This article aims to determine the phenolic, tocopherol contents, and antioxidant capacities from fruits (juices, peels, and seed oils) of 6 Tunisian pomegranate ecotypes. Total anthocyanins were determined by a differential pH method. Hydrolyzable tannins were determined with potassium iodate. The tocopherol (α-tocopherol, γ-tocopherol, and δ-tocopherol) contents were, respectively, 165.77, 107.38, and 27.29 mg/100 g from dry seed. Four phenolic compounds were identified and quantified in pomegranate peel and pulp using the high-performance liquid chromatography/ultraviolet method: 2 hydroxybenzoic acids (gallic and ellagic acids) and 2 hydroxycinnamic acids (caffeic and p-coumaric acids). Juice, peel, and seed oil antioxidants were confirmed by ferric reducing antioxidant power (FRAP) and oxygen radical absorbance capacity (ORAC) methods. The highest values were recorded in peels with 25.63 mmol trolox equivalent/100 g and 22.08 mmol TE/100 g for FRAP and ORAC assay, respectively. Results showed that the antioxidant potency of pomegranate extracts was correlated with their phenolic compound content. In particular, the highest correlation was reported in peels. High correlations were also found between peel hydroxybenzoic acids and FRAP ORAC antioxidant capacities. Identified tocopherols seem to contribute in major part to the antioxidant activity of seed oil. The results implied that bioactive compounds from the peel might be potential resources for the development of antioxidant function dietary food.

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Polyphenols Flavonoids HPLC-DAD/ESI-MS Phenolic acids Flavonol glycosides A B S T R A C T The total polyphenol and flavonoids in leaves of Morus alba var. alba, Morus alba var. rosa and Morus rubra were determined and identification of their components was carried out. The total content of phenolics varied between 345.20 and 631.53 mg gallic acid equivalents (GAE)/100 g dry weight (DW) basis. The total amount of flavonoids ranged between 193.87 and 398.33 mg rutin equivalents (RE)/100 g DW. Thirteen compounds were isolated by chromatography, and their structures determined to be mainly flavonol glycosides and phenolic acids. Three novel components were identified as kaempferol-7-O-glucoside, quercetin-3-O-b-glucoside-7-O-a-rhamnoside and quercetin-3-O-rhamnoside-7-O-glucoside, for the first time from mulberry leaves. Others known compounds were also identified.

Peels and fresh pomegranate extracts were used in the present study for the determination of the physic-chemical properties and DPPH-ABTS scavenging activities. Total sugars of juice are fructose (ca. 7 g/100 ml) and glucose (ca. 8 g/100 ml). Contents of soluble proteins in juice extracts are about 7 g/l (Bradford assays) and 22% (Kjeldhal assays) from dry pulp. Minerals in peel and juice are respectively 9.43+/-0.93 and 9.46+/-1.05 mg/100 ml for posphorus and 210.86+/-10.70 and 271.94+/-60.59 mg/100 g for potassium. The sodium contents are nearly 7 mg/100 ml in both peel and juice. Highly antioxidant contents in peels were confirmed. Free radical scavenging is about 3.58+/-0.38 microg/ml in peel. The antioxidant capacity value determined by ABTS was 7.364+/-0.403 mM Trolox equivalent antioxidant capacity/100 g dry weight. These findings implied that bio-active compounds from the peel might be potential resources for the development of antioxidant function dietary food.

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