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Table 4 Pharmacokinetic (PK) variables following intravenous (IV), intramuscular (IM) or subcutaneous (SC) administration of buprenorphine (Simbadol; 0.02 mg/kg) in dogs undergoing ovariohysterectomy. Data are reported as mean (95% confidence interval)

From: Pharmacokinetics and analgesic effects of intravenous, intramuscular or subcutaneous buprenorphine in dogs undergoing ovariohysterectomy: a randomized, prospective, masked, clinical trial

Parameter

Unit

IV (n = 8)

IM (n = 8)

SC (n = 6)*

AUC 0-t

ng/mL*h

14.49 (12.86–16.11)

9.32 (6.53–12.11)

5.79 (4.26–7.32)

AUC 0-∞

ng/mL*h

15.77 (13.87–17.67)

12.41 (10.39–14.43)

16.45 (8.00–24.90)

C0 or Cmax

ng/mL

35.92 (14.42–57.43)

6.24 (2.78–9.70)

1.37 (0.89–1.85)

F

%

62.6

40

Tmax

h

0.14 (0.01–0.26)

0.33 (0.20–0.47)

λ z

1/h

0.19 (0.17–0.21)

0.14 (0.10–0.18)

0.04 (0.02–0.06)

t1/2

h

3.69 (3.25–4.14)

5.66 (2.82–8.50)

21.95 (12.03–31.87)

MRT0-∞

h

3.59 (3.06–4.12)

7.37 (3.00–11.73)

30.02 (15.77–44.27)

Cl or Cl/F

L/h/kg

1.29 (1.14–1.45)

1.65 (1.40–1.91)

1.40 (0.91–1.88)

Vz or Vz/F

L/kg

6.82 (6.06–7.58)

14.16 (4.50–23.81)

40.13 (26.27–53.98)

Vss

L/kg

4.59 (3.98–5.19)

NC

NC

  1. * The PK of buprenorphine could not be derived in two dogs after subcutaneous administration due to erratic drug absorption. AUC, area under the plasma concentration-time curve from zero to infinity (0-∞) or to the last measurable concentration (0-t); MRT, mean residence time; Cl or Cl/F, plasma clearance or apparent clearance; t1/2, elimination half-life; λ z, elimination rate constant; F, bioavailability; Vz or Vz/F, apparent volume of distribution at pseudo equilibrium during the elimination phase; Tmax, time to maximal concentration; Cmax, maximal serum concentration; Vss, apparent volume of distribution at steady state; NC, non calculable