Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13221
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dc.contributor.authorJampasa S.
dc.contributor.authorSiangproh W.
dc.contributor.authorLaocharoensuk R.
dc.contributor.authorVilaivan T.
dc.contributor.authorChailapakul O.
dc.date.accessioned2021-04-05T03:22:46Z-
dc.date.available2021-04-05T03:22:46Z-
dc.date.issued2018
dc.identifier.issn399140
dc.identifier.other2-s2.0-85042707817
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13221-
dc.identifier.urihttps://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.abstractIn 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.subjectAmino acids
dc.subjectAntibodies
dc.subjectAromatic compounds
dc.subjectElectrochemical electrodes
dc.subjectElectrochemical sensors
dc.subjectGraphene
dc.subjectGraphite electrodes
dc.subjectKetones
dc.subjectMolecules
dc.subjectVoltammetry
dc.subjectAnthraquinone
dc.subjectC-reactive proteins
dc.subjectDifferential pulse voltammetry
dc.subjectELectrochemical detection
dc.subjectElectrochemical immunosensors
dc.subjectElectrochemical signals
dc.subjectSandwich format
dc.subjectScreen-printed graphene electrodes
dc.subjectChemical detection
dc.subjectanthraquinone derivative
dc.subjectantibody
dc.subjectC reactive protein
dc.subjectgraphite
dc.subjectchemistry
dc.subjectelectrochemical analysis
dc.subjectelectrode
dc.subjectgenetic procedures
dc.subjecthuman
dc.subjectprinting
dc.subjectAnthraquinones
dc.subjectAntibodies
dc.subjectBiosensing Techniques
dc.subjectC-Reactive Protein
dc.subjectElectrochemical Techniques
dc.subjectElectrodes
dc.subjectGraphite
dc.subjectHumans
dc.subjectPrinting
dc.titleElectrochemical detection of c-reactive protein based on anthraquinone-labeled antibody using a screen-printed graphene electrode
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationTalanta. Vol 183, (2018), p.311-319
dc.identifier.doi10.1016/j.talanta.2018.02.075
Appears in Collections:Scopus 1983-2021

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