Abstract
During the enantioselective analysis of whisky lactones after headspace in-tube extraction and gas chromatography with mass spectrometric detection using an ion trap mass analyzer (ITMS), an unusual effect led to peak suppression for one of the four enantiomers of whisky lactones. Using the ITMS in the selective ion monitoring (SIM) mode, one of the four targeted whisky lactone enantiomers could not be detected due to an abundant co-eluting matrix compound. For troubleshooting, detection with a quadrupole MS proved the presence of the missing enantiomer peak. A hypothetical explanation of this phenomenon is at present based on the different ion scanning mechanism of the two MS instruments. Considering the irregular sampling during the discontinuous scanning process of the ITMS being dictated by the ion current, this might have led to the suppression of the analyte. Furthermore, a solvent trapping effect of the target analyte with a co-chromatographing abundant matrix compound created a peak distortion (focusing) of the minor whisky lactone enantiomer. In our case, the inexplicably missing enantiomer peak triggered this investigation, but such matrix effects could easily be overseen with ITMS (SIM) detection, then eventually causing false-negative results.
References
Maga JA (1996) Oak lactones in alcoholic beverages. Food Rev Int 12(1):105–130
Guenther C, Mosandl A (1986) Stereoisomeric flavor substances. XII. 3-Methyl-4-octanolide quercuslactone, whiskey lactone-structure and properties of the stereoisomers. Liebigs Ann Chem 12:2112–2122
Mosandl A, Kustermann A, Palm U, Dorau HP, Koenig WA (1989) Stereoisomeric flavor compounds. XXVIII. Direct chirospecific HRGC analysis of natural γ-lactones. Z Lebensm Unters Forsch 188(6):517–520
Schmarr H-G, Eisenreich W, Engel K-H (2001) Synthesis and analysis of thio-, thiono-, and dithio-derivatives of whiskey lactone. J Agric Food Chem 49(12):5923–5928
Guichard E, Fournier N, Masson G, Puech JL (1995) Stereoisomers of β-methyl-γ-octalactone. I. Quantification in brandies as a function of wood origin and treatment of the barrels. Am J Enol Viticult 46(4):419–423
Commision Decision 2002/657/EC (2002) L 221/8, Official J. of the European Communities, 185 Document number C(2002) 3044, European Union
Laaks J, Jochmann MA, Schilling B, Schmidt TC (2010) In-tube extraction of volatile organic compounds from aqueous samples: an economical alternative to purge and trap enrichment. Anal Chem 82(18):7641–7648
Schmarr H-G, Mosandl A, Kaunzinger A (1991) Influence of derivatization on the chiral selectivity of cyclodextrins: alkylated/acylated cyclodextrins and γ-/δ-lactones as an example. J Microcolumn Sep 3(5):395–402
Hübschmann H-J (2008) Handbook of GC/MS—fundamentals and applications. Wiley, Weinheim
March RE (1997) An introduction to quadrupole ion trap mass spectrometry. J Mass Spectrom 32(4):351–369
March RE, Todd JFJ (2005) Quadrupole ion trap mass spectrometry, 2nd edn. In: Winefordner JD (ed) Chemical Analysis—Series of monographs on analytical chemistry and its applications, vol 165. Wiley-Interscience, Hoboken
Grob K (1987) On-column injection in capillary gas chromatography: basic technique, retention gaps, solvent effects. Hüthig Verlag, Heidelberg
Grob K Jr, Schilling B (1983) Solvent effects in capillary gas chromatography. Determination of trace amounts of chloroform as an example. J Chromatogr 264(1):7–18
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Financial support from the Ministerium für Umwelt, Landwirtschaft, Ernährung, Weinbau und Forsten (MULEWF), Rheinland-Pfalz, Germany is acknowledged.
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Slabizki, P., Potouridis, T. & Schmarr, HG. Ion Trap Mass Spectrometric Effect Leading to Peak Suppression and Solvent-Free Peak Focusing due to Co-Chromatography. Chromatographia 77, 1727–1730 (2014). https://doi.org/10.1007/s10337-014-2761-2
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DOI: https://doi.org/10.1007/s10337-014-2761-2