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.