Method Development and Validation for the Simultaneous Estimation of Ceftriaxone and Tazobactam in Bulk and Pharmaceutical Dosage Forms by Rp-Hplc

A simple, accurate and precise High Performance Liquid Chromatographic (HPLC) method was developed and validated for the simultaneous estimation of Ceftriaxone and Tazobactam in bulk and Pharmaceutical dosage forms. The method was developed using Waters HPLC system with Inertsil – C18, ODS column (250 x 4.6 mm, 5µ). Mobile phase containing Methanol and buffer in the ratio 80:20 v/v in isocratic elution mode at a flow rate of 1.0ml/min (load of 20µl) . The detection was carried out at 254 nm. Retention time of Ceftriaxone and Tazobactam were found to be 3.049 min and 4.317 min respectively. The developed method was validated with respect to linearity, robustness, precision and accuracy. It was successfully applied for the simultaneous quantitative estimation of Ceftriaxone and Tazobactam in the Pharmaceutical dosage form. Results show that the retention and run time were decreased, so it is evident that the method developed was simple and economical that can be adopted in regular Quality control test in Industries

Publication Details

Journal
International Journal of Pharmaceutical Research and Applications
Published
2025-05-01
DOI
https://doi.org/10.35629/4494-1005444450
Primary Topic
Geochemistry and Geologic Mapping
Type
article
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article

Method Development and Validation for the Simultaneous Estimation of Ceftriaxone and Tazobactam in Bulk and Pharmaceutical Dosage Forms by Rp-Hplc

International Journal of Pharmaceutical Research and Applications
Geochemistry and Geologic Mapping
article

Method Development and Validation for the Simultaneous Estimation of Ceftriaxone and Tazobactam in Bulk and Pharmaceutical Dosage Forms by Rp-Hplc

article en

Abstract

A simple, accurate and precise High Performance Liquid Chromatographic (HPLC) method was developed and validated for the simultaneous estimation of Ceftriaxone and Tazobactam in bulk and Pharmaceutical dosage forms. The method was developed using Waters HPLC system with Inertsil – C18, ODS column (250 x 4.6 mm, 5µ). Mobile phase containing Methanol and buffer in the ratio 80:20 v/v in isocratic elution mode at a flow rate of 1.0ml/min (load of 20µl) . The detection was carried out at 254 nm. Retention time of Ceftriaxone and Tazobactam were found to be 3.049 min and 4.317 min respectively. The developed method was validated with respect to linearity, robustness, precision and accuracy. It was successfully applied for the simultaneous quantitative estimation of Ceftriaxone and Tazobactam in the Pharmaceutical dosage form. Results show that the retention and run time were decreased, so it is evident that the method developed was simple and economical that can be adopted in regular Quality control test in Industries

International Journal of Pharmaceutical Research and ApplicationsVol. 10(5)
Industry, innovation and infrastructure
Openalex Percentile: Top 27%
Geochemistry and Geologic Mapping
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