Repository logo
Institutional Repository
Communities & Collections
Browse
Quick Links
  • Central Library
  • Digital Library
  • BHU Website
  • BHU Theses @ Shodhganga
  • BHU IRINS
  • Login
  • English
  • العربية
  • বাংলা
  • Català
  • Čeština
  • Deutsch
  • Ελληνικά
  • Español
  • Suomi
  • Français
  • Gàidhlig
  • हिंदी
  • Magyar
  • Italiano
  • Қазақ
  • Latviešu
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Srpski (lat)
  • Српски
  • Svenska
  • Türkçe
  • Yкраї́нська
  • Tiếng Việt
Log In
New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Komal Doifode"

Filter results by typing the first few letters
Now showing 1 - 1 of 1
  • Results Per Page
  • Sort Options
  • Loading...
    Thumbnail Image
    PublicationArticle
    ICH Guideline in Practice for Quantification of Ruxolitinib by applying Validated RP-HPLC Method on Commercial Tablet Formulation
    (Research Journal of Pharmacy and Technology, 2024) Minal Harde; Sameer Lakade; Ujwala Wasnik; Shejal Wakade; Komal Doifode; Kamlesh Palandurkar; Shrikant Joshi; Laxman Ingole
    Background: The current investigation explains the validation of High Pressure Liquid Chromatography (HPLC) technique for quantification of Ruxolitinib in active ingredient and marketed tablet dosage form. For assessment of Ruxolitinib, a specific column chromatographic method has been developed using UV detection. Methods: The chromatographic elution was executed on ODS Phenomenex analytical column (250mm × 4.6mm, 5μm particle size). The solvent ratio utilized was methanol: water (pH 3.5 adjusted with OPA) (70:30 V/V). A constant ratio of eluting phase flow rate 1.0ml/min was used to detect RTB at 236nm. Results: The developed method was justified using various variables such as accuracy, limit of detection, precision, specificity, robustness, limit of quantification. The retention time for Ruxolitinib was obtained at 8.59 min. The designed method was detected linear within 20 to 120μg/ml range. Correlation coefficient (r2) of the regression equation was found to be 0.9999. Detection and quantitation limit achieved was 0.1496 and 0.4483 respectively. The accuracy of the method was determined using recovery study. The % recovery obtained was in the range of 98.68 – 99.80%. All system suitability factors like tailing factor, retention factor, number of theoretical plates were obtained within acceptance range. The obtained result demonstrates that the presented method is reliable, precise, and economical. Conclusion: The specified method was effectively authenticated as per guidelines of ICH in practice and can be claimed successful for the determination of Ruxolitinib in commercial formulation. © RJPT All right reserved.
An Initiative by BHU – Central Library
Powered by Dspace