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Application of screen-printed electrodes as transducers in affinity flow-through sensor systems
J M Fernández Romero1, M Stiene, R Kast
1Department of Analytical Chemistry, Faculty of Sciences, University of Córdoba, Spain.
Biosensors & Bioelectronics
|December 8, 1998
Summary
This study presents a novel affinity flow-through sensor for detecting low molecular weight compounds like biotin and atrazine. The system utilizes competitive affinity assays and electrochemical detection for sensitive and efficient analysis.
Area of Science:
- Electrochemistry
- Biosensors
- Analytical Chemistry
Background:
- Low molecular weight compounds require sensitive detection methods.
- Affinity assays offer high specificity for analyte recognition.
- Flow-through systems enable automated and continuous analysis.
Purpose of the Study:
- To develop and optimize an affinity flow-through sensor system.
- To demonstrate the system's capability for determining biotin and atrazine.
- To establish a sensitive and reproducible analytical method.
Main Methods:
- Heterogeneous competitive affinity assay using immobilized binding proteins (streptavidin or antibody).
- Enzyme labeling (peroxidase) and electrochemical detection of reaction products.
- Amperometric measurement at -600 mV vs a screen-printed platinum electrode.
- Automated reagent delivery in an unsegmented flow-through system.
Main Results:
- Optimized biotin determination with a linear range of 0.045–2 µg/L and RSD < 3.8%.
- Developed atrazine assay with a linear range of 0.01–10 µg/L, IC50 = 0.4 µg/L, and RSD < 4.6%.
- Successful application to atrazine-spiked water samples.
- Sensor surface regeneration achieved by streptavidin removal.
Conclusions:
- The developed affinity flow-through sensor system is effective for sensitive determination of low molecular weight compounds.
- The system demonstrates high reproducibility and applicability to real-world samples.
- The sensor offers a promising platform for automated and efficient analytical applications.