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Electrochemical detection of c-reactive protein based on anthraquinone-labeled antibody using a screen-printed graphene electrode

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dc.contributor.author Jampasa S.
dc.contributor.author Siangproh W.
dc.contributor.author Laocharoensuk R.
dc.contributor.author Vilaivan T.
dc.contributor.author Chailapakul O.
dc.date.accessioned 2021-04-05T03:22:46Z
dc.date.available 2021-04-05T03:22:46Z
dc.date.issued 2018
dc.identifier.issn 399140
dc.identifier.other 2-s2.0-85042707817
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13221
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042707817&doi=10.1016%2fj.talanta.2018.02.075&partnerID=40&md5=1da3da462cb55f542acd0fa03c80ed06
dc.description.abstract In this present work, a novel electrochemical immunosensor employing a screen-printed graphene electrode (SPGE) for a simple and highly sensitive determination of C-reactive protein (CRP) in a sandwich-type format was proposed. The sensor comprised of two CRP-specific antibodies: an unlabeled capture primary antibody (Anti-1°Ab) and an electrochemically detectable anthraquinone-labeled signaling secondary (AQ-2°Ab) antibody. The Anti-1°Ab was first covalently anchored onto an L-cysteine/gold-modified disposable SPGE (L-Cys/Au/SPGE) to create the anti-CRP surface. After binding of the CRP and the AQ-2°Ab, the electrochemical signal response was measured using differential pulse voltammetry (DPV). In the presence of CRP, the sensor exhibited a significant increase in the AQ current at AQ-2°Ab compared to the negative control. The CRP concentration was detected in the range of 0.01–150 µg/mL, and the limit of detection (LOD) (S/N = 3) and limit of quantitation (LOQ) (10 SD/Slope) were 1.5 ng/mL and 10 ng/mL, respectively. This sensor exhibited very high sensitivity in determining CRP and was successfully applied to detect CRP in certified human serum with satisfactory results. The developed sensor is suitable as an alternative method for determination of CRP and the same principle may be further applied to determine other clinically important target molecules. © 2018 Elsevier B.V.
dc.subject Amino acids
dc.subject Antibodies
dc.subject Aromatic compounds
dc.subject Electrochemical electrodes
dc.subject Electrochemical sensors
dc.subject Graphene
dc.subject Graphite electrodes
dc.subject Ketones
dc.subject Molecules
dc.subject Voltammetry
dc.subject Anthraquinone
dc.subject C-reactive proteins
dc.subject Differential pulse voltammetry
dc.subject ELectrochemical detection
dc.subject Electrochemical immunosensors
dc.subject Electrochemical signals
dc.subject Sandwich format
dc.subject Screen-printed graphene electrodes
dc.subject Chemical detection
dc.subject anthraquinone derivative
dc.subject antibody
dc.subject C reactive protein
dc.subject graphite
dc.subject chemistry
dc.subject electrochemical analysis
dc.subject electrode
dc.subject genetic procedures
dc.subject human
dc.subject printing
dc.subject Anthraquinones
dc.subject Antibodies
dc.subject Biosensing Techniques
dc.subject C-Reactive Protein
dc.subject Electrochemical Techniques
dc.subject Electrodes
dc.subject Graphite
dc.subject Humans
dc.subject Printing
dc.title Electrochemical detection of c-reactive protein based on anthraquinone-labeled antibody using a screen-printed graphene electrode
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Talanta. Vol 183, (2018), p.311-319
dc.identifier.doi 10.1016/j.talanta.2018.02.075


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