Electrochemical determination of ibuprofen by batch‐injection analysis using a BORON‐doped ultrananocrystalline diamond electrode

Author:

Carolyne Prete Maiyara1ORCID,Rianne da Rocha Luana1,Gava Segatelli Mariana1,Antigo Medeiros Roberta1ORCID,Swain Greg M2ORCID,Tarley César Ricardo Teixeira13ORCID

Affiliation:

1. Department of Chemistry State University of Londrina (UEL) Exacts Science Center, Highway Celso Garcia Cid, PR 445 Km 380 CEP 86050–482 Londrina–PR Brazil

2. Department of Chemistry Michigan State University 578 S. Shaw Lane East Lansing, Michigan 48824 United States of America

3. National Institute of Science and Technology (INCT) of Bioanalytical State University of Campinas (UNICAMP) Institute of Chemistry Department of Analytical Chemistry Zeferino Vaz City, Vaz s/n CEP 13083–970 Campinas–SP Brazil

Abstract

AbstractIn this paper, the evaluation of a boron‐doped ultrananocrystalline diamond (BD‐UNCD) electrode for the determination of ibuprofen (IBU) in pharmaceutical formulations using batch‐injection analysis with amperometric detection (BIA‐AD) is presented. The BD‐UNCD electrode was characterized by Raman spectroscopy and the electrochemical measurements were carried out before and after anodic pretreatment. An improved electrochemical response for IBU oxidation was observed using BD‐UNCD as compared to commercial boron‐doped diamond electrode. The optimized method based on the BIA‐AD system was carried out by using 2.0 V as the detection potential, a dispensing rate of 211.9 μL s−1, and an injection volume of 40 μL in an electrochemical cell containing 30.0 mL of 1.0 mol L−1 HClO4 as the supporting electrolyte. The proposed method provided an analytical curve within a linear dynamic range from 1.84 to 20.0 μmol L−1 (R2=0.9967) and a limit of detection of 0.55 μmol L−1. The intra‐day (n=10) and inter‐day (n=2) precisions for IBU concentrations of 5.0 and 10.0 μmol L−1 assessed as relative standard deviation (%RSD) ranged from 2.65 to 5.84 %. The accuracy of the method was assessed through the determination of IBU in pharmaceutical samples (tablets and solutions), yielding results that were consistent with those obtained through the comparative method (HPLC‐DAD).

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

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