Fast dissolving eutectic compositions of curcumin

Int J Pharm. 2012 Dec 15;439(1-2):63-72. doi: 10.1016/j.ijpharm.2012.09.045. Epub 2012 Oct 3.

Abstract

The bioactive herbal ingredient curcumin was screened with pharmaceutically acceptable coformers to discover solid-state forms of high solubility. Mechano-chemical grinding of curcumin with cocrystal formers in a fixed stoichiometry ratio resulted in binary eutectic compositions of curcumin-coformer with nicotinamide (1:2), ferulic acid (1:1), hydroquinone (1:1), p-hydroxybenzoic acid (1:1), and l-tartaric acid (1:1). The eutectic nature of the product crystalline solids was established by differential scanning calorimetry, and the absence of hydrogen-bonded crystalline phases such as cocrystals/salts was ascertained by powder X-ray diffraction, IR-Raman, and solid-state NMR spectroscopy. The best case of CUR-NAM eutectic exhibits 10-fold faster IDR and 6-times higher AUC compared to crystalline curcumin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calorimetry, Differential Scanning
  • Crystallization
  • Curcumin / chemistry*
  • Magnetic Resonance Spectroscopy
  • Powder Diffraction
  • Solubility
  • Spectrum Analysis, Raman
  • X-Ray Diffraction

Substances

  • Curcumin