Structural Characterization of Electrochemically and in Vitro Biologically Generated Oxidation Products of Atorvastatin Using UHPLC/MS/MS
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F13%3A39896258" target="_blank" >RIV/00216275:25310/13:39896258 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11160/13:10190907
Výsledek na webu
<a href="http://link.springer.com/article/10.1007/s00216-013-7133-5" target="_blank" >http://link.springer.com/article/10.1007/s00216-013-7133-5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00216-013-7133-5" target="_blank" >10.1007/s00216-013-7133-5</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Structural Characterization of Electrochemically and in Vitro Biologically Generated Oxidation Products of Atorvastatin Using UHPLC/MS/MS
Popis výsledku v původním jazyce
Ultrahigh-performance liquid chromatography coupled with high-mass-accuracy tandem mass spectrometry (UHPLC-MS-MS) has been used for elucidation of the structures of oxidation products of atorvastatin (AT), one of the most popular commercially availabledrugs. The purpose of the study was identification of AT metabolites in rat hepatocytes and comparison with electrochemically generated oxidation products. AT was incubated with rat hepatocytes for 24 h. Electrochemical oxidation of AT was performed by use of a three-electrode off-line system with a glassy carbon working electrode. Three supporting electrolytes (0.1 mol L-1 H2SO4, 0.1 mol L-1 HCl, and 0.1 mol L-1 NaCl) were tested, and dependence on pH was also investigated. AT undergoes oxidation by asingle irreversible process at approximately +1.0 V vs. Ag/AgCl electrode. The results obtained revealed a simple and relatively fast way of determining the type of oxidation and its position, on the basis of characteristic neutral losses
Název v anglickém jazyce
Structural Characterization of Electrochemically and in Vitro Biologically Generated Oxidation Products of Atorvastatin Using UHPLC/MS/MS
Popis výsledku anglicky
Ultrahigh-performance liquid chromatography coupled with high-mass-accuracy tandem mass spectrometry (UHPLC-MS-MS) has been used for elucidation of the structures of oxidation products of atorvastatin (AT), one of the most popular commercially availabledrugs. The purpose of the study was identification of AT metabolites in rat hepatocytes and comparison with electrochemically generated oxidation products. AT was incubated with rat hepatocytes for 24 h. Electrochemical oxidation of AT was performed by use of a three-electrode off-line system with a glassy carbon working electrode. Three supporting electrolytes (0.1 mol L-1 H2SO4, 0.1 mol L-1 HCl, and 0.1 mol L-1 NaCl) were tested, and dependence on pH was also investigated. AT undergoes oxidation by asingle irreversible process at approximately +1.0 V vs. Ag/AgCl electrode. The results obtained revealed a simple and relatively fast way of determining the type of oxidation and its position, on the basis of characteristic neutral losses
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CB - Analytická chemie, separace
OECD FORD obor
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Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2013
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Analytical and Bioanalytical Chemistry
ISSN
1618-2642
e-ISSN
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Svazek periodika
405
Číslo periodika v rámci svazku
23
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
13
Strana od-do
7181-7193
Kód UT WoS článku
000323653400004
EID výsledku v databázi Scopus
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