Total antioxidant capacity of extracts was determined by phosphomolybdenum based method described previously [21]. The assay was performed by mixing 100 μl of extracts (4 mg/ml DMSO) with a reagent solution consisting of 28 mM sodium phosphate, 4 mM ammonium molybdate and 0.6 M sulphuric acid. Reaction mixture was then incubated at 95 °C for 90 min followed by cooling at room temperature. Absorbance was estimated at 695 nm using a microplate reader. The assay was executed in triplicate, ascorbic acid was used a positive control and calibration curve was drawn (y = 0.0096x + 0.1538, R2 = 0.9972). Negative control used in the experiment was DMSO and results were expressed as μg ascorbic acid equivalent (AAE) per mg extract.
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