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Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis

Serum level of CCL5 chemokine is considered an emerging biomarker for multiple sclerosis (MS). Due to the lack of specific assays for this disease, the development of a point-of-care test for rapid detection of MS could lead to avoiding diagnostics delays. In this paper, we report the first electroc...

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Autores principales: Guerrero, Sara, Sánchez-Tirado, Esther, Agüí, Lourdes, González-Cortés, Araceli, Yáñez-Sedeño, Paloma, Pingarrón, José M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406078/
https://www.ncbi.nlm.nih.gov/pubmed/36005006
http://dx.doi.org/10.3390/bios12080610
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author Guerrero, Sara
Sánchez-Tirado, Esther
Agüí, Lourdes
González-Cortés, Araceli
Yáñez-Sedeño, Paloma
Pingarrón, José M.
author_facet Guerrero, Sara
Sánchez-Tirado, Esther
Agüí, Lourdes
González-Cortés, Araceli
Yáñez-Sedeño, Paloma
Pingarrón, José M.
author_sort Guerrero, Sara
collection PubMed
description Serum level of CCL5 chemokine is considered an emerging biomarker for multiple sclerosis (MS). Due to the lack of specific assays for this disease, the development of a point-of-care test for rapid detection of MS could lead to avoiding diagnostics delays. In this paper, we report the first electrochemical immunoplatform for quantification of the CCL5 biomarker at the clinically required levels, able to discriminate between patients diagnosed with MS and healthy individuals. The immunosensing device involves protein capture from biological samples by complexation with biotinylated specific antibodies immobilized onto neutravidin-functionalized microparticles and sandwich assay with anti-CCL5 antibody and IgG labelled with horseradish peroxidase (HRP) for the enzyme-catalyzed amperometric detection of H(2)O(2) using hydroquinone (HQ) as the redox mediator. The method shows excellent analytical performance for clinical application with a wide linear range of concentrations (0.1–300 ng·mL(−1) CCL5, R(2) = 0.998) and a low detection limit (40 pg·mL(−1) CCL5). The biosensing platform was applied to the determination of the CCL5 endogenous content in 100-fold diluted sera both from healthy individuals and patients diagnosed with MS, with no further sample treatment in just two hours. The results were successfully compared with those obtained by the ELISA methodology.
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spelling pubmed-94060782022-08-26 Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis Guerrero, Sara Sánchez-Tirado, Esther Agüí, Lourdes González-Cortés, Araceli Yáñez-Sedeño, Paloma Pingarrón, José M. Biosensors (Basel) Article Serum level of CCL5 chemokine is considered an emerging biomarker for multiple sclerosis (MS). Due to the lack of specific assays for this disease, the development of a point-of-care test for rapid detection of MS could lead to avoiding diagnostics delays. In this paper, we report the first electrochemical immunoplatform for quantification of the CCL5 biomarker at the clinically required levels, able to discriminate between patients diagnosed with MS and healthy individuals. The immunosensing device involves protein capture from biological samples by complexation with biotinylated specific antibodies immobilized onto neutravidin-functionalized microparticles and sandwich assay with anti-CCL5 antibody and IgG labelled with horseradish peroxidase (HRP) for the enzyme-catalyzed amperometric detection of H(2)O(2) using hydroquinone (HQ) as the redox mediator. The method shows excellent analytical performance for clinical application with a wide linear range of concentrations (0.1–300 ng·mL(−1) CCL5, R(2) = 0.998) and a low detection limit (40 pg·mL(−1) CCL5). The biosensing platform was applied to the determination of the CCL5 endogenous content in 100-fold diluted sera both from healthy individuals and patients diagnosed with MS, with no further sample treatment in just two hours. The results were successfully compared with those obtained by the ELISA methodology. MDPI 2022-08-07 /pmc/articles/PMC9406078/ /pubmed/36005006 http://dx.doi.org/10.3390/bios12080610 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guerrero, Sara
Sánchez-Tirado, Esther
Agüí, Lourdes
González-Cortés, Araceli
Yáñez-Sedeño, Paloma
Pingarrón, José M.
Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis
title Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis
title_full Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis
title_fullStr Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis
title_full_unstemmed Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis
title_short Development of an Electrochemical CCL5 Chemokine Immunoplatform for Rapid Diagnosis of Multiple Sclerosis
title_sort development of an electrochemical ccl5 chemokine immunoplatform for rapid diagnosis of multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406078/
https://www.ncbi.nlm.nih.gov/pubmed/36005006
http://dx.doi.org/10.3390/bios12080610
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