Cellular kinetic 24 hs and 48 hs.

Once the optimum formulation and dosage were determined according to inhibitory action of growth up in BW cellular lines in 24 hours, it came the experimentation the kinetic in 48 hours.
In TABLE 1: "Growth up' inhibition of BW cellular line in 24 hours." They're presented the results of the 2 formulations (PF1 y PF3), as a percentage of growth up's inhibition of BW cellular lines in 24 hours, that in first phase of experimentation showed significant differences in reference to inhibition percentages of cellular growth up.

TABLE 1: Growth up's inhibition in BW cellular line in 24 hs.

Again as we see in TABLE 1: "Inhibition of BW cellular line's growth up in 24hs.", to bigger dilutions the following percentages of inhibition were decrecent, resulting the main efficacy with PF3 dilution.
In TABLE 2: "Inhibition of BW cellular line's growth up in 48 hs.", the results are expressed in percentages of inhibition of growth up in BW cellular lines in 48 hours. Once more were included PF1 and PF3 formulations as these one in the first phase of experimentation showed relevant differences in reference to the percentages of inhibition of cellular's growth up, trying to discharge the possibility of a different conduct at the 48 hours.

TABLE 2: Inhibition of BW cellular line's growth up in 48hs.

As a first conclusion in both formulations after 48 hours the inhibition effect at therapeutic dose was bigger than the one in 24 hours, that shows an accumulation effect (accumulation kinetic) to improve the wished objective that is an non proliferation effect. Also at 48 hours, the bigger inhibition of BW cellular line's growth up in absolutes terms at the therapeutic dose resulted in PF3 formulation
This way cellular kinetic is braked avoiding tumor's growth up.