Validation of analysis method for determining ketoprofen concentration in pharmaceutical dosage form using high performance liquid chromatography
European Journal of Chemistry , Volume 4, pp 58-60; doi:10.5155/eurjchem.4.1.58-60.678
Abstract: The study was conducted with the purpose to develop and validate a high performance liquid chromatography method with UV detector to determine ketoprofen content in tablet preparation using ethanol-phosphate buffer (pH = 6.0, 80:20, v:v). The method was validated toward parameters of accuracy, precision, linearity, selectivity, LOD and LOQ. The results obtained fulfill the validation requirement of the ketoprofen tablet in the form of LOD = 0.5302 ppm and LOQ = 1.7676 ppm.
Keywords: tablet / ethanol / Determining Ketoprofen / high performance liquid chromatography / Ketoprofen Concentration / Loq
Scifeed alert for new publicationsNever miss any articles matching your research from any publisher
- Get alerts for new papers matching your research
- Find out the new papers from selected authors
- Updated daily for 49'000+ journals and 6000+ publishers
- Define your Scifeed now
Click here to see the statistics on "European Journal of Chemistry" .