Development and Validation of New Analytical Method for Ceftriaxone Sodium in Bulk and Pharmaceutical Dosage Forms

Abstract

A simple, sensitive, accurate and precise LC assay method was developed for the quantitative determination of Ceftriaxone Sodium (CTS) in pharmaceutical dosage form. Chromatographic separation was achieved by use of XTerra RP-18 column (250 × 4.0 mm, 5 m). The described method was linear over a range of 1.0-120 g mL-1 for determination of CTS (r= 0.9992). F-test and t-test at 95% confidence level were used to check the intermediate precision data obtained under different experimental setups; the calculated value was found to be less than critical value. The developed method was found to be simple, specific, robust, linear, precise, and accurate for the determination of CTS in pharmaceutical formulations.

Issue :

2012 Volume-02

Article Subject :

Pharmacy

Keywords :

Ceftriaxone Sodium, validation, Assay, recovery studies.

Article PDF :

IJRRPAS 2.3.9