A Study on the Synergistic Cocrystallization of Chemically Related Curcuminoids with Hydroxybenzenes

Abstract

Cocrystallization of the curcuminoids (CURDs) curcumin (CUR), demethoxycurcumin (DMC), and bis(demethoxy)curcumin (BDMC) with the coformers resorcinol (RES) and hydroxyquinol (HYQ) from solution was investigated toward its potential of being used as a synergistic separation technique of the CURDs from their ternary mixtures. Therefore, solubilities of single CURDs with the respective coformer in toluene-ethyl acetate 90/10 v/v at 25 °C were measured, and ternary phase diagrams were constructed. CUR·RES and BDMC·HYQ cocrystals were identified, revealing an incongruent solubility behavior. All other CURD-coformer systems showed eutectic behavior. Separation experiments were performed using a CUR-rich and almost equimolar CURD mixture. Solubility measurements of CURD mixtures revealed large influences on each other’s solubility and high potential of DMC being integrated into CUR crystals and cocrystals. Cocrystallization of CUR·RES from the CUR-rich mixture outperformed direct CUR crystallization. In the case of BDMC·HYQ, the presence of the other CURDs suppressed cocrystal formation. Using the universal cocrystal solubility product K_s, CUR·RES cocrystal solubilities were predicted in ethanol, a solvent exhibiting large solubility differences between CUR and other CURDs. Subsequent separation experiments showed no benefit of cocrystallization over direct CUR crystallization.

Ternary phase diagrams of curcuminoids curcumin, demethoxycurcumin, and bis(demethoxy)curcumin with coformers resorcinol and hydroxyquinol in toluene-ethyl acetate 90/10 v/v solvent at 25 °C were determined. The formation of a curcumin-resorcinol cocrystal was exploited for separating curcumin from a curcuminoid mixture with an achieved purity of 86.4%. Solubility data were used to predict ternary phase diagrams in another solvent, ethanol.