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口服加巴喷丁在灰狗犬体内的药代动力学研究。

Pharmacokinetics of oral gabapentin in greyhound dogs.

机构信息

Kansas State University, College of Veterinary Medicine, Department of Anatomy and Physiology, 228 Coles Hall, Manhattan, KS 66506, USA.

出版信息

Vet J. 2011 Jan;187(1):133-5. doi: 10.1016/j.tvjl.2009.09.022. Epub 2009 Oct 23.

Abstract

The purpose of this study was to assess the pharmacokinetics of gabapentin in healthy greyhound dogs after single oral doses targeted at 10 and 20mg/kg PO. Six healthy greyhounds were enrolled (3 males, 3 females). Blood was obtained at predetermined times for the measurement of gabapentin plasma concentrations by liquid chromatography/mass spectrometry. Pharmacokinetic parameters were determined with computer software. The actual mean (and range) doses administered were 10.2 (9.1-12.0) mg/kg and 20.5 (18.2-24) mg/kg for the 10mg/kg and 20mg/kg targeted dose groups. The mean C(MAX) for the 10 and 20mg/kg groups were 8.54 and 13.22 microg/mL at 1.3 and 1.5h, and the terminal half-lives were 3.3 and 3.4h, respectively. The relative bioavailability of the 10mg/kg group was 1.13 compared to the 20mg/kg group. Gabapentin was rapidly absorbed and eliminated in dogs, indicating that frequent dosing is needed to maintain minimum targeted plasma concentrations.

摘要

本研究旨在评估单次口服 10 和 20mg/kg 剂量的加巴喷丁在健康灰狗犬体内的药代动力学。招募了 6 只健康灰狗(3 只雄性,3 只雌性)。通过液相色谱/质谱法在预定时间采集血液,以测量加巴喷丁的血浆浓度。使用计算机软件确定药代动力学参数。实际给予的平均(和范围)剂量为 10.2(9.1-12.0)mg/kg 和 20.5(18.2-24)mg/kg,分别为 10mg/kg 和 20mg/kg 目标剂量组。10mg/kg 和 20mg/kg 组的 C(MAX)均值分别为 1.3 和 1.5 小时时的 8.54 和 13.22μg/mL,终末半衰期分别为 3.3 和 3.4 小时。与 20mg/kg 组相比,10mg/kg 组的相对生物利用度为 1.13。加巴喷丁在犬体内吸收和消除迅速,表明需要频繁给药以维持最小的目标血浆浓度。

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