Development and validation of an UV spectrophotometric method for determination of gatifloxacin in tablets

Pharmazie. 2005 Apr;60(4):263-4.

Abstract

A simple, sensitive and accurate spectrophotometric method was developed for the assay of gatifloxacin in raw material and tablets. Validation of the method yielded good results concerning range, linearity, precision and accuracy. The absorbance was measured at 287 nm for gatifloxacin tablet solutions. The linearity range was found to be 4.0-14.0 microg/mL for gatifloxacin. It was also found that the excipients in the commercial tablets did not interfere with the method.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Infective Agents / analysis*
  • Calibration
  • Fluoroquinolones / analysis*
  • Gatifloxacin
  • Reference Standards
  • Reproducibility of Results
  • Spectrophotometry, Ultraviolet
  • Tablets

Substances

  • Anti-Infective Agents
  • Fluoroquinolones
  • Tablets
  • Gatifloxacin