Determination of 5-hydroxymethylfurfural using an electropolymerized molecularly imprinted polymer in combination with Salle

dc.contributor.authorFrancisco, Karen C.A. [UNESP]
dc.contributor.authorLobato, Alnilan
dc.contributor.authorTasić, Nikola
dc.contributor.authorCardoso, Arnaldo A. [UNESP]
dc.contributor.authorGonçalves, Luís M.
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionNational Institute of Chemistry
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversity of Belgrade
dc.date.accessioned2023-03-01T20:58:48Z
dc.date.available2023-03-01T20:58:48Z
dc.date.issued2022-12-01
dc.description.abstractCoffee, a beverage with a complex chemical composition, is appreciated for the sensory experience of its taste and aroma. The compound 5-(hydroxymethyl)-2-furfural (HMF) is essential for sensory characterization of the beverage, and is also used in the traceability of its production. In this work, a procedure combining salting-out assisted liquid-liquid extraction (SALLE) and an electropolymerized molecularly imprinted polymer (e-MIP) was developed for the detection and quantification of HMF in coffee samples. The sample preparation step using SALLE employed a combination of acetonitrile and phosphate-buffered saline, in a proportion of 70:30 (ACN:PBS), with addition of 0.02 g of NaCl. The new sensor (e-MIP) was prepared by electropolymerization of p-aminobenzoic acid onto a glassy carbon electrode (GCE) using cyclic voltammetry (CV). Analytical determinations were performed by differential pulse voltammetry (DPV). The linear regression correlation coefficient (r2) for the response was 0.9986. The limits of detection and quantification were 0.372 mg L−1 and 1.240 mg L−1, respectively. The repeatability and reproducibility values obtained were 6 and 10%, respectively. The recoveries for three concentration levels were between 97 and 101%. Analyses of different coffee samples showed that the HMF concentrations varied from 261.0 ± 41.0 to 770.2 ± 55.9 mg kg−1 in powdered coffee samples, and from 1510 ± 50 to 4445 ± 278 mg kg−1 in instant coffee samples. The advantages of this procedure, compared to other methods described in the literature, are its simplicity, easy operation, good selectivity and sensitivity, low cost, and minimal use of organic solvents.en
dc.description.affiliationDepartamento de Química Analítica Instituto de Química Universidade Estadual Paulista (UNESP), Araraquara
dc.description.affiliationDepartment of Analytical Chemistry National Institute of Chemistry
dc.description.affiliationDepartamento de Química Fundamental Instituto de Química Universidade de São Paulo (USP), SP
dc.description.affiliationDepartment of Materials Science Institute of Multidisciplinary Research University of Belgrade
dc.description.affiliationUnespDepartamento de Química Analítica Instituto de Química Universidade Estadual Paulista (UNESP), Araraquara
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2018/13922–7
dc.description.sponsorshipIdFAPESP: 2018/14425–7
dc.description.sponsorshipIdFAPESP: 2019/11214–8
dc.description.sponsorshipIdCNPq: 309168/2020–1
dc.identifierhttp://dx.doi.org/10.1016/j.talanta.2022.123723
dc.identifier.citationTalanta, v. 250.
dc.identifier.doi10.1016/j.talanta.2022.123723
dc.identifier.issn0039-9140
dc.identifier.scopus2-s2.0-85134489439
dc.identifier.urihttp://hdl.handle.net/11449/241365
dc.language.isoeng
dc.relation.ispartofTalanta
dc.sourceScopus
dc.subject5-(Hydroxymethyl)-2-furfural
dc.subjectElectroanalysis
dc.subjectElectropolymerization
dc.subjectMolecular recognition
dc.subjectSalting-out assisted liquid-liquid extraction
dc.subjectSample preparation
dc.titleDetermination of 5-hydroxymethylfurfural using an electropolymerized molecularly imprinted polymer in combination with Salleen
dc.typeArtigo
unesp.author.orcid0000-0002-8829-7536[1]
unesp.author.orcid0000-0002-4936-5647 0000-0002-4936-5647[2]
unesp.author.orcid0000-0003-2046-995X[4]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentQuímica Analítica - IQARpt

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