Molina-Calle María, Priego-Capote Feliciano, Luque de Castro María D
Department of Analytical Chemistry, University of Córdoba, Annex Marie Curie Building, Campus of Rabanales, 14071 Córdoba, Spain; Maimónides Institute for Research in Biomedicine of Córdoba (IMIBIC), Reina Sofía University Hospital, University of Córdoba, 14071 Córdoba, Spain; University of Córdoba, Agroalimentary Excellence Campus, ceiA3, Campus of Rabanales, 14071 Córdoba, Spain.
Department of Analytical Chemistry, University of Córdoba, Annex Marie Curie Building, Campus of Rabanales, 14071 Córdoba, Spain; Maimónides Institute for Research in Biomedicine of Córdoba (IMIBIC), Reina Sofía University Hospital, University of Córdoba, 14071 Córdoba, Spain; University of Córdoba, Agroalimentary Excellence Campus, ceiA3, Campus of Rabanales, 14071 Córdoba, Spain.
Talanta. 2015 Aug 15;141:150-7. doi: 10.1016/j.talanta.2015.03.045. Epub 2015 Apr 8.
An optimized method for extraction and characterization of compounds present in orange peel has been developed. The extraction method allows the simultaneous extraction of polar and non-polar compounds by using two immiscible extractants (a polar extractant-an 80:20 (v/v) methanol-water mixture, and a non-polar extractant-n-hexane). The method is ultrasound-assisted, thus facilitating both formation of a stable emulsion between the two immiscible extractants and favoring mass-transfer from the solid sample to the liquid phases by a wide contact surface. Optimization of the ultrasound-assisted emulsification-extraction (USAEE) led to the following values as desirability conditions for both extracts: 32% amplitude, 0.75s/s duty cycle and 7.5min of extraction time. The extracts obtained under these conditions were analyzed by LC-QTOF MS/MS in positive and negative ionization modes. Tentative identification of the most significant compounds present in each extract allowed their characterization by using high resolution tandem mass spectrometry. The optimum extracts provided by USAEE were compared by using Principal Component Analysis to those obtained by conventional extraction based on maceration. Thus, the composition of the polar extracts obtained after 7.5min ultrasonication was similar to that of conventional maceration for 4h in both the ionization modes. On the contrary, the analysis of non-polar extracts led to different results depending on the ionization mode: the ultrasound-assisted extract was similar to those of conventional maceration for 10h in negative and positive ionization. This behavior could be explained by the contribution of different groups of compounds to each ionization mode.
已开发出一种优化的方法,用于提取和表征橙皮中的化合物。该提取方法可通过使用两种不混溶的萃取剂(极性萃取剂——80:20(v/v)的甲醇 - 水混合物,以及非极性萃取剂——正己烷)同时提取极性和非极性化合物。该方法是超声辅助的,因此既有助于在两种不混溶的萃取剂之间形成稳定的乳液,又有利于通过广泛的接触表面使传质从固体样品转移到液相。超声辅助乳化萃取(USAEE)的优化得出了以下作为两种提取物期望条件的值:32%的振幅、0.75s/s的占空比和7.5分钟的萃取时间。在这些条件下获得的提取物通过LC - QTOF MS/MS在正离子和负离子模式下进行分析。通过使用高分辨率串联质谱对每种提取物中存在的最主要化合物进行初步鉴定,从而对其进行表征。通过主成分分析将USAEE提供的最佳提取物与基于浸渍法的传统提取方法所获得的提取物进行比较。因此,在两种电离模式下,超声处理7.5分钟后获得的极性提取物组成与传统浸渍4小时的提取物相似。相反,非极性提取物的分析根据电离模式得出不同结果:在负离子和正离子电离中,超声辅助提取物与传统浸渍10小时的提取物相似。这种行为可以通过不同组化合物对每种电离模式的贡献来解释。