Determination of volatile components of saffron by optimised ultrasound-assisted extraction in tandem with dispersive liquid-liquid microextraction followed by gas chromatography-mass spectrometry

被引:66
|
作者
Sereshti, Hassan [1 ]
Heidari, Reza [1 ]
Samadi, Soheila [1 ]
机构
[1] Univ Tehran, Fac Sci, Dept Chem, Tehran, Iran
关键词
Saffron; Ultrasonic-assisted extraction; Dispersive liquid-liquid microextraction; Gas chromatography-mass spectrometry; Central composite design; CROCUS-SATIVUS L; DIFFERENT GEOGRAPHICAL ORIGINS; ESSENTIAL OIL; QUALITY-CONTROL; SPICE; QUANTIFICATION; IDENTIFICATION; PRODUCTS; SAMPLES; AROMA;
D O I
10.1016/j.foodchem.2013.08.024
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present research, a combined extraction method of ultrasound-assisted extraction (UAE) in conjunction with dispersive liquid-liquid microextraction (DLLME) was applied to isolation and enrichment of saffron volatiles. The extracted components of the saffron were separated and determined by gas chromatography-mass spectrometry (GC-MS) technique. The mixture of methanol/acetonitrile was chosen for the extraction of the compounds and chloroform was used at the preconcentration stage. The important parameters, such as composition of extraction solvent, volume of preconcentration solvent, ultrasonic applying time, and salt concentration were optimised by using a half-fraction factorial central composite design (CCD). Under the optimal conditions, the linear dynamic ranges (LDRs) were 10-10,000 mg L-1. The determination coefficients (R-2) were from 0.9990 to 0.9997. The limits of detection (LODs) and limits, of quantification (LOQs) for the extracted compounds were 6-123 mg L-1 and 20-406 mg L-1, respectively. The relative standard deviations (RSDs) were 2.48-9.82% (n = 3). The enhancement factors (EFs) were 3.6-41.3. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:499 / 505
页数:7
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