Energetic aspects of diclofenac acid in crystal modifications and in solutions--mechanism of solvation, partitioning and distribution

J Pharm Sci. 2007 May;96(5):1031-42. doi: 10.1002/jps.20936.

Abstract

Temperature dependency of saturated vapor pressure and heat capacity for the diclofenac acid (Form II) were measured and thermodynamic functions of sublimation calculated (DeltaG(sub)(298) = 49.3 kJ x mol(-1); DeltaH(sub)(298) = 115.6 +/- 1.3 kJ x mol(-1); DeltaS(sub)(298) = 222 +/- 4 J x mol(-1) x K(-1)). Crystal polymorphic Forms I (P2(1)/c) and II (C2/c) of diclofenac acid have been prepared and characterized by X-ray diffraction experiments. The difference between crystal lattice energies of the two forms were obtained by solution calorimetry: DeltaDeltaH(sol)(I --> II) = 1.6 +/- 0.4 kJ x mol(-1). Temperature dependencies of the solubility in buffers with pH 2.0 and 7.4, n-octanol and n-hexane were measured. The thermodynamic functions of solubility, solvation, and transfer processes were deduced. Specific and non-specific solvation terms were distinguished using the transfer from the "inert" n-hexane to the other solvents. The transfer of diclofenac acid molecules from the buffers to n-octanol (partitioning and distribution) is an entropy driven process.

MeSH terms

  • 1-Octanol / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry*
  • Buffers
  • Calorimetry, Differential Scanning
  • Chemistry, Pharmaceutical
  • Crystallization
  • Crystallography, X-Ray
  • Diclofenac / chemistry*
  • Hexanes / chemistry
  • Hydrogen-Ion Concentration
  • Models, Chemical
  • Pressure
  • Solubility
  • Solutions
  • Solvents / chemistry*
  • Technology, Pharmaceutical
  • Temperature
  • Thermodynamics*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Buffers
  • Hexanes
  • Solutions
  • Solvents
  • Diclofenac
  • n-hexane
  • 1-Octanol