Development and validation of high performance liquid chromatography method for analysis of sibutramine hydrochloride and its impurity

A simple, Precise, Rapid reproducible and selective reverse phase HPLC method has been developed for the estimation of Sibutramine Hydrochloride monohydrate and its Impurity in Bulk as well as Formulation. The analyte was resolved by using Mobile phase [Sodium Dihydrogen phosphate and Acetonitrile] at the flow rate of 1.0 Ml/Min. on Isocratic HPLC system consisting of Jasco Make UV visible Detector of model UV 1575 and Jasco make HPLC pump of model PU 1580.An ODS C- 8 RP Column [4.6mm ID, 250mm L, particle size 5 Micron, at wavelength of 230 nm

sensitive HPLC method for simultaneous estimation of tamsulosin hydrochloride and its impurity

Tamsulosin hydrochloride is used to treat the symptoms of an enlarged prostate, a condition technically known as benign prostatic hyperplasia or BPH. The analyte was resolved by using Mobile phase [Potassium Dihydrogen Orthophosphate and Acetonitrile] at the flow rate of 1.2 Ml/Min. on Isocratic HPLC system consisting of Jasco Make UV visible Detector of model UV 1575 and Jasco make HPLC pump of model PU 1580. An ODS C- 8 RP Column [4.6mm ID, 250mm L, particle size 5 Micron, at wavelength of 280 Nm. The linearity range was found to be 0.4 Ml/Ml for Tamsulosin and 0.12 mg/ml to 2.0 mg/ml for its Impurity. The proposed method is simple, accurate, rapid and selective. Percent Relative standard Deviation was found to be very low, below 2.0%, which indicates that method is highly precise and specific. Short Analysis time [