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Journal of Pharmaceutical Sciences|September 11, 2007
Experimental and computational determination of blend time in USP Dissolution Testing Apparatus IIGe Bai, Piero M Armenante, Russell V PlankJournal of Pharmaceutical Sciences|September 11, 2007
Prediction of the possibility of the second peak of drug plasma concentration time curve after iv bolus administration from the standpoint of the traditional multi-compartmental linear pharmacokineticsLeonid M BerezhkovskiyJournal of Pharmaceutical Sciences|September 11, 2007
A framework to investigate drug release variability arising from hypromellose viscosity specifications in controlled release matrix tabletsShawn A Mitchell, Karen M BalwinskiJournal of Pharmaceutical Sciences|September 11, 2007
Theoretical dissolution model of poly-disperse drug particles in biorelevant mediaArimichi Okazaki, Takashi Mano, Kiyohiko SuganoJournal of Pharmaceutical Sciences|September 11, 2007
Pharmacokinetic/pharmacodynamic modeling of corticosterone suppression and lymphocytopenia by methylprednisolone in ratsZhenling Yao, Debra C DuBois, Richard R Almon, et al.Journal of Pharmaceutical Sciences|September 11, 2007
Effect of PEGylation on the solution conformation of antibody fragmentsYanling Lu, Stephen E Harding, Alison Turner, et al.Journal of Pharmaceutical Sciences|September 11, 2007
Heterogeneity of monoclonal antibodiesHongcheng Liu, Georgeen Gaza-Bulseco, Dinesh Faldu, et al.Journal of Pharmaceutical Sciences|November 6, 2007
Intravascular bioresorbable polymeric stents: a potential alternative to current drug eluting metal stentsTahmer Sharkawi, Frederick Cornhill, Antoine Lafont, et al.Journal of Pharmaceutical Sciences|November 9, 2007
Process induced disorder in crystalline materials: differentiating defective crystals from the amorphous form of griseofulvinTao Feng, Rodolfo Pinal, M Teresa CarvajalJournal of Pharmaceutical Sciences|November 15, 2007
Vibration effects on dissolution tests with USP apparatuses 1 and 2Zongming Gao, Terry W Moore, William H DoubPageof 1,699