4.7 Article

Electrochemical stripping analysis of nanogold label-induced silver deposition for ultrasensitive multiplexed detection of tumor markers

Journal

ANALYTICA CHIMICA ACTA
Volume 721, Issue -, Pages 1-6

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2012.01.048

Keywords

Biosensor; Multiplexed immunoassay; Stripping analysis; Gold nanoparticle; Silver deposition; Screen-printed electrode

Funding

  1. National Basic Research Program of China [2010CB732400]
  2. National Natural Science Foundation of China [21075055, 21135002]
  3. Department of Health of Jiangsu Province

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A multiplexed electrochemical immunoassay method was developed for simultaneous ultrasensitive measurement of tumor markers based on electrochemical stripping analysis of silver nanoparticles (Ag NPs). The Ag NPs were deposited on a disposable immunosensor array with a reduction reaction catalyzed by nanogold labels. The immunosensor array was prepared by covalently immobilizing capture antibodies on chitosan modified screen-printed carbon electrodes. Through a sandwich-type immunoreaction. antibody-functionalized Au NPs were captured onto immunosensor surface to induce the silver deposition from a silver enhancer solution. The deposited Ag NPs could be directly measured by anodic stripping analysis in KCl solution. The catalytic deposition enhanced the analytical sensitivity for detection of protein markers. The interference of dissolved oxygen could be avoided as the detection was performed with positive stripping potential range. Using carcinoembryonic antigen and alpha-fetoprotein as model analytes, the proposed multiplexed immunoassay method showed wide linear ranges of three orders of magnitude with the detection limits down to 3.5 and 3.9 pg mL(-1), respectively. The localized silver deposition, as well as the stripping detection process, eliminated completely the electrochemical cross talk between adjacent immunosensors. The immunosensor array exhibited acceptable reproducibility, stability and accuracy, showing a promising potential in multianalyte determination for clinical application. (C) 2012 Elsevier B.V. All rights reserved.

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