High-performance liquid-chromatographic determination of rifampicin in plasma and tissues

J Chromatogr A. 2004 Mar 26;1031(1-2):289-94. doi: 10.1016/j.chroma.2003.12.041.

Abstract

A HPLC-UV method has been developed for assaying rifampicin in plasma and liver. The assay involved a liquid-liquid extraction procedure with dichloromethane-pentane (1:1). An Ultrabase-C18 column and a simple mobile phase consisting of a water (pH 2.27)-acetonitrile (40:60, v/v) mixture were used. The flow-rate was 1 ml/min and the effluent was monitored at 333 nm. Results from the HPLC analyses showed that the assay method is linear in the ranges 0.1-1 and 1-50 microg/ml for plasma, and 0.6-40 microg/g for liver. Intra- and inter-day R.S.D. were below 15% for all the sample types. Recoveries averaged 83 and 95% for plasma and liver, respectively. The method is being successfully applied to determine rifampicin in plasma and liver samples taken during pharmacokinetic studies in rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibiotics, Antitubercular / analysis*
  • Antibiotics, Antitubercular / blood
  • Antibiotics, Antitubercular / pharmacokinetics
  • Chromatography, High Pressure Liquid
  • Liver / chemistry
  • Male
  • Rats
  • Rats, Wistar
  • Reference Standards
  • Reproducibility of Results
  • Rifampin / analysis*
  • Rifampin / blood
  • Rifampin / pharmacokinetics
  • Solutions
  • Solvents
  • Spectrophotometry, Ultraviolet
  • Tissue Distribution

Substances

  • Antibiotics, Antitubercular
  • Solutions
  • Solvents
  • Rifampin