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Excipients that facilitate amorphous drug stabilization

  • Yangjie Wei
  • , Bhaswati Dattachowdhury
  • , Kiran K. Vangara
  • , Niraja Patel
  • , Kenneth Alexander
  • , Sai Hs Boddu
  • University of Toledo
  • Inc

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

5 Scopus citations

Abstract

The importance of the amorphous state in studying bioavailability of poorly water-soluble drugs cannot be over-emphasized. The higher free energy and therefore the apparent high solubility of the amorphous phase are some of the advantages for promoting the amorphous phase, as compared to its crystalline counterpart. It is well known that the amorphous phase is thermodynamically unstable. This might result in the conversion of the metastable form to its stable crystalline form during storage. This conversion might also lead to product failure during storage owing to the poor dissolution properties of the crystalline form. Excipients can play a key role in preventing such a transformation during storage as well as maximizing the therapeutic efficacy of the amorphous material. This book chapter intends to highlight the delivery issues pertaining to amorphous drugs with a special emphasis on the most commonly used excipients in stabilizing amorphous drug substances in formulations.

Original languageEnglish
Title of host publicationExcipient Applications in Formulation Design and Drug Delivery
PublisherSpringer International Publishing
Pages463-495
Number of pages33
ISBN (Electronic)9783319202068
ISBN (Print)9783319202051
DOIs
StatePublished - 1 Jan 2015
Externally publishedYes

Keywords

  • Amorphicity index
  • Amorphous
  • Crystallization
  • Devitrification
  • Electrostatic spinning method
  • Excipient
  • Fusion
  • Glass transition temperature
  • Hot melt extrusion
  • Lyophilization
  • Mesoporous
  • Miscibility
  • Molecular mobility
  • Polymer
  • Porous silica
  • Silica
  • Solid dispersion
  • Spray drying
  • Stabilization
  • Supercritical fluid technology

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