2020
Highly sensitive simultaneous electrochemical determination of reduced and oxidized glutathione in urine samples using antimony trioxide modified carbon paste electrode
STOJANOVIC, Z.S., A.D. DUROVIC, A.M. ASHRAFI, Z. KOUDELKOVA, O. ZITKA et. al.Základní údaje
Originální název
Highly sensitive simultaneous electrochemical determination of reduced and oxidized glutathione in urine samples using antimony trioxide modified carbon paste electrode
Autoři
STOJANOVIC, Z.S., A.D. DUROVIC, A.M. ASHRAFI, Z. KOUDELKOVA, O. ZITKA a L. RICHTERA
Vydání
Sensors and Actuators B: Chemical, Lausanne, Elsevier, 2020, 0925-4005
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10405 Electrochemistry
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 7.460
Kód RIV
RIV/00216224:14740/20:00121457
Organizační jednotka
Středoevropský technologický institut
UT WoS
000539189500001
Klíčová slova anglicky
GSH; GSSG; Simultaneous determination; Modified carbon paste electrode; Square-wave voltammetry; Urine
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 29. 4. 2021 12:27, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
A simple and reproducible electroanalytical sensor using antimony trioxide modified-carbon paste electrode (Sb2O3-CPE) as sensing element was employed for the first time for simultaneous determination of glutathione (GSH) and glutathione disulphide (GSSG). The electrochemical response of Sb2O3-CPE was characterized by cyclic voltammetry and square-wave voltammetry. Scanning electron microscopy (SEM), scanning electrochemical microscopy (SECM) and Raman mapping were used to characterize the morphology and surface modification. A significant enhancement in the peak current response of GSH and GSSG accompanied with a good separation of the peaks were obtained at the modified electrode compared to the bare CPE. GSH and GSSG exhibited well-defined oxidation peaks at +1.08 V and +1.36 V (vs. Ag/AgCl, 3 mol/L) in Britton-Robinson buffer at pH 6.0. Parameters such as used supporting electrolyte and its pH value, amplitude and frequency were optimized for square-wave voltammetric determination. Under optimal conditions, voltammetric responses were linear in the concentration range of 2-200 mu mol/L for GSH and GSSG. The limits of detection were 0.34 mu mol/L and 0.10 mu mol/L for GSH and GSSG, respectively. Moreover, the proposed sensor also showed good reproducibility, stability and selectivity. Finally, the proposed sensor was applied for the simultaneous determination of GSH and GSSG in urine samples with satisfactory results.
Návaznosti
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