Volume : 12, Issue : 06, June – 2025
Title:
ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR THE ANALYSIS OF OXALIPLATIN IN PURE FORM AND MARKETED PHARMACEUTICAL DOSAGE FORMS BY USING RP-HPLC
Authors :
CH .Kantlam, D.Vinod Kumar*, J.Vasavi, Kavati. Ruchitha, Komarabenda. Ruchitha, Mamidi Anu
Abstract :
The present work includes a simple, economic, rapid, accurate and precise isocratic RP-HPLC method development for estimation of Oxaliplatin in bulk form and its marketed formulation. Estimation was done at 286nm which was found to be λmax of Oxaliplatin. The simple, selective, isocratic RP-HPLC method for Oxaliplatin was developed on Symmetry (C18) RP Column; 250 mm x 4.6 mm, 5µm with a mobile phase of Phosphate Buffer (pH-4.6) and Methanol were taken in the ratio of 70:30% v/v at a flow rate of 1.0 ml/min and detection wavelength 286nm. The developed method was validated successfully according to ICH Q2 (R1) guidelines. The chromatographic methods showed a good linear response with r2 values of 0.9995. The percentage relative standard deviation for method was found to be less than two, indicating that the methods were precise. The mean percentage recovery was for RP-HPLC method was 100.437%. From the results it could be concluded that both the developed method was specific, selective and robust. The method could be successfully applied for analysis of Bulk form and Marketed formulation of Oxaliplatin.
Key Words: Oxaliplatin, RP-HPLC, Method Development, Validation, ICH Guidelines.
Cite This Article:
Please cite this article in press Ch .Kantlam et al., Analytical Method Development And Validation For The Analysis Of Oxaliplatin In Pure Form And Marketed Pharmaceutical Dosage Forms By Using Rp-Hplc.,, Indo Am. J. P. Sci, 2025; 12(07).
Number of Downloads : 10
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