Voltammetric Investigation of Paracetamol Detection in Acidic Conditions by Using Cork-Modified Carbon Paste Electrodes

Author:

Monteiro Mayra K. S.1ORCID,Monteiro Mayara M. S.2,Henrique João M. M.3,Martínez-Huitle Carlos A.1ORCID,Ferro Sergio4ORCID,dos Santos Elisama Vieira1ORCID

Affiliation:

1. Laboratório de Eletroquímica Ambiental e Aplicada, Instituto de Química, Universidade Federal do Rio Grande do Norte, Natal CEP 59.072-900, RN, Brazil

2. Agência Brasileira de Apoio à Gestão do Sistema Único de Saúde (AgSUS), SBS Quadra 2, Bloco J, Lote 10, 7º andar, Edifício Carlton Tower Asa Sul, Brasília CEP 70.070-120, DF, Brazil

3. Instituto Federal do Sertão Pernambucano, IFSertãoPE, Estrada do Tamboril, s/n—Vila Quixada, Ouricuri CEP 56.200-000, PE, Brazil

4. Ecas4 Australia Pty. Ltd., Mile End South, SA 5031, Australia

Abstract

Developing new products that satisfy performance and durability expectations while also addressing environmental concerns is possible through the reuse of residues produced by industrial processes, aiming to fulfill the principles of circular economy. In this study, we improved the performance of a carbon paste sensor by incorporating untreated (RC) and regranulated/thermally treated (RGC) cork, which are considered biomass residues from the cork industry. We explored the electroanalytical behavior of paracetamol in sulfuric acid solutions using cyclic voltammetry and differential pulse techniques. The cork-modified carbon paste sensors showed greater sensitivity towards paracetamol. Both modified sensors allowed for an excellent resolution in distinguishing the voltammetric responses of paracetamol in sulfuric acid, showing for both an increase in peak currents compared to the unmodified carbon paste electrode. The quantification of paracetamol without interference has proved to be a feasible operation for the RC- and RGC-modified carbon paste sensors; notably, the first showed the most favorable limits of detection (LD = 2.4112 µM) and quantification (LQ = 8.0373 µM) for paracetamol in the sulfuric acid solution, performing significantly better than the second (LD = 10.355 µM, and LQ = 34.518 µM). Finally, the practical utility of the proposed sensors was assessed by analyzing paracetamol in pharmaceutical samples, obtaining satisfactory results that were in line with those obtainable using high-performance liquid chromatography.

Funder

National Council for Scientific and Technological Development

L’ORÉAL—ABC—UNESCO

Coordination for the Improvement of Higher Education Personnel

Human Resources Training Program for Oil, Natural Gas and Biofuels

Oronzio and Niccolò De Nora Foundation

Publisher

MDPI AG

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