4.6 Article

Sequential injection-differential pulse voltammetric immunosensor for hepatitis B surface antigen using the modified screen-printed carbon electrode

Journal

ELECTROCHIMICA ACTA
Volume 349, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2020.136335

Keywords

Reagentless electrochemical immunosensor; Hepatitis B surface antigen; Sequential injection; Silver nanoparticles probes; Gold nanoparticles/CNT composite

Funding

  1. Science Achievement Scholarship of Thailand (SAST)
  2. Graduate School, Chiang Mai, University
  3. Department of Chemistry, Faculty of Science, Chiang Mai, University
  4. Laboratory of Physicochemistry of Polymers and Interfaces (LPPI), CY Cergy Paris Universite [EA 2528]
  5. Thailand Research Fund [RSA6080007]
  6. Franco-Thai Mobility Program (SIAM) [35834SD]
  7. Chiang Mai University

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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. (c) 2020 Elsevier Ltd. All rights reserved.

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