Improving Dissolution

Poor aqueous solubility is a recurring and increasing challenge for drug developers. With 40% of marketed drugs and up to 90% of those in development exhibiting poor solubility(1), finding solutions to overcome this challenge and increasing the bioavailability of compounds is as important now as it ever has been.

Crystec have experience in overcoming solubility challenges across a  range of molecule classes (small and large molecules, natural products) and routes of administration (e.g. oral, inhaled, injectable). Crystec’s mSAS® (modified Supercritical Anti-Solvent) platform enables a range of strategies to be implemented, in isolation or in parallel, to improve rates of dissolution.

 
  • Novel solid state forms

  • Particle size and surface area

  • Manipulating particle shape

  • Scalable co-crystals 

  • Active-enhancer composites

  • Stabilised amorphous particles

References: 1 Kalepua. S, Nekkantib. V, Acta Pharm Sin B. 2015 Sep; 5(5): 442–453

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mSAS® Case Study: Improving Solubility

mSAS® Case Study: Improving Solubility

mSAS® Case Study: Polymorph Study

mSAS® Case Study: Polymorph Study

 
mSAS® Case Study: Scalable Co-crystals

mSAS® Case Study: Scalable Co-crystals

mSAS® strategies for addressing poor drug solubility

mSAS® strategies for addressing poor drug solubility

 
Video Demonstration: mSAS® For Improved Dissolution

Video Demonstration: mSAS® For Improved Dissolution