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Tyrosinase-Based Biosensors for Selective Dopamine Detection.
Monica Florescu1, Melinda David2
1Faculty of Medicine, Transilvania University of Brasov, 500019 Brasov, Romania. florescum@unitbv.ro.
Sensors (Basel, Switzerland)
|June 8, 2017
Summary
A new biosensor uses tyrosinase and cobalt-porphyrin to detect dopamine (DA) selectively. This method offers high sensitivity and accuracy for dopamine detection in real samples like urine and blood serum.
Area of Science:
- Electrochemistry
- Biosensor Technology
- Biomedical Engineering
Background:
- Dopamine (DA) detection is crucial for diagnosing neurological disorders.
- Existing detection methods often lack selectivity and sensitivity.
- Development of novel biosensors is needed for accurate DA monitoring.
Purpose of the Study:
- To develop a novel tyrosinase-based biosensor for selective dopamine detection.
- To enhance electrode selectivity using cobalt (II)-porphyrin (CoP) film.
- To validate the biosensor's performance in real biological samples.
Main Methods:
- Fabrication of a gold electrode modified with CoP film and cross-linked tyrosinase (Tyr).
- Electrochemical detection using differential pulse voltammetry to measure dopamine-quinone reduction current.
- Optimization of conditioning parameters for enhanced selectivity against ascorbic acid (AA).
Main Results:
- The CoP-modified electrode demonstrated improved selectivity for DA detection.
- A potential separation of 130 mV between AA and DA peaks was achieved.
- The biosensor exhibited a sensitivity of 1.22 ± 0.02 µA·cm-2·µM-1 and a detection limit of 0.43 µM.
- High recovery (96%) and low relative standard deviation (<5%) were observed in dopamine medication samples.
Conclusions:
- The developed tyrosinase-based biosensor offers selective and sensitive detection of dopamine.
- The CoP modification significantly enhances selectivity, enabling DA detection in complex matrices.
- The biosensor shows practical applicability for analyzing dopamine in human urine and blood serum.

