Asian Journal of Pharmaceutical Analysis
  • Year: 2024
  • Volume: 14
  • Issue: 3

UV spectrophotometric method development and validation for the determination of nirmatrelvir antiviral Drug in bulk and its in-house formulation

  • Author:
  • Priya R. Wani1,*, Vikram Jadhav2,**, Ashish Jain3,***, Vaishali Jadhav1,****
  • Total Page Count: 4
  • Page Number: 127 to 130

1Department of Quality Assurance, Shri D. D. Vispute College of Pharmacy and Research Center, Devad, Vichumbe, Gut No.104, Adjacent to Mumbai-Pune Express Highway, Tal. Panvel, Dist. Raigad, Maharashtra, India, 410 221

2Mini Drugs Testing LaboratoryOffice of the ADC (I), Central Drugs Standard Control Organization, M/s JWR Logistic Pvt Ltd 15-45, National Highway 4B, Panvel - JNPT Highway, Village Padeghar, Post - Vahal, Panvel - Maharashtra, India, 410206

3Department of Pharmacognosy and Phytochemistry, Shri D. D. Vispute College of Pharmacy and Research Center, Devad, Vichumbe, Gut No.104, Adjacent to Mumbai - Pune Express Highway, Tal. Panvel, Dist. Raigad, Maharashtra, India, 410 221

*Corresponding Author E-mail: priyawani703@gmail.com

**pharmavikram17@gmail.com

***drashishjain80@gmail.com

****vaishalikudekar@gmail.com

Online published on 9 April, 2025.

Abstract

UV spectrophotometry was performed by Lab India Analytical UV 3092 using methanol as medium. The resolution process was performed in the range of 200-400nm to determine the maximum absorption (λ max). The λmax of Nirmatrelvir was found to be 210nm. Measure the absorbance of 10, 20, 30, 40, 50, and 60μg/ml drug solution and measure the maximum absorbance at 210 nm with a blank control. Then draw a graph from the concentration on the X-axis and the absorbance on the Y-axis to get a straight line. Validation parameters such as linearity, precision, specificity, LOD and LOQ, accuracy and robustness were evaluated according to ICH guidelines.

Keywords

Nirmatrelvir, UV, Bulk and In-house tablet formulation, Development, Validation