HPLC-MS/MS METHOD FOR SIMULTANEOUS QUANTIFICATION OF VILDAGLIPTIN, METFORMIN, AND METFORMIN-RELATED COMPOUNDS IN TABLETS

Authors

  • Caroline Paola Uber Departamento de Farmacia, Universidade Federal do Parana, Curitiba, Parana, Brazil
  • Flavia Lada Degaut Pontes Departamento de Farmacia, Universidade Federal do Parana, Curitiba, Parana, Brazil
  • Joao Cleverson Gasparetto Departamento de Farmacia, Universidade Federal do Parana, Curitiba, Parana, Brazil
  • Thais Martins Guimaraes De Francisco Departamento de Farmacia, Universidade Federal do Parana, Curitiba, Parana, Brazil
  • MARIO SERGIO Piantavini Departamento de Farmacia, Universidade Federal do Parana, Curitiba, Parana, Brazil
  • Marco Andre Cardoso Instituto Pele Pequeno Principe, Curitiba, Parana, Brazil
  • Roberto Pontarolo Departamento de Farmacia, Universidade Federal do Parana, Curitiba, Parana, Brazil

Keywords:

Diabetes, HPLC-MSMS, Metformin, Metformin-related compound, Tablets, Vildagliptin

Abstract

Objective: The present study developed and validated a high-performance liquid chromatography-tandem mass spectrometry method for simultaneous determination of vildagliptin, metformin, and metformin-related compounds (A, B, and C) in tablets.

Methods: Chromatographic separations were achieved on a C8 column (150 × 4.6 mm, 5 µm particle size) maintained at 25°C. The isocratic mobile phase consisted of acetonitrile/water/formic acid (20:80:0.1, v/v/v), eluted at 800 μL/min. The volume of injection was 20 μL and the electrospray source was operated in positive ion mode.

Results: Data from validation studies demonstrated that the new method was highly selective, sensitive (limits of detection ≤ 0.6 ng/mL), precise (RSD < 5%), and accurate (RE < 5%). All of the calibration curves showed excellent coefficients of correlation (r ³ 0.99) over the ranges of 5‑150 ng/mL for vildagliptin, 250‑2000 ng/mL for metformin, and 2.5‑25 ng/mL for metformin-related compounds A, B, and C. Quantification of these compounds in tablets showed that they contained from 95.2‑101.2% (vildagliptin) and 97‑104.4% (metformin) of the stated level. No metformin-related compounds were detected using this highly sensitive method.

Conclusion: This new method is presented as an alternative approach to the quality control of tablets containing vildagliptin, metformin, and metformin-related compounds.

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Published

01-11-2014

How to Cite

Uber, C. P., F. L. D. Pontes, J. C. Gasparetto, T. M. G. D. Francisco, M. S. Piantavini, M. A. Cardoso, and R. Pontarolo. “HPLC-MS/MS METHOD FOR SIMULTANEOUS QUANTIFICATION OF VILDAGLIPTIN, METFORMIN, AND METFORMIN-RELATED COMPOUNDS IN TABLETS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 6, no. 11, Nov. 2014, pp. 203-7, https://journals.innovareacademics.in/index.php/ijpps/article/view/3068.

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