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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 metabolites
S 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 methods
P 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 methods
P 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 liver
Y 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 drug
A 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 compound
H 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 study
K 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 compound
P 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 dogs
D 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 levels
P Anderle, E Niederer, W Rubas, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 75) with videos related to
Sort By:
Page
of 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 metabolites
S 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 methods
P 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 methods
P 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 liver
Y 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 drug
A 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 compound
H 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 study
K 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 compound
P 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 dogs
D 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 levels
P Anderle, E Niederer, W Rubas, et al.
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of 8