Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care
Main Author: | |
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Publication Date: | 2021 |
Other Authors: | , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://hdl.handle.net/10316/95606 https://doi.org/10.1016/j.sbsr.2021.100445 |
Summary: | This work reports the development of a simple and rapid electrochemical immunosensor for the determination of breast cancer biomarker Cancer Antigen 15–3 (CA 15–3). Disposable and cost-effective chips, consisting of gold screen-printed electrodes (AuSPEs), were used to develop the portable electrochemical devices for monitoring the biomarker in point-of-care (PoC), under clinical context. The biosensor preparation consisted of two simple steps. First, a self-assembled monolayer (SAM) of mer-captosuccinic acid (MSA) was formed at the AuSPE surface. Then, the CA 15–3 antibody was covalently bound to the carboxylic groups standing at the electrode surface using EDC/NHS chemistry. The performance of the developed immunosensor was evaluated by assessing the sensor sensitivity, linear response interval, selectivity and detection limit (LOD). The developed immunosensor provided a wide linear concentration range (from 1.0 to 1000 U mL |
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Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-careCA 15-3Cancer biomarkerElectrochemical biosensorImmunosensorScreen-printed electrode (SPE)Point-of-care (PoC) analysisThis work reports the development of a simple and rapid electrochemical immunosensor for the determination of breast cancer biomarker Cancer Antigen 15–3 (CA 15–3). Disposable and cost-effective chips, consisting of gold screen-printed electrodes (AuSPEs), were used to develop the portable electrochemical devices for monitoring the biomarker in point-of-care (PoC), under clinical context. The biosensor preparation consisted of two simple steps. First, a self-assembled monolayer (SAM) of mer-captosuccinic acid (MSA) was formed at the AuSPE surface. Then, the CA 15–3 antibody was covalently bound to the carboxylic groups standing at the electrode surface using EDC/NHS chemistry. The performance of the developed immunosensor was evaluated by assessing the sensor sensitivity, linear response interval, selectivity and detection limit (LOD). The developed immunosensor provided a wide linear concentration range (from 1.0 to 1000 U mLElsevier2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/95606https://hdl.handle.net/10316/95606https://doi.org/10.1016/j.sbsr.2021.100445eng22141804https://www.sciencedirect.com/science/article/pii/S2214180421000507Rebelo, Tânia S.C.R.Ribeiro, José A.Sales, M. Goreti F.Pereira, Carlos M.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-24T16:51:11Zoai:estudogeral.uc.pt:10316/95606Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:43:37.497899Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
title |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
spellingShingle |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care Rebelo, Tânia S.C.R. CA 15-3 Cancer biomarker Electrochemical biosensor Immunosensor Screen-printed electrode (SPE) Point-of-care (PoC) analysis |
title_short |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
title_full |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
title_fullStr |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
title_full_unstemmed |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
title_sort |
Electrochemical immunosensor for detection of CA 15-3 biomarker in point-of-care |
author |
Rebelo, Tânia S.C.R. |
author_facet |
Rebelo, Tânia S.C.R. Ribeiro, José A. Sales, M. Goreti F. Pereira, Carlos M. |
author_role |
author |
author2 |
Ribeiro, José A. Sales, M. Goreti F. Pereira, Carlos M. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Rebelo, Tânia S.C.R. Ribeiro, José A. Sales, M. Goreti F. Pereira, Carlos M. |
dc.subject.por.fl_str_mv |
CA 15-3 Cancer biomarker Electrochemical biosensor Immunosensor Screen-printed electrode (SPE) Point-of-care (PoC) analysis |
topic |
CA 15-3 Cancer biomarker Electrochemical biosensor Immunosensor Screen-printed electrode (SPE) Point-of-care (PoC) analysis |
description |
This work reports the development of a simple and rapid electrochemical immunosensor for the determination of breast cancer biomarker Cancer Antigen 15–3 (CA 15–3). Disposable and cost-effective chips, consisting of gold screen-printed electrodes (AuSPEs), were used to develop the portable electrochemical devices for monitoring the biomarker in point-of-care (PoC), under clinical context. The biosensor preparation consisted of two simple steps. First, a self-assembled monolayer (SAM) of mer-captosuccinic acid (MSA) was formed at the AuSPE surface. Then, the CA 15–3 antibody was covalently bound to the carboxylic groups standing at the electrode surface using EDC/NHS chemistry. The performance of the developed immunosensor was evaluated by assessing the sensor sensitivity, linear response interval, selectivity and detection limit (LOD). The developed immunosensor provided a wide linear concentration range (from 1.0 to 1000 U mL |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10316/95606 https://hdl.handle.net/10316/95606 https://doi.org/10.1016/j.sbsr.2021.100445 |
url |
https://hdl.handle.net/10316/95606 https://doi.org/10.1016/j.sbsr.2021.100445 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
22141804 https://www.sciencedirect.com/science/article/pii/S2214180421000507 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
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