Sunada Hisakazu | Faculty Of Pharmacy Meijo University

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著作論文

Preparation of Rapidly Disintegrating Tablets Containing Itraconazole Solid Dispersions
Rapidly Disintegrating Tablets Prepared by a Surface-Modifying Method : Comparison of Disintegrants
Preparation and Evaluation of Solid Dispersions of Nitrendipine Prepared with Fine Silica Particles Using the Melt-Mixing Method
Preparation and Evaluation of Solid Dispersion for Nitrendipine-Carbopol and Nitrendipine-HPMCP Systems Using a Twin Screw Extruder
Evaluation of Bitterness Suppression of Macrolide Dry Syrups by Jellies
Preparation and Evaluation of a Compressed Tablet Rapidly Disintegrating in the Oral Cavity
Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules V. : Release Properties of Ethylcellulose Layered Matrix Granules
Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules IV. Evaluation of the Controlled Release Properties for in Vivo and in Vitro Release Systems
Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules III. Effects of the Dissolution Condition on the Release Process
Analysis of the Release Process of Phenylropanolamine Hydrochloride from Ethylcellulose Matrix Granules II. Effects of the Binder Solution on the Release Process
Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules
Preparation of Solid Dispersion for Ethenzamide-Carbopol and Theophylline-Carbopol Systems Using a Twin Screw Extruder
Improvement of the Dissolution Rate of Nitrendipine Using a New Pulse Combustion Drying Method
Effect of Several Cellulosic Binders and Method of Their Addition on the Properties and Binder Distribution of Granules Prepared in an Agitating Fluidized Bed
Effect of Process Variables on the Properties and Binder Distribution of Granules Prepared by a High-Speed Mixer
Preparation and Evaluation of Combination Tablet Containing Incompatible Active Ingredients
Release from or through a Wax Matrix System. IV. Generalized Expression of the Release Process for a Reservoir Device Tablet
Release from or through a Wax Matrix System. III. Basic Properties of Release through the Wax Matrix Layer
Release from or through a Wax Matrix System. II.^ Basic Properties of Release from or through the Wax Matrix Layer
Dissolution of Solid Dosage Form. VII. Effect of Shape on the Dissolution of Nondisintegrating Single Component Tablet under Non-sink Condition
Sustained-Release Progesterone Vaginal Suppositories 1 : Development of Sustained-Release Granule(Biopharmacy)
Influence of Physicochemical Properties on Drug Release Rate from Hydroxypropylmethylcellulose Matrix Tablets
Influence of Water-Soluble Polymers on the Dissolution of Nifedipine Solid Dispersions with Combined Carriers
Preparation and Evaluation of Ibuprofen Solid Dispersion Systems with Kollidon Particles Using a Pulse Combustion Dryer System
Some Factors Influencing the Dissolution of Solid Dispersions with Nicotinamide and Hydroxypropylmethylcellulose as Combined Carriers
Effect of Process Variables on the Properties and Binder Distribution of Granules Prepared in a Fluidized Bed
Release from or through a Wax Matrix System VI. : Analysis and Prediction of the Entire Release Process of the Wax Matrix Tablet
Release from or through a Wax Matrix System. V. Applicability of the Square-Root Time Law Equation for Release from a Wax Matrix Tablet
Release from or through a Wax Matrix System.I. Basic Release Properties of the Wax Matrix System
Mechanistic Studies on Hydrotropic Solubilization of Nifedipine in Nicotinamide Solution
Indomethacin Controlled Release Matrix Tablet Prepared by Wet Granulation Procedure
Comparison of Nicotinamide, Ethylurea and Polyethylene Glycol as Carriers for Nifedipine Solid Dispersion Systems

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