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Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection

Developing point-of-care (PoC) diagnostic platforms for carcinoembryonic antigen detection is essential. However, thefew implementations of transferring the signal amplification strategies in electrochemical sensing on paper-based platforms are not satisfactory in terms of detection limit (LOD). In...

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Autores principales: Chakraborty, B., Das, A., Mandal, N., Samanta, N., Das, N., Chaudhuri, C. Roy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859218/
https://www.ncbi.nlm.nih.gov/pubmed/33536505
http://dx.doi.org/10.1038/s41598-021-82580-y
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author Chakraborty, B.
Das, A.
Mandal, N.
Samanta, N.
Das, N.
Chaudhuri, C. Roy
author_facet Chakraborty, B.
Das, A.
Mandal, N.
Samanta, N.
Das, N.
Chaudhuri, C. Roy
author_sort Chakraborty, B.
collection PubMed
description Developing point-of-care (PoC) diagnostic platforms for carcinoembryonic antigen detection is essential. However, thefew implementations of transferring the signal amplification strategies in electrochemical sensing on paper-based platforms are not satisfactory in terms of detection limit (LOD). In the quest for pushing down LOD, majority of the research has been targeted towards development of improved nanostructured substrates for entrapping more analyte molecules and augmenting the electron transfer rate to the working electrode. But, such approaches have reached saturation. This paper focuses on enhancing the mass transport of the analyte towards the sensor surface through the application of an electric field, in graphene-ZnO nanorods heterostructure. These hybrid nanostructures have been deposited on flexible polyethylene terephthalate substrates with screen printed electrodes for PoC application. The ZnO nanorods have been functionalized with aptamers and the working sensor has been integrated with smartphone interfaced indigenously developed low cost potentiostat. The performance of the system, requiring only 50 µl analyte has been evaluated using electrochemical impedance spectroscopy and validated against commercially available ELISA kit. Limit of detection of 1 fg/ml in human serum with 6.5% coefficient of variation has been demonstrated, which is more than three orders of magnitude lower than the existing attempts on PoC device.
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spelling pubmed-78592182021-02-04 Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection Chakraborty, B. Das, A. Mandal, N. Samanta, N. Das, N. Chaudhuri, C. Roy Sci Rep Article Developing point-of-care (PoC) diagnostic platforms for carcinoembryonic antigen detection is essential. However, thefew implementations of transferring the signal amplification strategies in electrochemical sensing on paper-based platforms are not satisfactory in terms of detection limit (LOD). In the quest for pushing down LOD, majority of the research has been targeted towards development of improved nanostructured substrates for entrapping more analyte molecules and augmenting the electron transfer rate to the working electrode. But, such approaches have reached saturation. This paper focuses on enhancing the mass transport of the analyte towards the sensor surface through the application of an electric field, in graphene-ZnO nanorods heterostructure. These hybrid nanostructures have been deposited on flexible polyethylene terephthalate substrates with screen printed electrodes for PoC application. The ZnO nanorods have been functionalized with aptamers and the working sensor has been integrated with smartphone interfaced indigenously developed low cost potentiostat. The performance of the system, requiring only 50 µl analyte has been evaluated using electrochemical impedance spectroscopy and validated against commercially available ELISA kit. Limit of detection of 1 fg/ml in human serum with 6.5% coefficient of variation has been demonstrated, which is more than three orders of magnitude lower than the existing attempts on PoC device. Nature Publishing Group UK 2021-02-03 /pmc/articles/PMC7859218/ /pubmed/33536505 http://dx.doi.org/10.1038/s41598-021-82580-y Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chakraborty, B.
Das, A.
Mandal, N.
Samanta, N.
Das, N.
Chaudhuri, C. Roy
Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection
title Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection
title_full Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection
title_fullStr Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection
title_full_unstemmed Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection
title_short Label free, electric field mediated ultrasensitive electrochemical point-of-care device for CEA detection
title_sort label free, electric field mediated ultrasensitive electrochemical point-of-care device for cea detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859218/
https://www.ncbi.nlm.nih.gov/pubmed/33536505
http://dx.doi.org/10.1038/s41598-021-82580-y
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