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Journal of Pharmaceutical Sciences|March 1, 1977
Predictive conversion of in vitro drug dissolution data into in vivo drug response versus time profiles exemplified for plasma levels of warfarinV F Smolen, R J ErbJournal of Pharmaceutical Sciences|June 1, 1976
Attainment of highly uniform solid drug dispersions employing molecular scale drug entrapment in polymeric laticesA B Larson, G S BankerInternational Journal of Pharmaceutics|July 14, 2001
Examination of oxidized cellulose as a macromolecular prodrug carrier: preparation and characterization of an oxidized cellulose-phenylpropanolamine conjugateL Zhu, V Kumar, G S BankerJournal of Pharmaceutical Sciences|March 1, 1975
Drug-biomolecule interactions: bioelectrometric study of the mechanism of carbachol interactions with the cornea and its relation to miotic activityV F Smolen, C S Park, E J WilliamsThe Journal of Pharmacology and Experimental Therapeutics|December 11, 1975
Bioavailability analysis of chlorpromazine in humans from pupilometric dataV F Smolen, H R Murdock, E J WilliamsJournal of Pharmaceutical Sciences|March 1, 1977
Determination of porosity and pore-size distribution of aspirin tablets relevant to drug stabilityH Gucluyildiz, G S Banker, G E PeckAAPS Pharmscitech|January 20, 2004
Compression, compaction, and disintegration properties of low crystallinity celluloses produced using different agitation rates during their regeneration from phosphoric acid solutionsV Kumar, S H Kothari, G S BankerJournal of Pharmaceutical Sciences|January 1, 1982
Quantitative evaluation of pharmaceutical effervescent systems I: Design of testing apparatusN R Anderson, G S Banker, G E PeckJournal of Pharmaceutical Sciences|May 1, 1977
Bactericidal properties of quaternary ammonium compounds in dispersed systemsG J Baley, G E Peck, G S BankerJournal of Pharmaceutical Sciences|January 1, 1982
Quantitative evaluation of pharmaceutical effervescent systems II: Stability monitoring by reactivity and porosity measurementsN R Anderson, G S Banker, G E PeckPageof 2