| Literature DB >> 25236241 |
Isabella Vulcano1, Maria Halabalaki2, Leandros Skaltsounis2, Markus Ganzera3.
Abstract
The first CE procedure for the quantitative determination of pharmacologically relevant secoiridoids in olive oil, oleocanthal and oleacein, is described. Together with their precursors tyrosol and hydroxytyrosol they could be baseline separated in less than 15min using a borax buffer with pH 9.5, at 25kV and 30°C. Method validation confirmed that the procedure is selective, accurate (recovery rates from 94.0 to 104.6%), reproducible (σmax⩽6.8%) and precise (inter-day precision⩽6.4%), and that the compounds do not degrade quickly if non-aqueous acetonitrile is used as solvent. Quantitative results indicated a low occurrence of oleocanthal (0.004-0.021%) and oleacein (0.002-0.048%) in olive oil samples, which is in agreement to published HPLC data. The CE method impresses with its simple instrumental and methodological design, combined with reproducible and valid quantitative results.Entities:
Keywords: Capillary electrophoresis; Hydroxytyrosol (PubChem CID: 82755); Inflammation; Oleacein; Oleacein (no PubChem CID, CAS: 149183-75-5); Oleocanthal; Oleocanthal (PubChem CID: 16681728); Olive oil; Phenolic compounds; Tyrosol (PubChem CID: 10393)
Mesh:
Substances:
Year: 2014 PMID: 25236241 DOI: 10.1016/j.foodchem.2014.08.007
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514