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The bactericidal activity of PCL/RGO_Cu showed 78% reduction in viability of Escherichia coli.
There is a dose-dependent reduction in viability of dIMR32 cells.
The cytotoxicity was compared against control and percent reduction in viability of cells was calculated.
When the cells were protected with 10% γ-PGA, only 1.24 - 1.26 log CFU/ml reduction in viability was observed.
At the shorter time interval, activated chlorine dioxide demonstrates a 4-log reduction in viability compared to the control.
To study whether there was any further reduction in viability, cytotoxicity was also analysed after 48 h of exposure.
Therefore, the reduction in viability is perceived to be a result of NP interference and cannot be reported as cytotoxicity.
However, CaP-AgNP-1 has shown a slight reduction in viability compared to other samples (P < 0.05).
Exposure to AuNP Au[(Gly-Tyr-TrCys)2B] also resulted in a reduction in viability over time but not below interference levels.
When 10% sucrose was used to protect L. paracasei during freeze drying, 0.91 log CFU/ml reduction in viability was observed after freeze drying.
It was observed that when no cryoprotectant was used to protect the cells, L. paracasei showed a reduction in viability of 1.34 log CFU/ml.
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