Luo Xiaolin, Wang Xiaoyuan, Du Ming, Xu Xianbing
National Engineering Research Center of Seafood, School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, China.
Foods. 2022 May 22;11(10):1507. doi: 10.3390/foods11101507.
The determination of flavor compounds using headspace solid-phase microextraction (HS-SPME) combined with gas chromatography-mass spectrometry (GC-MS) can be severely interfered with by complex food matrices in food systems, especially solid samples. In this study, dispersive liquid-liquid microextraction (DLLME) was applied prior to HS-SPME to efficiently reduce the matrix effect in solid seafood samples. The method had high sensitivity (the quantification limits of maltol and ethyl maltol were 15 and 5 μg/kg, respectively), an excellent linear relationship (R2 ≥ 0.996), and the sample recovery rate was 89.0-118.6%. The relative standard deviation (RSD %) values for maltol and ethyl maltol were lower than 10%. Maltol (from 0.7 to 2.2 μg/g) and ethyl maltol (from 0.9 to 34.7 μg/g) in seafood were detected in the selected samples by the developed method. Finally, DLLME coupled with HS-SPME effectively removed the influence of sample matrix and improved the sensitivity of the method. The developed method was applicable in the analysis of flavor enhancers in complex matrix foods.
使用顶空固相微萃取(HS-SPME)结合气相色谱-质谱联用(GC-MS)测定食品体系中复杂食品基质(尤其是固体样品)中的风味化合物时,可能会受到严重干扰。在本研究中,在HS-SPME之前应用分散液液微萃取(DLLME),以有效降低固体海鲜样品中的基质效应。该方法具有高灵敏度(麦芽酚和乙基麦芽酚的定量限分别为15和5 μg/kg)、良好的线性关系(R2≥0.996),样品回收率为89.0-118.6%。麦芽酚和乙基麦芽酚的相对标准偏差(RSD%)值低于10%。通过所建立的方法在所选样品中检测到海鲜中的麦芽酚(0.7至2.2 μg/g)和乙基麦芽酚(0.9至34.7 μg/g)。最后,DLLME与HS-SPME联用有效消除了样品基质的影响,提高了方法的灵敏度。所建立的方法适用于复杂基质食品中风味增强剂的分析。