J 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

Štítky

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

90043, velká výzkumná infrastruktura
Název: CIISB