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Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection
This work describes for the first time the integration of Dye Sensitized Solar Cell (DSSC) technology in biosensors and biomimetic materials, opening doors towards a new dimension of autonomous screening devices that may be used in point-of-care, with zero-power requirements. DSSCs are fabricated wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033912/ https://www.ncbi.nlm.nih.gov/pubmed/29977025 http://dx.doi.org/10.1038/s41598-018-27884-2 |
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author | Moreira, Felismina T. C. Truta, Liliana A. A. N. A. Sales, M. Goreti F. |
author_facet | Moreira, Felismina T. C. Truta, Liliana A. A. N. A. Sales, M. Goreti F. |
author_sort | Moreira, Felismina T. C. |
collection | PubMed |
description | This work describes for the first time the integration of Dye Sensitized Solar Cell (DSSC) technology in biosensors and biomimetic materials, opening doors towards a new dimension of autonomous screening devices that may be used in point-of-care, with zero-power requirements. DSSCs are fabricated with a counter electrode (CE) of polypyrrole (PPy) that was made responsive to a specific protein by biomimetic material (BM) technology. Carcinogenic embryonic antigen (CEA) was selected as target protein. The resulting BM-PPy film acted as biomimetic artificial antibody for CEA. Rebinding of CEA into this film changed its intrinsic electrical properties and the subsequent electrical output of the DSSC using it as CE. The quantity of CEA in solution was deduced by I-V and electrochemical impedance spesctroscopy (EIS). Linear responses to CEA were observed down to 0.25 pg/mL, with 0.13 pg/mL detection limit. Control films of PPy (prepared without CEA in the electropolymerization step) confirmed the ability of the BM material to recognize the target protein. Accurate results were obtained in the analysis of urine samples. Further developments into this ground-breaking self-powered biosensor will display a huge impact in point-to-care medical applications, which may be extended to other fields of knowledge. |
format | Online Article Text |
id | pubmed-6033912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60339122018-07-12 Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection Moreira, Felismina T. C. Truta, Liliana A. A. N. A. Sales, M. Goreti F. Sci Rep Article This work describes for the first time the integration of Dye Sensitized Solar Cell (DSSC) technology in biosensors and biomimetic materials, opening doors towards a new dimension of autonomous screening devices that may be used in point-of-care, with zero-power requirements. DSSCs are fabricated with a counter electrode (CE) of polypyrrole (PPy) that was made responsive to a specific protein by biomimetic material (BM) technology. Carcinogenic embryonic antigen (CEA) was selected as target protein. The resulting BM-PPy film acted as biomimetic artificial antibody for CEA. Rebinding of CEA into this film changed its intrinsic electrical properties and the subsequent electrical output of the DSSC using it as CE. The quantity of CEA in solution was deduced by I-V and electrochemical impedance spesctroscopy (EIS). Linear responses to CEA were observed down to 0.25 pg/mL, with 0.13 pg/mL detection limit. Control films of PPy (prepared without CEA in the electropolymerization step) confirmed the ability of the BM material to recognize the target protein. Accurate results were obtained in the analysis of urine samples. Further developments into this ground-breaking self-powered biosensor will display a huge impact in point-to-care medical applications, which may be extended to other fields of knowledge. Nature Publishing Group UK 2018-07-05 /pmc/articles/PMC6033912/ /pubmed/29977025 http://dx.doi.org/10.1038/s41598-018-27884-2 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Moreira, Felismina T. C. Truta, Liliana A. A. N. A. Sales, M. Goreti F. Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
title | Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
title_full | Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
title_fullStr | Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
title_full_unstemmed | Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
title_short | Biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
title_sort | biomimetic materials assembled on a photovoltaic cell as a novel biosensing approach to cancer biomarker detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033912/ https://www.ncbi.nlm.nih.gov/pubmed/29977025 http://dx.doi.org/10.1038/s41598-018-27884-2 |
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