Analytical Method Development and Validation for Assay of Rufinamide Drug

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dc.contributor.authorJitender Singh
dc.contributor.authorSonia Sangwan
dc.contributor.authorParul Grover
dc.contributor.authorLovekesh Mehta
dc.contributor.authorDeepika Kiran
dc.contributor.authorAnju Goyal
dc.date.accessioned2025-12-15T09:03:55Z
dc.date.available2025-12-15T09:03:55Z
dc.date.issued2013-11
dc.description.abstractA 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 a mobile phase consisting of phosphate buffer: acetonitrile (60:40) was delivered at a flow rate of 1.0ml/ min. The analyte was detected by using a 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.
dc.identifier.issn2321-2217
dc.identifier.issn2321-2225
dc.identifier.otherhttps://doi.org/10.15415/jptrm.2013.12012
dc.identifier.urihttps://demodspace.chitkara.edu.in/handle/123456789/160
dc.language.isoen
dc.publisherChitkara University Publications
dc.subjectRP-HPLC
dc.subjectRufinamide
dc.subjectAPI
dc.subjectMethod Validation
dc.titleAnalytical Method Development and Validation for Assay of Rufinamide Drug
dc.typeArticle

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JPTRM Vol. 1 No. 2 (November 2013)