Utility of cyclodextrins in the formulation of genistein part 1. Preparation and physicochemical properties of genistein complexes with native cyclodextrins

J Pharm Biomed Anal. 2008 Nov 4;48(3):636-40. doi: 10.1016/j.jpba.2008.06.007. Epub 2008 Jun 24.

Abstract

Isoflavones are suitable guest molecules for inclusion complex formation with cyclodextrins (CDs). The molecular encapsulation with CDs results in a solid, molecularly dispersed form and in a significantly improved aqueous solubility of isoflavones. Genistein, a key isoflavone constituent of Ononidis spinosae radix was found to form a supramolecular, non-covalent inclusion complex with both beta-cyclodextrin (beta-CD) and gamma-cyclodextrin (gamma-CD), while it did not form a stable complex with alpha-CD. The guest genistein was found to spatially located in the less polar cavity of cyclodextrin. The isolated binary genistein/CD complexes appeared novel crystalline lattices. The in vitro dissolution of genistein entrapped into both beta- and gamma-CD, significantly surpassed that of the plain isoflavone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chemical Phenomena*
  • Chemistry, Pharmaceutical*
  • Cyclodextrins / chemistry*
  • Genistein / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Solubility
  • Spectrophotometry, Ultraviolet
  • beta-Cyclodextrins / chemistry*

Substances

  • Cyclodextrins
  • beta-Cyclodextrins
  • Genistein
  • betadex