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. 2015 May 5;18(4):290–302. doi: 10.1177/1098612X15581206

Table 4.

Pharmacokinetic parameters from cats after treatment with subcutaneous buprenorphine at 0.02, 0.06, 0.12 and 0.24 mg/kg body weight and using formulations containing 0.3, 0.6 and 1.2 mg/kg with and without preservatives

Buprenorphine
Group dose (formulation ID)* Cmax (ng/ml) Tmax (h) AUC ng/ml/h k(el)/h Ratio norbuprenorphine/ buprenorphine
AG6 0.02 mg/kg (standard/low) (A) 1.3 (1.0–1.7) 0.42 (0.25–0.50) 6.43 ± 3.90 0.37570 (0.1300–0.5144) 0
AG4 0.06 mg/kg (medium) (D) 3.4 (1.4–4.9) 0.70 (0.25–2.00) 61.8 ± 13.2 0.0324 (0.0222–0.0431)
AG2 0.12 mg/kg (high) (A) 6.5 (5.7–7.7) 0.75 (0.5–1.00) 115.6 ± 32.1 0.03394 (0.0221–0.0471) 0.45 (0.17–0.34)
AG3 0.12 mg/kg (high) (C) 20.8 (4.5–51.4) 0.67 (0.50–1.00) 163.55 ± 64.40 0.04152 (0.0310–0.05063) 0.5 (0.21–0.99)
AG3 0.12 mg/kg (high) (D) 10.3 (6.1–22.6) 0.7 (0.5–1.0) 139.6 ± 11.7 0.0371 (0.0204–0.0584)
AG7 0.12 mg/kg (high) (B) 14.9 (6.6–29.5) 0.83 (0.50–1.00) 160.74 ± 19.80 0.04851 (0.0348–0.0688) 0.32 (0.21–0.53)
AG5 0.24 mg/kg (very high) (D) 15.6 (5.3–22.4) 0.63 (0.25–1.00) 265.07 ± 53.60 0.04206 (0.0302–0.0497) 0.40 (0.18–0.61)
*

See footnote to Table 1 for formulation IDs

Mean (range)

Mean ± SD

Cmax = peak concentration; Tmax = time to peak concentration; AUC = area under the concentration time curve