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Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker

[Image: see text] The traditional three-electrode electrochemical system used in the development of biosensors for detecting various biomarkers of interest necessitates the use of bulk electrodes, which precludes the deployment of handheld electrochemical devices in clinical applications. Affordable...

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Autores principales: Lakshmanakumar, Muthaiyan, Nesakumar, Noel, Sethuraman, Swaminathan, S, Rajan K., Krishnan, Uma Maheswari, Rayappan, John Bosco Balaguru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655768/
https://www.ncbi.nlm.nih.gov/pubmed/34901602
http://dx.doi.org/10.1021/acsomega.1c04043
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author Lakshmanakumar, Muthaiyan
Nesakumar, Noel
Sethuraman, Swaminathan
S, Rajan K.
Krishnan, Uma Maheswari
Rayappan, John Bosco Balaguru
author_facet Lakshmanakumar, Muthaiyan
Nesakumar, Noel
Sethuraman, Swaminathan
S, Rajan K.
Krishnan, Uma Maheswari
Rayappan, John Bosco Balaguru
author_sort Lakshmanakumar, Muthaiyan
collection PubMed
description [Image: see text] The traditional three-electrode electrochemical system used in the development of biosensors for detecting various biomarkers of interest necessitates the use of bulk electrodes, which precludes the deployment of handheld electrochemical devices in clinical applications. Affordable screen-printed carbon electrodes (SPCEs) modified with functional interfaces are being developed to enhance the sensitivity of a compact sensing system as a whole. In this work, SPCEs were fabricated on an overhead projection (OHP) sheet in three different active areas of 2 × 2, 3 × 3, and 4 × 4 mm(2) using a screen printing technique, and then ∼2 nm sized graphene quantum dots (GQDs) were electrodeposited over the SPCE surface to add functionality for the detection of ultralow levels of one of the cardiac biomarkers, C-reactive protein (CRP). The proposed mediator-dependent voltammetric biosensor exhibited good sensitivity, a low detection limit, and a linear range of 2.45 μA ng(–1) mL(–1) cm(–2), 0.036 ng mL(–1), and 0.5–10 ng mL(–1), respectively. The fabricated SPCE/GQDs/anti-CRP biosensor could rapidly detect CRP in less than 25 s. The intra- and interassays were performed with five sensor strips, which showed a minimum standard deviation of 1.85 and 2.8%, respectively. The SPCE/GQDs/anti-CRP electrode was used to detect CRP concentrations in a ringer lactate solution. Thus, the developed biosensor has all of the characteristics such as rapidity, inexpensive disposable electrodes, miniaturization, and a lower detection limit needed to evolve as a point-of-care (PoC) application.
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spelling pubmed-86557682021-12-10 Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker Lakshmanakumar, Muthaiyan Nesakumar, Noel Sethuraman, Swaminathan S, Rajan K. Krishnan, Uma Maheswari Rayappan, John Bosco Balaguru ACS Omega [Image: see text] The traditional three-electrode electrochemical system used in the development of biosensors for detecting various biomarkers of interest necessitates the use of bulk electrodes, which precludes the deployment of handheld electrochemical devices in clinical applications. Affordable screen-printed carbon electrodes (SPCEs) modified with functional interfaces are being developed to enhance the sensitivity of a compact sensing system as a whole. In this work, SPCEs were fabricated on an overhead projection (OHP) sheet in three different active areas of 2 × 2, 3 × 3, and 4 × 4 mm(2) using a screen printing technique, and then ∼2 nm sized graphene quantum dots (GQDs) were electrodeposited over the SPCE surface to add functionality for the detection of ultralow levels of one of the cardiac biomarkers, C-reactive protein (CRP). The proposed mediator-dependent voltammetric biosensor exhibited good sensitivity, a low detection limit, and a linear range of 2.45 μA ng(–1) mL(–1) cm(–2), 0.036 ng mL(–1), and 0.5–10 ng mL(–1), respectively. The fabricated SPCE/GQDs/anti-CRP biosensor could rapidly detect CRP in less than 25 s. The intra- and interassays were performed with five sensor strips, which showed a minimum standard deviation of 1.85 and 2.8%, respectively. The SPCE/GQDs/anti-CRP electrode was used to detect CRP concentrations in a ringer lactate solution. Thus, the developed biosensor has all of the characteristics such as rapidity, inexpensive disposable electrodes, miniaturization, and a lower detection limit needed to evolve as a point-of-care (PoC) application. American Chemical Society 2021-11-22 /pmc/articles/PMC8655768/ /pubmed/34901602 http://dx.doi.org/10.1021/acsomega.1c04043 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Lakshmanakumar, Muthaiyan
Nesakumar, Noel
Sethuraman, Swaminathan
S, Rajan K.
Krishnan, Uma Maheswari
Rayappan, John Bosco Balaguru
Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker
title Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker
title_full Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker
title_fullStr Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker
title_full_unstemmed Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker
title_short Fabrication of GQD-Electrodeposited Screen-Printed Carbon Electrodes for the Detection of the CRP Biomarker
title_sort fabrication of gqd-electrodeposited screen-printed carbon electrodes for the detection of the crp biomarker
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655768/
https://www.ncbi.nlm.nih.gov/pubmed/34901602
http://dx.doi.org/10.1021/acsomega.1c04043
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