Gleeson Molly D, Guzman David Sanchez-Migallon, Knych Heather K, Kass Philip H, Drazenovich Tracy L, Hawkins Michelle G
Am J Vet Res. 2018 Jan;79(1):13-20. doi: 10.2460/ajvr.79.1.13.
OBJECTIVE To determine the pharmacokinetics and sedative effects of 2 doses of a concentrated buprenorphine formulation after SC administration to red-tailed hawks (Buteo jamaicensis). ANIMALS 6 adult red-tailed hawks. PROCEDURES Concentrated buprenorphine (0.3 mg/kg, SC) was administered to all birds. Blood samples were collected at 10 time points over 24 hours after drug administration to determine plasma buprenorphine concentrations. After a 4-week washout period, the same birds received the same formulation at a higher dose (1.8 mg/kg, SC), and blood samples were collected at 13 time points over 96 hours. Hawks were monitored for adverse effects and assigned agitation-sedation scores at each sample collection time. Plasma buprenorphine concentrations were quantified by liquid chromatography-tandem mass spectrometry. RESULTS Mean time to maximum plasma buprenorphine concentration was 7.2 minutes and 26.1 minutes after administration of the 0.3-mg/kg and 1.8-mg/kg doses, respectively. Plasma buprenorphine concentrations were > 1 ng/mL for mean durations of 24 and 48 hours after low- and high-dose administration, respectively. Mean elimination half-life was 6.23 hours for the low dose and 7.84 hours for the high dose. Mean agitation-sedation scores were higher (indicating some degree of sedation) than the baseline values for 24 hours at both doses. No clinically important adverse effects were observed. CONCLUSIONS AND CLINICAL RELEVANCE Concentrated buprenorphine was rapidly absorbed, and plasma drug concentrations considered to have analgesic effects in other raptor species were maintained for extended periods. Most birds had mild to moderate sedation. Additional studies are needed to evaluate the pharmacodynamics of these doses of concentrated buprenorphine in red-tailed hawks.
目的 确定向红尾鵟(Buteo jamaicensis)皮下注射2种剂量的浓缩丁丙诺啡制剂后的药代动力学和镇静效果。动物 6只成年红尾鵟。方法 向所有鸟类皮下注射浓缩丁丙诺啡(0.3 mg/kg)。给药后24小时内的10个时间点采集血样,以测定血浆丁丙诺啡浓度。经过4周的洗脱期后,相同的鸟类接受更高剂量(1.8 mg/kg,皮下注射)的相同制剂,并在96小时内的13个时间点采集血样。监测鵟的不良反应,并在每个采样时间点评定激动 - 镇静评分。通过液相色谱 - 串联质谱法定量血浆丁丙诺啡浓度。结果 分别给予0.3 mg/kg和1.8 mg/kg剂量后,血浆丁丙诺啡浓度达到峰值的平均时间分别为7.2分钟和26.1分钟。低剂量和高剂量给药后,血浆丁丙诺啡浓度分别在24小时和48小时内平均持续高于1 ng/mL。低剂量的平均消除半衰期为6.23小时,高剂量为7.84小时。两种剂量下,平均激动 - 镇静评分均高于基线值24小时(表明有一定程度的镇静)。未观察到具有临床意义的不良反应。结论及临床意义 浓缩丁丙诺啡吸收迅速,在其他猛禽物种中被认为具有镇痛作用的血浆药物浓度可维持较长时间。大多数鸟类有轻度至中度镇静。需要进一步研究来评估这些剂量的浓缩丁丙诺啡在红尾鵟中的药效学。