Development of RP-HPLC method for the estimation of Oseltamivir in pharmaceutical dosage form

Journal Title: Indian Journal of Research in Pharmacy and Biotechnology - Year 2017, Vol 5, Issue 5

Abstract

A rapid and precise Reverse Phase High Performance Liquid Chromatographic method has been developed for the validated of Oseltamivir, in its pure form as well as in tablet dosage form. Chromatography was carried out on a Phenomenex Luna C18 (4.6 x 250mm, 5µm) column using a mixture of Methanol and Water (75:25% v/v) as the mobile phase at a flow rate of 1.0ml/min, the detection was carried out at 223nm. The retention time of the Oseltamivir was 2.7 ±0.02 minutes. The method produce linear responses in the concentration range of 20-100ppm of Oseltamivir. The method precision for the determination of assay was below 2.0%RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.

Authors and Affiliations

Sumera Kousar, Hareesha, M. Anusha, Lavasri, Shabaz

Keywords

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  • EP ID EP33485
  • DOI -
  • Views 366
  • Downloads 0

How To Cite

Sumera Kousar, Hareesha, M. Anusha, Lavasri, Shabaz (2017). Development of RP-HPLC method for the estimation of Oseltamivir in pharmaceutical dosage form. Indian Journal of Research in Pharmacy and Biotechnology, 5(5), -. https://www.europub.co.uk/articles/-A-33485