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. 2016 Mar 4;18(3):737–745. doi: 10.1208/s12248-016-9876-3

Table III.

Relevant Plasma Compartmental Pharmacokinetic Parameters of S-AR-42 in Rats (n = 6) Following I.V. and P.O. Administration

PK parameters Average SD CV (%)
I.V. administration (20 mg/kg)
C 0 (μM) 35.6 24.9 70.0
 α (h−1) 7.6 4.7 62.2
T 1/2 α (h) 0.12 0.07 57.1
 β (h−1) 0.22 0.09 40.5
T 1/2 β (h) 5.1 2.6 51.0
 MRT (h) 6.5 3.7 56.7
 Cl (l/h/kg) 1.8 0.6 33.0
 Vss (l/kg) 11.0 5.5 49.5
 AUC0-∞ (μM×h) 39.8 14.4 36.1
P.O. administration (50 mg/kg)
C max (μM) 7.1 1.6 23.2
T max (h) 3.3 4.5 137
 λz (h−1) 0.09 0.04 37.4
 HL-λz (h) 9.3 6.4 68.5
 Vz/F (L/kg) 13.7 12.1 88.2
 AUMC (μM×h2) 3242 704 21.7
 MRT (h) 19.5 5.6 28.7
 Cl/F (l/h/kg) 1.0 0.2 17.7
 AUC0-∞ (μM×h) 171 30.9 18.1

SD standard deviation determined from n = 6 estimates; CV (%) coefficient of variation determined by SD/average*100%