostic platforms with reduced assay time and reagent amounts, leading to higher throughput analysis of clinical samples. It may also open new avenues in point of care diagnostic devices, where kinetics and sampling size/volume play a critical role.
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spelling pubmed-69345262019-12-29 Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay Yasun, Emir Trusty, Travis Abolhosn, Rania W. Clarke, Nigel J. Mezić, Igor Sci Rep Article The efficiency of the diagnostic platforms utilizing ELISA technique or immunoassays depends highly on incubation times of the recognition elements or signaling molecules and volume of the patient samples. In conventional immunoassays, long incubation times and excess amounts of the recognition and signaling molecules are used. The technology proposed here uses electrokinetic mixing of the reagents involved in a sandwich immunoassay based diagnostic assay in electrode-enabled microwell plates in such a way that the incubation times and volumes can be reduced substantially. The integration of the electrodes at the bottom of the conventional microwell plates ensures that the motions of the liquid flows in the wells can be controlled through the application of high frequency AC current along these electrodes. The strategy to generate chaotic mixing by modification of standard multiwell plates, enables its use in high throughput screening, in contrast to microfluidic channel-based technologies that are difficult to incorporate into conventional plates. An immunoassay for detection of glycated hemoglobin (HbA1c) that can reveal a patient’s average level of blood sugar from the past 2–3 months instead of just measuring the current levels and thereby constitutes a reliable diabetes monitoring platform was chosen as a pilot assay for technology demonstration. The overall incubation time for the assay was reduced by approximately a factor of five when electrokinetic mixing was employed. Furthermore, when the quantity of the reagents was reduced by half, almost no distinguishable signals could be obtained with conventional immunoassay, while electrokinetic mixing still facilitated acquisition of signals while varying concentration of the glycated hemoglobin. There was also a substantial difference in the signal intensities especially for the low concentrations of the HbA1c obtained from electrokinetic mixing assisted and conventional immunoassay when the quantity of the reagents and incubation times were kept constant, which is also an indication of the increase in bioassay efficiency. The electrokinetic mixing technique has the potential to improve the efficiency of immunoassay based diagnostic platforms with reduced assay time and reagent amounts, leading to higher throughput analysis of clinical samples. It may also open new avenues in point of care diagnostic devices, where kinetics and sampling size/volume play a critical role. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934526/ /pubmed/31882622 http://dx.doi.org/10.1038/s41598-019-56205-4 Text en © The Author(s) 2019 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
Yasun, Emir
Trusty, Travis
Abolhosn, Rania W.
Clarke, Nigel J.
Mezić, Igor
Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay
title Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay
title_full Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay
title_fullStr Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay
title_full_unstemmed Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay
title_short Electrokinetic Mixing for Improving the Kinetics of an HbA1c Immunoassay
title_sort electrokinetic mixing for improving the kinetics of an hba1c immunoassay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934526/
https://www.ncbi.nlm.nih.gov/pubmed/31882622
http://dx.doi.org/10.1038/s41598-019-56205-4
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