TY - JOUR
T1 - Sensitive and Profitable Electrochemical Detection of Uric Acid in the Presence of Dopamine with a Novel Carbon Paste Electrode Decorated with a Copper(II) Complex
AU - Tamayo, Lenka V.
AU - Torres, Juan F.
AU - Llanos-Penagos, Johisner
AU - Calderón, Jorge A.
AU - Nagles, Edgar
AU - García-Beltrán, Olimpo
AU - Hurtado, John J.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim A new microcomposite with copper(II) complex and carbon paste (CuC/CPE) was developed to determine the uric acid (UA) content in the presence of dopamine (DP) and was characterized via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and energy dispersive spectroscopy (EDS). The results showed high selectivity for UA compared with DP because the anodic peak currents for DP were near those of a CPE without Cuc and were considerably increased for UA. The UA and DP increases were 86.9 % and 14.3 %, respectively, according to CV and 96.6 % and 25.5 %, respectively, according to square wave voltammetry (SWV) with the CuC/CPE. Moreover, the anodic peak separation for UA and DP was 0.17 V. With optimal parameters (pH, 3.3; adsorption time(tADS), 30 s;adsorption potential (EADS), 0.10 V), the anodic peak currents for UA were proportional to concentrations between 1.6 and 14.4 μmol L−1 using standard solutions with UA concentrations ranging from 8.0–40.5 μmol L−1 and real samples. The UA detection limit was 0.13 μmol L−1. The new sensor was used to determine the UA contentin human urine samples, and the method was checked with a urine chemistry control from Bio-Rad based on human urine spiked with quantities of UA and showed a recovery between 84 % and 106 % at concentrations below 10.0 μmol L−1.
AB - © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim A new microcomposite with copper(II) complex and carbon paste (CuC/CPE) was developed to determine the uric acid (UA) content in the presence of dopamine (DP) and was characterized via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and energy dispersive spectroscopy (EDS). The results showed high selectivity for UA compared with DP because the anodic peak currents for DP were near those of a CPE without Cuc and were considerably increased for UA. The UA and DP increases were 86.9 % and 14.3 %, respectively, according to CV and 96.6 % and 25.5 %, respectively, according to square wave voltammetry (SWV) with the CuC/CPE. Moreover, the anodic peak separation for UA and DP was 0.17 V. With optimal parameters (pH, 3.3; adsorption time(tADS), 30 s;adsorption potential (EADS), 0.10 V), the anodic peak currents for UA were proportional to concentrations between 1.6 and 14.4 μmol L−1 using standard solutions with UA concentrations ranging from 8.0–40.5 μmol L−1 and real samples. The UA detection limit was 0.13 μmol L−1. The new sensor was used to determine the UA contentin human urine samples, and the method was checked with a urine chemistry control from Bio-Rad based on human urine spiked with quantities of UA and showed a recovery between 84 % and 106 % at concentrations below 10.0 μmol L−1.
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U2 - 10.1002/elan.201900348
DO - 10.1002/elan.201900348
M3 - Article
SN - 1040-0397
SP - 2429
EP - 2436
JO - Electroanalysis
JF - Electroanalysis
ER -