Profiling of urinary amino-carboxylic metabolites by in-situ heptafluorobutyl chloroformate mediated sample preparation and gas chromatography-mass spectrometry
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F16%3A00458358" target="_blank" >RIV/60077344:_____/16:00458358 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00843989:_____/16:E0105395
Výsledek na webu
<a href="http://www.sciencedirect.com/science/article/pii/S0021967316302692" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0021967316302692</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.chroma.2016.03.019" target="_blank" >10.1016/j.chroma.2016.03.019</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Profiling of urinary amino-carboxylic metabolites by in-situ heptafluorobutyl chloroformate mediated sample preparation and gas chromatography-mass spectrometry
Popis výsledku v původním jazyce
A novel heptafluorobutyl chloroformate reagent (HFBCF) was examined for in-situ derivatization of amino-carboxylic metabolites in human urine. The sample preparation protocol provides cleaner extracts than other urinary GC–MS based methods. Reaction products of 153 urinary metabolites with HFBCF and two internal standards were investigated in detail by GC–MS and LC–MS. The new method was validated for 132 metabolites in artificial urine with special attention to potential disease biomarker candidates. The sample preparation protocol was finally evaluated by means of a certified organic acid standard mixture in urine and by GC–MS analysis of 100 morning urines obtained from healthy patients, where 112 physiological metabolites were quantified in a 25 µL sample aliquot. Most metabolites were found within the range reported in the reference human metabolome (HMDB) database and literature. The described method has been a promising tool for targeted GC–MS based metabolomic analysis in urine.n
Název v anglickém jazyce
Profiling of urinary amino-carboxylic metabolites by in-situ heptafluorobutyl chloroformate mediated sample preparation and gas chromatography-mass spectrometry
Popis výsledku anglicky
A novel heptafluorobutyl chloroformate reagent (HFBCF) was examined for in-situ derivatization of amino-carboxylic metabolites in human urine. The sample preparation protocol provides cleaner extracts than other urinary GC–MS based methods. Reaction products of 153 urinary metabolites with HFBCF and two internal standards were investigated in detail by GC–MS and LC–MS. The new method was validated for 132 metabolites in artificial urine with special attention to potential disease biomarker candidates. The sample preparation protocol was finally evaluated by means of a certified organic acid standard mixture in urine and by GC–MS analysis of 100 morning urines obtained from healthy patients, where 112 physiological metabolites were quantified in a 25 µL sample aliquot. Most metabolites were found within the range reported in the reference human metabolome (HMDB) database and literature. The described method has been a promising tool for targeted GC–MS based metabolomic analysis in urine.n
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CE - Biochemie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/GA13-18509S" target="_blank" >GA13-18509S: Nové strategie značení alkylchlorformiáty pro cílenou a srovnávací metabolomiku technikami hmotnostní spektrometrie</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Chromatography A
ISSN
0021-9673
e-ISSN
—
Svazek periodika
1443
Číslo periodika v rámci svazku
April 22
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
22
Strana od-do
211-232
Kód UT WoS článku
000374362600025
EID výsledku v databázi Scopus
2-s2.0-84977962792