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单剂量静脉注射和口服美洛昔康在红尾鹰(赤肩鵟)和大角鸮中的药代动力学

Pharmacokinetics of a single dose of intravenous and oral meloxicam in red-tailed hawks (Buteo jamaicensis) and great horned owls (Bubo virginianus).

作者信息

Lacasse Claude, Gamble Kathryn C, Boothe Dawn M

机构信息

Lincoln Park Zoo, 2001 N Clark St, Chicago, IL 60614, USA.

Clinical Pharmacology Laboratory, College of Veterinary Medicine, Auburn University, 109 Greene Hall, Auburn, AL 36489, USA.

出版信息

J Avian Med Surg. 2013 Sep;27(3):204-10. doi: 10.1647/2012-044.

Abstract

Pharmacokinetic data were determined after a single dose of meloxicam in red-tailed hawks (RTH; Buteo jamaicensis) and great horned owls (GHO; Bubo virginianus). In a nonrandomized crossover design, individual birds of each species received 1 dose of intravenous meloxicam (0.5 mg/kg i.v.; n = 7 for each species) followed by a 2-week washout period, and then each received 1 dose of oral meloxicam (0.5 mg/kg PO; n = 5 for each species). Blood samples were collected intermittently after administration, and meloxicam was detected in plasma by high-performance liquid chromatography. Time versus plasma concentration data were subjected to noncompartmental analysis. Red-tailed hawks were determined to have the shortest elimination half-life for meloxicam (0.49 +/- 0.5 hours) of any species documented. Great horned owls also eliminated meloxicam very rapidly (0.78 +/- 0.52 hours). Great horned owls achieved higher plasma concentrations (368 +/- 87 ng/mL) of meloxicam than RTH (182 +/- 167 ng/mL) after oral administration, although RTH had a markedly higher volume of distribution (832 +/- 711 mL/kg) than GHO (137.6 +/- 62.7 mL/kg). The differences in meloxicam pharmacokinetics between these 2 raptor species supports the need for species-dependent studies and underlines the challenges of extrapolating drug dosages between species. Results of this study suggest that the current recommended once-daily dosing interval of oral meloxicam is unlikely to maintain plasma concentrations anticipated to be therapeutic in either RTH or GHO, and practical dosing options are questionable for this nonsteriodal anti-inflammatory drug in these raptor species.

摘要

在红尾鹰(RTH;美洲赤褐鹰)和大角鸮(GHO;大角鸮)单次给予美洛昔康后测定了药代动力学数据。在非随机交叉设计中,每个物种的个体鸟类接受1剂静脉注射美洛昔康(0.5 mg/kg静脉注射;每个物种n = 7),随后有2周的洗脱期,然后每个个体接受1剂口服美洛昔康(0.5 mg/kg口服;每个物种n = 5)。给药后间歇性采集血样,并通过高效液相色谱法在血浆中检测美洛昔康。时间与血浆浓度数据进行非房室分析。已确定红尾鹰是所有记录物种中美洛昔康消除半衰期最短的(0.49±0.5小时)。大角鸮消除美洛昔康也非常迅速(0.78±0.52小时)。口服给药后,大角鸮的美洛昔康血浆浓度(368±87 ng/mL)高于红尾鹰(182±167 ng/mL),尽管红尾鹰的分布容积(832±711 mL/kg)明显高于大角鸮(137.6±62.7 mL/kg)。这两种猛禽物种之间美洛昔康药代动力学的差异支持了进行物种依赖性研究的必要性,并强调了在不同物种间推断药物剂量的挑战。本研究结果表明,目前推荐的口服美洛昔康每日一次给药间隔不太可能维持预期在红尾鹰或大角鸮中具有治疗作用的血浆浓度,对于这些猛禽物种中的这种非甾体抗炎药,实际给药方案存在疑问。

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