Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor

Detalhes bibliográficos
Autor(a) principal: Pacheco, João
Data de Publicação: 2018
Outros Autores: Rebelo, Patrícia, Freitas, Maria, Nouws, Henri, 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/10400.22/14573
Resumo: The extracellular domain of the human epidermal growth factor receptor 2 (HER2-ECD) is a protein breast cancer biomarker. Its quantification in peripheral blood could provide an important contribution to diagnostics and patient follow-up. In this work an electrochemical molecularly imprinted polymer (MIP) sensor for the quantification of HER2-ECD was developed. The MIP was electropolymerized by cyclic voltammetry using a solution containing phenol and HER2-ECD on a screen-printed gold electrode (AuSPE). The sensor was characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The analysis of HER2-ECD was performed by differential pulse voltammetry using ([Fe(CN)6]3−/4−as redox probe. The linear range was established in the concentration interval from 10 to 70 ng/mL HER2-ECD, with a limit of detection of 1.6 ng/L and a limit of quantification of 5.2 ng/mL. Through the analysis of other protein biomarkers, the MIP sensor was found to be selective. Furthermore, these proteins did not interfere in the analysis of the selected biomarker. The developed sensor was used for the analysis of spiked human serum samples, providing adequate recovery values and precise results. The outcomes of this study indicate that the developed MIP sensor could be useful in the non-invasive analysis of HER2-ECD in breast cancer patients.
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spelling Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensorBreast cancerMolecularly imprinted polymerHER2Electrochemical sensorVoltammetryThe extracellular domain of the human epidermal growth factor receptor 2 (HER2-ECD) is a protein breast cancer biomarker. Its quantification in peripheral blood could provide an important contribution to diagnostics and patient follow-up. In this work an electrochemical molecularly imprinted polymer (MIP) sensor for the quantification of HER2-ECD was developed. The MIP was electropolymerized by cyclic voltammetry using a solution containing phenol and HER2-ECD on a screen-printed gold electrode (AuSPE). The sensor was characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The analysis of HER2-ECD was performed by differential pulse voltammetry using ([Fe(CN)6]3−/4−as redox probe. The linear range was established in the concentration interval from 10 to 70 ng/mL HER2-ECD, with a limit of detection of 1.6 ng/L and a limit of quantification of 5.2 ng/mL. Through the analysis of other protein biomarkers, the MIP sensor was found to be selective. Furthermore, these proteins did not interfere in the analysis of the selected biomarker. The developed sensor was used for the analysis of spiked human serum samples, providing adequate recovery values and precise results. The outcomes of this study indicate that the developed MIP sensor could be useful in the non-invasive analysis of HER2-ECD in breast cancer patients.Maria Freitas is grateful to FCT (Fundação para a Ciência e a Tecnologia) for her PhD grant (SFRH/BD/111942/2015). Patrícia Rebelo is grateful to FCT (Fundação para a Ciência e a Tecnologia) for her PhD grant (SFRH/BD/132384/2017). João Pacheco is grateful to FCT for his Postdoc. grant (SFRH/BPD/101419/2014), 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.ElsevierRepositório Científico do Instituto Politécnico do PortoPacheco, JoãoRebelo, PatríciaFreitas, MariaNouws, HenriDelerue-Matos, Cristina2019-09-12T13:27:50Z2018-062018-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/14573eng0925-400510.1016/j.snb.2018.06.113info: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:RCAAP2023-03-13T12:57:06Zoai:recipp.ipp.pt:10400.22/14573Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:34:06.433027Repositório 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 Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
title Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
spellingShingle Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
Pacheco, João
Breast cancer
Molecularly imprinted polymer
HER2
Electrochemical sensor
Voltammetry
title_short Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
title_full Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
title_fullStr Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
title_full_unstemmed Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
title_sort Breast cancer biomarker (HER2-ECD) detection using a molecularly imprinted electrochemical sensor
author Pacheco, João
author_facet Pacheco, João
Rebelo, Patrícia
Freitas, Maria
Nouws, Henri
Delerue-Matos, Cristina
author_role author
author2 Rebelo, Patrícia
Freitas, Maria
Nouws, Henri
Delerue-Matos, Cristina
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Pacheco, João
Rebelo, Patrícia
Freitas, Maria
Nouws, Henri
Delerue-Matos, Cristina
dc.subject.por.fl_str_mv Breast cancer
Molecularly imprinted polymer
HER2
Electrochemical sensor
Voltammetry
topic Breast cancer
Molecularly imprinted polymer
HER2
Electrochemical sensor
Voltammetry
description The extracellular domain of the human epidermal growth factor receptor 2 (HER2-ECD) is a protein breast cancer biomarker. Its quantification in peripheral blood could provide an important contribution to diagnostics and patient follow-up. In this work an electrochemical molecularly imprinted polymer (MIP) sensor for the quantification of HER2-ECD was developed. The MIP was electropolymerized by cyclic voltammetry using a solution containing phenol and HER2-ECD on a screen-printed gold electrode (AuSPE). The sensor was characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The analysis of HER2-ECD was performed by differential pulse voltammetry using ([Fe(CN)6]3−/4−as redox probe. The linear range was established in the concentration interval from 10 to 70 ng/mL HER2-ECD, with a limit of detection of 1.6 ng/L and a limit of quantification of 5.2 ng/mL. Through the analysis of other protein biomarkers, the MIP sensor was found to be selective. Furthermore, these proteins did not interfere in the analysis of the selected biomarker. The developed sensor was used for the analysis of spiked human serum samples, providing adequate recovery values and precise results. The outcomes of this study indicate that the developed MIP sensor could be useful in the non-invasive analysis of HER2-ECD in breast cancer patients.
publishDate 2018
dc.date.none.fl_str_mv 2018-06
2018-06-01T00:00:00Z
2019-09-12T13:27:50Z
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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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.22/14573
url http://hdl.handle.net/10400.22/14573
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0925-4005
10.1016/j.snb.2018.06.113
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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