Microwave-Vacuum Drying Kinetics of Pharmaceutical Powders

Abstract

The drying kinetics (maximum drying rate, drying constants) and center temperature of selected powder (aspirin, paracetamol, lactose, and maize starch)–solvent (water, ethanol, methanol, and acetone) systems were monitored during microwave-vacuum drying. An experimental microwave-vacuum system (650 W and 2.45 GHz) operated at 61–81 kPa was used. The drying rate profile did not vary with the powder–solvent system; an initial warming-up period was followed by a constant-rate stage and two falling-rate periods. However, the drying kinetics were found to be both powder and solvent dependent, with the drying times for acetone-, ethanol-, and methanol-wetted materials being considerably shorter (up to 89.8%) than those of samples containing water. Although the general form of the temperature profile (short warming-up period, constant-rate stage, and decreasing temperature phase) was similar for all systems, the maximum temperatures varied quite significantly with solvent type, ranging from highest to lowest in the order water-ethanol-methanol-acetone. For most powder–solvent systems, reduced operating pressure facilitated increased drying rates and thus shorter drying times.

Keywords:

• Drying
• Kinetics
• Internal temperature
• Microwave-vacuum
• Pharmaceutical powders

ACKNOWLEDGEMENTS

The authors gratefully acknowledge the support of AstraZeneca.