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酮洛芬赖氨酸缓释制剂在人体中的药代动力学

Pharmacokinetics of a slow-release preparation of ketoprofen lysine in man.

作者信息

Borsa M, Tonon G C, Ronchi C, Zanolo G, Canali S

出版信息

Arzneimittelforschung. 1983;33(10):1497-500.

PMID:6418181
Abstract

The lysine salt of 2-(3-benzoylphenyl)propionic acid (ketoprofen lysine) was administered at the dose of 160 mg either in two conventional capsules (Artrosilene) or in one slow-release capsule in a randomized sequence to 8 volunteers. Serum and urine concentrations of ketoprofen were determined by HPLC. The slow-release preparation had a bioavailability greater than 90% as compared with the conventional capsule and produced lower and longer lasting ketoprofen serum levels. These results suggest that two daily administrations of the new formulation should be suitable for therapeutic use.

摘要

2-(3-苯甲酰基苯基)丙酸赖氨酸盐(酮洛芬赖氨酸盐)以160毫克的剂量,采用随机顺序,给8名志愿者分别服用两个常规胶囊(Artrosilene)或一个缓释胶囊。通过高效液相色谱法测定血清和尿液中酮洛芬的浓度。与常规胶囊相比,缓释制剂的生物利用度大于90%,且产生的酮洛芬血清水平更低、持续时间更长。这些结果表明,每日服用两次这种新制剂应适用于治疗用途。

相似文献

7
Urinary pharmacokinetics of orally administered ketoprofen in man.口服酮洛芬在人体中的尿液药代动力学。
Eur J Drug Metab Pharmacokinet. 1984 Jul-Sep;9(3):201-4. doi: 10.1007/BF03189642.
9
Circadian changes in the pharmacokinetics of oral ketoprofen.口服酮洛芬药代动力学的昼夜变化
Clin Pharmacokinet. 1987 May;12(5):367-78. doi: 10.2165/00003088-198712050-00003.

引用本文的文献

1
Clinical pharmacokinetics of ketoprofen and its enantiomers.酮洛芬及其对映体的临床药代动力学。
Clin Pharmacokinet. 1990 Sep;19(3):197-217. doi: 10.2165/00003088-199019030-00004.

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