Development and validation of Ombitasvir In RP- HPLC

Authors

  • Raja shekar A Department of Pharmaceutical analysis, Mother Teresa college of Pharmacy,Ghatkesar, Medchal Telangana-501301
  • Chaithanya M Assistant Professor,Department of Pharmaceutical analysis, Mother Teresa college of Pharmacy,Ghatkesar ,Medchal Telangana-501301
  • Bhandhavi D Assistant Professor,Department of Pharmaceutical analysis, Mother Teresa college of Pharmacy,Ghatkesar ,Medchal Telangana-501301

Keywords:

RP- HPLC, Ombitasvir

Abstract

Ombitasvir (OMB) in mass and measurement structure now have a reliable, specific, rapid, and actual Streams stage - elite execution fluid chromatographic method. At a circulation charge per unit of 1.0 mL/min, a mixture of support arrangement (1 ml of Orthophosphoric corrosive changed into taken in a 1000 ml volumetric flagon and alternate the PH with Weakened NaOH upto three) and Acetonitrile as a transportable degree were used to attain chromatographic approval on Inertsil ODS C-18 insightful phase (4.6250 mm; fivem). The discovery of ultraviolet light occurred at 252 nanometers. Ombitasvir had respective storage durations of 2.315 minutes, 2.89 minutes, and 5.483 minutes. Over the fixation range of 6.25-37.five g/mL, 37.5-225 g/mL, and 25-150 g/mL for Ombitasvir, the adjustment plot became direct (r2=0.999). The approach had been permitted almost around ICH rules and carried out to the measurement of Ombitasvir, Paritaprevir and Ritonavir in unadulterated shape and dose shape

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Published

2023-09-30

How to Cite

A, R. shekar, M, C., & D, B. (2023). Development and validation of Ombitasvir In RP- HPLC. Frontier Journal of Pharmaceutical Sciences and Research, 6(2), 30–33. Retrieved from https://frontierjournals.org/index.php/fjpsr/article/view/46