Avital Beig
University of Michigan(US)BioSurfaces (United States)(US)
Publications by Year
Research Areas
Drug Solubulity and Delivery Systems, Advanced Drug Delivery Systems, Drug Transport and Resistance Mechanisms, Crystallization and Solubility Studies, Analytical Chemistry and Chromatography
Most-Cited Works
- → A Win–Win Solution in Oral Delivery of Lipophilic Drugs: Supersaturation via Amorphous Solid Dispersions Increases Apparent Solubility without Sacrifice of Intestinal Membrane Permeability(2012)250 cited
- → The Solubility–Permeability Interplay: Mechanistic Modeling and Predictive Application of the Impact of Micellar Solubilization on Intestinal Permeation(2011)201 cited
- → The solubility–permeability interplay and oral drug formulation design: Two heads are better than one(2016)189 cited
- → Oral Delivery of Lipophilic Drugs: The Tradeoff between Solubility Increase and Permeability Decrease When Using Cyclodextrin-Based Formulations(2013)130 cited
- → The Solubility–Permeability Interplay When Using Cosolvents for Solubilization: Revising the Way We Use Solubility-Enabling Formulations(2012)129 cited
- → Accounting for the solubility–permeability interplay in oral formulation development for poor water solubility drugs: The effect of PEG-400 on carbamazepine absorption(2012)103 cited
- → The Twofold Advantage of the Amorphous Form as an Oral Drug Delivery Practice for Lipophilic Compounds: Increased Apparent Solubility and Drug Flux Through the Intestinal Membrane(2012)83 cited
- → Head-To-Head Comparison of Different Solubility-Enabling Formulations of Etoposide and Their Consequent Solubility–Permeability Interplay(2015)77 cited
- → In-situ intestinal rat perfusions for human Fabs prediction and BCS permeability class determination: Investigation of the single-pass vs. the Doluisio experimental approaches(2015)75 cited
- → The use of captisol (SBE7-β-CD) in oral solubility-enabling formulations: Comparison to HPβCD and the solubility–permeability interplay(2015)61 cited