Voltammetric Method for Determination of Glutathione on a Gold-Carbon-Containing Electrode; Inorganic Materials; Vol. 56, iss. 11

Detaylı Bibliyografya
Parent link:Inorganic Materials
Vol. 56, iss. 11.— 2020.— [P. 1362-1368]
Müşterek Yazar: Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение химической инженерии
Diğer Yazarlar: Gashevskaya A. S. Anna Sergeevna, Dorozhko E. V. Elena Vladimirovna, Korotkova E. I. Elena Ivanovna, Pashkovskaya E. A. Elvira Aleksandrovna, Voronova O. A. Olesya Aleksandrovna, Plotnikov E. V. Evgeny Vladimirovich, Derina K. V. Kseniya Vladimirovna, Lipskikh O. I. Olga Ivanovna
Özet:Title screen
Glutathione (GSH) is one of the most important thiol-containing antioxidants involved in various biochemical processes in the human body. Glutathione determination in biological fluids (saliva, urine, serum) and pharmaceutical preparations is rather important for clinical practice. Various analytical methods such as spectrophotometry, fluorimetry, high-performance liquid chromatography, NMR spectroscopy, capillary electrophoresis, and electrochemical methods are widely used for this purpose. Electrochemical methods are characterized by easy implementation, low cost, and possibility of miniaturization. The electrochemical behavior of reduced (GSH) and oxidized (GSSG) glutathione on a gold-carbon-containing electrode (AuCE) was studied using cathodic voltammetry with different methods of removing oxygen from an electrochemical cell: nitrogen sparging and addition of sodium sulfite (4 mol/dm3). It has been shown that traces of H2O2 that remain in the near-electrode layer on the AuCE even after oxygen removal influence the electrochemical properties of GSH at a cathode sweep of the potential from 0 to –1.8 V: GSH is oxidized by H2O2 to GSSG; the most important product of this reaction is O2. An indirect determination of GSH by the current of oxygen reduction in the Na2SO3 medium in the concentration range from 0.5 Ч 10–8 to 4.2 Ч 10–8 mol/dmm3 with a detection limit of 2.5 Ч 10–9 mol/dm3 is proposed. The developed voltammetric method is approved for the determination of GSH in certain pharmaceutical preparations.
Режим доступа: по договору с организацией-держателем ресурса
Dil:İngilizce
Baskı/Yayın Bilgisi: 2020
Konular:
Online Erişim:https://doi.org/10.1134/S0020168520140071
Materyal Türü: Elektronik Kitap Bölümü
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=665041

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200 1 |a Voltammetric Method for Determination of Glutathione on a Gold-Carbon-Containing Electrode  |f A. S. Gashevskaya, E. V. Dorozhko, E. I. Korotkova [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 42 tit.] 
330 |a Glutathione (GSH) is one of the most important thiol-containing antioxidants involved in various biochemical processes in the human body. Glutathione determination in biological fluids (saliva, urine, serum) and pharmaceutical preparations is rather important for clinical practice. Various analytical methods such as spectrophotometry, fluorimetry, high-performance liquid chromatography, NMR spectroscopy, capillary electrophoresis, and electrochemical methods are widely used for this purpose. Electrochemical methods are characterized by easy implementation, low cost, and possibility of miniaturization. The electrochemical behavior of reduced (GSH) and oxidized (GSSG) glutathione on a gold-carbon-containing electrode (AuCE) was studied using cathodic voltammetry with different methods of removing oxygen from an electrochemical cell: nitrogen sparging and addition of sodium sulfite (4 mol/dm3). It has been shown that traces of H2O2 that remain in the near-electrode layer on the AuCE even after oxygen removal influence the electrochemical properties of GSH at a cathode sweep of the potential from 0 to –1.8 V: GSH is oxidized by H2O2 to GSSG; the most important product of this reaction is O2. An indirect determination of GSH by the current of oxygen reduction in the Na2SO3 medium in the concentration range from 0.5 Ч 10–8 to 4.2 Ч 10–8 mol/dmm3 with a detection limit of 2.5 Ч 10–9 mol/dm3 is proposed. The developed voltammetric method is approved for the determination of GSH in certain pharmaceutical preparations. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Inorganic Materials 
463 |t Vol. 56, iss. 11  |v [P. 1362-1368]  |d 2020 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a glutathione 
610 1 |a voltammetry 
610 1 |a gold-carbon-containing electrode 
610 1 |a sodium sulfite 
610 1 |a thiol compounds 
610 1 |a глутатионы 
610 1 |a вольтамперометрия 
610 1 |a сульфиты 
610 1 |a тиоловые соединения 
701 1 |a Gashevskaya  |b A. S.  |g Anna Sergeevna 
701 1 |a Dorozhko  |b E. V.  |c chemist  |c Engineer of Tomsk Polytechnic University  |f 1979-  |g Elena Vladimirovna  |3 (RuTPU)RU\TPU\pers\32174  |9 16175 
701 1 |a Korotkova  |b E. I.  |c chemist  |c Professor of Tomsk Polytechnic University, Doctor of chemical science  |f 1965-  |g Elena Ivanovna  |3 (RuTPU)RU\TPU\pers\31278  |9 15456 
701 1 |a Pashkovskaya  |b E. A.  |g Elvira Aleksandrovna 
701 1 |a Voronova  |b O. A.  |c chemist  |c Assistant of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1979-  |g Olesya Aleksandrovna  |3 (RuTPU)RU\TPU\pers\32169  |9 16170 
701 1 |a Plotnikov  |b E. V.  |c chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1983-  |g Evgeny Vladimirovich  |3 (RuTPU)RU\TPU\pers\32469  |9 16417 
701 1 |a Derina  |b K. V.  |c chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1989-  |g Kseniya Vladimirovna  |3 (RuTPU)RU\TPU\pers\33919  |9 17492 
701 1 |a Lipskikh  |b O. I.  |c chemist  |c engineer of Tomsk Polytechnic University  |f 1984-  |g Olga Ivanovna  |3 (RuTPU)RU\TPU\pers\38489 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Инженерная школа природных ресурсов  |b Отделение химической инженерии  |3 (RuTPU)RU\TPU\col\23513 
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856 4 |u https://doi.org/10.1134/S0020168520140071 
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