Predicting the solubility-permeability interplay when using cyclodextrins in solubility-enabling formulations: Model validation

Keyphrases

• Model Validation 100%
• Cyclodextrin 100%
• Solubility-enabling Formulations 100%
• Solubility-permeability Interplay 100%
• Molecular Complexation 66%
• Mass Transport Model 66%
• Intestinal Permeability 33%
• Mathematical Model 33%
• Predictive Ability 33%
• Method Validation 33%
• Carbamazepine 33%
• Progesterone 33%
• Hydrocortisone 33%
• Opposing Effects 33%
• Apparent Permeability 33%
• Solubilizer 33%
• Solubility Advantage 33%
• Oral Drug Absorption 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Cyclodextrin 100%
• Complexation 66%
• Mass Transfer 66%
• Drug Absorption 33%
• Intestinal Permeability 33%
• Hydrocortisone 33%
• Progesterone 33%
• Carbamazepine 33%
• Solubilizer 33%