A Stability Indicating RP-HPLC Method Validation for Simultaneous Estimation of Metformin HCl, Dapagliflozin and Saxagliptin in Pharmaceutical Dosage Form
Darshak Patel
Department of Quality Assurance & Pharm. Chem., Faculty of Pharmacy, Nootan Pharmacy College, Sankalchand Patel University, S. K. Campus, Visnagar-384315, Gujarat, India.
Ujashkumar Shah *
Department of Quality Assurance & Pharm. Chem., Faculty of Pharmacy, Nootan Pharmacy College, Sankalchand Patel University, S. K. Campus, Visnagar-384315, Gujarat, India.
Jayvadan Patel
Department of Quality Assurance & Pharm. Chem., Faculty of Pharmacy, Nootan Pharmacy College, Sankalchand Patel University, S. K. Campus, Visnagar-384315, Gujarat, India.
Darshana Patel
Department of Quality Assurance & Pharm. Chem., Faculty of Pharmacy, Nootan Pharmacy College, Sankalchand Patel University, S. K. Campus, Visnagar-384315, Gujarat, India.
Pavan Patel
Restech Pharmaceuticals, Plot No. 407 New Ahmedabad Industrial Estate, Sarkhej-Bavala Road, Moraiya-382 210, Dist-Ahmedabad, Gujarat, India.
*Author to whom correspondence should be addressed.
Abstract
Aims: Metformin HCl, Dapagliflozin and Saxagliptin is a new drug combination for the treatment of Diabetes Mellitus which is one of the oldest and lethal diseases of mankind. Aim of the research work was to develop and validate novel, rapid, sensitive, specific, robust stability indicating analytical method for simultaneous estimation of: Metformin HCl, Dapagliflozin and Saxagliptin in pharmaceutical dosage form as fixed dose formulation.
Study Design: Method development and validation was performed as recommended in ICH guideline “Validation of analytical procedures: Test and Methodology Q2 (R1)”.
Methodology: Method develop with chromatographic parameters as C18 column (250mm×4.6 mm, 5mm particle size), HPLC system with PDA detector and mobile phase contained a mixture of Phosphate Buffer pH 3.5 and Acetonitrile (80:20 v/v) + 1 ml triethylamine per 100 ml mobile phase. The flow rate was set to 1 ml/min with responses measured at 265 nm, injection volume was 20 µl, and run time of 15 mins.
Results: The retention time of Metformin HCl, Dapagliflozin and Saxagliptin was 5.8 min, 6.8 mins and 8.4 min respectively with resolution of 3.5 between Metformin HCl and Dapagliflozin and 4.5 between Dapagliflozin and Saxagliptin. Linearity was established in the range of 250-1500 µg/ml for Metformin HCl, 1.25-7.5 µg/ml for Dapagliflozin and Saxagliptin with correlation coefficients more than 0.999. The percentage recoveries were between 98.39-101.66 for Metformin HCl, 99.01-101.77 for Dapagliflozin and 98.88-101.87 for Saxagliptin Validation parameters were evaluated according to the International Conference on Harmonization (ICH) Q2 R1 guidelines. The forced degradation studies were performed by using HCl, NaOH, H2O2, thermal and UV Radiation. The developed method was successfully applied for the quantification and hyphenated instrumental analysis.
Conclusion: Significance of developed method is that it can be utilize for routine or unknown sample analysis of assay of Metformin HCl, Dapagliflozin and Saxagliptin in pharmaceutical dosage form developed by various Pharmaceutical Industry.
Keywords: Metformin HCl, dapagliflozin, saxagliptin, RP-HPLC, stability, diabetes mellitus