Development and Validation of method for Simultaneous estimation of Remogliflozin, Vildagliptin and Metformin and its validation using ICH Q2R1

This study reports the method development and validation for anti-diabetic drugs by UPLC. A new, simple, rapid, selective, precise and accurate ultra-performance liquid chromatography assay has been developed for simultaneous estimation of remogliflozin, vildagliptin and metformin. The separation was achieved by using ODS 3V column with dimensions 5 µm, 4.6 mm x 250 mm. The pH of mobile phase was adjusted to 4.5 with acetonitrile. The flow rate was 0.4 mL/min, and the separated drugs were detected using UPLC detector at the wavelength of 260 nm. The method was validated as per ICH guidelines. The proposed method was found to be accurate, reproducible, and consistent. It was successfully applied for the analysis of these drugs in marketed formulations and could be effectively used for the routine analysis of formulations.

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Publication Details

Journal
Asian Journal of Pharmaceutical Analysis
Published
2025-03-04
DOI
https://doi.org/10.52711/2231-5675.2025.00007
Primary Topic
Diabetes Treatment and Management
Type
article
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article

Development and Validation of method for Simultaneous estimation of Remogliflozin, Vildagliptin and Metformin and its validation using ICH Q2R1

B. Mounika, Kommineni Vinutha, Priya Sridevi, Rayeesa Seema
Asian Journal of Pharmaceutical Analysis
Diabetes Treatment and Management
article

Development and Validation of method for Simultaneous estimation of Remogliflozin, Vildagliptin and Metformin and its validation using ICH Q2R1

B. Mounika, Kommineni Vinutha, Priya Sridevi, Rayeesa Seema
article en

Abstract

This study reports the method development and validation for anti-diabetic drugs by UPLC. A new, simple, rapid, selective, precise and accurate ultra-performance liquid chromatography assay has been developed for simultaneous estimation of remogliflozin, vildagliptin and metformin. The separation was achieved by using ODS 3V column with dimensions 5 µm, 4.6 mm x 250 mm. The pH of mobile phase was adjusted to 4.5 with acetonitrile. The flow rate was 0.4 mL/min, and the separated drugs were detected using UPLC detector at the wavelength of 260 nm. The method was validated as per ICH guidelines. The proposed method was found to be accurate, reproducible, and consistent. It was successfully applied for the analysis of these drugs in marketed formulations and could be effectively used for the routine analysis of formulations.

Asian Journal of Pharmaceutical Analysis
Shri Venkateshwara University (IN)
Openalex Percentile: Top 89%
Diabetes Treatment and Management
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