León-Camacho Manuel, Del Carmen Pérez-Camino María
Lipid Characterization and Quality Department, Instituto de la Grasa, Spanish National Research Council, 41013 Seville, Spain.
Foods. 2021 Aug 27;10(9):2019. doi: 10.3390/foods10092019.
The unsaponifiable fraction of oils and fats constitutes a very small fraction but it is an essential part of the healthy properties of some specific oils. It is a complex fraction formed by a large number of minor compounds and it is a source of information to characterize and authenticate the oil sample. Specially, the composition of sterols of any oil or fat is a distinctive feature of itself and, therefore, it has become a useful tool for detecting contaminants and adulterants in oils. A new supported liquid extraction (SLE) technique for the analysis and characterization of the unsaponifiable fraction of fats and oils is proposed. The SLE system includes, as a stationary phase, a combination of adsorbent materials which allow a highly purified unsaponifiable matter ready to be isolated by high performance liquid chromatography (HPLC) and quantified by gas chromatography (GC). This method ensures the removal of fatty acids, avoiding possible interferences and making the analysis of sterols and triterpenic dialcohols easier. The procedure uses a small sample size (0.2 g), reduces the volume of solvents and reagents, and reduces the handling of samples subjected to analytical control. All this is achieved without losing either precision-a relative standard deviation of each compound lower than the reference value (≤16.4%)-or recovery, being for all compounds higher than 88.00%. Therefore, this new technique represents a significant economic and time saving in business control laboratories, a larger productivity and enhancement of working safety.
油脂的不皂化物部分占比非常小,但却是某些特定油脂健康特性的重要组成部分。它是一个由大量次要化合物构成的复杂部分,是表征和鉴定油样的信息来源。特别地,任何油脂的甾醇组成都是其独特特征,因此,它已成为检测油脂中污染物和掺假物的有用工具。本文提出了一种用于分析和表征油脂不皂化物部分的新型支撑液液萃取(SLE)技术。该SLE系统包括作为固定相的吸附材料组合,可得到高度纯化的不皂化物,便于通过高效液相色谱(HPLC)分离并通过气相色谱(GC)定量。该方法可确保去除脂肪酸,避免可能的干扰,使甾醇和三萜二醇的分析更加容易。该方法使用的样品量小(0.2 g),减少了溶剂和试剂的用量,并减少了分析控制样品的操作。所有这些都在不损失精度(每种化合物的相对标准偏差低于参考值(≤16.4%))或回收率(所有化合物的回收率高于88.00%)的情况下实现。因此,这项新技术在商业控制实验室中显著节省了经济成本和时间,提高了生产力并增强了工作安全性。