Drug solubility in compressed carbon dioxide is usually low, and for this reason, CO2 is not considered a suitable solvent. However, it can be used as antisolvent to crystallize a solute from a liquid solution. The choice of optimal pressure and the CO2/drug solution ratio is a crucial point of the process, and these values must be optimized. An estimation method based on the Peng–Robinson’s equation of state is presented here with which to calculate the solubility of drugs such as Acetaminophen, Acyclovir, Atenolol, Carbamazepine, Ibuprofen, Naproxen, Nimesulide, and Sotalol hydrochloride in mixtures of CO2 and common organic solvents at a constant temperature but a variable pressure. The model temperature was 298K for Ibuprofen and Naproxen, 315K for Acetaminophen and 313K for any other systems. This method is a practical and rapid alternative to experimental determination.

Solubility estimation of drugs in ternary systems of interest for the antisolvent precipitation processes

KIKIC, IRENEO;DE ZORDI, NICOLA;MONEGHINI, MARIAROSA;SOLINAS, DARIO
2010-01-01

Abstract

Drug solubility in compressed carbon dioxide is usually low, and for this reason, CO2 is not considered a suitable solvent. However, it can be used as antisolvent to crystallize a solute from a liquid solution. The choice of optimal pressure and the CO2/drug solution ratio is a crucial point of the process, and these values must be optimized. An estimation method based on the Peng–Robinson’s equation of state is presented here with which to calculate the solubility of drugs such as Acetaminophen, Acyclovir, Atenolol, Carbamazepine, Ibuprofen, Naproxen, Nimesulide, and Sotalol hydrochloride in mixtures of CO2 and common organic solvents at a constant temperature but a variable pressure. The model temperature was 298K for Ibuprofen and Naproxen, 315K for Acetaminophen and 313K for any other systems. This method is a practical and rapid alternative to experimental determination.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2305770
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