Electrochemical Analysis of Curcumin in Real Samples Using Intelligent Materials

Author:

Jara-Cornejo Eduardo1ORCID,Peña-Bedón Erick1ORCID,Torres Moya Mahely1,Espinoza-Torres Sergio1ORCID,Sotomayor Maria D. P. T.23ORCID,Picasso Gino1ORCID,Tuesta Juan C.4,López Rosario1ORCID,Khan Sabir156

Affiliation:

1. Technology of Materials for Environmental Remediation (TecMARA) Research Group, Faculty of Sciences, National University of Engineering, Lima 150128, Peru

2. Institute of Chemistry, State University of São Paulo (UNESP), Araraquara 14801-970, SP, Brazil

3. National Institute for Alternative Technologies of Detection, Toxicological Evaluation and Removal of Micropollutantans Radioactives (INCT-DATREM), Araraquara 14801-970, SP, Brazil

4. Laboratorio de Biotecnología, Universidad Nacional Autónoma de Alto Amazonas, Calle Prolongación Libertad 1220, Yurimaguas 16501, Peru

5. Department of Natural Sciences, Mathematics, and Statistics, Federal Rural University of the Semi-Arid, Mossoro 59625-900, RN, Brazil

6. Department of Exact Sciences and Technology, State University of Santa Cruz, Ilhéus 45662-900, BA, Brazil

Abstract

Curcumin is a compound of great importance in the food industry due to its biological and pharmacological properties, which include being an antioxidant, anti-inflammatory, antibacterial, antiviral, and anticarcinogenic. This paper proposes the synthesis of an electrochemical sensor based on molecularly imprinted polymers (MIPs) and MWCNT by drop casting deposited on a glassy carbon electrode (GCE) for the selective quantification of curcumin in food samples. The synthesized compounds are characterized by Fourier transform infrared (IR), Brunauer–Emmett–Teller (BET), and electrochemical techniques such as cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The optimal conditions for further experiments were determined by selecting these parameters. We examined three food products, commercial capsules, turmeric rhizomes, and commercial turmeric powder, employing both electrochemical and HPLC methods for the analysis. The electrochemical method revealed a limit of detection (LOD) value of 0.1365 µmol L−1, compared with the HPLC analysis, which gave a value of 3.55 µmol L−1. Furthermore, the MIP material demonstrated superior selectivity for the analyte compared to potential interferents. The recovery percentage, determined using the HPLC method, fell within the range of 87.5% to 102.6%

Funder

CONCYTEC through the PROCIENCIA program in the framework of the award Special Projects: Visiting Researchers contest

Central Office of Research Management of National University of Engineering (DIGI) of Lima-Perú

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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