“…Additionally, the salt formation of an API affects the stability and dissolution performance of the solid dispersion. 10 In addition to the previous ingenuities of solid states, measures such as hydrotropes, [11][12][13] nanoparticulation, 2 chemical modications, 14 cyclodextrin inclusion complexes, 15 and pH adjustment 16 can be used to manipulate solubility. 17,18 Approximately 40% of market-approved medicines and 90% of molecules in the discovery pipeline have low aqueous solubility, while only 8% of new drug candidates exhibit high aqueous solubility and intestinal permeability.…”