Departamento de Química Analítica, Facultad de Química, Universitat de València, 46100 Burjassot, Valencia, Spain.
Departamento de Química Analítica, Facultad de Química, Universitat de València, 46100 Burjassot, Valencia, Spain.
Anal Chim Acta. 2014 May 15;826:28-34. doi: 10.1016/j.aca.2014.03.042. Epub 2014 Apr 4.
A new analytical method based on simultaneous derivatization and dispersive liquid-liquid microextraction (DLLME) followed by gas chromatography-mass spectrometry (GC-MS), for the determination of the allergenic compounds atranol and chloroatranol in perfumes, is presented. Derivatization of the target analytes by means of acetylation with anhydride acetic in carbonate buffer was carried out. Thereby volatility and detectability were increased for improved GC-MS sensitivity. In addition, extractability by DLLME was also enhanced due to a less polar character of the solutes. A liquid-liquid extraction was performed before DLLME to clean up the sample and to obtain an aqueous sample solution, free of the low polar matrix from the essential oils, as donor phase. Different parameters, such as the nature and volume of both the extraction and disperser solvents, the ionic strength of the aqueous donor phase or the effect of the derivatization reagent volume, were optimized. Under the selected conditions (injection of a mixture of 750μL of acetone as disperser solvent, 100μL of chloroform as extraction solvent and 100μL of anhydride acetic as derivatization reagent) the figures of merit of the proposed method were evaluated. Limits of detection in the low ngmL(-1) range were obtained. Matrix effect was observed in real perfume samples and thus, standard addition calibration is recommended.
一种基于同时衍生化和分散液相微萃取(DLLME)的新分析方法,随后是气相色谱-质谱(GC-MS),用于测定香水中的过敏原化合物阿特拉醇和氯阿特拉醇。通过在碳酸盐缓冲液中用乙酸酐对目标分析物进行乙酰化衍生化。由此增加了挥发性和可检测性,提高了 GC-MS 的灵敏度。此外,由于溶质的极性较小,通过 DLLME 萃取的能力也得到了增强。在 DLLME 之前进行液液萃取,以净化样品并获得水性样品溶液,该溶液不含精油的低极性基质,作为供体相。优化了不同的参数,例如萃取和分散溶剂的性质和体积、水性供体相的离子强度或衍生化试剂体积的影响。在选择的条件下(注入 750μL 丙酮作为分散溶剂、100μL 氯仿作为萃取溶剂和 100μL 乙酸酐作为衍生化试剂),评估了所提出方法的优点。在低 ngmL(-1)范围内获得了检测限。在实际香水样品中观察到基质效应,因此建议采用标准添加校准。