Equilibrium solubility measurement of compounds with low dissolution rate by Higuchi's Facilitated Dissolution Method. A validation study

• Published in: European journal of pharmaceutical sciences 2017-08, Vol.106, p.133-141
• Main Authors: Takács-Novák, Krisztina, Urac, Maria, Horváth, Péter, Völgyi, Gergely, Anderson, Bradley D., Avdeef, Alex
• Format: Article
• Language: English
• Subjects: Drug Liberation; Ethylene Dichlorides - chemistry; Facilitated Dissolution Method; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Kinetics; Low dissolution rate; Low solubility; Method validation; Octanes - chemistry; Octanols - chemistry; Progesterone - chemistry; Solubility; Solvents; Water - chemistry
• ISSN: 0928-0987; 1879-0720
• DOI: 10.1016/j.ejps.2017.05.064

Incubation time plays a critical role in the accurate measurement of equilibrium solubility of compounds. Substances which dissolve very slowly generally need long incubation times (days or weeks) to reach equilibrium. However, long times may pose several problems, such as decomposition of solute, molding of buffer, and drifting of pH. Higuchi in 1979 proposed the Facilitated Dissolution Method (FDM) to dramatically reduce incubation time. It employs a small volume of water-immiscible organic solvent to partly solubilize the sample and thereby increase the surface area available for dissolution. The method has been used only rarely. In this study we performed a systematic validation of FDM using progesterone as model compound. The reference solubility value, 7.95±0.21μg/mL (p200 solubility experiments, supports the validity of Higuchi's method. In this study we propose a standardized protocol for the FDM, where 1% v/v of organic solvent is used. Octane (or isooctane) was found to be suitable for highly hydrophobic compounds. Alternatively, octanol or 1,2-dichloroethane can be used for less lipophilic compounds. [Display omitted]