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Quantitative determination of α-ionone, β-ionone, and β-damascenone and enantiodifferentiation of α-ionone in wine for authenticity control using multidimensional gas chromatography with tandem mass spectrometric detection. | LitMetric

Quantitative determination of α-ionone, β-ionone, and β-damascenone and enantiodifferentiation of α-ionone in wine for authenticity control using multidimensional gas chromatography with tandem mass spectrometric detection.

Anal Bioanal Chem

Dienstleistungszentrum Ländlicher Raum (DLR) Rheinpfalz, Institut für Weinbau und Oenologie, Breitenweg 71, 67435, Neustadt an der Weinstraße, Germany.

Published: September 2016

AI Article Synopsis

  • The study examined the presence of α-ionone, β-ionone, and β-damascenone in various authentic and commercial wines, focusing on their potential as aroma markers.
  • A specialized technique called headspace solid-phase microextraction (HS-SPME) was used to extract these compounds, which were then analyzed using advanced gas chromatography and mass spectrometry.
  • Results showed that authentic wines had a higher presence of the (R)-enantiomer of α-ionone, suggesting that changes in its ratio could indicate potential wine adulteration, especially in wines with stronger flavors.

Article Abstract

Native concentrations of α-ionone, β-ionone, and β-damascenone were studied in various authentic and commercial wines. In addition, the enantiomeric distribution of α-ionone was determined and its merits as a potential marker for aroma adulteration in wine were discussed. For extraction of volatiles, headspace solid-phase microextraction (HS-SPME) was applied, followed by heart-cut multidimensional gas chromatography coupled to tandem mass spectrometric detection for trace-level analysis. The enantioselective analysis of α-ionone was achieved with octakis(2,3-di-O-pentyl-6-O-methyl)-γ-cyclodextrin as the chiral selector in the separation column for gas chromatography (GC). In all the authentic wines studied, α-ionone showed a high enantiomeric ratio in favor of the (R)-enantiomer. Since an illegal addition of α-ionone in a racemic form changes the enantiomeric ratio, this ratio may serve as an adulteration marker. Concentrations varied between

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Source
http://dx.doi.org/10.1007/s00216-016-9767-6DOI Listing

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