Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers

The multiplexed immunosensor array was fabricated on a carbon electrode array containing three graphite working electrodes, which was prepared with screen-printed technology. This immunosensor was achieved using graphene (GR) to modify the immunosensor surface for accelerating electron transfer. The...

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Main Authors: Ge, Shenguang, Yu, Feng, Ge, Lei, Yan, Mei, Yu, Jinghua, Chen, Dairong
Other Authors: School of Mechanical and Aerospace Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/95959
http://hdl.handle.net/10220/10752
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-959592020-03-07T13:22:16Z Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers Ge, Shenguang Yu, Feng Ge, Lei Yan, Mei Yu, Jinghua Chen, Dairong School of Mechanical and Aerospace Engineering The multiplexed immunosensor array was fabricated on a carbon electrode array containing three graphite working electrodes, which was prepared with screen-printed technology. This immunosensor was achieved using graphene (GR) to modify the immunosensor surface for accelerating electron transfer. The in situ synthesis of AuNPs on GR modified electrode surface aimed at the immobilization of capture antibody (Ab1). With a sandwich-type immunoreaction, the alkaline phosphatase (ALP)-labeled antibody (Ab2) functionalized Au cluster (AuCs)/GR was captured on the immunosensor surface to catalyze the hydrolysis of 3-indoxyl phosphate in substrate, which produced an indoxyl intermediate to reduce Ag ion. The silver deposition process was catalyzed by both ALP and AuCs/GR, which amplified the detection signal. The deposited silver was then measured by anodic linear sweep voltammetric stripping analysis in KCl solution. The increase of stripping peak currents was proportional to the logarithm value of the CA 153, CA 125 and CEA concentration in the range 5.0 × 10−3 to 50 U mL−1 for CA 153, 1.0 × 10−3 to 100 U mL−1 for CA 125, and 4.0 × 10−3 to 200 ng mL−1 for CEA, with a limit detection of 1.5 × 10−3 U mL−1 for CA 153, 3.4 × 10−4 U mL−1 for CA 125, and 1.2 × 10−3 ng mL−1 for CEA. The disposable immunosensor array and simple detection method for fast measurement of a panel of tumor markers avoided cross-talk and the need for deoxygenation for the electrochemical immunoassay, and showed significant clinical value for application in cancer screening, providing great potential for convenient point-of-care testing and commercial application. 2013-06-27T01:51:48Z 2019-12-06T19:23:44Z 2013-06-27T01:51:48Z 2019-12-06T19:23:44Z 2012 2012 Journal Article Ge, S., Yu, F., Ge, L., Yan, M., Yu, J., & Chen, D. (2012). Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers. Analyst, 137(20), 4727-4733. 0003-2654 https://hdl.handle.net/10356/95959 http://hdl.handle.net/10220/10752 10.1039/c2an35967g en Analyst © 2012 The Royal Society of Chemistry.
institution Nanyang Technological University
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description The multiplexed immunosensor array was fabricated on a carbon electrode array containing three graphite working electrodes, which was prepared with screen-printed technology. This immunosensor was achieved using graphene (GR) to modify the immunosensor surface for accelerating electron transfer. The in situ synthesis of AuNPs on GR modified electrode surface aimed at the immobilization of capture antibody (Ab1). With a sandwich-type immunoreaction, the alkaline phosphatase (ALP)-labeled antibody (Ab2) functionalized Au cluster (AuCs)/GR was captured on the immunosensor surface to catalyze the hydrolysis of 3-indoxyl phosphate in substrate, which produced an indoxyl intermediate to reduce Ag ion. The silver deposition process was catalyzed by both ALP and AuCs/GR, which amplified the detection signal. The deposited silver was then measured by anodic linear sweep voltammetric stripping analysis in KCl solution. The increase of stripping peak currents was proportional to the logarithm value of the CA 153, CA 125 and CEA concentration in the range 5.0 × 10−3 to 50 U mL−1 for CA 153, 1.0 × 10−3 to 100 U mL−1 for CA 125, and 4.0 × 10−3 to 200 ng mL−1 for CEA, with a limit detection of 1.5 × 10−3 U mL−1 for CA 153, 3.4 × 10−4 U mL−1 for CA 125, and 1.2 × 10−3 ng mL−1 for CEA. The disposable immunosensor array and simple detection method for fast measurement of a panel of tumor markers avoided cross-talk and the need for deoxygenation for the electrochemical immunoassay, and showed significant clinical value for application in cancer screening, providing great potential for convenient point-of-care testing and commercial application.
author2 School of Mechanical and Aerospace Engineering
author_facet School of Mechanical and Aerospace Engineering
Ge, Shenguang
Yu, Feng
Ge, Lei
Yan, Mei
Yu, Jinghua
Chen, Dairong
format Article
author Ge, Shenguang
Yu, Feng
Ge, Lei
Yan, Mei
Yu, Jinghua
Chen, Dairong
spellingShingle Ge, Shenguang
Yu, Feng
Ge, Lei
Yan, Mei
Yu, Jinghua
Chen, Dairong
Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
author_sort Ge, Shenguang
title Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
title_short Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
title_full Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
title_fullStr Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
title_full_unstemmed Disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
title_sort disposable electrochemical immunosensor for simultaneous assay of a panel of breast cancer tumor markers
publishDate 2013
url https://hdl.handle.net/10356/95959
http://hdl.handle.net/10220/10752
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