Development of a UV- HPLC method for assay and dissolution in Dapoxetine tablets

The aim of this work was to develop and validate of assay and dissolution tests for Dapoxetine Hydrochloride in the pharmaceutical dosage by using HPLC and spectrophotometric analyses, respectively. The assay method by HPLC was found to be linear in the concentration range of 05 to 005 μg/ml. All the parameters of validation were in the acceptance range. This developed method was successfully applied to estimate the amount of Dapoxetine Hydrochloride in the tablets. Moreover, a simple and precise UV spectrophotometric technique was used for the determination in dissolution studies. Linear dependency of UV spectrophotometric method lies in the concentration range of 05 to 05μg/ml. This proposed methods was sensitive, accurate, repeatable and useful for the routine determination of Dapoxetine Hydrochloride in the tablets.

کلیدواژه ها:

Dapoxetine Hydrochloride ، High performance liquid chromatography (HPLC) ، spectrophotometric