On the stability of the bioactive flavonoids quercetin and luteolin under oxygen-free conditions
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F12%3A10127724" target="_blank" >RIV/00216208:11310/12:10127724 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61388955:_____/12:00375920
Výsledek na webu
<a href="http://dx.doi.org/10.1007/s00216-011-5504-3" target="_blank" >http://dx.doi.org/10.1007/s00216-011-5504-3</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00216-011-5504-3" target="_blank" >10.1007/s00216-011-5504-3</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
On the stability of the bioactive flavonoids quercetin and luteolin under oxygen-free conditions
Popis výsledku v původním jazyce
The natural flavonoid compounds quercetin (3,3',4',5,7-pentahydroxyflavone) and luteolin (3',4',5,7-tetrahydroxyflavone) are important bioactive compounds with antioxidative, anti-allergic, and anti-inflammatory properties. However, both are unstable when exposed to atmospheric oxygen, which causes degradation and complicates their analytical determinations. The oxidative change of these flavonoids was observed and followed by UV-visible spectrophotometry, both in aqueous and ethanolic solutions. The distribution of the degradation products in aqueous media was monitored by LC-MS and LC-DAD analysis. The amounts of oxidative reaction products increase with the exposure time. The oxidative degradation reduces the pharmacological efficiency of these antioxidants and renders analytical determination inaccurate. The oxidative changes in flavonoid test solutions can explain the inconsistent dissociation constants reported in the literature. Dissociation constants of quercetin and luteolin w
Název v anglickém jazyce
On the stability of the bioactive flavonoids quercetin and luteolin under oxygen-free conditions
Popis výsledku anglicky
The natural flavonoid compounds quercetin (3,3',4',5,7-pentahydroxyflavone) and luteolin (3',4',5,7-tetrahydroxyflavone) are important bioactive compounds with antioxidative, anti-allergic, and anti-inflammatory properties. However, both are unstable when exposed to atmospheric oxygen, which causes degradation and complicates their analytical determinations. The oxidative change of these flavonoids was observed and followed by UV-visible spectrophotometry, both in aqueous and ethanolic solutions. The distribution of the degradation products in aqueous media was monitored by LC-MS and LC-DAD analysis. The amounts of oxidative reaction products increase with the exposure time. The oxidative degradation reduces the pharmacological efficiency of these antioxidants and renders analytical determination inaccurate. The oxidative changes in flavonoid test solutions can explain the inconsistent dissociation constants reported in the literature. Dissociation constants of quercetin and luteolin w
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CF - Fyzikální chemie a teoretická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/GA203%2F09%2F1607" target="_blank" >GA203/09/1607: Elektrochemie přírodních barviv a jejich inkluzní komplexy.</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2012
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
402
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
8
Strana od-do
975-982
Kód UT WoS článku
000298645300039
EID výsledku v databázi Scopus
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