Document details

Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample

Author(s): Hudari, Felipe Fantinato [UNESP] ; da Silva, Bianca Ferreira [UNESP] ; Pividori, Maria Isabel ; Zanoni, Maria Valnice Boldrin [UNESP]

Date: 2018

Persistent ID: http://hdl.handle.net/11449/177599

Origin: Oasisbr

Subject(s): Diuretic; Graphite-epoxy composite electrode; Magnetic particles; Multivariate optimization; Triamterene; Voltammetric sensor; Diuretic; Diuretic; Graphite-epoxy composite electrode; Graphite-epoxy composite electrode; Magnetic particles; Magnetic particles; Multivariate optimization; Multivariate optimization; Triamterene; Triamterene; Voltammetric sensor; Voltammetric sensor


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Made available in DSpace on 2018-12-11T17:26:16Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-09-01

Some diuretic substances are controlled and monitored by the World Anti-Doping Agency as prohibited substances for use by athletes, such as triamterene (TRT). Thus, this work describes a voltammetric method based on graphite-epoxy composite electrode modified by tosyl-functionalized magnetic particles (GECE/MPs-To) for determination of TRT diuretic in urine sample. The TRT presented an oxidation peak at +1.24 V at GECE/MPs-To with irreversible behavior. Controlled potential electrolysis of the TRT at +1.26 V indicated the two electrons are transferred during amine group oxidation and the main product was identified by LC-MS/MS. The anodic peak current is 25 % higher at the modified electrode, suggesting that TRT is adsorbed on the magnetic particles. Using optimized conditions by using multivariate optimization of the parameters inherent of the square wave voltammetry, a calibration curve was constructed with a linear relationship for TRT from 0.500 to 99.8 μmol L−1. The limits of detection and quantification were 1.47 and 4.91 × 10−7 mol L−1, respectively. The proposed method was applied to urine sample and validated by LC-MS/MS technique where the values found and compared between the two techniques showed no significant difference at 95 % confidence.

Departamento de Química UNESP Universidade Estadual Paulista Júlio Mesquita Filho Instituto de Química de Araraquara, Rua Francisco Degni, 55, Bairro Quitandinha,

Departamento de Química Grupo de Sensor e Biosensor Universidade Autônoma de Barcelona, Bellaterra

Departamento de Química UNESP Universidade Estadual Paulista Júlio Mesquita Filho Instituto de Química de Araraquara, Rua Francisco Degni, 55, Bairro Quitandinha,

Document Type Journal article
Language English
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