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RESEARCH JOURNAL OF PHARMACY AND TECHNOLOGY
Year : 2021, Volume : 14, Issue : 2
First page : ( 1045) Last page : ( 1049)
Print ISSN : 0974-3618. Online ISSN : 0974-360X.
Article DOI : 10.5958/0974-360X.2021.00187.6

Stability indicating simultaneous method development and validation of dapagliflozin and saxagliptin by RP-HPLC

Manasa Merugu1, Aanandhi Vijey M2*

1Research Scholar, Department of Pharmaceutical Chemistry and Analysis, School of Pharmaceutical Sciences, Vels Institute of Science, Technology and Advanced Studies (VISTAS), Pallavaram, Chennai, Tamil Nadu, India.

2Department of Pharmaceutical Chemistry and Analysis, School of Pharmaceutical Sciences, Vels Institute of Science Technology and Advanced Studies (VISTAS), Chennai, India.

*Corresponding Author E-mail: hodpchemistry@velsuniv.ac.in

Online published on 30 April, 2021.

Abstract

The developed method was validated according to ICH guidelines with respect to specificity, linearity, limits of detection, quantification, accuracy, precision, and robustness. The stability indicating simultaneous method development and validation of Dapagliflozin and Saxagliptin by RP-HPLC in drug substance and product. The chromatographic separation was done in an isocratic mode using the BDS C18 (150 x 4.6mm, 5.0μ) column with mobile phase containing a Ammonium acetate buffer: ACN (40: 60%v/v) used for efficient chromatographic separation. The flow rate of the mobile phase was adjusted to 1.0mL/min with 30oC column temperature and detection of wavelength at 220nm, injection volume 10μl was fixed for achieving good elution of eluents. The retention time for DAPA and SAXA were found to be 2.207 min and 2.889 min respectively. DAPA and SAXA were linear in the concentration ranges from 0–15μg/ml and 0–8μg/ml respectively. Regression analysis showed that R2 value (correlation coefficient) for DAPA and SAXA were found to be 0.999. LOD and LOQ of DAPA was found to be 21.6μg/ml and 9.1μg/ml, SAXA was found to be 11.5μg/ml 9.1μg/ml. The developed method was validated and found to be accurate, specific and robust. Both the drugs were subjected to the stress conditions like acidic, basic, oxidative, photolytic and thermal conditions. The degradation results were found to be satisfactory. In acidic, alkaline and peroxide stress conditions. The forced degradation test results confirmed that the DAPA and SAXA peaks were homogenous in all stress conditions, thus proving the stability-indicating nature of the method. This method could be applied for the simultaneous estimation of DAPA and SAXA in drug substance.

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Keywords

RP-HPLC, Dapagliflozin (DAPA) and Saxagliptin (SAXA), Stability indicating, Analytical method development, Analytical method validation.

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