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(A) AO/EB staining of apoptotic HepG2 cells incubated with free DOX, CDs-DOX, and laser irradiated CDs-ICG-LPs for 24 h. (B) Flow cytometric analysis of apoptotic/necrotic cells in HepG2 cells treated with free DOX, CDs-DOX, and CDs-ICG-LPs for 24 h, untreated cells were used as a control and photothermal was evaluated as well.
