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Arch Pharm Res ; 40(3): 364-372, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28205012

ABSTRACT

A high performance liquid chromatographic method was developed and validated for the determination of urazamide in pharmaceutical preparation with novel green aqueous mobile phase modified with room temperature ionic liquids (RTILs). 1-Ethyl-3-methyl-imidazolium tetrafluoroborate ([EMIM][BF4]) was selected as a mobile phase additive to improve retention and avoid baseline disturbances at t0. Various mobile phase parameters such as cation moiety, chaotropic anion moiety, pH and concentration of RTILs were optimized to determine urazamide at the proper retention time. The assay was validated according to International Conference on Harmonization guidelines. The linearity of the calibration curve was good (r2 > 0.999). Intra-day precision varied between 0.50 and 1.23%. Relative standard deviations of inter-day precision ranged between 1.07 and 1.66%. Recoveries in tablets ranged between 99.7 and 101.2% and it was successfully applied to determine urazamide in pharmaceutical preparations.


Subject(s)
Aminoimidazole Carboxamide/chemistry , Aspartic Acid/analogs & derivatives , Ionic Liquids/chemistry , Aspartic Acid/chemistry , Chromatography, High Pressure Liquid , Hydrogen-Ion Concentration , Imidazoles , Indicators and Reagents , Pharmaceutical Preparations/analysis , Reference Standards , Reproducibility of Results , Spectrophotometry, Ultraviolet , Tablets/analysis
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