摘要
Paracetamol （PCM） was crystallized from an isopropanol （IPA） solution containing various small amounts of metacetamol as an additive. The effect on the nucleation kinetics was studied by measuring the induction time to nucleation and the metastable zone width using focused beam reflectance measurements （FBRM） and attenuated total reflectance （ATR-UV/Vis） spectroscopy. Both the induction time and the metastable zone width were expressed as functions of the additive concentration. Small amounts ofmetacetamol （1-4 tool-%） were found to cause significant inhibition to the nucleation by extending both the induction time and the metastable zone width. A progressive change in the morphology of the paracetamol crystals from tabular to columnar habit was observed with increasing metacetamol concentration. The solvent also had a significant effect on the size of the paracetamol crystals as smaller crystals were obtained in IPA than in aqueous solution. The dissolution rate of paracetamol was improved by the incorporation of metacetamol with 4 tool-% having the most effect. A supersaturation control （SSC） approach was implemented for the PCM-IPA system with and without metacetamol in an attempt to control and obtain larger metacetamol-doped paraeetamol crystals.
Paracetamol （PCM） was crystallized from an isopropanol （IPA） solution containing various small amounts of metacetamol as an additive. The effect on the nucleation kinetics was studied by measuring the induction time to nucleation and the metastable zone width using focused beam reflectance measurements （FBRM） and attenuated total reflectance （ATR-UV/Vis） spectroscopy. Both the induction time and the metastable zone width were expressed as functions of the additive concentration. Small amounts ofmetacetamol （1-4 tool-%） were found to cause significant inhibition to the nucleation by extending both the induction time and the metastable zone width. A progressive change in the morphology of the paracetamol crystals from tabular to columnar habit was observed with increasing metacetamol concentration. The solvent also had a significant effect on the size of the paracetamol crystals as smaller crystals were obtained in IPA than in aqueous solution. The dissolution rate of paracetamol was improved by the incorporation of metacetamol with 4 tool-% having the most effect. A supersaturation control （SSC） approach was implemented for the PCM-IPA system with and without metacetamol in an attempt to control and obtain larger metacetamol-doped paraeetamol crystals.
