Fig. 7. Lipid peroxidation measured on samples of MSSA with: A) 0.2 mg/mL P25TiO₂NPs; B) 0.02 mg/mL P25TiO₂NPs; C) 0.2 mg/mL VitaminB2@P25TiO₂NPs; D) VitaminB2@P25TiO₂NPs 0.02 mg/mL after 3 h of irradiation (red) and 6 h (blue). MDA could not be detected after 6 h of irradiation in a sample with P25TiO₂NPs. Error bars are too small to be seen in graphic and p < 0.05 between C-D and A-B.

The vitaminB2@TiO₂NPs were obtained at room temperature, by a method developed after trying several ratios of reactants. Briefly, 0.02 g of P25TiO₂NPs were dispersed in 1 mL of ultra-pure water and stirred in a Vortex. Next, 200 μl of vitamin B2 dissolved in ultra-pure water (5.3 × 10⁻³ M) were added to 200 μL of P25TiO2NPs and the mixture was ultrasonicated for 1 hour to achieve a deep-yellow homogeneous suspension. The pellet obtained after centrifuging the suspension for 10 min at 4500 rpm was resuspended in ultrapure water, centrifuged again, and then lyophilized.