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P Langguth

Showing results (51-60 of 75) with videos related to

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International Journal of Clinical Pharmacology and Therapeutics|April 28, 2000
Affinities at the verapamil binding site of MDR1-encoded P-glycoprotein: drugs and analogs, stereoisomers and metabolitesS Neuhoff, P Langguth, C Dressler, et al.
Die Pharmazie|March 12, 2011
IVIVR in oral absorption for fenofibrate immediate release tablets using dissolution and dissolution permeation methodsP Buch, P Holm, J Q Thomassen, et al.
Die Pharmazie|November 26, 2010
IVIVR in oral absorption for fenofibrate immediate release tablets using dissolution and dissolution permeation methodsP Buch, P Holm, J Q Thomassen, et al.
The Journal of Pharmacy and Pharmacology|November 12, 1998
First-pass metabolism of peptide drugs in rat perfused liverY Taki, T Sakane, T Nadai, et al.
Advanced Drug Delivery Reviews|June 15, 2007
Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drugA Hanafy, H Spahn-Langguth, G Vergnault, et al.
International Journal of Clinical Pharmacology and Therapeutics|February 26, 1998
P-glycoprotein transporters and the gastrointestinal tract: evaluation of the potential in vivo relevance of in vitro data employing talinolol as model compoundH Spahn-Langguth, G Baktir, A Radschuweit, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|October 15, 2009
Greeen tea extracts lower serum folates in rats at very high dietary concentrations only and do not affect plasma folates in a human pilot studyK Augustin, J Frank, S Augustin, et al.
Drug Development and Industrial Pharmacy|April 16, 2005
Nanosuspension formulations for low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compoundP Langguth, A Hanafy, D Frenzel, et al.
International Journal of Pharmaceutics|May 15, 2018
The effects of three absorption-modifying critical excipients on the in vivo intestinal absorption of six model compounds in rats and dogsD Dahlgren, C Roos, P Johansson, et al.
Journal of Pharmaceutical Sciences|June 11, 1998
P-Glycoprotein (P-gp) mediated efflux in Caco-2 cell monolayers: the influence of culturing conditions and drug exposure on P-gp expression levelsP Anderle, E Niederer, W Rubas, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
International Journal of Clinical Pharmacology and Therapeutics|April 28, 2000
Affinities at the verapamil binding site of MDR1-encoded P-glycoprotein: drugs and analogs, stereoisomers and metabolitesS Neuhoff, P Langguth, C Dressler, et al.
Die Pharmazie|March 12, 2011
IVIVR in oral absorption for fenofibrate immediate release tablets using dissolution and dissolution permeation methodsP Buch, P Holm, J Q Thomassen, et al.
Die Pharmazie|November 26, 2010
IVIVR in oral absorption for fenofibrate immediate release tablets using dissolution and dissolution permeation methodsP Buch, P Holm, J Q Thomassen, et al.
The Journal of Pharmacy and Pharmacology|November 12, 1998
First-pass metabolism of peptide drugs in rat perfused liverY Taki, T Sakane, T Nadai, et al.
Advanced Drug Delivery Reviews|June 15, 2007
Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drugA Hanafy, H Spahn-Langguth, G Vergnault, et al.
International Journal of Clinical Pharmacology and Therapeutics|February 26, 1998
P-glycoprotein transporters and the gastrointestinal tract: evaluation of the potential in vivo relevance of in vitro data employing talinolol as model compoundH Spahn-Langguth, G Baktir, A Radschuweit, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|October 15, 2009
Greeen tea extracts lower serum folates in rats at very high dietary concentrations only and do not affect plasma folates in a human pilot studyK Augustin, J Frank, S Augustin, et al.
Drug Development and Industrial Pharmacy|April 16, 2005
Nanosuspension formulations for low-soluble drugs: pharmacokinetic evaluation using spironolactone as model compoundP Langguth, A Hanafy, D Frenzel, et al.
International Journal of Pharmaceutics|May 15, 2018
The effects of three absorption-modifying critical excipients on the in vivo intestinal absorption of six model compounds in rats and dogsD Dahlgren, C Roos, P Johansson, et al.
Journal of Pharmaceutical Sciences|June 11, 1998
P-Glycoprotein (P-gp) mediated efflux in Caco-2 cell monolayers: the influence of culturing conditions and drug exposure on P-gp expression levelsP Anderle, E Niederer, W Rubas, et al.
Pageof 8