STOJANOVIC, Z.S., A.D. DUROVIC, A.M. ASHRAFI, Z. KOUDELKOVA, O. ZITKA and L. RICHTERA. Highly sensitive simultaneous electrochemical determination of reduced and oxidized glutathione in urine samples using antimony trioxide modified carbon paste electrode. Sensors and Actuators B: Chemical. Lausanne: Elsevier, 2020, vol. 318, SEP, p. 128141-128152. ISSN 0925-4005. Available from: https://dx.doi.org/10.1016/j.snb.2020.128141.
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Basic information
Original name Highly sensitive simultaneous electrochemical determination of reduced and oxidized glutathione in urine samples using antimony trioxide modified carbon paste electrode
Authors STOJANOVIC, Z.S., A.D. DUROVIC, A.M. ASHRAFI, Z. KOUDELKOVA, O. ZITKA and L. RICHTERA.
Edition Sensors and Actuators B: Chemical, Lausanne, Elsevier, 2020, 0925-4005.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10405 Electrochemistry
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 7.460
RIV identification code RIV/00216224:14740/20:00121457
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1016/j.snb.2020.128141
UT WoS 000539189500001
Keywords in English GSH; GSSG; Simultaneous determination; Modified carbon paste electrode; Square-wave voltammetry; Urine
Tags ne MU, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 29/4/2021 12:27.
Abstract
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.
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