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For laboratory and industrial strains, a sharp decrease in the viability and trehalose concentration was observed above 90 g l− 1 and 140 g l− 1 ethanol, respectively.
A significant decrease in the cell viability was observed after 60, 180 min upon incubation with tuffted carpet dust, while knotted carpet dust caused a significant decrease in the viability after 180 min. LDH leakage was parallel to the cell viability.
At 25 to 100 μg/mL of Fe, Fe3O4 NPs both before and after coating with HLC showed no obvious decrease in the viability of the NIH3T3 cells.
However, there was a gradual decrease in the viability of cells with the increasing dose of Cu-MWCNTs and Ag-MWCNTs.
Noticeably, ΔvosA causes a radical decrease in the viability of spores.
The H2O2 treatment led to a dose-dependent decrease in the viability of differentiated SK-N-SH cells (Fig. 1B).
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Decreases in the viability of rapidly-multiplying cells result from cell proliferation arrest, cell death or both.
Both types of CNTs induced significant dose-dependent decreases in the viability of PC-12 cells, whereas graphene exerted adverse effects on the neural cells just at over 62.5 ppm.
However, it was seen that the surface-coated SWSB nanocomposites demonstrated a gradual decrease in the cell viability as the concentration increases, with the lowest cell viability of 54.7% observed in SWSB-PEG at concentration of 100 μg mL−1.
This coincided with a ∼2 fold decrease in the microbial viability.
The results from the study indicated a decrease in the cell viability [134].
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