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Drug Development and Industrial Pharmacy|July 20, 2000
Sustained-release butorphanol microparticlesH C Chang, L C Li
Drug Development and Industrial Pharmacy|July 20, 2000
Preparation of polymeric microcapsules: formulation studiesK Bjerknes, K Dyrstad, G Smistad, et al.
Drug Development and Industrial Pharmacy|July 20, 2000
A stability-indicating HPLC method to determine cyproterone acetate in tablet formulationsA Segall, M Vitale, V Perez, et al.
Drug Development and Industrial Pharmacy|July 20, 2000
Optimization of the formulation and characterization of the physicochemical properties of the novel platelet-activating factor receptor antagonist E5880Y Asai, N Murahashi, K Iwamoto
Drug Development and Industrial Pharmacy|July 20, 2000
Simultaneous determination of thiabendazole and mebendazole in tablets by high-performance liquid chromatographyE M Orsine, E R Kedor-Hackmann, M I Santoro
Drug Development and Industrial Pharmacy|May 2, 2000
Formulation and development of tablets based on Ludipress and scale-up from laboratory to production scaleR Heinz, H Wolf, H Schuchmann, et al.
Drug Development and Industrial Pharmacy|May 2, 2000
Comparing HPLC and UV spectrophotometric analysis methods for determining the stability of sorbic acid in nonionic creams containing lactic acidM M de Villiers, J J Bergh
Drug Development and Industrial Pharmacy|May 2, 2000
A temperature study on critical micellization concentration of the novel platelet-activating factor receptor antagonist E5880 in water by electric conductivity measurementsY Asai, T Nomura, N Murahashi, et al.
Drug Development and Industrial Pharmacy|May 2, 2000
Formulation optimization of controlled-release pellets of metoclopramide hydrochloride using dissolution fit factor approachM T Wang, F H Tsai, D P Wang
Drug Development and Industrial Pharmacy|April 9, 2001
Spray-drying as a method for microparticulate controlled release systems preparation: advantages and limits. I. Water-soluble drugsG F Palmieri, G Bonacucina, P Di Martino, et al.
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