Abstract

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.

Highlights

  • The authentication of foodstuff has been developed according to market tendencies, and analytical methods have evolved to detect adulterations.The unsaponifiable fraction of oils or fats constitutes a very small fraction but an essential part of oils’ healthy properties

  • Among all the possibilities for the determination of sterols in vegetable oils, gas chromatography with a FID detector is the last step in the process of their quantification and, it is, with minor differences, common to all proposals

  • The official methods [5,6,7] described several liquid–liquid extractions with diethyl ether where the unsaponifiable fraction is extracted almost free of the saponified part, which is solubilized into the water

Read more

Summary

Introduction

The authentication of foodstuff has been developed according to market tendencies, and analytical methods have evolved to detect adulterations. The unsaponifiable fraction of oils or fats constitutes a very small fraction but an essential part of oils’ healthy properties. It is a complex fraction formed by a large number of minor compounds. These compounds rarely represent more than 2% of the oil composition and include many compounds of a different nature [1]. In the case of olive oils, the analytical methods to determine the content in several sterols and triterpenic dialcohols and their values are described in detail in the official regulations [4,5,6,7,8]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call