DSC, X-ray and FTIR studies of a gemfibrozil/dimethyl-β-cyclodextrin inclusion complex produced by co-grinding

J Pharm Biomed Anal. 2012 Jan 5:57:62-7. doi: 10.1016/j.jpba.2011.08.034. Epub 2011 Aug 30.

Abstract

The steps of formation of an inclusion complex produced by the co-grinding of gemfibrozil and dimethyl-β-cyclodextrin were investigated by differential scanning calorimetry (DSC), X-ray powder diffractometry (XRPD) and Fourier transform infrared (FTIR) spectroscopy with curve-fitting analysis. The endothermic peak at 59.25°C reflecting the melting of gemfibrozil progressively disappeared from the DSC curves of the products on increase of the duration of co-grinding. The crystallinity of the samples too gradually decreased, and after 35min of co-grinding the product was totally amorphous. Up to this co-grinding time, XRPD and FTIR investigations indicated a linear correlation between the cyclodextrin complexation and the co-grinding time. After co-grinding for 30min, the ratio of complex formation did not increase. These studies demonstrated that co-grinding is a suitable method for the complexation of gemfibrozil with dimethyl-β-cyclodextrin. XRPD analysis revealed the amorphous state of the gemfibrozil-dimethyl-β-cyclodextrin product. FTIR spectroscopy with curve-fitting analysis may be useful as a semiquantitative analytical method for discriminating the molecular and amorphous states of gemfibrozil.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calorimetry, Differential Scanning / methods*
  • Gemfibrozil / chemistry*
  • Hypolipidemic Agents / chemistry*
  • Powder Diffraction / methods*
  • Spectroscopy, Fourier Transform Infrared / methods*
  • beta-Cyclodextrins / chemistry*

Substances

  • Hypolipidemic Agents
  • beta-Cyclodextrins
  • heptakis(2,6-O-dimethyl)beta-cyclodextrin
  • Gemfibrozil