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用高效液相色谱法测定血浆中的酮洛芬。与气液色谱法的比较(作者译)

[Determination of ketoprofen in plasma using high-performance liquid chromatography. Comparison with gas--liquid chromatography (author's transl)].

作者信息

Bannier A, Brazier J L, Ribon B

出版信息

J Chromatogr. 1978 Aug 11;155(2):371-8. doi: 10.1016/s0021-9673(00)87998-4.

Abstract

A new method of determination of ketoprofen 2-(3-benzoyl phenyl) propionic acid in plasma using high-performance liquid chromatography (HPLC) is described. After extraction by diethyl either in acidic medium, ketoprofen and the internal standard, 2-(4-benzoyl phenyl) butyric acid, are methylated with gaseous diazomethane and their concentrations measured by HPLC using in LiChrosorb Si 60 (5 micrometer) column and dichloromethane-hexane (60:40) as the mobile phase. The absolute retention times of the internal standard and ketoprofen are 11.6 and 12.8 min, respectively. The precision of the methods is +/- 4% and the lower detection limit ranges from 0.06 to 0.10 microgram/ml. The results obtained by HPLC show a very good correlation with those obtained by gas--liquid chromatography. The proposed method is sensitive, reproducible and rapid and very suitable for ketoprofen determination in pharmacokinetic studies.

摘要

本文描述了一种使用高效液相色谱法(HPLC)测定血浆中酮洛芬(2-(3-苯甲酰基苯基)丙酸)的新方法。在酸性介质中用乙醚萃取后,酮洛芬和内标物2-(4-苯甲酰基苯基)丁酸用气态重氮甲烷进行甲基化,然后使用LiChrosorb Si 60(5微米)柱,以二氯甲烷-己烷(60:40)作为流动相,通过HPLC测定它们的浓度。内标物和酮洛芬的绝对保留时间分别为11.6分钟和12.8分钟。该方法的精密度为±4%,检测下限范围为0.06至0.10微克/毫升。HPLC获得的结果与气-液色谱法获得的结果具有很好的相关性。所提出的方法灵敏、可重现且快速,非常适合在药代动力学研究中测定酮洛芬。

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