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. 2018 Apr 17;8(26):14268–14279. doi: 10.1039/c8ra00911b

Fig. 6. (A) Cell viabilities of U87MG cells after CuS-apoferritin (100 μg mL−1) and CuS-apoferritin-MBA (100 μg mL−1) induced photothermal ablation at different laser power densities (0.2, 0.5, 0.8, and 1.0 W cm−2). (B) Cell viabilities of U87MG cells incubated with different concentrations (10, 20, 40, 80, and 100 μg mL−1) of CuS-apoferritin and CuS-apoferritin-MBA under exposure to the 808 nm laser at a power density of 1 W cm−2. (C) Cell viabilities of U87MG cells after CuS-apoferritin (100 μg mL−1) and CuS-apoferritin-MBA (100 μg mL−1) with anti-TfR induced photothermal ablation at different laser power densities (0.2, 0.5, 0.8, and 1.0 W cm−2). (D) Cell viabilities of U87MG cells incubated with different concentrations (10, 20, 40, 80, and 100 μg mL−1) of CuS-apoferritin and CuS-apoferritin-MBA under exposure to the 808 nm laser at the a power density of 1 W cm−2. (E) Confocal fluorescence images of Calcein AM/PI co-stained U87MG cells incubated with CuS-apoferritin (100 μg mL−1) and CuS-apoferritin-MBA (100 μg mL−1) after being exposed to the 808 nm laser (1 W cm−2) for 5 min. Error bar is 20 μm.

Fig. 6