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Analytical procedure for the in-vial derivatization—extraction of phenolic acids and flavonoids in methanolic and aqueous plant extracts followed by gas chromatography with mass-selective detection
An in-vial simple method for the combined derivatization and extraction of phenolic acids and flavonoids from plant extracts and their direct determination with GC–MS, is described. The method is taking advantage of the beneficial potentials of phase transfer catalysis (PTC). Catalysts in soluble an...
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Published in: | Journal of Chromatography A 2004-07, Vol.1041 (1), p.11-18 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | An in-vial simple method for the combined derivatization and extraction of phenolic acids and flavonoids from plant extracts and their direct determination with GC–MS, is described. The method is taking advantage of the beneficial potentials of phase transfer catalysis (PTC). Catalysts in soluble and polymer-bound form were tested with the latter being the format of choice due to its high reaction yield and facile separation from the rest of the reaction system. Optimization of experimental conditions was established. Chromatographic separation of eight phenolic acids and four flavonoids methylated via the PTC derivatization step was achieved in 45
min. The detection limits for the described GC–MS(SIM) method of analysis ranged between 2 and 40
ng/ml whereas limits of quantitation fall in the range 5–118
ng/ml, with flavonoids accounting for the lowest sensitivity due to their multiple reaction behavior. Four methanolic extracts from
Tilia europea,
Urtica dioica,
Mentha spicata and
Hypericum perforatum grown wild in north-western Greece and four aquatic infusions from commercially available
Mentha spicata,
Origanum dictamnus,
Rosemarinus officinalis and
Sideritis cretica were analyzed. Good trueness of the method was demonstrated as no matrix effects were found for the analytes concerned. |
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ISSN: | 0021-9673 |
DOI: | 10.1016/j.chroma.2004.04.041 |