TY - JOUR
T1 - Voltammetric sensor based on magnetic particles modified composite electrode for determination of triamterene in biological sample
AU - Hudari, Felipe Fantinato
AU - da Silva, Bianca Ferreira
AU - Pividori, Maria Isabel
AU - Zanoni, Maria Valnice Boldrin
PY - 2016/9/1
Y1 - 2016/9/1
N2 - © 2015, Springer-Verlag Berlin Heidelberg. 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.
AB - © 2015, Springer-Verlag Berlin Heidelberg. 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.
KW - Diuretic
KW - Graphite-epoxy composite electrode
KW - Magnetic particles
KW - Multivariate optimization
KW - Triamterene
KW - Voltammetric sensor
U2 - 10.1007/s10008-015-3078-2
DO - 10.1007/s10008-015-3078-2
M3 - Article
SN - 1432-8488
VL - 20
SP - 2491
EP - 2501
JO - Journal of Solid State Electrochemistry
JF - Journal of Solid State Electrochemistry
IS - 9
ER -