Stanovení redukovaného a oxidovaného glutathionu v biologickém materiálu pomocí HPLC s elektrochemickou detekcí
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F07%3A00006240" target="_blank" >RIV/00216275:25310/07:00006240 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Determination of reduced and oxidized glutathione in biological material by HPLC with electrochemical detection
Popis výsledku v původním jazyce
Background. Tripeptid glutathione plays an important role in biological systems. It protects against the action of some reactive oxygen and nitrogen species and is involved in detoxication of harmful compounds. Methods. A method for determination of bothreduced and oxidized glutathione in whole blood and hepatocytes has been developed and evaluated. Chromatography of both reduced and oxidized glutathione was accomplished using isocratic elution on Polaris 5u C18-A, 250 x 4.6 mm, i.d. column. The mixture of methanol and 25 mmol/L sodium dihydrogen phosphate, pH 3.0 (6:94 v/v) was used as a mobile phase. Results. The analytical performance of this method is satisfactory. The intra-assay coefficients of variation in whole blood and rat hepatocytes were 2.1% and 2.2% for reduced and 4.7% and 4.9% for oxidized glutathione. The recoveries were following: 91.2% (CV 3.3%) for reduced and 94.1% (CV 8.3%) for oxidized glutathione in the whole blood. The calibration curve was linear in the whole
Název v anglickém jazyce
Determination of reduced and oxidized glutathione in biological material by HPLC with electrochemical detection
Popis výsledku anglicky
Background. Tripeptid glutathione plays an important role in biological systems. It protects against the action of some reactive oxygen and nitrogen species and is involved in detoxication of harmful compounds. Methods. A method for determination of bothreduced and oxidized glutathione in whole blood and hepatocytes has been developed and evaluated. Chromatography of both reduced and oxidized glutathione was accomplished using isocratic elution on Polaris 5u C18-A, 250 x 4.6 mm, i.d. column. The mixture of methanol and 25 mmol/L sodium dihydrogen phosphate, pH 3.0 (6:94 v/v) was used as a mobile phase. Results. The analytical performance of this method is satisfactory. The intra-assay coefficients of variation in whole blood and rat hepatocytes were 2.1% and 2.2% for reduced and 4.7% and 4.9% for oxidized glutathione. The recoveries were following: 91.2% (CV 3.3%) for reduced and 94.1% (CV 8.3%) for oxidized glutathione in the whole blood. The calibration curve was linear in the whole
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
CE - Biochemie
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2007
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
Clinical Chemistry and Laboratory Medicine
ISBN
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ISSN
1434-6621
e-ISSN
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Počet stran výsledku
1
Strana od-do
"S195"
Název nakladatele
Walter de Gruyter GmbH & Co. KG
Místo vydání
Berlin
Místo konání akce
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Datum konání akce
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Typ akce podle státní příslušnosti
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Kód UT WoS článku
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