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To corroborate these findings, cell viability experiments were conducted at different PFA concentrations.
In addition, cell proliferation and viability experiments were not performed under mild hyperoxic (30% O2) conditions.
The cell viability experiments demonstrated excellent biocompatibility of hollow capsules with mouse embryonic fibroblast cells.
Bacterial retention and viability experiments were correlated with the force measurements.
Cell viability experiments indicated that blank APA-CPNPs possessed excellent biocompatibility with normal cells.
Cell viability experiments indicated that all complexes showed significant dose dependent cytotoxicity in selected cell lines.
The results of both cell proliferation and cell viability experiments indicate that GO-chitosan film is suitable for cell proliferation.
The chemical proteomics and cell viability experiments demonstrated that free heme could effectively activate ART, while free ferrous iron has minimal effects on the activation of ART, and the modulation of endogenous heme could also affect anticancer activity of ART.
The preliminary haemolysis and cell viability experiments show that BSA conjugation mitigates the haemolytic effect of the iron oxide nanoparticles on erythrocytes and is non-cytotoxic to the healthy Baby Hamster Kidney cells.
Interestingly, in cell viability experiments, using HL-60 cells (expressing exclusively CB2 receptors), all synthesised compounds were shown to be cytotoxic, suggesting that a CB2 agonist response may be involved.
For cell viability experiments, A549 and HK2 cells were grown to confluence in 96-well flat-bottom tissue culture plates (Sarstedt, Nümbrecht, Germany) and cultured in pre-equilibrated and prewarmed RPMI, DMEM and a 1 1 mixture of DMEM Ham's F12 media, respectively.
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