Analysis of volatile compounds of pineapple wine using solid-phase microextraction techniques

An analytical procedure based on headspace solid-phase microextraction (HS-SPME) method combined with GC–MS was developed for the extraction and quantification of volatile compounds from pineapple wine. Different sample preparation (SPME fibre type, addition of sodium chloride, extraction time and t...

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Veröffentlicht in:Food chemistry 2010-10, Vol.122 (4), p.1241-1246
Hauptverfasser: Pino, Jorge A., Queris, Oscar
Format: Artikel
Sprache:eng
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Zusammenfassung:An analytical procedure based on headspace solid-phase microextraction (HS-SPME) method combined with GC–MS was developed for the extraction and quantification of volatile compounds from pineapple wine. Different sample preparation (SPME fibre type, addition of sodium chloride, extraction time and temperature) were evaluated to optimise the method. For the final method, 8 ml of pineapple wine were placed in a 15 ml headspace vial with addition of 1 g of NaCl; a polydimethylsiloxane SPME fibre was used for extraction at 30 °C for 30 min with continuous stirring. The volatile compounds have shown a good linearity in the range of concentrations studied with regression coefficients higher than 0.98, and the reproducibility expressed as relative standard deviation ranged from 4.2% (2-phenylethyl acetate) to 7.1% (ethyl benzoate). The values obtained for detection and quantification limits were low enough to permit the determination of volatiles in pineapple wine. Using this method, 18 volatiles were identified, including 13 esters, 4 alcohols and one acid. Ethyl octanoate, ethyl acetate, 3-methyl-1-butanol and ethyl decanoate were the major constituents. A tentative study to estimate the contribution of the identified compounds to the aroma of the wine, on the basis of their odour activity values (OAV), indicated that the compounds potentially most important to pineapple wine included ethyl octanoate, ethyl acetate and ethyl 2-methylpropanoate.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2010.03.033