Antioxidant activity of plant extract was analysed using DPPH free radical scavenging assay, according to the method described by Brand-Williams et al. [25]. 167 μL of 4 mM ethanol solution of DPPH was mixed with 33 μL analysed samples in different concentrations (250 μg·ml− 1 – 5000 μg·ml− 1). The absorbance was measured at λ = 516 nm in every 5 min for 30 min using UV-Vis spectrophotometer Filter Max 5 (Thermo Scientific). DPPH solution mixed with equal volume of distilled water was served as a control. The percentage of the DPPH radical scavenging were calculated using the equation:
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.