| Literature DB >> 26877176 |
Antoni Pastor1, Jose Rodríguez-Morató2, Eulàlia Olesti3, Mitona Pujadas4, Clara Pérez-Mañá5, Olha Khymenets6, Montserrat Fitó7, María-Isabel Covas8, Rosa Solá9, María-José Motilva10, Magí Farré11, Rafael de la Torre12.
Abstract
Hydroxytyrosol (HT) from olive oil, a potent bioactive molecule with health benefits, has a poor bioavailability, its free form (free HT) being undetectable so far. This fact leads to the controversy whether attained HT concentrations after olive oil polyphenol ingestion are too low to explain the observed biological activities. Due to this, an analytical methodology to determine free HT in plasma is crucial for understanding HT biological activity. Plasma HT instability and low concentrations have been major limitations for its quantification in clinical studies. Here, we describe a method to detect and quantify free HT in human plasma by using liquid chromatography coupled to tandem mass spectrometry. The method encompasses different steps of sample preparation including plasma stabilization, protein precipitation, selective derivatization with benzylamine, and purification by solid-phase extraction. A high sensitivity (LOD, 0.3ng/mL), specificity and stability of HT is achieved following these procedures. The method was validated and its applicability was demonstrated by analyzing human plasma samples after olive oil intake. A pharmacokinetic comparison was performed measuring free HT plasma concentrations following the intake of 25mL of ordinary olive oil (nearly undetectable concentrations) versus an extra-virgin olive oil (Cmax=4.40ng/mL). To our knowledge, this is the first time that an analytical procedure for quantifying free HT in plasma after olive oil dietary doses has been reported. The present methodology opens the door to a better understanding of the relationship between HT plasma concentrations and its beneficial health effects.Entities:
Keywords: Benzylamine derivatization; Health; Humans; Hydroxytyrosol; LC–MS/MS; Virgin olive oil
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Year: 2016 PMID: 26877176 DOI: 10.1016/j.chroma.2016.02.016
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759