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. Author manuscript; available in PMC: 2017 Oct 24.
Published in final edited form as: J Biomed Nanotechnol. 2015 Feb;11(2):274–281. doi: 10.1166/jbn.2015.1903

Table II.

Pharmacokinetic parameter estimates of O2 levels in Hs-766T tumors in mice dosed with NVX-108. Note these values have been normalized to tumor volume size (mm3).

NVX-108 dose mL/kg Mouse ID t1/2 elim. min/mm3 Tmax min/mm3 Cmax mmHg/mm3 AUC mmHg × min/mm3) Vd mL/kg · mm3 Tumor volume mm3 Avg. blood perfusion BPU
0.3 015 0.021a 0.14 0.007 0.84 0.09 1307.5 40 ± 18
009 0.017 0.03 0.003 0.17 0.58 863.6 236 ± 68
0.45 022 0.007 0.07 0.047 2.37 0.03 775.8 50 ± 9
011 0.003 0.06 0.013 0.44 0.06 1088.3 80 ± 38
012 0.002 0.02 0.017 0.22 0.07 1155.1 68 ± 18
0.6 014 0.056 0.03 0.002b 0.20b 2.84b 898.5 285 ± 201
002 0.020 0.05 0.003b 0.09b 2.28b 800.2 59 ± 103
020 0.098a 0.19 0.054 9.02 0.17 503.4 92 ± 26
024 0.034a 0.11 0.037 5.05 0.06 992.8 127 ± 89
MEAN 0.02 0.08 0.005c,g 0.501c,f 0.15 931.7
0.026d,g 1.010d,f
0.046e,g 7.033e,f

Notes:

a

values automatically calculated by the modeling software but not used in determining statistics;

b

values likely to have been caused by large fluctuations in blood perfusion thorough out measurement period (SD higher than 70%). These were not used in determining statistics;

c

at 0.3 mL/kg dose of NVX-108;

d

at 0.45 mL/kg dose of NVX-108;

e

at 0.6 mL/kg dose of NVX-108;

f

significant difference at p = 0.03 (ANOVA);

g

significant difference at p = 0.11 (ANOVA).