Figure 1.

Comparison of the scavenging capacity of the test compounds. (a) DPPH radical scavenging assay. The test compounds (0–10 mg/mL) were added to 100 μM DPPH and absorbance was read at 490 nm after 3 h of incubation with the test compounds. (b) Fenton reaction assay. A comparison of the effect of 10 mg/mL α-tocopherol, CO₂-SFE mussel oil, and scymnol on the degradation of deoxyribose by a Fenton reaction. Absorbance was read at 532 nm. Results expressed as the means ± SD of triplicate samples.