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Review article

https://doi.org/10.5599/admet.686

Perspectives in solubility measurement and interpretation

Christel A.S. Bergström ; Department of Pharmacy, Uppsala University, BMC P.O. Box 580, SE-751 23 Uppsala, Sweden
Alex Avdeef orcid id orcid.org/0000-0002-3139-5442 ; in-ADME Research, 1732 First Avenue, #102, New York, NY 10128, USA


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Abstract

Several key topics in solubility measurement and interpretation are briefly summarized and illustrated with case studies drawing on published solubility determinations as a function of pH. Featured are examples of ionizable molecules that exhibit solubility-pH curve distortion from that predicted by the traditionally used Henderson-Hasselbalch equation and possible interpretations for these distortions are provided. The scope is not exhaustive; rather it is focused on detailed descriptions of a few cases. Topics discussed are limitations of kinetic solubility, ‘brick-dust and grease-balls,’ applications of simulated and human intestinal fluids, supersaturation and the relevance of pre-nucleation clusters and sub-micellar aggregates in the formation of solids, drug-buffer/excipient complexation, hydrotropic solubilization, acid-base ‘supersolubilization,’ cocrystal route to supersaturation, as well as data quality assessment and solubility prediction. The goal is to highlight principles of solution equilibria – graphically more than mathematically – that could invite better assay design, to result in improved quality of measurements, and to impart a deeper understanding of the underlying solution chemistry in suspensions of drug solids. The value of solid state characterizations is stressed but not covered explicitly in this mini-review.

Keywords

Solubility-pH; shake-flask solubility; intrinsic solubility; thermodynamic solubility; Henderson-Hasselbalch equation; supersaturation; pre-nucleation clusters, drug aggregates; drug salts; pharmaceutical cocrystals

Hrčak ID:

218702

URI

https://hrcak.srce.hr/218702

Publication date:

5.4.2019.

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