A new method for immediate derivatization of hydroxyl groups by fluoroalkyl chloroformates and its application for the determination of sterols and tocopherols in human serum and amniotic fluid by gas chromatography-mass spectrometry
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, validační studie
PubMed
24666939
DOI
10.1016/j.chroma.2014.03.007
PII: S0021-9673(14)00370-7
Knihovny.cz E-zdroje
- Klíčová slova
- Alkyl chloroformate derivatization, Amniotic fluid, Gas chromatography–mass spectrometry, Human serum, Liquid–liquid microextraction, Steroid hydroxyl group,
- MeSH
- fluorokarbony chemie MeSH
- formiáty chemie MeSH
- indikátory a reagencie MeSH
- lidé MeSH
- mikroextrakce kapalné fáze MeSH
- plodová voda chemie MeSH
- plynová chromatografie s hmotnostně spektrometrickou detekcí MeSH
- sérum MeSH
- steroly analýza krev MeSH
- těhotenství MeSH
- tokoferoly analýza krev MeSH
- Check Tag
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- validační studie MeSH
- Názvy látek
- fluorokarbony MeSH
- formiáty MeSH
- heptafluorobutyl chloroformate MeSH Prohlížeč
- indikátory a reagencie MeSH
- steroly MeSH
- tokoferoly MeSH
A new method has been described for efficient derivatization of secondary alicyclic hydroxyl groups in steroids by alkyl chloroformates (RCFs). Cholesterol, an essential human sterol and a steroid precursor in eukaryotic cells, was used as a model for treatment with various RCFs in an aqueous and non-aqueous environment. While the cholesterol hydroxyl group did not react completely with any of the tested RCFs reagents in the former case, trifluoroethyl chloroformate (TFECF) or heptafluorobutyl chloroformate (HFBCF) fully converts cholesterol and related metabolites into the corresponding mixed carbonates under anhydrous conditions in seconds. The acylation reaction was combined with liquid-liquid microextraction (LLME) between isooctane and acetonitrile phase. The sample preparation requires just a stepwise addition of 50μl isooctane with 5μl of a pyridine catalyst, 100μl acetonitrile and 100μl isooctane with dissolved 5μl of the fluoroalkyl chloroformate reagent to a dried sample. The protocol developed in this study was successfully tested for GC-MS analysis of 12 important model steroids and four main tocopherols. Each analyte provided a single peak with excellent GC separation properties, well defined EI spectra containing diagnostic fragment ions suitable for their identification and quantitation. The new method was further validated for the determination of six diagnostic non-cholesterol sterols and four main tocopherols in human serum and in amniotic fluid. Satisfactory data were obtained in terms of calibration, quantitation limits (for sterols and tocopherols, 0.05 and 0.15μg/ml, respectively), within-run precision (0.9-19.5%) and between-run precision (0.2-19.0%), accuracy (82-115%) and recovery (90-110%). The validated method was successfully applied to GC-MS analysis of the analytes in woman sera and amniotic fluids and the results are well-comparable with those reported by other authors. The presented work demonstrates for the first time capability of the RCFs to derivatize alicyclic hydroxyls in steroids and tocopherols metabolites for GC-MS with excellent reaction rates, highest reaction yields, minor reagent consumption and easy conjunction with LLME methods.
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