The DPPH radical scavenging activity of LOs was investigated by a previous method with slight modification (19 (link)). In brief, 100 μL different concentrations (0.1–2.0 mg/mL) of LOs were added to 100 μL of 50 mmol/L DPPH in ethanol. Then the mixture was shaken and incubated in dark place for 30 min, and the value of absorbance was measured at 517 nm. Ascorbic acid was used as a positive control. The ability of DPPH scavenging was calculated using the following equation:
Where A0 was the absorbance of blank (ethanol instead of sample), Ai was the absorbance of sample (sample with DPPH-methanol solution), Aj was the absorbance of control (sample without DPPH-methanol solution).
The potential of LOs in scavenging ABTS radicals was evaluated as described earlier with some adjustments (20 (link)). Briefly, ABTS radical solution was prepared as follows: 7 mmol/L of ABTS solution (5 mL) was incubated with 2.45 mmol/L of potassium persulfate (88 μL) at room temperature for 16 h. Next, 2 mL ABTS radical solution were added into LOs samples (1 mL) with various concentrations (0.0625, 0.125, 0.25, 0.5, 1, and 2 mg/mL), respectively. After rection at room temperature (in dark place) for 10 min, the value of absorbance was measured at 734 nm. Ascorbic acid was used as the positive control. The ABTS radical scavenging activity (%) was calculated as DPPH radical scavenging activity equation above.
Where A0 was the absorbance of blank (ethanol instead of sample), Ai was the absorbance of sample (sample with DPPH-methanol solution), Aj was the absorbance of control (sample without DPPH-methanol solution).
The potential of LOs in scavenging ABTS radicals was evaluated as described earlier with some adjustments (20 (link)). Briefly, ABTS radical solution was prepared as follows: 7 mmol/L of ABTS solution (5 mL) was incubated with 2.45 mmol/L of potassium persulfate (88 μL) at room temperature for 16 h. Next, 2 mL ABTS radical solution were added into LOs samples (1 mL) with various concentrations (0.0625, 0.125, 0.25, 0.5, 1, and 2 mg/mL), respectively. After rection at room temperature (in dark place) for 10 min, the value of absorbance was measured at 734 nm. Ascorbic acid was used as the positive control. The ABTS radical scavenging activity (%) was calculated as DPPH radical scavenging activity equation above.