Electrochemical Sensing of Dopamine Neurotransmitter by Deep Eutectic Solvent–Carbon Black–Crosslinked Chitosan Films: Charge Transfer Kinetic Studies and Biological Sample Analysis
Dopamine (DA) is a neurotransmitter responsible for important functions in mammals’ bodies, including mood, movement and motivation. High or low dopamine levels are associated mainly with mental illnesses such as schizophrenia and depression. Therefore, contributing to the development of electrochem...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-07-01
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| Series: | Chemosensors |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2227-9040/13/7/254 |
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| Summary: | Dopamine (DA) is a neurotransmitter responsible for important functions in mammals’ bodies, including mood, movement and motivation. High or low dopamine levels are associated mainly with mental illnesses such as schizophrenia and depression. Therefore, contributing to the development of electrochemical devices to precisely determine the DA levels in urine samples, a simple and low-cost sensor is proposed in this work. The proposed sensor design is based on crosslinked chitosan films combining carbon black (CB) and deep eutectic solvents (DESs), incorporated onto the surface of a glassy carbon electrode (GCE). Fourier Transform Infrared Spectroscopy (FT-IR) was applied to characterize the produced DESs and their precursors, while the films were characterized by scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The sensor modified with CB and DES–ethaline (DES (ETHA)-CB/GCE) showed a significantly enhanced analytical signal for DA using differential pulse voltammetry under the optimized working conditions. Moreover, a better heterogeneous electron transfer rate constant (<i>k</i><sup>0</sup>) was obtained, about 45 times higher than that of the bare GCE. The proposed sensor achieved a linear response range of 0.498 to 26.8 µmol L<sup>−1</sup> and limits of detection and quantification of 80.7 and 269 nmol L<sup>−1</sup>, respectively. Moreover, the sensor was successfully applied in the quantification of DA in the synthetic urine samples, with recovery results close to 100%. Furthermore, the sensor presented good precision, as shown from the repeatability tests. The presented method to electrochemically detect DA has proven to be efficient and simple compared to the conventional methods commonly reported. |
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| ISSN: | 2227-9040 |