Wilson K E, Davis J L, Crisman M V, Kvaternick V, Zarabadipour C, Cheramie H, Hodgson D R
Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA, USA.
North Carolina State College of Veterinary Medicine, Raleigh, NC, USA.
J Vet Pharmacol Ther. 2017 Dec;40(6):e23-e29. doi: 10.1111/jvp.12410. Epub 2017 Apr 29.
The purpose of this study was to determine the pharmacokinetic profile of intravenous firocoxib in neonatal foals. Six healthy foals were administered 0.09 mg/kg firocoxib intravenously once a day for 7 days. Blood was collected for plasma firocoxib analysis using high-performance liquid chromatography with fluorescence detection at times 0 (day 1 of study only) and 0.08, 0.25, 1, 2, 4, 6, 8, 16 and 24 hr on dose numbers 1, 5 and 7. Blood was also collected immediately prior to doses 3, 4, 5 and 7. Final samples were collected at 36, 48, 72 and 96 hr following the final dose. Noncompartmental analysis using the trapezoidal method with linear interpolation revealed a moderate half-life (15.9 ± 9.1 hr) with a large volume of distribution at steady state (1.79 ± 0.57 L/kg) and a clearance (96.0 ± 59.2 ml h kg ) that was more rapid than that observed in adult horses.
本研究的目的是确定静脉注射氟罗昔康在新生马驹体内的药代动力学特征。六匹健康马驹每天静脉注射0.09 mg/kg氟罗昔康,持续7天。在给药第1、5和7次时,于0小时(仅研究第1天)以及0.08、0.25、1、2、4、6、8、16和24小时采集血液,采用高效液相色谱荧光检测法分析血浆中的氟罗昔康。在第3、4、5和7次给药前也采集血液。在最后一次给药后36、48、72和96小时采集最终样本。使用梯形法和线性内插法进行的非房室分析显示,半衰期适中(15.9±9.1小时),稳态分布容积较大(1.79±0.57 L/kg),清除率(96.0±59.2 ml h kg)比成年马更快。