All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Abstract

Development and Validation of RP HPLC Method for the Estimation of Cefetamet in Bulk and Tablet Dosage Form

Author(s): N. Prudhvi, K. P. Channabasavaraj, Y. N. Manohara, A. L. Rao and D. B. Raju

A simple, rapid, sensitive and precise High Performance Liquid Chromatography (HPLC) method has been developed for the estimation of cefetamet in bulk and tablet dosage form. In this method, RP-C18 column (150 mm x 4.6 mm I.D., 5 7m particle size) with mobile phase consisting of acetonitrile, methanol and phosphate buffer (pH 3.60) in the ratio of 50 : 20 : 30 v/v/v in isocratic mode was used. The detection wavelength is 236 nm and the flow rate was 0.8 mL/min. In the range of 5-25 7g/mL, the linearity of cefetamet shows a correlation coefficient of 0.9995. The proposed method was validated by determining sensitivity, accuracy, precision and system suitability parameters. The method is simple, fast, accurate and precise and hence, it can be applied for routine analysis of cefetamet in bulk drug and its tablet dosage form.


Share this       
Google Scholar citation report
Citations : 9398

International Journal of Chemical Sciences received 9398 citations as per Google Scholar report

Indexed In

  • Google Scholar
  • Open J Gate
  • China National Knowledge Infrastructure (CNKI)
  • Cosmos IF
  • Geneva Foundation for Medical Education and Research
  • ICMJE

View More