Ether soluble polyphenols from leaves of Eucalyptus camaldulensis, E. globulus and E. rudis have been studied. The phenolic aldehyde vanillin, the phenolic acids gallic, protocatechuic and ellagic acids, some flavonol glycosides (rutin, quercetin-3-arabinoside, quercetin-3,7-dirhamnoside, quercitrin, kaempferol-3-arabinoside and their aglycones), one flavanone (naringenin) and two flavones (luteolin and apigenin) were identified and quantified. Some ellagitannins, flavonols and flavanones were recognized according to their ultra-violet spectra. E. camaldulensis and E. rudis showed the highest concentrations and varieties of flavonol glycosides, whilst E. globulus was characterized by high concentrations of ellagitannins.
Polyphenols of adult leaves from Eucalyptus globulus, E. camaldulensis and E. rudis grown in Spain, in two areas with different edaphoclimatical characteristics, were estimated by chemical methods and by high pressure liquid chromatography. Leaf extracts consisted mainly of proanthocyanidins, ellagitannins and flavonol glycosides. Knowledge of the ellagitannins allows the discrimination of the three species, with E. globulus being well differentiated from the other two. However, the pattern of flavonol glycosides only permitted the discrimination of E. rudis with respect to E. camaldulensis and E. globulus. EXPERIMENTALSamples. Adult leaves of E. camaldulensis, E. globulus and E. rudis were collected in two Spanish arboreta. The climate at one of the sites, located in the South Western province of Huelva, is warmer and drier than that of the other, which is in the North Eastern province of Pontevedra. Five samples, each from a different tree, were collected for each species at each geographical origin, with the exception of E. camaldulensis from Pontevedra where only two trees were sampled.Extraction. Tannins were extracted from dried and ground leaf samples (10 g) with 300 mL methanol:water (80:20), at room temperature in the dark for 24 h (Conde et al., 1995). The suspensions were filtered, the methanol was removed by vacuum distillation and the aqueous solution was extracted with ethyl ether and freeze dried. The aqueous solution was used for the quantitative analysis of total phenols, proanthocyanidins and ellagitannins, whilst the lyophilized material was used for HPLC analysis after redissolving in methanol:water (1:1).Total phenol content. This was determined by the Folin-Ciocalteu method (Singleton and Rossi, 1965) using aqueous solutions of gallic acid (2-40 g/mL) as standard. The molar absorbance obtained in our analysis conditions was 22.3ϫ 10 3 /mol/cm. Proanthocyanidin content. The evaluation of proanthocyanidins was carried out using the vanillin method (Swain and Hillis, 1959). Calibration was achieved with aqueous solutions of catechin (2-40 g/mL) and a molar absorbance of 34.3ϫ 10 3 /mol/cm was obtained under our conditions. Ellagitannin content. Ellagitannins were estimated by the HPLC evaluation of the ellagic acid obtained following acid hydrolysis.
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