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. Author manuscript; available in PMC: 2021 May 1.
Published in final edited form as: Small. 2020 Apr 26;16(21):e2000528. doi: 10.1002/smll.202000528

Figure 1. Characterization of nanoparticle morphology, dissolution characteristics, and cellular uptake.

Figure 1.

Figure 1.

(A) TEM images of 16 nanoparticles provided by the consortium. The images were captured using a JEOL 1200-EX TEM with accelerating voltage of 80 kV. (B) ICP-OES analysis of nanoparticle dissolution. The graph shows the % metal dissolution for the individual nanoparticles in water and complete DMEM (DMEM with 10 % FBS) at two time points (0 and 24 h). The analysis was performed by suspending 100 μg/mL of each material in deionized H2O, followed by incubation at 37 °C for 0 or 24 h. The supernatants were collected by centrifugation at 15, 000 g for 30 min and digested by concentrated nitric acid at 90 °C for 3 h. The digested solutions were dried by evaporation at 120 °C and dissolved in 3 mL of 5% nitric acid for ICP-OES analysis. (C) Cellular uptake of nanoparticles. After 4 h treatment with 12.5 μg/mL nanoparticles, KUP5 and Hepa 1–6 cell pellets were collected and acid digested for assessment of their metal content by ICP-OES.