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Lecture 7: Complexation for the Delivery of Poorly Soluble Drugs

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Upon completion of this lecture of the eCourse, the participant should be able to:
  • Review how you can make a solid intermediate or make a liquid form.
  • Discuss drug solubilization using cyclodextrins. 
  • Explain the structure and physicochemical properties of cyclodextrins, phase solubility, drug stability, toxicology and pharmacokinetics.
  • Analyze a case study with downstream formulation and processing of complexation intermediates.