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Determination of Rufinamide in the Presence of 1-[(2,6-Difluorophenyl)Methyl]-1H-1,2,3-Triazole-4 Carboxylic Acid Using RP-HPLC and Derivative Ratio Methods as Stability Indicating Assays to Be Applied on Dosage Form

BACKGROUNDRufinamide is a triazole derivative that is structurally dissimilar to other marketed antiepileptic drugs, has been assumed a marketing authorization, by the European Union and FDA, for use as a complementary therapy for seizures associated with Lennox-Gastaut syndrome. OBJECTIVEThis work...

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Bibliographic Details
Published in:Journal of AOAC International 2020-09, Vol.103 (5), p.1215-1222
Main Authors: Hassib, Sonia T, Hashem, Hanaa M A, Mahrouse, Marianne A, Mostafa, Eman A
Format: Article
Language:English
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Summary:BACKGROUNDRufinamide is a triazole derivative that is structurally dissimilar to other marketed antiepileptic drugs, has been assumed a marketing authorization, by the European Union and FDA, for use as a complementary therapy for seizures associated with Lennox-Gastaut syndrome. OBJECTIVEThis work is concerned with development of two methods for determination of rufinamide (RUF) in presence of 1-[(2,6-difluorophenyl)methyl]-1H-1,2,3-triazole-4 carboxylic acid as its alkaline degradation product in dosage form. METHODSThe first method was capable of determing RUF in the presence of its alkaline degradation product and in dosage form. Kromasil C8 column and mobile phase consisting of acetonitrile-water (50:50, v/v) were used and UV detection at 210 nm. In the second method, first derivative ratio spectrophotometry, RUF was determined by measuring peak amplitude at 269.5 nm over 5-30 μg/mL. RESULTSThe linearity range of RUF was 10-90 μg/mL for HPLC method covering its therapeutic range with r2 = 0.9999. Forced degradation under alkaline conditions was carried out, the degradation product was isolated and its structure was confirmed. Both methods were validated in accordance to ICH guidelines. Statistical analysis revealed no significant difference between obtained results and reported ones. CONCLUSIONThe present study is useful for therapeutic drug monitoring and routine analysis of RUF in quality control laboratories. HIGHLIGHTSKinetics of the alkaline degradation of RUF was studied by following the concentration of the remaining drug until complete degradation was achieved.
ISSN:1944-7922
DOI:10.1093/jaoacint/qsaa020