2014
Determination of sterols using liquid chromatography with off-line surface-assisted laser desorption/ionization mass spectrometry
VRBKOVÁ, Blanka, Vendula ROBLOVÁ, Edward S. YEUNG a Jan PREISLERZákladní údaje
Originální název
Determination of sterols using liquid chromatography with off-line surface-assisted laser desorption/ionization mass spectrometry
Autoři
VRBKOVÁ, Blanka (203 Česká republika, domácí), Vendula ROBLOVÁ (203 Česká republika, domácí), Edward S. YEUNG (840 Spojené státy) a Jan PREISLER (203 Česká republika, garant, domácí)
Vydání
Journal of Chromatography A, Amsterdam, Elsevier, 2014, 0021-9673
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10406 Analytical chemistry
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.169
Kód RIV
RIV/00216224:14740/14:00073825
Organizační jednotka
Středoevropský technologický institut
UT WoS
000340979200013
Klíčová slova anglicky
sterols; SALDI MS; HPLC
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 15. 2. 2018 22:08, prof. Mgr. Jan Preisler, Ph.D.
Anotace
V originále
A new method, reversed phase liquid chromatography with off-line surface-assisted laser desorption/ionization mass spectrometry (RPLC–SALDI MS) for the determination of brassicasterol (BR), cholesterol (CH), stigmasterol (ST), campesterol (CA) and b-sitosterol (SI) in oil samples has been developed. The sample preparation consisted of alkaline saponification followed by extraction of the unsaponificable fraction with diethyl ether. The recovery of the sterols ranged from 91 to 95% with RSD less than 4%. Separation of the five major sterols on a C18 column using methanol-water gradient was achieved in about 10 min. An on-line UV detector was employed for the initial sterol detection prior to effluent deposition using a laboratory-built spotter with 1:73 splitter. Off-line SALDI MS was then applied for mass determination/identification and quantification of the separated sterols. Ionization of the nonpolar analytes was achieved by silver ion cationization with silver nanoparticles used as the SALDI matrix providing limits of detection 12, 6 and 11 fmol for CH, ST and SI, respectively. Because of the incorporated splitter, the effective limits of detection of the RPLC–SALDI MS analysis were 4, 3 and 4 pmol (or 0.08, 0.06 and 0.08 ug/mL) for CH, ST and SI, respectively. For quantification, 6-ketocholestanol (KE) was used as the internal standard. The method has been applied for the identification and quantification of sterols in olive, linseed and sunflower oil samples. The described off-line coupling of RPLC to SALDI MS represents an alternative to GC–MS for analysis of nonpolar compounds.
Návaznosti
ED1.1.00/02.0068, projekt VaV |
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GAP206/12/0538, projekt VaV |
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