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Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor
Tuberculosis (TB) remains a leading cause of death globally, especially in underdeveloped nations. The main impediment to TB eradication is a lack of efficient diagnostic tools for disease diagnosis. In this work, label free and ultrasensitive electrochemical DNA biosensor for detecting Mycobacteriu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720118/ https://www.ncbi.nlm.nih.gov/pubmed/36479437 http://dx.doi.org/10.3389/fchem.2022.1046930 |
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author | Sharif, M. N. Taufiq, S. Sohail, M. Abbas, S. R. |
author_facet | Sharif, M. N. Taufiq, S. Sohail, M. Abbas, S. R. |
author_sort | Sharif, M. N. |
collection | PubMed |
description | Tuberculosis (TB) remains a leading cause of death globally, especially in underdeveloped nations. The main impediment to TB eradication is a lack of efficient diagnostic tools for disease diagnosis. In this work, label free and ultrasensitive electrochemical DNA biosensor for detecting Mycobacterium tuberculosis has been developed based on the electrodeposition of gold nanoparticles on the surface of carbon screen-printed carbon electrode (Zensors) for signal amplification. Particularly, screen-printed electrodes were modified by electrochemical deposition of Au to enhance the conductivity and facilitate the immobilization of ssDNA probes via Au-S bonds. The electrochemically modified SPEs were characterized using Scanning electron microscopy/Energy Dispersive X-Ray Analysis (SEM/EDX) and X-Ray Diffraction (XRD). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques were used to investigate the DNA hybridization between single-stranded (ssDNA) probe and target DNA (tDNA). Under the ideal conditions, DPV exhibited a correlation coefficient R2 = 0.97, when analyzed with different tDNA concentrations. The proposed DNA biosensor exhibits a good detection range from 2 to 10 nm with a low detection limit of 1.91 nm, as well as high selectivity that, under ideal conditions, distinguishes non-complementary DNA from perfectly matched tDNA. By eliminating the need for DNA purification, this work paves the path for creating disposable biosensors capable of detecting DNA from raw sputum samples. |
format | Online Article Text |
id | pubmed-9720118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97201182022-12-06 Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor Sharif, M. N. Taufiq, S. Sohail, M. Abbas, S. R. Front Chem Chemistry Tuberculosis (TB) remains a leading cause of death globally, especially in underdeveloped nations. The main impediment to TB eradication is a lack of efficient diagnostic tools for disease diagnosis. In this work, label free and ultrasensitive electrochemical DNA biosensor for detecting Mycobacterium tuberculosis has been developed based on the electrodeposition of gold nanoparticles on the surface of carbon screen-printed carbon electrode (Zensors) for signal amplification. Particularly, screen-printed electrodes were modified by electrochemical deposition of Au to enhance the conductivity and facilitate the immobilization of ssDNA probes via Au-S bonds. The electrochemically modified SPEs were characterized using Scanning electron microscopy/Energy Dispersive X-Ray Analysis (SEM/EDX) and X-Ray Diffraction (XRD). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques were used to investigate the DNA hybridization between single-stranded (ssDNA) probe and target DNA (tDNA). Under the ideal conditions, DPV exhibited a correlation coefficient R2 = 0.97, when analyzed with different tDNA concentrations. The proposed DNA biosensor exhibits a good detection range from 2 to 10 nm with a low detection limit of 1.91 nm, as well as high selectivity that, under ideal conditions, distinguishes non-complementary DNA from perfectly matched tDNA. By eliminating the need for DNA purification, this work paves the path for creating disposable biosensors capable of detecting DNA from raw sputum samples. Frontiers Media S.A. 2022-11-21 /pmc/articles/PMC9720118/ /pubmed/36479437 http://dx.doi.org/10.3389/fchem.2022.1046930 Text en Copyright © 2022 Sharif, Taufiq, Sohail and Abbas. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Sharif, M. N. Taufiq, S. Sohail, M. Abbas, S. R. Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor |
title | Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor |
title_full | Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor |
title_fullStr | Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor |
title_full_unstemmed | Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor |
title_short | Tuberculosis detection from raw sputum samples using Au-electroplated screen-printed electrodes as E-DNA sensor |
title_sort | tuberculosis detection from raw sputum samples using au-electroplated screen-printed electrodes as e-dna sensor |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720118/ https://www.ncbi.nlm.nih.gov/pubmed/36479437 http://dx.doi.org/10.3389/fchem.2022.1046930 |
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