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. 2020 Jan 27;22(2):34. doi: 10.1208/s12248-020-0417-8

Table II.

Effect of Interplay Between BDM and Drug-Substance Properties on Dissolution

BDM property Drug-substance property Effect of BDM-drug-substance interplay
pH • pKaa Extent of drug ionization across pH range of GI tract
• Acid/base character
Buffer capacity • pKa Extent of surface pH alteration by charged drug species
• Acid/base character
• Intrinsic solubility
Concentration of bile salts and phospholipids • Log Pb/log Dc Extent of drug solubilization in mixed lipidic aggregates

pKa, negative log of the acid dissociation constant (Ka); log P, logarithm of the partition coefficient between octanol and water for a completely non-ionized molecule; log D, logarithm of the pH-adjusted partition coefficient of a molecule between octanol and water