Mendonça Carla R B, Bica Clara I D, Piatnicki Clarisse M S, Simó-Alfonso Ernesto F, Ramis-Ramos Guillermo
Departament de Química Analítica, Universitat de València, Burjassot, Spain.
Electrophoresis. 2005 Sep;26(17):3307-14. doi: 10.1002/elps.200410394.
The separation of hydroxyaromatic compounds in vegetable oils, including synthetic antioxidants (3-tert-butyl-4-hydroxyanisol and 2,6-di-tert-butyl-4-hydroxytoluene), E-vitamers and other natural oil components, by nonaqueous capillary electrophoresis in an oil-miscible background electrolyte (BGE) was investigated. The BGE contained 40 mM KOH in a methanol/1-propanol (PrOH) mixture (15:85 v/v). The oil samples were 1:1 diluted with PrOH and directly injected in the capillary. Under negative polarity (cathode at the injection end), the anionic solutes moved faster than the electroosmotic flow, being well-resolved among them and from the triacylglycerols. Using virgin palm, extra virgin olive, wheat germ, virgin soybean and other oils, the capability of the procedure to quickly yield a characteristic profile of the biophenols present in the sample was demonstrated. The alpha-, (beta + gamma)- (as unresolved pair) and delta-tocopherols of a soybean oil sample were quantified.
研究了在与油混溶的背景电解质(BGE)中,通过非水毛细管电泳法分离植物油中的羟基芳香族化合物,包括合成抗氧化剂(3-叔丁基-4-羟基茴香醚和2,6-二叔丁基-4-甲基苯酚)、维生素E异构体和其他天然油成分。BGE在甲醇/1-丙醇(PrOH)混合物(15:85 v/v)中含有40 mM氢氧化钾。油样用PrOH按1:1稀释后直接注入毛细管。在负极性(注入端为阴极)下,阴离子溶质的移动速度比电渗流快,它们之间以及与三酰甘油之间都得到了很好的分离。使用初榨棕榈油、特级初榨橄榄油、小麦胚芽油、初榨大豆油和其他油类,证明了该方法能够快速生成样品中存在的生物酚的特征图谱。对一个大豆油样品中的α-、(β+γ)-(作为未分离的一对)和δ-生育酚进行了定量分析。