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. Author manuscript; available in PMC: 2010 Sep 1.
Published in final edited form as: Antivir Chem Chemother. 2009 Sep 25;20(1):37–46. doi: 10.3851/IMP782

Table 6.

Two compartmental analysis of cyclopropavir (5) plasma levels after IV bolus dosing of prodrug (6). See text for model description.

Parameter Best Fit CV%
Volume of distribution, V, L/kg 2.61 21.0
Area under the curve, AUC, mg.min/L 874 22.3
Input rate constant, K01, min.−1 0.21 121
Elimination rate constant, K10, min.−1 0.0071 32.7
Elimination Half-life of T1/2K10, min. 97 32.7
Time of maximum plasma concentration, Tmax, min. 16.7 85.8
Maximum plasma concentration, Cmax, mg/L 5.52 15.0
Clearance (Cl), L/min. 0.0185 22.3
a

A complete conversion of the prodrug (6) to cyclopropavir (5) is assumed, which would result in a equivalent dose of cyclopropavir (5) of 16.2 mg/kg.