Author(s): Dave Vidhi, Paresh Patel

Email(s): vidhidave1988@gmail.com

DOI: 10.52711/0974-360X.2021.00362   

Address: Dave Vidhi*, Dr. Paresh Patel
Department of Quality Assurance, S.K. Patel College of Pharmaceutical Education and Research, Ganpat University, Kherva , Gujarat, India.
*Corresponding Author

Published In:   Volume - 14,      Issue - 4,     Year - 2021


ABSTRACT:
A simple, precise and sensitive UV spectrophotometric method has been developed for the estimation of Remogliflozin etabonate in bulk and pharmaceutical dosage Form. Remogliflozin etabonate shows Maximum Absorbance at 229nm. Beer’s law was obeyed in range of 2-10µg/ml. The correlation coefficient was found to be 0.9990. The result of interday and intraday precision shows standard deviation ranging from 0.050% - 0.254% and 0.058% - 0.258% for three concentration and three replicates. The Percentage recovery was found to be in the range of 98.94% - 99.86%. The LOD and LOQ were found to be 0.037µg/ml and 0.113µg/ml respectively. The purposed method was novel and successfully applied for the determination of Remogliflozin Etabonate in Tablet Dosage Form. The method was successfully validated according to ICH guidelines.


Cite this article:
Dave Vidhi, Paresh Patel. Method development and Validation of UV Spectrophotometric estimation of Remogliflozin Etabonate in bulk and its tablet dosage form. Research Journal of Pharmacy and Technology. 2021; 14(4):2042-4. doi: 10.52711/0974-360X.2021.00362

Cite(Electronic):
Dave Vidhi, Paresh Patel. Method development and Validation of UV Spectrophotometric estimation of Remogliflozin Etabonate in bulk and its tablet dosage form. Research Journal of Pharmacy and Technology. 2021; 14(4):2042-4. doi: 10.52711/0974-360X.2021.00362   Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-4-38


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