Department of Analytical Chemistry and Food Technology, University of Castilla-La Mancha, Campus de Ciudad Real, E-13004 Ciudad Real, Spain.
J Chromatogr A. 2009 Oct 23;1216(43):7179-85. doi: 10.1016/j.chroma.2009.08.053. Epub 2009 Aug 27.
A new, simple and versatile method is presented for the determination of different concentration levels of alkenylbenzenes (eugenol, isoeugenol, eugenol methyl ether, myristicin, anethole and estragole) and the related flavour compounds (coumarin and pulegone) in food samples. The method involves the use of a stationary phase (capillary column) for the enrichment with appropriate elution. After the sample had completely passed through the capillary column the eluent was changed and the separation/detection was achieved. Excellent linearity was obtained under the proposed conditions for a direct determination method and a method including on-line preconcentration. The limits of detection were in the ranges 97-148 and 9.5-14.2 ng/mL, respectively. Evidence for a matrix effect was not found and recoveries between 92 and 110% were obtained. The precision of the method, expressed as relative standard deviation values, was below 5% in all cases. The applicability of this methodology was tested by analyzing synthetic and real food samples.
本文提出了一种新的、简单且通用的方法,用于测定食品样品中不同浓度水平的烯基苯(丁香酚、异丁香酚、丁香酚甲醚、肉豆蔻醚、茴香脑和黄樟素)和相关风味化合物(香豆素和薄荷酮)。该方法涉及使用固定相(毛细管柱)进行适当洗脱的富集。在样品完全通过毛细管柱后,改变洗脱液并实现分离/检测。在所提出的条件下,对于直接测定方法和在线预浓缩方法,均获得了极好的线性。检测限范围分别为 97-148 和 9.5-14.2 ng/mL。未发现基质效应的证据,回收率在 92%至 110%之间。该方法的精密度,以相对标准偏差值表示,在所有情况下均低于 5%。通过分析合成和真实食品样品,验证了该方法的适用性。