Author:
Dobrinas Simona,Soceanu Alina,Popescu Viorica,Carazeanu Popovici Ionela,Jitariu Daniela
Abstract
The purpose of this study was to investigate the antioxidant capacity of different tea plant: mint, linden, chamomile, St. John’s wort, green and black tea in relation to total phenolic content. The antioxidant capacity of the tea infusions at different brewing times was determined using DPPH assay while the total phenolic content (TPC) was assessed using the modified Folin-Ciocalteu method. The results showed that there were significant statistical differences in antioxidant capacity depending on infusion time, according to one-way ANOVA analysis. Leaves used as components of tea infusions were analyzed by FAAS for their content of iron and copper in the dry product and in the infusion. The correlation between TPC and DPPH capacity of tea plant infusions was evaluated by Pearson correlation matrix. Total phenolics compounds content was positively and significantly correlated with DPPH capacity for all infusions time. Significant correlation was observed between TPC and the copper concentration (p < 0.05). Consequently, the correlations between the physicochemical parameters, TPC, DPPH capacity, Fe and Cu content suggested that the TPC may be a good indicator of the DPPH capacity in the tea infusions and also, suggested the influence of antioxidant compounds on mineral bioavailability.
Subject
Process Chemistry and Technology,Chemical Engineering (miscellaneous),Bioengineering
Reference50 articles.
1. Chemical composition and sensory evaluation of tea (CAMELLIA SINENSIS) commercialized in Pakistan;Adnan;Pak. J. Bot.,2013
2. Characterisation of white tea – Comparison to green and black tea
3. Medicinal Benefits of Green Tea: Part I. Review of Noncancer Health Benefits
4. Inhibition of carcinogenesis by tea: Bioavailability of tea polyphenols and mechanisms of actions;Yang;Proc. Soc. Exp. Biol. Med.,2010
5. Evaluation of antioxidant activity of ten compounds in different tea samples by means of an on-line HPLC–DPPH assay