Development and Validation of visible Spectrophotometric method of Tapentadol Hydrochloride in bulk and Pharmaceutical dosage form
Kavita M. Babu, S. Kathirvel
Abstract
Kavita M. Babu, S. Kathirvel
Abstract
A simple, sensitive, accurate spectrophotometric method has been developed for the estimation of Tapentadol hydrochloride in bulk and pharmaceutical formulation. The method is based on the formation of blue colored chromogen with Folin-Ciocalteu reagent in the presence of NaOH and obeys beer ’s law in the range of 5 -35 μg/mL exhibiting the maximum absorbance at 763nm. The limit of detection and quantification were found to be 0.76 μg/mL and 2.33 μg/mL respectively. The calibration curve demonstrated a linear relationship between the absorbance and concentration, with the correlation coefficient higher than 0.9999. The Regression Equation of the curve was Y=0.0248x-0.0436. The method was fully validated according to ICH guidelines.
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A simple, sensitive, accurate spectrophotometric method has been developed for the estimation of Tapentadol hydrochloride in bulk and pharmaceutical formulation. The method is based on the formation of blue colored chromogen with Folin-Ciocalteu reagent in the presence of NaOH and obeys beer ’s law in the range of 5 -35 μg/mL exhibiting the maximum absorbance at 763nm. The limit of detection and quantification were found to be 0.76 μg/mL and 2.33 μg/mL respectively. The calibration curve demonstrated a linear relationship between the absorbance and concentration, with the correlation coefficient higher than 0.9999. The Regression Equation of the curve was Y=0.0248x-0.0436. The method was fully validated according to ICH guidelines.
Key concepts: Absorbance, Calibration curve, Pharmaceutical formulation, Correlation coefficient, Dosage form, Chromatography, Reagent, Tapentadol