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Simultaneous Electrochemical Determination of Dopamine, Acetaminophen, and Caffeine with a PVP/rGO-Modified Electrode
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Metadata
Document Title
Simultaneous Electrochemical Determination of Dopamine, Acetaminophen, and Caffeine with a PVP/rGO-Modified Electrode
Author
Lisnund S.
Name from Authors Collection
Affiliations
Department of Applied Chemistry, Faculty of Science and Liberal Arts, Rajamangala University of Technology Isan, 744 Suranarai Rd, Nakhon Ratchasima, 30000, Thailand; Department of Microbiology and Environmental Toxicology, University of California at Santa Cruz, Santa Cruz, 95064, CA, United States; National Nanotechnology Center, National Science and Technology Development Agency Thailand Science Park, Pathum Thani, 12120, Thailand; School of Chemistry, Institute of Science, Suranaree University of Technology, 111 University Avenue, Suranari, Muang, Nakhon Ratchasima, 30000, Thailand
Type
Article
Source Title
ACS Omega
ISSN
24701343
Year
2025
Volume
10
Issue
28
Page
30717-30727
Open Access
All Open Access; Gold Open Access; Green Open Access
Publisher
American Chemical Society
DOI
10.1021/acsomega.5c02812
Abstract
The simultaneous and cost-effective determination of Dopamine (DA), Acetaminophen (APAP), and Caffeine (CAF) could be useful in several areas such as pain management, clinical diagnostics, and pharmaceutical quality control. In this study, reduced graphene oxide (rGO) was synthesized from graphite and graphene oxide (GO) using ascorbic acid as reducing agent. The rGO was characterized using FT-IR spectroscopy, Raman spectroscopy, scanning electron microscopy, and thermogravimetry. rGO and polyvinylpyrrolidone (PVP) were then combined to modify a glassy carbon electrode (rGO-PVP/GCE), which was studied using cyclic voltammetry, electrochemical impedance spectroscopy, and square-wave voltammetry (SWV). The modified electrode rGO-PVP/GCE exhibited favorable electron transfer kinetics and electrocatalytic activity in the oxidation of DA, APAP, and CAF compared to GO/GCE, PVP/GCE, and rGO/GCE. The SWV results showed three distinct anodic peaks at 0.44, 0.63, and 1.49 V (vs Ag/AgCl 3 M KCl), corresponding to the oxidation of DA, APAP, and CAF, respectively. The responses showed good linearity in the investigated concentration ranges and the limits of detection for DA, APAP, and CAF were 0.81, 0.16, and 19.6 μM, respectively. Finally, the proposed sensor was applied to simultaneously determine DA, APAP, and CAF in artificial urine, a pharmaceutical syrup, and an energy beverage. © 2025 The Authors. Published by American Chemical Society
License
CC BY-NC-ND
Rights
Authors
Publication Source
Scopus