Open AccessSPECTROPHOTOMETRIC EVALUATION OF NIMESULIDE IMPURITY D: 4-NITRO-2- PHENOXYANILINE USING 8-HYDROXYQUINOLINE AS OXIDATIVE COUPLING REAGENT
Author(s) -
Anil Kumar S,
Bhaskar Bl
Publication year - 2017
Publication title -
asian journal of pharmaceutical and clinical research
Language(s) - English
Resource type - Journals
eISSN - 2455-3891
pISSN - 0974-2441
DOI - 10.22159/ajpcr.2017.v10i7.18540
Subject(s) - nimesulide , absorbance , chemistry , reagent , detection limit , chromatography , impurity , oxidative coupling of methane , nuclear chemistry , organic chemistry , biochemistry , catalysis
Objective: Spectrophotometric investigation of 4-nitro-2-phenoxyaniline (4N2PA), a probable intermediate during the synthesis of anti-inflammatory drug nimesulide, both in pure form and in the presence of nimesulide has been attempted. Methods: 4N2PA on diazotization followed by coupling with 8-hydroxyquinoline produces a crimson-colored complex which changes to deep violet on diluting with ethanol. Results: The complex showed maximum absorbance at 560 nm when evaluated spectrophotometrically with a detection limit of 0.005 μg/ml and quantification range of 0.05-3.0 μg/ml. The method has been statistically evaluated with respect to the International Council for Harmonisation guidelines and found to be accurate and precise. Conclusion: Pure tablet formulations of nimesulide do not respond to the method; however, the presence of minute amounts of 4N2PA in the drug as added impurity could be spectrophotometrically analyzed. Hence, the authors suggest that the reported technique could be a marker test for detecting the presence of 4N2PA in nimesulide formulations.