Simultaneous Analysis of Remogliflozin Etabonate and Vildagliptin in Tablets by HPTLC: Method Development and Validation

Recently, Vildagliptin and Remogliflozin together have become a viable treatment choice for diabetes. The invention of HPTLC (High Performance Thin Layer Chromatography) approach for the concurrent measurement of Vildagliptin (VILG) and Remogliflozin (REMO) in both their pure API (Active Pharmaceutical Ingredient) forms and in a commercially accessible formulation is shown in the present work. The method is robust, selective, sensitive, and fast. Utilizing a solvent solution consisting of toluene: ethyl acetate: methanol and glacial acetic acid (2.0: 6.0: 0.5: 0.1, v/v/v/v), the separation was successfully accomplished on silica gel F254. The chromatographic bands were observed at a wavelength of 250nm in short-wave ultraviolet light. With retention factor Rf values of 0.36 and 0.71 for REMO and VILG, correspondingly, proposed method showed clearly delineated spots.

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Publication Details

Journal
Research Journal of Pharmacy and Technology
Published
2024-12-27
DOI
https://doi.org/10.52711/0974-360x.2024.00867
Citations
1
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
Field-Weighted Citation Impact
0.24
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article

Simultaneous Analysis of Remogliflozin Etabonate and Vildagliptin in Tablets by HPTLC: Method Development and Validation

Parixit Prajapati, Pankaj Kapupara, Hitesh Vekariya
1 citations
Research Journal of Pharmacy and Technology
Analytical Methods in Pharmaceuticals
0.24
article

Simultaneous Analysis of Remogliflozin Etabonate and Vildagliptin in Tablets by HPTLC: Method Development and Validation

Parixit Prajapati, Pankaj Kapupara, Hitesh Vekariya
article en
1 citations

Abstract

Recently, Vildagliptin and Remogliflozin together have become a viable treatment choice for diabetes. The invention of HPTLC (High Performance Thin Layer Chromatography) approach for the concurrent measurement of Vildagliptin (VILG) and Remogliflozin (REMO) in both their pure API (Active Pharmaceutical Ingredient) forms and in a commercially accessible formulation is shown in the present work. The method is robust, selective, sensitive, and fast. Utilizing a solvent solution consisting of toluene: ethyl acetate: methanol and glacial acetic acid (2.0: 6.0: 0.5: 0.1, v/v/v/v), the separation was successfully accomplished on silica gel F254. The chromatographic bands were observed at a wavelength of 250nm in short-wave ultraviolet light. With retention factor Rf values of 0.36 and 0.71 for REMO and VILG, correspondingly, proposed method showed clearly delineated spots.

Research Journal of Pharmacy and Technology
RK University (IN)
Openalex Percentile: Top 48%
Analytical Methods in Pharmaceuticals
0.24
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