Polymorphism of spironolactone: An unprecedented case of monotropy turning to enantiotropy with a huge difference in the melting temperatures

Int J Pharm. 2018 Dec 1;552(1-2):193-205. doi: 10.1016/j.ijpharm.2018.09.059. Epub 2018 Sep 25.

Abstract

Spironolactone form I melts at about 70 degrees lower than form II, which is very unusual for two co-existing polymorphs. The phase relationships involving this unprecedented case of dimorphism have been investigated by constructing a topological pressure-temperature phase diagram. The transition from polymorph I to polymorph II is unambiguously exothermic while it is accompanied with an increase in the specific volume. This indicates that the dP/dT slope of the I-II equilibrium curve is negative. The convergence of the melting equilibrium lines at high pressure leads to a topological P-T diagram in which polymorph I possesses a stable phase region at high pressure. Thus, forms I and II are monotropically related at ordinary pressure and turn to an enantiotropic relationship at high pressure. Given that polymorph I is the densest form, it negates the rule of thumb that the densest form is also the most stable form at room temperature, similar to the case of paracetamol.

Keywords: Heat capacity; Phase diagram; Polymorph; Specific volume; Stability; Thermodynamics.

MeSH terms

  • Calorimetry, Differential Scanning
  • Crystallization
  • Diuretics / chemistry*
  • Spironolactone / chemistry*
  • Transition Temperature

Substances

  • Diuretics
  • Spironolactone