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. Author manuscript; available in PMC: 2018 Aug 17.
Published in final edited form as: ACS Nano. 2018 Mar 12;12(3):2922–2938. doi: 10.1021/acsnano.8b00516

Figure 7.

Figure 7

Inhibition of exocytosis increases the accumulation of MoS2-based NSs. Schematic representation of exocytosis pathways in (a) HeLa and (b) MCF-7 cells. (c) HeLa and (d) MCF-7 cells were pretreated with Exo1 for 2 h, and then cells were incubated with fluorescent MoS2-based NSs (10 μg/mL) for 3 h. Cytoplasmic fluorescence was measured by flow cytometer. (e) HeLa and (f) MCF-7 cells were incubated in the presence or absence of Exo1 for 2 h after fluorescent MoS2-based NS treatment. After that, we renewed the culture medium with fresh DMEM and incubated the cells for 3 h. Cytoplasmic fluorescence was then measured by flow cytometer.