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“Pazufloxacin is chemically, (3R)-10-(1-aminocyclopropyl)-9-fluoro-2,3-dihydro-3-methyl-7-oxo7H-pyrido[1,2,3-de]1,4-benzoxazine-6-carboxylic acid. 1 Pazufloxacin is broad spectrum fluoroquinolone antibiotic and it exhibits antibacterial activity by inhibiting DNA gyrase thus preventing DNA replication and synthesis. 2 The literature survey reveals that the drug can be estimated in human plasma and urine by check details HPLC 3 and a validated stability-indicating RP-HPLC method for the estimation of pazufloxacin in presence of its degradation products. 4 Based on the literature survey authors

found that there was no any RP-HPLC method to quantify the drug in pure and formulation. The aim of the study was to develop a simple, precise and accurate RP-HPLC method for the estimation of pazufloxacin in pure drug and in injectable dosage form. Waters 2695 HPLC system equipped with Kromasil C18, 150 × 4.6 mm, 5 μm column, Rheodyne injector with 20 μL loop, 2996 PDA detector and Empower-2 software was used. The mobile phase consisted of 0.05 M phosphate buffer (pH 3) and acetonitrile in the ratio of 80:20% v/v that was set at a flow rate of 1 mL/min. All the

regents and solvents used are analytical and HPLC grade. The mobile phase buffer was prepared by dissolving 6.8 g potassium dihydrogen orthophosphate in 1000 ml selleck compound of water and pH adjusted to 3 with orthophosphoric acid. The pure drug of pazufloxacin was obtained from commercial supplier India. Injectable formulation of the drug was obtained from local pharmacy. Stock solution of pazufloxacin was prepared by dissolving accurately

weighed 100 mg of the drug in 100 mL of HPLC grade water (final concentration, 1 mg/mL). The prepared Mephenoxalone stock solution was stored at 4 °C protected from light. Calibration plot was constructed by analysis of appropriate working solutions (concentration 12.5, 25, 50, 75, 100, 125 and 150 μg/mL) of pazufloxacin in the mobile phase and plotting concentration against peak area response for each injection. Unknown samples were quantified by reference to this calibration plot. The pazufloxacin injectable dosage form was diluted with mobile phase to get 50 μg/mL of drug and filtered through a 0.2 μm membrane filter. From this solution 20 μL was injected for HPLC analysis. The developed method was optimised to obtain the best chromatographic conditions, the wavelength for detection of drug without any interference of additives used for the preparation of formulation, the column and the mobile phase composition must be effectively selected. Column chemistry, solvent type, solvent strength, detection wavelength and flow rate were varied to determine the chromatographic conditions giving the best separation of pazufloxacin.