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高效液相色谱法测定人血浆中的布洛芬:方法验证及其在药代动力学研究中的应用

Determination of Ibuprofen in human plasma by high-performance liquid chromatography: validation and application in pharmacokinetic study.

作者信息

Canaparo R, Muntoni E, Zara G P, Della Pepa C, Berno E, Costa M, Eandi M

机构信息

Department of Anatomy, Pharmacology and Forensic Medicine, University of Torino, Torino, Italy.

出版信息

Biomed Chromatogr. 2000 Jun;14(4):219-26. doi: 10.1002/1099-0801(200006)14:4<219::AID-BMC969>3.0.CO;2-Z.

Abstract

A specific method for the simultaneous determination of S-(+)Ibuprofen and R-(-)Ibuprofen enantiomers in human plasma is described. Adopting a high-performance liquid chromatographic (HPLC) system with spectrofluorometer detector, the compounds were extracted from plasma in alcohol medium and were separated on C18 column, using a solution of acetonitrile-water-acetic acid-triethylamine as mobile phase. The limit of quantitation was 0.1 microg/mL for both compounds. The method was validated by intra-day assays at three concentration levels and was used in a kinetic study in healthy volunteers. During the study we carried out inter-day assays to confirm the feasibility of the method.

摘要

描述了一种同时测定人血浆中S-(+)布洛芬和R-(-)布洛芬对映体的具体方法。采用配备荧光分光光度计检测器的高效液相色谱(HPLC)系统,化合物在乙醇介质中从血浆中提取出来,并在C18柱上分离,使用乙腈-水-乙酸-三乙胺溶液作为流动相。两种化合物的定量限均为0.1μg/mL。该方法通过在三个浓度水平进行日内测定进行验证,并用于健康志愿者的动力学研究。在研究过程中,我们进行了日间测定以确认该方法的可行性。

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