4.5 Article

Prediction of Solubility of Drugs and Other Compounds in Organic Solvents

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 99, Issue 3, Pages 1500-1515

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1002/jps.21922

Keywords

physicochemical properties; solubility; structure-property relationship (SPR); distribution; QSPR

Ask authors/readers for more resources

We have set out a procedure for the prediction of solubilities of drugs and other compounds in a wide range of solvents, based on the Abraham solvation equations. The method requires a knowledge of solubilities of a given compound in a few solvents, as shown by our own experimental data on apocynin, diapocynin, dehydrodivanillin, and dehydrodi(methyl vanillate). The procedure is especially useful for very hydrophobic compounds such as cholesteryl acetate and cholesterol that we give as examples. Other examples include vanillin and 3,4-dichlorobenzoic acid. If the solubility in water is available, then this alone is sufficient to predict solubilities in organic solvents, provided that the Abraham descriptors are available for the compound. Predictions can be made for solubilities in some 85 solvents. (C) 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:1500-1515, 2010

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available