Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection

Detalhes bibliográficos
Autor(a) principal: Freitas, Maria
Data de Publicação: 2019
Outros Autores: Nouws, Henri P. A., Delerue-Matos, Cristina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/16660
Resumo: Screening and early diagnosis are crucial to increase the success of cancer patients’ treatments and improve the survival rate. To contribute to this success, distinct electrochemical immunosensing platforms were developed for the analysis of the ExtraCellular Domain of the Human Epidermal growth factor Receptor 2 (HER2‐ECD) through sandwich assays on nanomaterial‐modified screen‐printed carbon electrodes (SPCEs). The most promising platforms showed to be SPCEs modified with (i) gold nanoparticles (AuNPs) and (ii) multiwalled carbon nanotubes combined with AuNPs. The antibody‐antigen interaction was detected using a secondary antibody labelled with alkaline phosphatase and 3‐indoxyl phosphate and silver ions as the enzymatic substrate. The electrochemical signal of the enzymatically generated metallic silver was recorded by linear sweep voltammetry. Under the optimized conditions, linear calibration plots were obtained between 7.5 and 50 ng/mL and the total assay time was 2 h 20 min, achieving LODs of 0.16 ng/mL (SPCE‐MWCNT/AuNP) and 8.5 ng/mL (SPCE‐AuNP), which are well below the established cut‐off value of 15 ng/mL for this cancer biomarker.
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spelling Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker DetectionElectrochemical Sensing PlatformsBreast CancerBiomarker DetectionScreening and early diagnosis are crucial to increase the success of cancer patients’ treatments and improve the survival rate. To contribute to this success, distinct electrochemical immunosensing platforms were developed for the analysis of the ExtraCellular Domain of the Human Epidermal growth factor Receptor 2 (HER2‐ECD) through sandwich assays on nanomaterial‐modified screen‐printed carbon electrodes (SPCEs). The most promising platforms showed to be SPCEs modified with (i) gold nanoparticles (AuNPs) and (ii) multiwalled carbon nanotubes combined with AuNPs. The antibody‐antigen interaction was detected using a secondary antibody labelled with alkaline phosphatase and 3‐indoxyl phosphate and silver ions as the enzymatic substrate. The electrochemical signal of the enzymatically generated metallic silver was recorded by linear sweep voltammetry. Under the optimized conditions, linear calibration plots were obtained between 7.5 and 50 ng/mL and the total assay time was 2 h 20 min, achieving LODs of 0.16 ng/mL (SPCE‐MWCNT/AuNP) and 8.5 ng/mL (SPCE‐AuNP), which are well below the established cut‐off value of 15 ng/mL for this cancer biomarker.Maria Freitas is grateful to FCT‐Fundação para a Ciência e a Tecnologia for her PhD grant (SFRH/BD/111942/2015), financed by POPH‐QREN‐Tipologia 4.1‐Formação Avançada, subsidized by Fundo Social Europeu and Ministério da Ciência, Tecnologia e Ensino Superior. This work received financial support from the European Union (FEDER funds through COMPETE) and National Funds (FCT) through project UID/QUI/50006/2013.WileyRepositório Científico do Instituto Politécnico do PortoFreitas, MariaNouws, Henri P. A.Delerue-Matos, Cristina2021-01-05T16:40:06Z20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/16660eng10.1002/elan.201800537info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T13:02:40Zoai:recipp.ipp.pt:10400.22/16660Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:35:51.572747Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
title Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
spellingShingle Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
Freitas, Maria
Electrochemical Sensing Platforms
Breast Cancer
Biomarker Detection
title_short Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
title_full Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
title_fullStr Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
title_full_unstemmed Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
title_sort Electrochemical Sensing Platforms for HER2-ECD Breast Cancer Biomarker Detection
author Freitas, Maria
author_facet Freitas, Maria
Nouws, Henri P. A.
Delerue-Matos, Cristina
author_role author
author2 Nouws, Henri P. A.
Delerue-Matos, Cristina
author2_role author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Freitas, Maria
Nouws, Henri P. A.
Delerue-Matos, Cristina
dc.subject.por.fl_str_mv Electrochemical Sensing Platforms
Breast Cancer
Biomarker Detection
topic Electrochemical Sensing Platforms
Breast Cancer
Biomarker Detection
description Screening and early diagnosis are crucial to increase the success of cancer patients’ treatments and improve the survival rate. To contribute to this success, distinct electrochemical immunosensing platforms were developed for the analysis of the ExtraCellular Domain of the Human Epidermal growth factor Receptor 2 (HER2‐ECD) through sandwich assays on nanomaterial‐modified screen‐printed carbon electrodes (SPCEs). The most promising platforms showed to be SPCEs modified with (i) gold nanoparticles (AuNPs) and (ii) multiwalled carbon nanotubes combined with AuNPs. The antibody‐antigen interaction was detected using a secondary antibody labelled with alkaline phosphatase and 3‐indoxyl phosphate and silver ions as the enzymatic substrate. The electrochemical signal of the enzymatically generated metallic silver was recorded by linear sweep voltammetry. Under the optimized conditions, linear calibration plots were obtained between 7.5 and 50 ng/mL and the total assay time was 2 h 20 min, achieving LODs of 0.16 ng/mL (SPCE‐MWCNT/AuNP) and 8.5 ng/mL (SPCE‐AuNP), which are well below the established cut‐off value of 15 ng/mL for this cancer biomarker.
publishDate 2019
dc.date.none.fl_str_mv 2019
2019-01-01T00:00:00Z
2021-01-05T16:40:06Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.22/16660
url http://hdl.handle.net/10400.22/16660
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1002/elan.201800537
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dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
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