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Updated: Aug 10, 2025

An Aptamer-based Sensor for Unchelated GadoliniumIII
Published on: January 9, 2017
A dual-functional module cellular electrochemical sensing platform for simultaneous detection guanine and xanthine
Shumeng Zhang1, Jiwen Cui2, Shi Zhou2
1College of Materials Science and Engineering Technology, Jiamusi University, Jiamusi, Heilongjiang, 154007, China.
This study developed a dual-functional module cellular electrochemical sensing platform (DMCEP) to separate and detect intracellular guanine and xanthine without interference. The DMCEP enables sensitive and simultaneous monitoring of these biomarkers, advancing cell electrochemistry applications.
Area of Science:
- Electrochemistry
- Biomarker Detection
- Molecular Imprinting Technology
Background:
- Separating superimposed electrochemical signals of intracellular guanine (G) and xanthine (X) is challenging, hindering cell electrochemistry applications.
- Existing methods struggle with the interference between G and X signals within cells.
Purpose of the Study:
- To develop a novel dual-functional module cellular electrochemical sensing platform (DMCEP) for sensitive and interference-free detection of intracellular G and X.
- To enable simultaneous signal separation and analysis of G and X within living cells.
- To establish a foundation for electrochemical cell viability detection and simultaneous tracking of multiple biomarkers.
Main Methods:
- Construction of independent G-functional module (G-FM) and X-functional module (X-FM) using molecular imprinting technology.
- Integration of G-FM and X-FM into a DMCEP for synchronous signal transmission via two channels.
- Utilizing DMCEP to separate superimposed G and X signals within cells.
Main Results:
- DMCEP demonstrated satisfactory reproducibility (RSD 3.10% for G, 2.22% for X) and repeatability (RSD 3.72% for G, 3.05% for X).
- Achieved low detection limits of 0.05 μM for G and 0.06 μM for X.
- Established good linear relationships between cell concentrations and G/X signals over specific ranges.
- Successfully tracked MCF-7 cell growth, showing earlier detection of viability changes compared to traditional cell counting.
Conclusions:
- The developed DMCEP effectively separates and detects intracellular G and X without interference, overcoming a major obstacle in cell electrochemistry.
- This strategy provides a robust method for electrochemical cell viability detection and offers new possibilities for simultaneous monitoring of multiple intracellular analytes.
- The platform opens avenues for simultaneous recording of superimposed signals and tracking of multiple biomarkers in biological systems.
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