Antinociceptive efficacy and plasma concentrations of transdermal buprenorphine in dogs

被引:29
作者
Pieper, Korbinian [1 ]
Schuster, Tibor [2 ]
Levionnois, Olivier [3 ]
Matis, Ulrike [1 ]
Bergadano, Alessandra
机构
[1] Univ Munich, Fac Vet Med, Dept Small Anim Surg, Munich, Germany
[2] Tech Univ Munich, Dept Med Stat & Epidemiol, Munich, Germany
[3] Univ Bern, Dept Clin Vet Med, Div Anaesthesiol, Vetsuisse Fac, CH-3012 Bern, Switzerland
关键词
Buprenorphine; Dog; Thermal threshold; Transdermal; Antinociception; EXPERIMENTAL PAIN MODELS; VON-FREY DEVICE; OPEN-LABEL; FENTANYL; MORPHINE; PHARMACOKINETICS; CANCER; CATS; NORBUPRENORPHINE; MULTICENTER;
D O I
10.1016/j.tvjl.2010.01.013
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
To assess the antinociceptive efficacy of transdermal (TD) buprenorphine (B) in dogs, a prospective, positive-controlled experimental study was performed in 10 healthy Beagles. In an open label crossover design, the dogs initially received intravenous B (IVB, 0.02 mg kg(-1)) as a positive control, followed by TDB (52.5 mu g h(-1)) 4 months later. Blood was collected at regular intervals for determination of the plasma concentrations of B ([B]) and its metabolite norbuprenorphine. The antinociceptive efficacy was assessed using thermal and mechanical models of nociception. The peak concentration [B] was 1.54 ng mL(-1) (+/- 1.98) 60 h after TDB application, although three dogs had no measurable [B] after TDB. Maximum thermal threshold (TT) was 52.6 degrees C (+/- 0.48) at 1 h after IVB administration and 51.63 degrees C (+/- 1.01) 72 h after TDB application. The significant increase in TT indicated that effective antinociception was achieved beyond 36 h after the application of TDB, lasting until patch removal. There was hysteresis between [B] and the antinociceptive effect. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:335 / 341
页数:7
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