静脉注射盐酸哌替啶在犬体内的药代动力学:正常和手术病例。

W. Kaithum, A.E. Waterman
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引用次数: 8

摘要

正常犬和术后即刻犬单次静脉注射哌啶的血药浓度-时间曲线可拟合为双指数方程,Cp = Ae -at+ be -βt。当正常犬使用较高的剂量率(3.5 mg/kg)时,分布率显著降低,但在其他动力学参数中未见其他差异。在相同剂量率(2 mg/kg)下,正常犬和术后犬的∝相和β相动力学常数无显著差异,β半衰期分别为36.59±5.98 min和52.54±11.94 min,但手术犬的分布体积和全身清除率明显低于正常犬。因此,与接受手术操作的狗相比,正常情况下哌替啶的药代动力学存在差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The pharmacokinetics of intravenous pethidine HC1 in dogs: normal and surgical cases.

The plasma concentration-time profiles of pethidine following a single bolus dose by intravenous injection in normal dogs and in dogs in the immediate postoperative period can be fitted into a biexponential equation, Cp = Ae -at+ Be-βt. The rate of distribution was significantly reduced when a comparatively higher dose rate (3.5 mg/kg) was used in normal dogs but no other differences were seen in the rest of the kinetic parameters. On the other hand using the same dose rate (2 mg/kg) the kinetic constants of both ∝ and β phases in normal and post-surgical dogs were not significantly different, with their respective β half-lives of 36.59 ± 5.98 min and 52.54 ± 11.94 min. However, the distribution volumes and the total body clearance were markedly reduced in surgical as compared to normal dogs. Thus there were differences between the pharmacokinetics of pethidine in normal when compared to dogs undergoing surgical manipulations.

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