4.7 Article

One-step electrochemical immunosensing for simultaneous detection of two biomarkers using thionine and ferrocene as distinguishable signal tags

Journal

MICROCHIMICA ACTA
Volume 178, Issue 3-4, Pages 357-365

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-012-0839-9

Keywords

Alpha-fetoprotein; Carcinoembryonic antigen; Electrochemical immunosensor; Multiplexed immunoassay

Funding

  1. Research Fund for the Doctoral Program of Higher Education of China [20103514120003]
  2. National Science Foundation of Fujian Province [2011J06003]
  3. National Natural Science Foundation of China [21075019, 41176079]
  4. 973 National Basic Research Program of China [2010CB732403]
  5. Program for Changjiang Scholars and Innovative Research Team in University [IRT1116]

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We report on a new kind of electrochemical immunosensors for simultaneous determination of the biomarkers carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP). Thionine and ferrocene were applied as distinguishable electrochemical tags (and mediators) which were covalently conjugated on anti-AFP and anti-CEA antibodies, respectively, via carboxy groups. The resulting conjugates were co-immobilized on a glassy carbon electrode functionalized with gold nanoparticles. Finally, horseradish peroxidase (HRP) was immobilized onto the modified electrode. Labeled thionine and ferrocene, respectively, act as distinguishable tags for simultaneous determination of AFP and CEA due to the difference in the location of their voltammetric peaks. With a one-step immunoassay format, the analytes in the sample produced transparent immunoaffinity reaction with the corresponding antibodies on the electrode. Once the immunocomplex is formed, it partially inhibits the active center of the immobilized HRP, and this decreased the activity of HRP in terms of reduction of hydrogen peroxide. This immunosensor enables the simultaneous determination of AFP and CEA in a single run and within the same dynamic range (0.01-50 ng mL(-1)) and the same lower detection limit (0.01 ng mL(-1)). The reproducibility and stability of the immunosensors are acceptable. The dual immunosensor was applied to evaluate several specimens, and the assay results are in acceptable agreement with clinical data.

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