- Accelerating the introduction of new drugs through efficient production processes
- Requiring the use of smaller production facilities with lower building and capital costs
- Minimizing waste, energy consumption, and raw material use
- Monitoring drug quality on a continuous basis rather than through post-production batch-based testing
- Enhancing process reliability and flexibility to respond to market needs
Our group, in cooperation with the Novartis-MIT Center is exploring the use of various types of continuous crystallization for pharmaceutical intermediates and final crystallization of active pharmaceutical ingredients (APIs). Issues related to purity, polymorphism, crystal size distribution, crystal shape, and scale-up and recycle are being studied.
Areas of focus:
- Process design of continuous crystallization to increase yield of active pharmaceutical ingredients
- Process design of continuous crystallization to enhance product purity
- Novel Crystallizer Designs