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Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification

Prostate cancer is a disease with a high incidence and mortality rate in men worldwide. Serum prostate-specific antigens (PSA) are the main circulating biomarker for this disease in clinical practices. In this work, we present a portable and reusable microfluidic device for PSA quantification. This...

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Autores principales: Felici, Emiliano, Regiart, Matías D., Pereira, Sirley V., Ortega, Francisco G., Angnes, Lúcio, Messina, Germán A., Fernández-Baldo, Martín A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046291/
https://www.ncbi.nlm.nih.gov/pubmed/36979602
http://dx.doi.org/10.3390/bios13030390
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author Felici, Emiliano
Regiart, Matías D.
Pereira, Sirley V.
Ortega, Francisco G.
Angnes, Lúcio
Messina, Germán A.
Fernández-Baldo, Martín A.
author_facet Felici, Emiliano
Regiart, Matías D.
Pereira, Sirley V.
Ortega, Francisco G.
Angnes, Lúcio
Messina, Germán A.
Fernández-Baldo, Martín A.
author_sort Felici, Emiliano
collection PubMed
description Prostate cancer is a disease with a high incidence and mortality rate in men worldwide. Serum prostate-specific antigens (PSA) are the main circulating biomarker for this disease in clinical practices. In this work, we present a portable and reusable microfluidic device for PSA quantification. This device comprises a polymethyl methacrylate microfluidic platform coupled with electrochemical detection. The platinum working microelectrode was positioned in the outflow region of the microchannel and was modified with carbon nanofibers (CNF)-decorated gold nanoporous (GNP) structures by the dynamic hydrogen bubble template method, through the simultaneous electrodeposition of metal precursors in the presence of CNF. CNF/GNP structures exhibit attractive properties, such as a large surface to volume ratio, which increases the antibody’s immobilization capacity and the electroactive area. CNFs/GNP structures were characterized by scanning electron microscopy, energy dispersive spectrometry, and cyclic voltammetry. Anti-PSA antibodies and HRP were employed for the immune-electrochemical reaction. The detection limit for the device was 5 pg mL(−1), with a linear range from 0.01 to 50 ng mL(−1). The coefficients of variation within and between assays were lower than 4.40%, and 6.15%, respectively. Additionally, its clinical performance was tested in serum from 30 prostate cancer patients. This novel device was a sensitive, selective, portable, and reusable tool for the serological diagnosis and monitoring of prostate cancer.
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spelling pubmed-100462912023-03-29 Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification Felici, Emiliano Regiart, Matías D. Pereira, Sirley V. Ortega, Francisco G. Angnes, Lúcio Messina, Germán A. Fernández-Baldo, Martín A. Biosensors (Basel) Article Prostate cancer is a disease with a high incidence and mortality rate in men worldwide. Serum prostate-specific antigens (PSA) are the main circulating biomarker for this disease in clinical practices. In this work, we present a portable and reusable microfluidic device for PSA quantification. This device comprises a polymethyl methacrylate microfluidic platform coupled with electrochemical detection. The platinum working microelectrode was positioned in the outflow region of the microchannel and was modified with carbon nanofibers (CNF)-decorated gold nanoporous (GNP) structures by the dynamic hydrogen bubble template method, through the simultaneous electrodeposition of metal precursors in the presence of CNF. CNF/GNP structures exhibit attractive properties, such as a large surface to volume ratio, which increases the antibody’s immobilization capacity and the electroactive area. CNFs/GNP structures were characterized by scanning electron microscopy, energy dispersive spectrometry, and cyclic voltammetry. Anti-PSA antibodies and HRP were employed for the immune-electrochemical reaction. The detection limit for the device was 5 pg mL(−1), with a linear range from 0.01 to 50 ng mL(−1). The coefficients of variation within and between assays were lower than 4.40%, and 6.15%, respectively. Additionally, its clinical performance was tested in serum from 30 prostate cancer patients. This novel device was a sensitive, selective, portable, and reusable tool for the serological diagnosis and monitoring of prostate cancer. MDPI 2023-03-16 /pmc/articles/PMC10046291/ /pubmed/36979602 http://dx.doi.org/10.3390/bios13030390 Text en © 2023 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
Felici, Emiliano
Regiart, Matías D.
Pereira, Sirley V.
Ortega, Francisco G.
Angnes, Lúcio
Messina, Germán A.
Fernández-Baldo, Martín A.
Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification
title Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification
title_full Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification
title_fullStr Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification
title_full_unstemmed Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification
title_short Microfluidic Platform Integrated with Carbon Nanofibers-Decorated Gold Nanoporous Sensing Device for Serum PSA Quantification
title_sort microfluidic platform integrated with carbon nanofibers-decorated gold nanoporous sensing device for serum psa quantification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046291/
https://www.ncbi.nlm.nih.gov/pubmed/36979602
http://dx.doi.org/10.3390/bios13030390
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