Polymorph transformation in paracetamol monitored by in-line NIR spectroscopy during a cooling crystallization process

AAPS PharmSciTech. 2011 Jun;12(2):764-70. doi: 10.1208/s12249-011-9642-x. Epub 2011 Jun 14.

Abstract

The reliable in-line monitoring of pharmaceutical processes has been regarded as a key tool toward the full implementation of process analytical technology. In this study, near-infrared (NIR) spectroscopy was examined for use as an in-line monitoring method of the paracetamol cooling crystallization process. The drug powder was dissolved in ethanol-based cosolvent at 60°C and was cooled by 1°C/min for crystallization. NIR spectra acquired by in-line measurement were interpreted by principal component analysis combined with off-line characterizations via X-ray diffraction, optical microscopy, and transmission electron microscopy. The whole crystallization process appeared to take place in three steps. A metastable form II polymorph of paracetamol was formed and transformed into the stable form I polymorph on the way to the growth of pure form I by cooling crystallization. These observations are consistent with a previous focused beam reflectance method-based study (Barthe et al., Cryst Growth Des 8:3316-3322, 2008).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / chemistry*
  • Acetaminophen / standards
  • Cold Temperature*
  • Crystallization / methods*
  • Crystallization / standards
  • Reproducibility of Results
  • Spectroscopy, Near-Infrared / methods*
  • Spectroscopy, Near-Infrared / standards
  • X-Ray Diffraction / methods
  • X-Ray Diffraction / standards

Substances

  • Acetaminophen