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. Author manuscript; available in PMC: 2013 Jul 29.
Published in final edited form as: Pharm Res. 2011 Mar 1;28(7):1622–1630. doi: 10.1007/s11095-011-0396-7

Table I.

Pharmacokinetic Parameter Estimates for Etanercept in CIA Rats

Parameter Definition Estimate CV%
CLD (mL/day/kg) Distributional clearance 1.15 759
V1 (mL/kg) Volume of central compartment 46.3 3.19
V2 (mL/kg) Volume of peripheral compartment 53.9 1722
Vmax (µg/day) Capacity Michaelis-Menten constant 1200 143
Km (µg/mL) Affinity Michaelis-Menten constant 59.5 104
ka (day−1) First-order absorption rate constant 1.41 72.4
F Bioavailability of SC administration 0.42 7.93
Fr Fractional dose undergoing k1 process 0.201 330
T (day) Time period for k0 process 3 FIXED

CV% coefficient of variation percentage