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Pharmaceutical Research
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July 10, 2001
Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration
E Nicolaides, M Symillides, J B Dressman, et al.
The Journal of Pharmacy and Pharmacology
|
April 1, 1991
Unusual solubility behaviour of cyclosporin A in aqueous media
G Ismailos, C Reppas, J B Dressman, et al.
Advanced Drug Delivery Reviews
|
June 30, 2007
Estimating drug solubility in the gastrointestinal tract
J B Dressman, M Vertzoni, K Goumas, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
May 12, 2009
Simulation of gastric lipolysis and prediction of felodipine release from a matrix tablet in the fed stomach
A Diakidou, M Vertzoni, B Abrahamsson, et al.
Pharmaceutical Research
|
January 22, 2000
Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data
E Nicolaides, E Galia, C Efthymiopoulos, et al.
Gastroenterology
|
May 1, 1991
Effect of hydroxypropylmethylcellulose on gastrointestinal transit and luminal viscosity in dogs
C Reppas, J H Meyer, P J Sirois, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
October 31, 1998
Effect of elevated viscosity in the upper gastrointestinal tract on drug absorption in dogs
C Reppas, G Eleftheriou, P Macheras, et al.
Pharmaceutical Research
|
March 6, 1998
Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms
J B Dressman, G L Amidon, C Reppas, et al.
Journal of Pharmaceutical Sciences
|
August 6, 2008
Postprandial evolution in composition and characteristics of human duodenal fluids in different nutritional states
S Clarysse, J Tack, F Lammert, et al.
Pharmaceutical Research
|
January 1, 1995
Evaluation of different metrics as indirect measures of rate of drug absorption from extended release dosage forms at steady-state
C Reppas, L F Lacey, O N Keene, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Pharmaceutical Research
|
July 10, 2001
Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration
E Nicolaides, M Symillides, J B Dressman, et al.
The Journal of Pharmacy and Pharmacology
|
April 1, 1991
Unusual solubility behaviour of cyclosporin A in aqueous media
G Ismailos, C Reppas, J B Dressman, et al.
Advanced Drug Delivery Reviews
|
June 30, 2007
Estimating drug solubility in the gastrointestinal tract
J B Dressman, M Vertzoni, K Goumas, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
May 12, 2009
Simulation of gastric lipolysis and prediction of felodipine release from a matrix tablet in the fed stomach
A Diakidou, M Vertzoni, B Abrahamsson, et al.
Pharmaceutical Research
|
January 22, 2000
Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data
E Nicolaides, E Galia, C Efthymiopoulos, et al.
Gastroenterology
|
May 1, 1991
Effect of hydroxypropylmethylcellulose on gastrointestinal transit and luminal viscosity in dogs
C Reppas, J H Meyer, P J Sirois, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|
October 31, 1998
Effect of elevated viscosity in the upper gastrointestinal tract on drug absorption in dogs
C Reppas, G Eleftheriou, P Macheras, et al.
Pharmaceutical Research
|
March 6, 1998
Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms
J B Dressman, G L Amidon, C Reppas, et al.
Journal of Pharmaceutical Sciences
|
August 6, 2008
Postprandial evolution in composition and characteristics of human duodenal fluids in different nutritional states
S Clarysse, J Tack, F Lammert, et al.
Pharmaceutical Research
|
January 1, 1995
Evaluation of different metrics as indirect measures of rate of drug absorption from extended release dosage forms at steady-state
C Reppas, L F Lacey, O N Keene, et al.
Page
of 4