A validated RP-HPLC method for simultaneous estimation of ofloxacin and satranidazole from tablets
A. Sanjay A. Sanjay, K. Vinitha Prakash, Sutar Ravindra, Syad N.Lateef, Rahul Keshav Godge
Abstract
A. Sanjay A. Sanjay, K. Vinitha Prakash, Sutar Ravindra, Syad N.Lateef, Rahul Keshav Godge
Abstract
A simple, selective, rapid, precise and accurate reverse phase high performance liquid chromatographic method has been developed for simultaneous estimation of ofloxacin and satranidazole in combined tablet dosage form. The method was carried out on Jasco HPLC system with HiQ Sil C18Wcolumn (250i´4.6mm i.d.), usingAcetonitrile:Ammonium acetate 65:35v/v as a mobile phase. The detectionwas carried out usingUV detector set at 305nm. Clonazepamwas used as internal standard. BeerÂÂs law is obeyed in the concentration range of 2.0 to 20.0iÂg mL-1 and 3.0 to 30iÂg mL-1 of Ofloxacin and Satranidazole, respectively. The method has been successfully applied for the analysis of drugs in pharmaceutical formulations. Results of analysis were validated statistically and by recovery studies.
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A simple, selective, rapid, precise and accurate reverse phase high performance liquid chromatographic method has been developed for simultaneous estimation of ofloxacin and satranidazole in combined tablet dosage form. The method was carried out on Jasco HPLC system with HiQ Sil C18Wcolumn (250i´4.6mm i.d.), usingAcetonitrile:Ammonium acetate 65:35v/v as a mobile phase. The detectionwas carried out usingUV detector set at 305nm. Clonazepamwas used as internal standard. BeerÂÂs law is obeyed in the concentration range of 2.0 to 20.0iÂg mL-1 and 3.0 to 30iÂg mL-1 of Ofloxacin and Satranidazole, respectively. The method has been successfully applied for the analysis of drugs in pharmaceutical formulations. Results of analysis were validated statistically and by recovery studies.
Key concepts: Ofloxacin, Chromatography, Ammonium acetate, High-performance liquid chromatography, Chemistry, Pharmaceutical formulation, Materials science, Biochemistry