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. 2017 May;45(5):484–491. doi: 10.1124/dmd.116.074526

TABLE 2.

Pharmacodynamic parameter estimates for unbound ISF effects of NPX in healthy and CIA rats

Parameter Definition Estimate (CV%)
Females Males
tonset (h) Time of disease onset 289 (1.07) 308 (0.5)
kout (l h) Loss of edema rate constant 0.013 (41.3) 0.007 (20.6)
kdeg (l/h) Loss of production rate constant 0.001 (29.0) 0.001 (16.6)
kg (l/h) Natural growth rate constant 0.003 (33.8) 0.002 (41.8)
Imax Maximum inhibition on production of paw edema 0.75 (40.1) 1.0 (Fixed)
IC50 (µg/ml) Unbound NPX concentration at 50% maximum inhibition 0.221 (56.4) 0.136 (45.9)
Pawss (mm2) Paw size at steady state 70.2 (4.6) 102.2 (7.9)
kin0,c (mm2/h) Disease production rate constant at tonset for control group 2.21 (24.6) 1.36 (12.0)
Paw0,c (mm2) Paw size on day 0 for control group 58.92 (1.6) 73.49 (1.8)
kin0,t (mm2/h) Disease production rate constant at tonset for treatment group 2.31 (23.3) 1.44 (11.6)
Paw0,t (mm2) Paw size on day 0 for treatment group 59.99 (1.6) 76.02 (1.6)
Paw0,ng (mm2) Paw size on day 0 for natural growth group 50.38 (2.9) 77.43 (1.8)