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. 2018 Dec 26;8(2):246–261. doi: 10.1039/c8tx00267c

Fig. 4. ZnONP induced cell death, reactive oxygen species, and inhibition of cellular respiration in treated clinical isolates. The ZnONP (1.0 mg ml–1) mediated increase in the number of dead cells as a result of increased membrane permeability. Panels A and C show the residual fluorescence of PI in K. pneumoniae and S. aureus cells. Panel C and D present an increase in PI fluorescence due to the damaged cell membrane. Panels E and G show the residual fluorescence of DCF in K. pneumoniae and S. aureus cells. Panel F and H show a significant increase in intracellular ROS when exposed to 1 mg ml–1 of ZnONPs. Panel I shows the inhibition of cellular respiration of E. coli, S. aureus, K. pneumoniae, and P. aeruginosa by green synthesized ZnONPs at 0.125–1.5 mg ml–1. The decrease in red color intensity in microtitre wells represents the loss of metabolic activity of bacterial cells.

Fig. 4