Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70332
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dc.contributor.authorJantima Upanen_US
dc.contributor.authorPhilippe Baneten_US
dc.contributor.authorPierre Henri Auberten_US
dc.contributor.authorKontad Ounnunkaden_US
dc.contributor.authorJaroon Jakmuneeen_US
dc.date.accessioned2020-10-14T08:27:42Z-
dc.date.available2020-10-14T08:27:42Z-
dc.date.issued2020-07-20en_US
dc.identifier.issn00134686en_US
dc.identifier.other2-s2.0-85084257271en_US
dc.identifier.other10.1016/j.electacta.2020.136335en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85084257271&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70332-
dc.description.abstract© 2020 Elsevier Ltd A label-free electrochemical immunosensor was developed for the determination of hepatitis B surface antigen (HBsAg), a biomarker of hepatitis B virus (HBV). It is based on the specific binding of antigen-antibody on the electrode surface, which hindered the oxidation of silver nanoparticles (AgNPs) used as redox probe and hence reduced its oxidation current. The screen-printed carbon electrode (SPCE) was modified with carbon nanotube decorated with gold nanoparticles (AuNPs-CNT) and silver nanoparticles. The AuNPs provide good biocompatibility and large surface area for densely immobilizing the hepatitis B surface antibody (HBsAb) on the electrode, which helps to improve the signal. AgNPs act as a sensing probe in differential pulse voltammetric (DPV) detection. In addition, a sequential injection (SI) system was employed as an automated solution handling and minimizing chemical consumption. Characterization of the developed immunosensor by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) confirmed the successful modification/immobilization in various steps of immunosensor fabrication. The percentage of the decrease in oxidative peak current of AgNPs was directly proportional to the HBsAg concentration. The linear range of 1–40 ng mL−1 with a detection limit of 0.86 ng mL−1 HBsAg were achieved. The proposed method is economical, efficient, and useful for clinical analysis.en_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleSequential injection-differential pulse voltammetric immunosensor for hepatitis B surface antigen using the modified screen-printed carbon electrodeen_US
dc.typeJournalen_US
article.title.sourcetitleElectrochimica Actaen_US
article.volume349en_US
article.stream.affiliationsLaboratoire de Physicochimie des Polymères et des Interfacesen_US
article.stream.affiliationsChiang Mai Universityen_US
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