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Pharmaceutical Research|April 1, 1990
Drug-excipient incompatibility studies of the dipeptide angiotensin-converting enzyme inhibitor, moexipril hydrochloride: dry powder vs wet granulationL Gu, R G Strickley, L H Chi, et al.Pharmaceutical Development and Technology|July 1, 1996
Compaction simulator studies of a new drug substance: effect of particle size and shape, and its binary mixtures with microcrystalline celluloseM Celik, J T Ong, Z T Chowhan, et al.Journal of Pharmaceutical Sciences|February 1, 1993
Effect of the mode of super disintegrant incorporation on dissolution in wet granulated tabletsM S Gordon, V S Rudraraju, K Dani, et al.Journal of Pharmaceutical Sciences|December 1, 1982
Effect of moisture and crushing strength on tablet friability and in vitro dissolutionZ T Chowhan, I C Yang, A A Amaro, et al.Journal of Pharmaceutical Sciences|May 1, 1991
Effect of formulation solubility and hygroscopicity on disintegrant efficiency in tablets prepared by wet granulation, in terms of dissolutionJ R Johnson, L H Wang, M S Gordon, et al.Pageof 3