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. Author manuscript; available in PMC: 2019 Jul 28.
Published in final edited form as: J Control Release. 2018 Apr 19;282:62–75. doi: 10.1016/j.jconrel.2018.04.032

Fig. 5.

Fig. 5

Intracellular trafficking of GSH-sensitive HMSiO2 NPs in MCF-7 cells: (A–D) Representative CLSM images of the cells treated with GSH-sensitive HMSiO2 NPs; (A) Cells were treated with 50 μg mL−1 of NPs and incubated for 4 h; (B) Cells were treated with 50 μg mL−1 of NPs and incubated for 24 h; (C) Cells were treated with 250 μg mL−1 of NPs and incubated for 4 h; and (D) Cells were treated with 250 μg mL−1 of NPs and incubated for 24 h. (A1-D1) Merge CLSM images under higher magnifications. Nuclei were stained in blue with Hoechst 33342 dye. NPs appeared with the green fluorescence of FITC. LysoTracker Deep Red dye was used to stain the lysosomes. As illustrated, NPs accumulated in the endolysosomal compartments and perinuclear regions. GSH-sensitive HMSiO2 NP uptake rate in MCF-7 cells measured by ICP-MS in terms of (E) NP concentration in the range of 0–1000 μg mL−1 with constant incubation time of 24 h and (F) incubation time in the range of 0–24 h with constant NP concentration of 100 μg mL−1. Results indicate that there is a threshold for the internalization of GSH-sensitive HMSiO2 NPs with the maximum uptake of c.a. 2.1% after incubation for 24 h. Cells without NP treatment were used as control. Data are mean ± SD (n = 3).