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The DPPH assay was performed by using the method of Molyneux [42], with some modifications. The stock solution was prepared by dissolving 4 mg DPPH with 100 mL of 100% methanol. Shortly, for each Berberis spp. fruit sample, a 750 µL standard solution was added to a 750 µL DPPH methanolic solution and the mixtures were shaken vigorously and left to stand in the dark for 50 min at room temperature. Then, the absorbance was read at 517 nm. Six different concentrations were used to calculate the inhibition values of the Berberis spp. fruit samples. To calculate DPPH radical activity, Trolox was used as a standard.

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