肌注吡罗昔康的药代动力学。

J B Fourtillan
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引用次数: 0

摘要

在18名健康男性志愿者体内研究了吡罗昔康两种制剂(口服胶囊20 mg和肌肉注射溶液20 mg)的药代动力学和生物利用度。在头两天的早晨服用40毫克的剂量,在随后的五天服用20毫克的剂量。根据交叉设计,在第一次给药四周后,重复该方案。采用高效液相色谱法测定吡罗昔康的血浆浓度,紫外检测波长为340 nm。方差分析、Westlake检验和Wilcoxon检验结果表明,两种制剂具有生物等效性。然而,在第一次40mg注射后45分钟,第二次40mg注射后30分钟,以及20mg维持剂量后15分钟,肌内溶液产生相对较高的吡罗西康血浆浓度。肌内给药后半衰期为58.1 +/- 2.3小时,口服给药后半衰期为60.2 +/- 2.5小时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics of intramuscular piroxicam.

The pharmacokinetics and bioavailability of two piroxicam formulations, 20-mg capsules for oral administration and 20-mg solution for intramuscular injection, were studied in 18 healthy male volunteers. A 40-mg dose was administered on the morning of the first two days, and a 20-mg dose on five subsequent days. Four weeks after the first dose was administered, the regimen was repeated, according to a crossover design. Plasma levels of piroxicam were measured with high performance liquid chromatography (HPLC) using ultraviolet detection at 340 nm. Results of ANOVA, Westlake, and Wilcoxon tests show that the two preparations are bioequivalent. The intramuscular solution, however, produces comparatively higher piroxicam plasma concentrations up to 45 minutes after the first 40-mg dose, up to 30 minutes after the second 40-mg injection, and up to 15 minutes after the 20-mg maintenance doses. The terminal half-lives were found to be 58.1 +/- 2.3 hours after intramuscular administration and 60.2 +/- 2.5 hours after oral dosing.

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