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James E Polli

Showing results (1-10 of 187) with videos related to

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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 Polli
The 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 Polli
Molecular Pharmaceutics|November 6, 2023
Virtual Issue Honoring Gordon L. Amidon: First Editor-in-Chief of <i>Molecular Pharmaceutics</i>James E Polli
The AAPS Journal|January 6, 2022
Evaluation of Excipient Risk in BCS Class I and III BiowaiversMelissa Metry, James E Polli
The Journal of Pharmacology and Experimental Therapeutics|April 30, 2008
Impact of impurity on kinetic estimates from transport and inhibition studiesPablo González, James E Polli
Journal 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 Polli
Journal of the American Pharmacists Association : Japha|May 19, 2007
Evaluation of a novel tablet splitterJing Shao, James E Polli
Molecular Pharmaceutics|June 6, 2006
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug targetAnand Balakrishnan, James E Polli
International Journal of Pharmaceutics|April 13, 2016
Prediction of positive food effect: Bioavailability enhancement of BCS class II drugsSiddarth Raman, James E Polli
European 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 Polli
Pageof 19

Showing results (1-10 of 187) with videos related to

Sort By:
Pageof 19
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 Polli
The 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 Polli
Molecular Pharmaceutics|November 6, 2023
Virtual Issue Honoring Gordon L. Amidon: First Editor-in-Chief of <i>Molecular Pharmaceutics</i>James E Polli
The AAPS Journal|January 6, 2022
Evaluation of Excipient Risk in BCS Class I and III BiowaiversMelissa Metry, James E Polli
The Journal of Pharmacology and Experimental Therapeutics|April 30, 2008
Impact of impurity on kinetic estimates from transport and inhibition studiesPablo González, James E Polli
Journal 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 Polli
Journal of the American Pharmacists Association : Japha|May 19, 2007
Evaluation of a novel tablet splitterJing Shao, James E Polli
Molecular Pharmaceutics|June 6, 2006
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug targetAnand Balakrishnan, James E Polli
International Journal of Pharmaceutics|April 13, 2016
Prediction of positive food effect: Bioavailability enhancement of BCS class II drugsSiddarth Raman, James E Polli
European 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 Polli
Pageof 19