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. Author manuscript; available in PMC: 2015 Apr 1.
Published in final edited form as: J Vet Pharmacol Ther. 2013 Nov 18;37(2):196–200. doi: 10.1111/jvp.12088

Table 1.

Calculated mean ± standard deviation non-compartmental pharmacokinetic parameters for serum suberoylanilidehydroxamic acid (SAHA) concentration data after IV and PO administration to adult cats (n=6). Doses and administration routes were 2 mg/kg intravenous (IV) SAHA (solvated at 20 mg/mL in DMSO) or 250 mg/m2 oral (PO) SAHA in gelatin capsules.

Parameter IV PO
Dose 2 mg/kg 250 mg/m2 = 17±2 mg/kg
T1/2λz (hr) 0.15 ± 0.03 2 ±1
Clobs (mL/hr/kg) 14,000 ± 5,000 -
VDss,obs (mL/kg) 1600 ± 800 -
Cmaxobs (ng/mL) - 40 ± 10
Tmaxobs (hr) - 0.6 ± 0.3
AUC0 → τ (hr*ng/mL) 150 ± 40 70 ± 10
AUC0 → ∞ (hr*ng/mL) 150 ± 50 80 ± 20
Percent Extrapolated (%) 0.6 ± 0.2 17 ± 7
F (%), n=5 - 8 ± 4

T1/2λz, elimination half-life, CLobs: Observed clearance, VDss,obs: Observed volume of distribution at steady state, Cmax(obs), observed maximum serum concentration; Tmax(obs), time to observed maximal serum concentration; AUC0 → τ area under the serum concentration vs. time curve to the last value; AUC0 → ∞ area under the serum concentration vs. time curve extrapolated to infinity; F(%): oral bioavailability