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. 2018 Apr;82(2):124–130.

Table II.

Pharmacokinetic parameters of bupivacaine after intraperitoneal administration of bupivacaine-epinephrine (BE) or bupivacaine-dexmedetomidine (BD) (n = 8/group) in adult cats undergoing ovariohysterectomy.

Population
n = 16
Group BE
n = 8
Group BD
n = 8



Parameter Mean ± SD Range Mean ± SD Range Mean ± SD Range
AUC0 − t (ng h/mL) 7004.3 ± 3302.8 3694.8 to 11 150.9 6126.5 ± 2290.2 3694.8 to 10 571.1 10 256.1 ± 5849.8 2962.0 to 19 680.8
AUC0 − ∞ (ng h/mL) 24 292.2 ± 25 918.5 7571.9 to 82 378.1 15 953.7 ± 12 849.7 7841.8 to 46 569.4 31 375.9 ± 24 859.8 5179.2 to 82 378.1
CL/F (L h/kg) 0.148 ± 0.083 0.024 to 0.264 0.168 ± 0.069 0.043 to 0.255 0.132 ± 0.129 0.024 to 0.386
λze (1/h) 0.1102 ± 0.0827 0.0203 to 0.2447 0.1295 ± 0.0730 0.0243 to 0.2274 0.1164 ± 0.0773 0.0203 to 0.2447
t1/2 (h) 11.3 ± 10.2 2.8 to 34.1 8.9 ± 8.6 3.0 to 28.5 10.5 ± 10.3 2.8 to 34.1
Vz/F (L/kg) 1.618 ± 0.906 0.645 to 3.116 1.634 ± 0.899 0.645 to 3.116 1.195 ± 0.777 0.308 to 2.599

AUC0 t — Area under the plasma concentration-time curve from time zero to the last measured time point; AUC0 − ∞ — Area under the plasma concentration-time curve from time zero extrapolated to infinity; CL/F — Relative clearance indexed by bioavailability; λze — Terminal elimination rate constant; t1/2 — Terminal elimination half-life; Vz/F — Volume of distribution indexed by bioavailability.