• Optimized lipid carrier formulation improving cyclosporine bioavailability by 38% while maintaining ophthalmic safety parameters.
• Conducted stability and in-vitro release studies, improving formulation uniformity by 42% using analytical characterization techniques.
• Performed particle size and zeta potential optimization, reducing PDI variation by 27% to ensure long-term formulation stability.
• Formulation Development
• Stability Studies
• Drug Release Kinetics
• Particle Size Analysis
• Pharmaceutical Documentation