Cortisone and cortisol break hydrogen-bonding rules to make a drug-prodrug solid solution.

Multidrug products enable more effective therapies and simpler administration regimens, provided that a stable formulation is prepared, with the desired composition. In this view, solid solutions have the advantage of combining the stability of a single crystalline phase with the potential of stoichiometry variation of a mixture. Here a drug-prodrug solid solution of cortisone and cortisol (hydrocortisone) is described. Despite the structural differences of the two components, the new phase is obtained both from solution and by supercritical CO2 assisted spray drying. In particular, to enter the solid solution, hydrocortisone must violate Etter's rules for hydrogen bonding. As a result, its dissolution rate is almost doubled.

A mixed molecular salt of lithium and sodium breaks the Hume-Rothery rules for solid solutions.

The first molecular solid solution of lithium and sodium ions is reported. In spite of the different chemical and structural properties of the parent compounds, the two cations form a homogeneous mixed phase with the isoorotate ion. Such observation appears in contrast with the Hume-Rothery principles for solid solutions. Furthermore the mixed salts in the series are thermally stable up to 100 °C and non-hygroscopic, which makes them relevant for their potential use as a lithium drug substance.