Determination of furfural in beers, vinegars and infant formulas by solid-phase microextraction and gas chromatography/mass spectrometry

被引:14
|
作者
Tsai, Shih-Wei [1 ]
Kao, Kuo-Yuan [2 ]
机构
[1] Natl Taiwan Univ, Inst Environm Hlth, Coll Publ Hlth, Taipei 100, Taiwan
[2] China Med Univ, Dept Occupat Safety & Hlth, Taichung 404, Taiwan
关键词
solid-phase microextraction; O-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride; furfural; gas chromatography; food samples; ON-FIBER DERIVATIZATION; CARBONYL-COMPOUNDS; VOLATILE; WATER; ALDEHYDES; AIR;
D O I
10.1080/03067319.2010.496050
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The solid-phase microextraction (SPME) technique with on-fibre derivatisation was evaluated for the analysis of furfural in infant formulas, beers, and vinegars. The poly(dimethylsiloxane)/divinylbenzene (PDMS/DVB) fibre was used and O-2,3,4,5,6-(pentafluorobenzyl) hydroxylamine hydrochloride (PFBHA) was first loaded onto the fibre. Food sample of 2mL was then placed in a 4mL PTFE-capped glass vial. Headspace extraction by the SPME fibre was performed at 80 degrees C for 20 min under 1100 rpm magnetic stirring with the addition of 40% sodium chloride. Afterwards, the SPME fibre was directly desorbed at the injection port of a gas chromatography/mass spectrometer (GC/MS), followed by the analysis of derivatives formed on-fibre. To avoid matrix interferences, standard addition method was performed. The adsorption-time profiles were examined. The precision, recovery and method detection limits (MDLs) were evaluated with spiked food samples. The relative standard deviations from different spiked samples were all less than 5% and the recoveries were 100 +/- 5%. With 2mL of food sample, MDLs were in the range of 3.09 similar to 14.05 mu g L(-1). Compared with other techniques, the study shown here provided
引用
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页码:76 / 84
页数:9
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