Abstract

In this paper, the development of a nanoporous TiO2 array-modified Ti electrode for photo-electrochemical (PEC) sensing of dopamine (DA) is reported. A porous TiO2 array-modified electrode was fabricated from the controlled anodic oxidation of a Ti working electrode of commercial screen-printed electrodes (SPE). The anodization process and the related morphological and microstructural transformation of the bare Ti electrode into a TiO2/Ti electrode was followed by scanning electron microscopy (SEM) and UV-visible reflectance spectroscopy (DR-UV-Vis). The modified electrode was irradiated with a low-power (120 mW) UV-Vis LED lamp (λ = 400 nm) and showed good performance for the detection of DA with a large linear response range, a sensitivity of 462 nA mM−1 cm−2, and a limit of detection of 20 µM. Moreover, it showed higher photocurrents in the presence of DA in comparison to some foreign species such as ascorbic acid, uric acid, glucose, K+, Na+, and Cl−. Thus, this proposed low-cost photo-electrochemical sensor, with the advantage of very simple fabrication, demonstrates potential applications for the determination of dopamine in real samples.

Highlights

  • The sensitive determination of biomolecules using electrochemical sensors based on nanostructured sensing materials has acquired high importance for disease diagnoses and drug screening [1,2]

  • One widely investigated subject in the field of electroanalysis is the determination of neurotransmitters [3,4]

  • It is vital to many neuronal functions like memory, learning, cognition, behaviour, attention, emotion, and movement

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Summary

Introduction

The sensitive determination of biomolecules using electrochemical sensors based on nanostructured sensing materials has acquired high importance for disease diagnoses and drug screening [1,2]. In this respect, one widely investigated subject in the field of electroanalysis is the determination of neurotransmitters [3,4]. Abnormal responses of dopamine may cause several diseases like epilepsy, schizophrenia, and Parkinson’s disease [5]. This explains the huge investigative efforts deployed during the last three decades for the determination of dopamine

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