Analytical Method Development and Validation for Assay of Rufinamide Drug
Journal Title: JOURNAL OF PHARMACEUTICAL TECHNOLOGY, RESEARCH AND MANAGEMENT - Year 2013, Vol 1, Issue 2
Abstract
A simple, rapid, sensitive, cost effective and reproducible reverse phase high performance liquid chromatographic (RP-HPLC) method was developed and validated for the stability testing of rufinamide. The proposed RP-HPLC method was developed on phenome-nex LunaR C-18 5μm ,250 mm × 4.6 mm id. Column (at ambient temperature) and mobile phase consisting of phosphate buffer: acetonitrile (60:40) was delivered at a flow rate 1.0ml/ min. The analyte was detected by using UV detector at the wavelength of 293 nm. The method was found to be linear over the concentration range of 50- 150 μgml-1 (r2=0.999). 30. The retention time of rufinamide was 4.717 min.
Authors and Affiliations
Jitender Singh , Sonia Sangwan , Parul Grover , Lovekesh Mehta , Deepika Kiran , Anju Goyal
Keywords
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- EP ID EP596678
- DOI 10.15415/jptrm.2013.12012
- Views 211
- Downloads 0
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