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The AAPS Journal|November 17, 2022
A Simple One-Parameter Percent Dissolved Versus Time Dissolution Equation that Accommodates Sink and Non-sink Conditions via Drug Solubility and Dissolution VolumeJames E PolliThe AAPS Journal|May 27, 2008
In vitro studies are sometimes better than conventional human pharmacokinetic in vivo studies in assessing bioequivalence of immediate-release solid oral dosage formsJames E PolliJournal of Pharmaceutical Sciences|April 2, 2011
Synthesis and in vitro characterization of drug conjugates of l-carnitine as potential prodrugs that target human Octn2Lei Diao, James E PolliMolecular Pharmaceutics|June 6, 2006
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug targetAnand Balakrishnan, James E PolliThe AAPS Journal|January 6, 2022
Evaluation of Excipient Risk in BCS Class I and III BiowaiversMelissa Metry, James E PolliThe Journal of Pharmacology and Experimental Therapeutics|April 30, 2008
Impact of impurity on kinetic estimates from transport and inhibition studiesPablo González, James E PolliInternational Journal of Pharmaceutics|April 13, 2016
Prediction of positive food effect: Bioavailability enhancement of BCS class II drugsSiddarth Raman, James E PolliEuropean Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|August 9, 2022
Prediction of food effect on in vitro drug dissolution into biorelevant media: Contributions of solubility enhancement and relatively low colloid diffusivityRaqeeb Jamil, James E PolliEuropean Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|August 30, 2014
Mechanistic interpretation of conventional Michaelis-Menten parameters in a transporter systemDiana Vivian, James E PolliInternational Journal of Pharmaceutics|April 15, 2022
Sources of dissolution variability into biorelevant mediaRaqeeb Jamil, James E PolliPageof 78