Abstract

It was proven that sterols subjected to high-temperature treatment can be concatenated, which results in polymeric structures, e.g., 3β,3′β-disteryl ethers. However, it was also proven that due to increased temperature in oxygen-containing conditions, sterols can undergo various oxidation reactions. This study aimed to prove the existence and perform quantitative analysis of oxidized 3β,3′β-disteryl ethers, which could form during high-temperature treatment of sterol-rich samples. Samples were heated at 180, 200 and 220 °C for 0.5 to 4 h. Quantitative analyses of the oxidized 3β,3′β-disteryl ethers were performed with liquid extraction, solid-phase extraction and liquid chromatography coupled with mass spectrometry. Additionally, to perform this analysis, the appropriate standards of all oxidized 3β,3′β-disteryl ethers were prepared. Eighteen various oxidized 3β,3′β-disteryl ethers (derivatives of 3β,3′β-dicholesteryl ether, 3β,3′β-disitosteryl ether and 3β,3′β-distigmasteryl ether) were prepared. Additionally, the influence of metal compounds on the mechanism of ether formation at high temperatures was investigated.

Highlights

  • It was already proven that oxysterols and oxyphytosterols are formed through the oxidation of sterol molecules and possess various functions or influences in the human body

  • Based on the molecular mass obtained by high-resolution mass spectrometry (HRMS), one of the found dimers was suggested to consist of two stigmasterol moieties linked with ether bonds, which could correspond to the structure of 3β,30 β-distigmasteryl ether

  • Using gas chromatography coupled with mass spectrometry (GC-MS), we recently proved the formation of 3β,30 β-disteryl ethers in sterol-rich samples after high-temperature treatment [4]

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Summary

Introduction

It was already proven that oxysterols and oxyphytosterols are formed through the oxidation of sterol molecules and possess various functions or influences in the human body. Using gas chromatography coupled with mass spectrometry (GC-MS), we recently proved the formation of 3β,30 β-disteryl ethers in sterol-rich samples after high-temperature treatment [4]. In addition to the polymerization reaction, formed ethers could be oxidized or, as presumed, formed oxysterols during heat treatment could react with native sterol to form oxidized 3β,30 β-disteryl ethers because only one sterol particle needs the 3β-hydroxyl and double bond at positions 5–6 [4]. This possibility was confirmed by Struijs, who found

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