Heptafluorobutyl Chloroformate-Based Sample Preparation Protocol for Nonchiral and Chiral Amino Acid Analysis by Gas Chromatography-Mass Spectrometry
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
- Klíčová slova
- 2,3-Dimercapto-1-propanesulfonic acid, Amino acid, Amino acid analysis, Chiral analysis, Derivatization, Enantiomer, Gas chromatography, Heptafluorobutyl chloroformate, Mass spectrometry, Plasma, Serum,
- MeSH
- aminokyseliny krev chemie izolace a purifikace MeSH
- deuterium analýza chemie MeSH
- extrakce kapalina-kapalina přístrojové vybavení metody MeSH
- fluorokarbony chemie MeSH
- formiáty chemie MeSH
- izotopy uhlíku analýza chemie MeSH
- kalibrace MeSH
- lidé MeSH
- plynová chromatografie s hmotnostně spektrometrickou detekcí přístrojové vybavení metody MeSH
- stereoizomerie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aminokyseliny MeSH
- Carbon-13 MeSH Prohlížeč
- deuterium MeSH
- fluorokarbony MeSH
- formiáty MeSH
- heptafluorobutyl chloroformate MeSH Prohlížeč
- izotopy uhlíku MeSH
Gas chromatography (GC) is a commonly used technique in amino acid analysis (AAA). However, one of the requirements of the application of GC for AAA is a need for the polar analytes to be converted into their volatile, thermally stable derivatives. In the last two decades, alkyl chloroformates (RCFs) have become attractive derivatization reagents. The reagents react immediately with most amino acid functional groups in aqueous matrices, and the process can easily be coupled with liquid-liquid extraction of the resulting less polar derivatives into immiscible organic phase. Here we describe a simple protocol for in situ derivatization of amino acids with heptafluorobutyl chloroformate (HFBCF) followed by subsequent chiral as well as nonchiral GC/MS (mass spectrometric) analysis on a respective nonpolar fused silica and an enantioselective Chirasil-Val capillary column.
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