Simultaneous determination of mushroom toxins ?-amanitin, ?-amanitin and muscarine in human urine by solid-phase extraction and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F15%3A33155700" target="_blank" >RIV/61989592:15110/15:33155700 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00098892:_____/15:#0000975
Výsledek na webu
<a href="http://www.sciencedirect.com/science/article/pii/S037907381500153" target="_blank" >http://www.sciencedirect.com/science/article/pii/S037907381500153</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.forsciint.2015.04.007" target="_blank" >10.1016/j.forsciint.2015.04.007</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Simultaneous determination of mushroom toxins ?-amanitin, ?-amanitin and muscarine in human urine by solid-phase extraction and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry
Popis výsledku v původním jazyce
This paper presents a method for the simultaneous determination of ?-amanitin, ?-amanitin and muscarine in human urine by solid-phase extraction (SPE) and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry. The method can be used for a diagnostics of mushroom poisonings. Different SPE cartridges were tested for sample preparation, namely hydrophilic modified reversed-phase (Oasis HLB) and polymeric weak cation phase (Strata XCW).The latter gave better results and therefore it was chosen for the subsequent method optimization and partial validation. In the course of validation, limits of detection, linearity, intraday and interday precisions and recoveries were evaluated. The obtained LOD values of ?-amanitin and ?-amanitin were1 ng/mL and of muscarine 0.09 ng/mL. The intraday and interday precisions of human urine spiked with ?-amanitin (10 ng/mL), ?-amanitin (10 ng/mL) and muscarine (1 ng/mL) ranged from 6% to 10% and from 7% to 13%,
Název v anglickém jazyce
Simultaneous determination of mushroom toxins ?-amanitin, ?-amanitin and muscarine in human urine by solid-phase extraction and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry
Popis výsledku anglicky
This paper presents a method for the simultaneous determination of ?-amanitin, ?-amanitin and muscarine in human urine by solid-phase extraction (SPE) and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry. The method can be used for a diagnostics of mushroom poisonings. Different SPE cartridges were tested for sample preparation, namely hydrophilic modified reversed-phase (Oasis HLB) and polymeric weak cation phase (Strata XCW).The latter gave better results and therefore it was chosen for the subsequent method optimization and partial validation. In the course of validation, limits of detection, linearity, intraday and interday precisions and recoveries were evaluated. The obtained LOD values of ?-amanitin and ?-amanitin were1 ng/mL and of muscarine 0.09 ng/mL. The intraday and interday precisions of human urine spiked with ?-amanitin (10 ng/mL), ?-amanitin (10 ng/mL) and muscarine (1 ng/mL) ranged from 6% to 10% and from 7% to 13%,
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CB - Analytická chemie, separace
OECD FORD obor
—
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Forensic Science International
ISSN
0379-0738
e-ISSN
—
Svazek periodika
2015
Číslo periodika v rámci svazku
251
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
5
Strana od-do
209-213
Kód UT WoS článku
000354125900031
EID výsledku v databázi Scopus
—