Development of headspace solid-phase microextraction-gas chromatography-mass spectrometry methodology for analysis of terpenoids in Madeira wines

被引:114
作者
Câmara, JS
Alves, MA
Marques, JC
机构
[1] Univ Madeira, Dept Quim, P-9000390 Funchal, Madeira, Portugal
[2] Univ Porto, Dept Engn Quim, Fac Engn, P-4200465 Oporto, Portugal
关键词
solid-phase microextraction; optimisation; varietal compounds; must; wine;
D O I
10.1016/j.aca.2005.09.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A dynamic headspace solid-phase microextraction methodology was developed for analysis of varietal aroma compounds in must and Madeira wine samples, a spirit wine with an ethanol content of 18% (v/v). The factors with influence in the headspace solid-phase microextraction efficiency such as: fibre coating, extraction time and temperature, pH, ionic strength, ethanol content, desorption time and temperature, were optimised and the method validated. The best results were obtained for a 85 Run polyacrylate fibre, with a 60 min headspace for must and 120 min for wine samples, in a 2.4 ml sample at 40 degrees C with 30% of NaCl. The extract is injected in the splitless mode in a GC-MS Varian system, Saturn III, and separated on a Stabilwax capillary column. The linear dynamic range of the method covers the normal range of occurrence of analytes in wine with typical r(2) between 0.985 (beta-ionone) and 0.998 (linalool) for musts and between 0.980 (alpha-terpineol) and 0.999 (linalool) for must and wine samples, respectively. For must samples the reproducibility ranges from 2.5% (citronellol) to 14.4% (nerolidol) (as R.S.D.), and from 4.8% (citronellol) to 14.2% (neiolidol) for wine samples. The analysis of spiked samples has shown that matrix effects do not significantly affect method performance. Limits of detection obtained are in low mu g I-1 range for all compounds analysed in this study. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:191 / 200
页数:10
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