Improvement of Class II Drug Properties by Crystal Agglomeration Design

Strategies to Improve solubility of Oral Drugs

Enhancement of The Solubility and The Dissolution Rate of Oral Nimodipine Formulation with Solid Dispersion

Theoretical Construction of Thermodynamic Relations for a Solvent-controlled Phase Transition to Improve the Bioavailability of Drugs: A Case Study of Indomethacin

Different Approaches for Enhancement of Curcumin Aqueous Solubility and Dissolution rate

Critical Appraisal of Physiochemical Characteristics of Statins and Drug Delivery Systems for Improving Their Bioavailability

“Examples of Drug Delivery Systems for Delivery of Certain Poorly Water-Soluble Drugs”

Amino Acid as Co-Crystal Coformer for Ebastine Solubility Enhancement

NANOCRYSTALLIZATION OF DAPSONE; A NOVEL APPROACH TO BOOST SOLUBILITY, DISSOLUTION, AND IN-VITRO ANTI-INFLAMMATORY ACTIVITY

Development of a nanostructured double-layer coated tablet based on polyethylene glycol/gelatin as a platform for hydrophobic molecules delivery