QbD-Enhanced HPLC Method Development for Vildagliptin and Metformin HCl Formulations

Indian Journal of Pharmaceutical Education and Research

  • Pankaj Sopan Hasabe2Research and Development, Integrated Product Development, Dr. Reddy’s Laboratories Ltd., Bachupally, Hyderabad, Telangana, INDIA.
  • Kishor Vinayak Gaikwad1Department of Chemistry, Rajarshi Chhatrapati Shahu College, Kolhapur, Maharashtra, INDIA.
  • Venketa Satyanarayana Nandmuri2Research and Development, Integrated Product Development, Dr. Reddy’s Laboratories Ltd., Bachupally, Hyderabad, Telangana, INDIA.
  • Akanksha Govind Kolekar3Department of Chemistry, Fluorescence Spectroscopy Research Laboratory, Shivaji University, Kolhapur, Maharashtra, INDIA.
  • Kalyanraman Lakshmi Narayanan2Research and Development, Integrated Product Development, Dr. Reddy’s Laboratories Ltd., Bachupally, Hyderabad, Telangana, INDIA.
  • Samadhan Prakash Pawar3Department of Chemistry, Fluorescence Spectroscopy Research Laboratory, Shivaji University, Kolhapur, Maharashtra, INDIA.

Volume 59 Issue 2s Pages s724-s732

DOI: 10.5530/ijper.20256263

Abstract

Objectives: This research employs the Quality by Design strategy to design an optimized High-Performance Liquid Chromatography method aimed at analyzing vildagliptin and metformin hydrochloride in pharmaceutical dosage forms. Materials and Methods: The mobile phases A and B comprised a buffer-acetonitrile mixture in ratios of 950:50 v/v and 600:400 v/v, respectively. Chromatographic separation was achieved using an YMC Triart C-18 column, with Vildagliptin detection conducted at 210 nm via UV absorbance. Various independent parameters were selected for investigation and risk assessment was employed to evaluate their impact on the analytical responses. Results: QbD prioritizes product understanding, risk management and process control to enhance quality assurance and regulatory tractability. Analytical Quality by Design principles ensure robust and flexible methods throughout the product lifecycle. Conclusion: This study developed a robust HPLC method for Vildagliptin using a Quality by Design (QbD) approach. Key factors like mobile phase composition and buffer pH were optimized through multivariate analysis. The resulting method, validated for accuracy, precision and robustness, outperformed traditional methods and is suitable for routine pharmaceutical analysis.

Keywords

  • HPLC method development
  • Metformin hydrochloride
  • Pharmaceutical dosage forms
  • Product understanding
  • Quality by Design
  • Risk management
  • Vildagliptin
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