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Updated: Apr 19, 2026

Development and Validation of an Ultrasensitive Single Molecule Array Digital Enzyme-linked Immunosorbent Assay for Human Interferon-α
Published on: June 14, 2018
Single electrode biosensor for simultaneous determination of interferon gamma and lysozyme
Jianfei Xia1, Daimin Song1, Zonghua Wang1
1Laboratory of Fiber Materials and Modern Textile, The Growing Base for State Key Laboratory, College of Chemical Science and Engineering, Shandong Sino-Japanese Center for Collaborative Research of Carbon Nanomaterials, Collaborative Innovation Center for Marine Biomass Fiber Materials and Textiles, Qingdao University, Qingdao, Shandong 266071, China.
A novel biosensor enables simultaneous electrochemical detection of interferon gamma (IFN-γ) and lysozyme (Lys) for acute leukemia evaluation. This aptamer-based sensor uses combined "signal-on" and "signal-off" modes for reliable results.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Molecular Diagnostics
Background:
- Acute leukemia diagnosis requires sensitive and specific biomarker detection.
- Simultaneous analysis of multiple biomarkers can improve diagnostic accuracy.
- Existing methods for biomarker detection may lack efficiency or specificity.
Purpose of the Study:
- To develop a novel electrochemical biosensor for simultaneous detection of interferon gamma (IFN-γ) and lysozyme (Lys).
- To utilize aptamer recognition with coupled "signal-on" and "signal-off" modes for enhanced detection.
- To provide a reliable tool for acute leukemia evaluation.
Main Methods:
- Fabrication of a gold electrode modified with aptamers and signaling probes (ferrocene and methylene blue).
- Electrochemical detection using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and square wave voltammetry (SWV).
- Exploitation of target-induced aptamer release leading to altered redox signals of signaling probes.
Main Results:
- The biosensor achieved simultaneous detection of IFN-γ and Lys with linear ranges of 0.01–10 nM and 0.1–100 nM, respectively.
- Detection limits were as low as 1.14×10⁻³ nM for IFN-γ and 0.0164 nM for Lys.
- The biosensor demonstrated good regeneration and successful application in practical analyses.
Conclusions:
- The developed aptamer-based biosensor offers a sensitive and simultaneous method for detecting key biomarkers in acute leukemia.
- The combined "signal-on" and "signal-off" strategy provides reliable and integrated information for clinical evaluation.
- This approach holds promise for improving the diagnosis and management of acute leukemia.
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