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

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.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / blood*
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics*
  • Calibration
  • Chromatography, High Pressure Liquid
  • Humans
  • Ibuprofen / blood*
  • Ibuprofen / pharmacokinetics*
  • Quality Control
  • Reference Standards
  • Reproducibility of Results

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Ibuprofen