Abstract: This research manuscript explains simple yet sensitive & speedy, accurate, precise, repeatable & reproducible RP-UPLC method for the analysis of Levofloxacin and Ornidazole in combine pharmaceutical dosage form. The sample was analyzed by reverse phase C18 column (Purospher Star 100×2.1 mm, Merck Specialities) as stationary phase and Phosphate Buffer: Acetonitrile (65:35 v/v) as a mobile phase [where PH of of the buffer was adjusted to 2.5 by using Tri ethylamine (1ml for 1 lit buffer) and ortho-phosphoric acid] at a flow rate of 0. 44 ml/min. TUV detector was used for the detection at 294 nm. The retention time for Levofloxacin and Ornidazole was found to be 0.537 and 0.938 minute respectively. The linearity for both the drugs was obtained in the concentration range of 2-14 μg/ml and 4-28 μg/ml. The method was successfully applied to pharmaceutical formulation because no significant interferences from suspension excipient were found. The method retained its accuracy and precision when certain variations in method parameters were applied.
Keywords: Combined dosage forms; Levofloxacin and Ornidazole; Method development & validation, RP-UPLC,Stability Study.
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