Using colloidal packings as templates for structuring drugs

ORAL

Abstract

Many pharmaceutical compounds are poorly soluble in water; this is problematic because most pharmaceuticals are delivered orally and must dissolve in the gastrointestinal fluid in order to be taken up by the body. We introduce a simple method for increasing the dissolution rates of poorly water-soluble organic actives. We demonstrate that by structuring the compounds within the interconnected, nanoscale pore space of a colloidal packing we create composites which rapidly disintegrate in water, exposing the nanostructured organic active and leading to improved dissolution rates.

Authors

  • James Wilking

    • Harvard University
  • Andr\'e Studart

    • ETH
  • Sebastian Koltzenburg

    • BASF
  • Rodrigo Guerra

    • Harvard University
  • Esther Amstad

    • Harvard University
  • Jens Rieger

    • BASF
  • David Weitz

    • Harvard University
    • Department of Physics and Division of Engineering and Applied Science, Harvard University, Cambridge, MA 02138
    • School of Engineering and Applied Sciences, Harvard University
    • Department of Physics, Harvard University, Cambridge, MA, United States
    • Department of Physics and School of Engineering and Applied Sciences, Harvard University, Cambridge, MA