Thermodynamics of risperidone and solubility in pure organic solvents

Donal Mealey, Michael Svärd, A. C. Rasmuson

Research output: Contribution to journalArticlepeer-review

Abstract

The solid-liquid solubility of the thermodynamically stable form I of the drug risperidone has been determined by a gravimetric method in nine pure organic solvents in the temperature range 278.15-323.15K. The melting temperature and associated enthalpy of fusion of risperidone form I has been determined by differential scanning calorimetry (DSC) to be 442.38K and 43.94kJmol-1, respectively. The heat capacity of the solid form I and the melt have been determined over a range of temperatures by temperature-modulated DSC, and extrapolated data has been used to calculate the Gibbs energy, enthalpy and entropy of fusion from ambient temperature up to the melting point. The ideal solubility within a Raoult's law framework is obtained from the Gibbs energy of fusion, and the solution activity coefficient at equilibrium in the nine solvents quantified. Solutions in all solvents exhibit positive deviation from Raoult's law, with the highest solubility (closest to ideality) in toluene, an aprotic apolar solvent. The solubility curves plotted in a van't Hoff graph show non-linear behaviour and are well-approximated by a second order polynomial.

Original languageEnglish
Pages (from-to)73-79
Number of pages7
JournalFluid Phase Equilibria
Volume375
DOIs
Publication statusPublished - 15 Aug 2014

Keywords

  • Activity coefficient
  • Heat capacity
  • Ideality
  • Solubility
  • Thermodynamics

Fingerprint

Dive into the research topics of 'Thermodynamics of risperidone and solubility in pure organic solvents'. Together they form a unique fingerprint.

Cite this