Search

Unprocessed olives are well-known sources of phenolic antioxidants with important biological properties. Processing methods to prepare table olives may cause a reduction of valuable phenols and may deprive the food of precious biological functions. The present work was undertaken to evaluate table olives produced in Greece as sources of biophenols. Commercially available olives were analyzed for their total phenol content by using the Folin-Ciocalteu reagent and for individual phenols by RP-HPLC. Samples were Spanish-style green olives in brine, Greek-style naturally black olives in brine, and Kalamata olives in brine. Most of the types of olives analyzed were found to be good sources of phenols. Hydroxytyrosol, tyrosol, and luteolin were the prevailing phenols in almost all of the samples examined. High levels of hydroxytyrosol were determined mainly in Kalamata olives and Spanish-style green olives, cultivar Chalkidiki (250-760 mg/kg).

Essential oils and extracts of aromatic herbs obtained by organic solvents have been extensively studied for their antioxidant activity in lipid substrates. Very little is known about the possible presence of antioxidants in polar extracts from herbs used in preparation of infusions and decoctions. In this work water extracts of six different herbs of the Lamiaceae family (dittany, lemon balm, mint, sage, sideritis and sweet marjoram) were prepared. The extracts were examined for their effect against lipid oxidation in comparison to a tea water extract. Sweet marjoram, sage and dittany extracts were found to have a remarkable capacity in retarding lipid oxidation. Examination by thin-layer chromatography of the freeze-dried extracts, before and after hydrolysis, showed that the extracts were rich in bound forms of phenolic compounds such as hydroxycinnamic acids and flavonoids. Rosmarinic and caffeic acids were detected in all extracts with the exception of those from mint and sideritis. These results indicate that certain plants used for the preparation of infusions could be further studied like tea as sources of antioxidants.

A combination of advanced nuclear magnetic resonance (NMR) methodologies for the analysis of complex phenolic mixtures that occur in natural products is described, with particular emphasis on caffeic acid and its ester derivative, rosmarinic acid. The combination of variable-temperature two-dimensional proton-proton double quantum filter correlation spectroscopy (H-1-H-1 DQF COSY) and proton-carbon heteronuclear multiple quantum coherence (H-1-C-13 HMQC) gradient NMR spectroscopy allows the identification and tentative quantification of caffeic and rosmarinic acids at 243 K in extracts from plants of the Lamiaceae family, without resorting to previous chromatographic separation of the components. The use of proton-carbon heteronuclear multiple bond correlation (H-1-C-13 HMBC) gradient NMR spectroscopy leads to the complete assignment of the correlations of the spins of H-2a and H-3a with the ester and carboxyl carbons of rosmarinic and caffeic acid, even at room temperature, and confirms the results of the above methodology. Quantitative results are in reasonable agreement with reverse phase HPLC measurements. J Agric Food Chem