4.4 Article

Determination of volatile compounds in antioxidant rosemary extracts by multiple headspace solid-phase microextraction and gas chromatography

期刊

FLAVOUR AND FRAGRANCE JOURNAL
卷 21, 期 4, 页码 626-633

出版社

WILEY
DOI: 10.1002/ffj.1630

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volatile compounds; multiple solid-phase microextraction; consecutive extractions; odour; gas chromatography; rosemary extract; Rosmarinus officinalis

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Rosemary extracts are commercialized as natural antioxidants that delay the lipid oxidation process. Residual amounts of rosemary odour-responsible volatile compounds, such as borneol, camphor and verbenone, can remain in the final extract. The presence of these compounds may be undesirable when the extracts are used as food or cosmetic additives. In this paper a MHS-SPME method is proposed to quantify 10 rosemary odour-responsible compounds in a commercial solid rosemary extract. Multiple headspace solid-phase microextraction (MHS-SPME) is a recent technique proposed to eliminate the matrix effect on the quantitative analysis of solid samples. This technique performs few consecutive extractions from the same sample, and the total area corresponding to an exhaustive extraction is calculated as the sum of individual area values obtained from each extraction or by using an equation. The most influential variables of the extraction process, such as type of fibre, temperature and extraction time, were studied. Extraction was carried out using 2.5 mg solid extract and a divinylbenzene-carboxen-polydimethylsiloxane (DVB-CAR-PDMS) fibre at 55 degrees C for 60 min; calibration was carried out using aqueous standard solutions containing 1% (v/v) ethanol at 40 degrees C for 45 min. The features of the method were established using aqueous standards solutions. Precision was 4-15 %, expressed as RSD, and the method allowed detection limits of 0.4-47 ng for p-cyrnene and verbenone, respectively. Finally, the method was applied to analyse a rosemary solid extract, and verbenone (356 mu g/g), borneol (190 mu g/g) and camphor (136 mu g/g) were found to be the most abundant compounds. Copyright (c) 2006 John Wiley & Sons, Ltd.

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