NEW STABILITY INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY METHOD FOR THE DETERMINATION OF NIRMATRELVIR AND RITONAVIR IN BULK AND TABLET DOSAGE FORM

Authors

  • Arthi M. Pharmacy, Department of Pharmaceutical Analysis, Malla Reddy College of Pharmacy, Maisammaguda, Secunderabad, Hyderabad, 500100, Medchal District, Secunderabad, Hyderabad, 500100, Medchal District.

Keywords:

Nirmatrelvir, Ritonavir, Rp HPLC, Validation, Method Development.

Abstract

Nirmatrelvir and Ritonavir are prescribed to treat COVID-19. An cheap HPLC approach was developed and is utilized for validation. KH2PO4 and MeCN are combined in an Agilent C18 150x4.6mm, 5m column at a flow rate of 1 ml/min at a temperature of 30 oC using a 60:40 v/v ratio. Its length was 215.0 nm. Nirmatrelvir had a holding time of 2.243 hours, whereas Ritonavir took 2.815 hours. It was discovered that the %RSD was 0.5% and 0.5%. The Nirmatrelvir regression equation was: y = 58409x + 2794. It was also discovered that ritonavir was y = 59191x + 774.23. Additionally, the LOD and LOQ values were discovered, and all tests passed and met ICH criteria.

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Published

2024-12-26

How to Cite

Arthi. (2024). NEW STABILITY INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY METHOD FOR THE DETERMINATION OF NIRMATRELVIR AND RITONAVIR IN BULK AND TABLET DOSAGE FORM. World Journal of Pharmaceutical Sciences, 13(01). Retrieved from https://wjpsonline.com/index.php/wjps/article/view/1714

Issue

Section

Research Article