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Immunomagnetic bead-based bioassay for the voltammetric analysis of the breast cancer biomarker HER2-ECD and tumour cells using quantum dots as detection labels
An electrochemical magnetic immunosensing strategy was developed for the determination of HER2-ECD, a breast cancer biomarker, and breast cancer cells in human serum. A sandwich assay was performed on carboxylic acid-functionalized magnetic beads (MBs) using a screen-printed carbon electrode (SPCE)...
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Published in: | Mikrochimica acta (1966) 2020-02, Vol.187 (3), p.184-184, Article 184 |
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container_title | Mikrochimica acta (1966) |
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creator | Freitas, Maria Nouws, Henri P. A. Keating, Elisa Fernandes, Virginia Cruz Delerue-Matos, Cristina |
description | An electrochemical magnetic immunosensing strategy was developed for the determination of HER2-ECD, a breast cancer biomarker, and breast cancer cells in human serum. A sandwich assay was performed on carboxylic acid-functionalized magnetic beads (MBs) using a screen-printed carbon electrode (SPCE) as transducer surface. The affinity process was detected using electroactive labels; core/shell streptavidin-modified CdSe@ZnS Quantum Dots (QDs). Cd
2+
ions, released from the QDs, were determined by differential pulse anodic stripping voltammetry (DPASV). An assay time of 90 min, with an actual hands-on time of about 20 min, a linear range between 0.50–50 ng·mL
−1
of HER2-ECD and a limit of detection of 0.29 ng·mL
−1
were achieved. Analysis of live breast cancer cells was also performed using the optimized assay. Breast cancer cell lines SK-BR-3 (a HER2-positive cell line), MDA-MB-231 (a HER2-negative cell line) and MCF-7 (a cell line with low HER2 expression) were tested. The selectivity of the assay towards SK-BR-3 cells was confirmed. A concentration-dependent signal that was 12.5× higher than the signal obtained for the HER2-negative cells (MDA-MB-231) and a limit of detection of 2 cells·mL
−1
was obtained.
Graphical abstract
Schematic representation of the electrochemical immunomagnetic assay for the determination of the breast cancer biomarker HER2-ECD and cancer cells using magnetic beads (MBs), a screen-printed carbon electrode (SPCE) as transducer surface and quantum dots (QD) as electroactive labels. |
doi_str_mv | 10.1007/s00604-020-4156-4 |
format | article |
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2+
ions, released from the QDs, were determined by differential pulse anodic stripping voltammetry (DPASV). An assay time of 90 min, with an actual hands-on time of about 20 min, a linear range between 0.50–50 ng·mL
−1
of HER2-ECD and a limit of detection of 0.29 ng·mL
−1
were achieved. Analysis of live breast cancer cells was also performed using the optimized assay. Breast cancer cell lines SK-BR-3 (a HER2-positive cell line), MDA-MB-231 (a HER2-negative cell line) and MCF-7 (a cell line with low HER2 expression) were tested. The selectivity of the assay towards SK-BR-3 cells was confirmed. A concentration-dependent signal that was 12.5× higher than the signal obtained for the HER2-negative cells (MDA-MB-231) and a limit of detection of 2 cells·mL
−1
was obtained.
Graphical abstract
Schematic representation of the electrochemical immunomagnetic assay for the determination of the breast cancer biomarker HER2-ECD and cancer cells using magnetic beads (MBs), a screen-printed carbon electrode (SPCE) as transducer surface and quantum dots (QD) as electroactive labels.</description><identifier>ISSN: 0026-3672</identifier><identifier>EISSN: 1436-5073</identifier><identifier>DOI: 10.1007/s00604-020-4156-4</identifier><identifier>PMID: 32088788</identifier><language>eng</language><publisher>Vienna: Springer Vienna</publisher><subject>Analytical Chemistry ; Breast cancer ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Electric properties ; Ethylenediaminetetraacetic acid ; IX NyNA 2019. International Congress on Analytical Nanoscience and Nanotechnology ; Microengineering ; Nanochemistry ; Nanotechnology ; Original Paper</subject><ispartof>Mikrochimica acta (1966), 2020-02, Vol.187 (3), p.184-184, Article 184</ispartof><rights>Springer-Verlag GmbH Austria, part of Springer Nature 2020</rights><rights>COPYRIGHT 2020 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-e211c36340eac3df835def638ce02a19a0ec1f3fbab25685acfd63b692dc1b133</citedby><cites>FETCH-LOGICAL-c411t-e211c36340eac3df835def638ce02a19a0ec1f3fbab25685acfd63b692dc1b133</cites><orcidid>0000-0002-3904-9907 ; 0000-0002-3924-776X ; 0000-0003-3979-7523 ; 0000-0002-0628-2753 ; 0000-0002-1472-8866</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32088788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Freitas, Maria</creatorcontrib><creatorcontrib>Nouws, Henri P. A.</creatorcontrib><creatorcontrib>Keating, Elisa</creatorcontrib><creatorcontrib>Fernandes, Virginia Cruz</creatorcontrib><creatorcontrib>Delerue-Matos, Cristina</creatorcontrib><title>Immunomagnetic bead-based bioassay for the voltammetric analysis of the breast cancer biomarker HER2-ECD and tumour cells using quantum dots as detection labels</title><title>Mikrochimica acta (1966)</title><addtitle>Microchim Acta</addtitle><addtitle>Mikrochim Acta</addtitle><description>An electrochemical magnetic immunosensing strategy was developed for the determination of HER2-ECD, a breast cancer biomarker, and breast cancer cells in human serum. A sandwich assay was performed on carboxylic acid-functionalized magnetic beads (MBs) using a screen-printed carbon electrode (SPCE) as transducer surface. The affinity process was detected using electroactive labels; core/shell streptavidin-modified CdSe@ZnS Quantum Dots (QDs). Cd
2+
ions, released from the QDs, were determined by differential pulse anodic stripping voltammetry (DPASV). An assay time of 90 min, with an actual hands-on time of about 20 min, a linear range between 0.50–50 ng·mL
−1
of HER2-ECD and a limit of detection of 0.29 ng·mL
−1
were achieved. Analysis of live breast cancer cells was also performed using the optimized assay. Breast cancer cell lines SK-BR-3 (a HER2-positive cell line), MDA-MB-231 (a HER2-negative cell line) and MCF-7 (a cell line with low HER2 expression) were tested. The selectivity of the assay towards SK-BR-3 cells was confirmed. A concentration-dependent signal that was 12.5× higher than the signal obtained for the HER2-negative cells (MDA-MB-231) and a limit of detection of 2 cells·mL
−1
was obtained.
Graphical abstract
Schematic representation of the electrochemical immunomagnetic assay for the determination of the breast cancer biomarker HER2-ECD and cancer cells using magnetic beads (MBs), a screen-printed carbon electrode (SPCE) as transducer surface and quantum dots (QD) as electroactive labels.</description><subject>Analytical Chemistry</subject><subject>Breast cancer</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Electric properties</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>IX NyNA 2019. International Congress on Analytical Nanoscience and Nanotechnology</subject><subject>Microengineering</subject><subject>Nanochemistry</subject><subject>Nanotechnology</subject><subject>Original Paper</subject><issn>0026-3672</issn><issn>1436-5073</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kc-KFDEQhxtR3HH1AbxIwIuXXvOnO91zXMbRXVgQRM-hOqmMvXYnu6m0MG_jo5p2VkEQySGh8v2Kor6qein4heC8e0uca97UXPK6Ea2um0fVRjRK1y3v1ONqw7nUtdKdPKueEd1yLjotm6fVmZK877u-31Q_rud5CXGGQ8A8WjYguHoAQseGMQIRHJmPieWvyL7HKcM8Y04FhADTkUZi0f_6HBICZWYhWExrdob0rbyu9p9kvd-9KwHH8jLHJTGL00RsoTEc2P0CoZSZi5kYEHOY0eYxBjbBgBM9r554mAhfPNzn1Zf3-8-7q_rm44fr3eVNbRshco1SCKu0ajiCVc73qnXoteotcgliCxyt8MoPMMhW9y1Y77Qa9FY6Kwah1Hn15tT3LsX7BSmbeaR1UAgYFzKyNC9La7a6oK9P6AEmNGPwMSewK24uO9Hytmv4tlAX_6DKcTiPNgb0Y6n_FRCngE2RKKE3d2ksWzwawc3q25x8m-LbrL5NUzKvHqZehhndn8RvwQWQJ4DKVzhgMrfFQHFH_-n6ExEgt0s</recordid><startdate>20200222</startdate><enddate>20200222</enddate><creator>Freitas, Maria</creator><creator>Nouws, Henri P. A.</creator><creator>Keating, Elisa</creator><creator>Fernandes, Virginia Cruz</creator><creator>Delerue-Matos, Cristina</creator><general>Springer Vienna</general><general>Springer</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3904-9907</orcidid><orcidid>https://orcid.org/0000-0002-3924-776X</orcidid><orcidid>https://orcid.org/0000-0003-3979-7523</orcidid><orcidid>https://orcid.org/0000-0002-0628-2753</orcidid><orcidid>https://orcid.org/0000-0002-1472-8866</orcidid></search><sort><creationdate>20200222</creationdate><title>Immunomagnetic bead-based bioassay for the voltammetric analysis of the breast cancer biomarker HER2-ECD and tumour cells using quantum dots as detection labels</title><author>Freitas, Maria ; Nouws, Henri P. A. ; Keating, Elisa ; Fernandes, Virginia Cruz ; Delerue-Matos, Cristina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-e211c36340eac3df835def638ce02a19a0ec1f3fbab25685acfd63b692dc1b133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Analytical Chemistry</topic><topic>Breast cancer</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Electric properties</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>IX NyNA 2019. International Congress on Analytical Nanoscience and Nanotechnology</topic><topic>Microengineering</topic><topic>Nanochemistry</topic><topic>Nanotechnology</topic><topic>Original Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Freitas, Maria</creatorcontrib><creatorcontrib>Nouws, Henri P. A.</creatorcontrib><creatorcontrib>Keating, Elisa</creatorcontrib><creatorcontrib>Fernandes, Virginia Cruz</creatorcontrib><creatorcontrib>Delerue-Matos, Cristina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Mikrochimica acta (1966)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Freitas, Maria</au><au>Nouws, Henri P. A.</au><au>Keating, Elisa</au><au>Fernandes, Virginia Cruz</au><au>Delerue-Matos, Cristina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunomagnetic bead-based bioassay for the voltammetric analysis of the breast cancer biomarker HER2-ECD and tumour cells using quantum dots as detection labels</atitle><jtitle>Mikrochimica acta (1966)</jtitle><stitle>Microchim Acta</stitle><addtitle>Mikrochim Acta</addtitle><date>2020-02-22</date><risdate>2020</risdate><volume>187</volume><issue>3</issue><spage>184</spage><epage>184</epage><pages>184-184</pages><artnum>184</artnum><issn>0026-3672</issn><eissn>1436-5073</eissn><abstract>An electrochemical magnetic immunosensing strategy was developed for the determination of HER2-ECD, a breast cancer biomarker, and breast cancer cells in human serum. A sandwich assay was performed on carboxylic acid-functionalized magnetic beads (MBs) using a screen-printed carbon electrode (SPCE) as transducer surface. The affinity process was detected using electroactive labels; core/shell streptavidin-modified CdSe@ZnS Quantum Dots (QDs). Cd
2+
ions, released from the QDs, were determined by differential pulse anodic stripping voltammetry (DPASV). An assay time of 90 min, with an actual hands-on time of about 20 min, a linear range between 0.50–50 ng·mL
−1
of HER2-ECD and a limit of detection of 0.29 ng·mL
−1
were achieved. Analysis of live breast cancer cells was also performed using the optimized assay. Breast cancer cell lines SK-BR-3 (a HER2-positive cell line), MDA-MB-231 (a HER2-negative cell line) and MCF-7 (a cell line with low HER2 expression) were tested. The selectivity of the assay towards SK-BR-3 cells was confirmed. A concentration-dependent signal that was 12.5× higher than the signal obtained for the HER2-negative cells (MDA-MB-231) and a limit of detection of 2 cells·mL
−1
was obtained.
Graphical abstract
Schematic representation of the electrochemical immunomagnetic assay for the determination of the breast cancer biomarker HER2-ECD and cancer cells using magnetic beads (MBs), a screen-printed carbon electrode (SPCE) as transducer surface and quantum dots (QD) as electroactive labels.</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><pmid>32088788</pmid><doi>10.1007/s00604-020-4156-4</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3904-9907</orcidid><orcidid>https://orcid.org/0000-0002-3924-776X</orcidid><orcidid>https://orcid.org/0000-0003-3979-7523</orcidid><orcidid>https://orcid.org/0000-0002-0628-2753</orcidid><orcidid>https://orcid.org/0000-0002-1472-8866</orcidid></addata></record> |
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subjects | Analytical Chemistry Breast cancer Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Electric properties Ethylenediaminetetraacetic acid IX NyNA 2019. International Congress on Analytical Nanoscience and Nanotechnology Microengineering Nanochemistry Nanotechnology Original Paper |
title | Immunomagnetic bead-based bioassay for the voltammetric analysis of the breast cancer biomarker HER2-ECD and tumour cells using quantum dots as detection labels |
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