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L J Leeson

Showing results (1-10 of 11) with videos related to

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Pharmacology|January 1, 1972
PhenylbutazoneL J Leeson
Journal of Pharmaceutical Sciences|April 1, 1973
Product dissolution methodsL J Leeson
Journal of Pharmaceutical Sciences|September 1, 1973
Significance of dissolution standardsL J Leeson
Pharmaceutical Research|May 1, 1990
A better way to present postersL J Leeson, G Levy
Journal of Pharmaceutical Sciences|December 1, 1973
Calculating absorption rate constants for drugs with incomplete availabilityL J Leeson, H Weintraub
Journal of Pharmacokinetics and Biopharmaceutics|October 1, 1985
The in vitro development of extended-release solid oral dosage formsL J Leeson, D Adair, J Clevenger, et al.
Drug Metabolism Reviews|January 1, 1975
The objective and timing of drug disposition studies, appendix IV. Phenylbutazone formulations: in vitro dissolution and in vivo performanceL J Leeson, E C Shinal, G Lukas, et al.
British Journal of Clinical Pharmacology|January 1, 1985
Oros controlled-release formulations of metoprolol: an approach to the development of a system for once daily administrationW Good, L J Leeson, S L Zak, et al.
Journal of Pharmaceutical Sciences|January 1, 1991
Development of a new controlled-release formulation of chlorpheniramine maleate using in vitro/in vivo correlationsR L Williams, R A Upton, L Ball, et al.
Pharmaceutical Research|October 1, 1990
The development of USP dissolution and drug release standardsJ L Cohen, B B Hubert, L J Leeson, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pharmacology|January 1, 1972
PhenylbutazoneL J Leeson
Journal of Pharmaceutical Sciences|April 1, 1973
Product dissolution methodsL J Leeson
Journal of Pharmaceutical Sciences|September 1, 1973
Significance of dissolution standardsL J Leeson
Pharmaceutical Research|May 1, 1990
A better way to present postersL J Leeson, G Levy
Journal of Pharmaceutical Sciences|December 1, 1973
Calculating absorption rate constants for drugs with incomplete availabilityL J Leeson, H Weintraub
Journal of Pharmacokinetics and Biopharmaceutics|October 1, 1985
The in vitro development of extended-release solid oral dosage formsL J Leeson, D Adair, J Clevenger, et al.
Drug Metabolism Reviews|January 1, 1975
The objective and timing of drug disposition studies, appendix IV. Phenylbutazone formulations: in vitro dissolution and in vivo performanceL J Leeson, E C Shinal, G Lukas, et al.
British Journal of Clinical Pharmacology|January 1, 1985
Oros controlled-release formulations of metoprolol: an approach to the development of a system for once daily administrationW Good, L J Leeson, S L Zak, et al.
Journal of Pharmaceutical Sciences|January 1, 1991
Development of a new controlled-release formulation of chlorpheniramine maleate using in vitro/in vivo correlationsR L Williams, R A Upton, L Ball, et al.
Pharmaceutical Research|October 1, 1990
The development of USP dissolution and drug release standardsJ L Cohen, B B Hubert, L J Leeson, et al.
Pageof 2