Asian Journal of Research in Chemistry
  • Year: 2009
  • Volume: 2
  • Issue: 3

Development and Validation of RP-HPLC Method for Simultaneous Determination of Ceftriaxone Sodium and Sulbactam Sodium in Bulk and Pharmaceutical Formulation

  • Author:
  • Jagjitsingh C Girase1, G Venkateshwarlu2, Saurabh Kumar Banerjee1,
  • Total Page Count: 5
  • Page Number: 280 to 284

1School of Pharmacy Technology and Management, SVKM's, NMIMS University, Shirpur Campus, Babulde, Near Bank of Tapi River, Shirpur, Dist: Dhule (M.S), India- 425405

2Research and Development Division, Concept Pharmaceuticals Ltd, Aurangabad

*Corresponding Author E-mail: saurabhk77@gmail.com

Online published on 13 March, 2013.

Abstract

A reverse phase high performance liquid chromatographic method was developed for simultaneous determination of Ceftriaxone Sodium and Sulbactam Sodium in bulk and Pharmaceutical Formulation. The separation was done by a Kromasil C18 column (250 mm × 4.6 mm, 5μm) using Acetonitrile: Buffer PH 7: Distilled Water (400:50:550, v/v/v) as mobile phase. The validation of the method was performed, and specificity, reproducibility, precision and accuracy were confirmed. The limit of detection was approximately 0.39 μg/ml for Ceftriaxone Sodium and 0.08 μg/ml for Sulbactam sodium. Due to simplicity and accuracy the method particularly suitable for routine pharmaceutical quality control.

Keywords

RP-HPLC, Ceftriaxone Sodium, Sulbactam sodium