金庭 延慶 | School Of Pharmaceutical Sciences Showa University

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• 同名の論文著者
• School Of Pharmaceutical Sciences Showa Universityの論文著者

関連著者

• 金庭 延慶

  School Of Pharmaceutical Sciences Showa University

• 金庭 延慶

  School of pharmaceutical Sciences, Showa University

• 池川 昭子

  School Of Pharmaceutical Sciences Showa University

• 森口 郁生

  School of Pharmaceutical Sciences, Kitasato University

• 森口 郁生

  School Of Pharmaceutical Sciences Kitasato University

• 大塚 誠

  School of pharmaceutical Sciences, Showa University

• 伏見 静夫

  School of Pharmaceutical Sciences, Showa University

• 伏見 静夫

  School Of Pharmaceutical Sciences Showa University

• 渉 信敏

  昭和大学薬学部

• 渉 信敏

  School of Pharmaceutical Sciences, Showa University

• 今川 歓二

  School of Pharmaceutical Sciences, Showa University

• 今川 歓二

  School Of Pharmaceutical Sciences Showa University

• 市川 順一

  School of Pharmaceutical Sciences, Showa University

• 市川 順一

  School Of Pharmaceutical Sciences Showa University

• 松本 崇弘

  School of Pharmaceutical Sciences, Showa University

• 松本 崇弘

  昭和大 薬

• 鷲見 正宏

  昭和大学歯科病院薬局

• 鷲見 正宏

  School of Pharmaceutical Sciences, Showa University

• 青木 晴子

  School of Pharmaceutical Sciences, Showa University

• 青木 晴子

  School Of Pharmaceutical Sciences Showa University

• 林 哲男

  昭和大学薬学部

• 林 哲男

  School of Pharmaceutical Sciences, Showa University

• 花野 学

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 花野 学

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 早瀬 夫抄子

  School of Pharmaceutical Sciences, Showa University

• 富田 豊

  School of Pharmaceutical Sciences, Showa University

• 鍋山 義一郎

  School of Pharmaceutical Sciences, Showa University

• 橋本 勝代

  School of Pharmaceutical Sciences, Showa University

• 大森 利枝

  School of Pharmaceutical Sciences, Showa University

• 増川 喜久弥

  School of Pharmaceutical Sciences, Showa University

• 橋本 勝代

  School Of Pharmaceutical Sciences Showa University

• 富田 豊

  School Of Pharmaceutical Sciences Showa University

• 日浦 満

  昭和大学薬学部

• 大森 利枝

  School Of Pharmaceutical Sciences Showa University

• 早瀬 夫抄子

  School Of Pharmaceutical Sciences Showa University

• 梅原 玲子

  School Of Pharmaceutical Sciences Showa University

• 池川 明子

  School Of Pharmaceutical Sciences Showa University

• 日浦 満

  School of Pharmaceutical Sciences, Showa University

• 船木 朋雄

  School of Pharmaceutical Sciences, Showa University

• 大島 千恵子

  School of Pharmaceutical Sciences, Showa University

• 荒木 良枝

  School of Pharmaceutical Sciences, Showa University

• 名雪 美穂子

  School of Pharmaceutical Sciences, Showa University

• 飯島 寿子

  School of Pharmaceutical Sciences, Showa University

• 飯島 寿子

  School Of Pharmaceutical Sciences Showa University

• 荒木 良枝

  School Of Pharmaceutical Sciences Showa University

• 鍋山 義一郎

  School Of Pharmaceutical Sciences Showa University

• 名雪 美穂子

  School Of Pharmaceutical Sciences Showa University

• 増川 喜久弥

  School Of Pharmaceutical Sciences Showa University

• 大島 千恵子

  School Of Pharmaceutical Sciences Showa University

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著作論文

• The Dehydration Kinetics of Theophylline Monohydrate Powder and Tablet
• A Kinetic Study of the Crystallization Process of Noncrystalline Indomethacin under Isothermal Conditions
• Effect of Environmental Temperature on the Polymorphic Transformation of Phenylbutazone during Grinding
• Effect of Environmental Temperature on Polymorphic Solid-State Transformation of Indomethacin during Grinding
• Physicochemical Characterization of Indomethacin Polymorphs and the Transformation Kinetics in Ethanol
• Effect of Tabletting on the Degree of Crystallinity and on the Dehydration and Decomposition Points of Cephalexin Crystalline Powder
• Compression Properties of Cephalexin Powder and Physical Properties of the Tablet
• The Interaction between Water and Cephalexin in the Crystalline and Noncrystalline States
• Effects of Grinding on the Physicochemical Properties of Cephalexin Powder
• Effect of Grinding on the Degree of Crystallinity of Cephalexin Powder
• Hygroscopicity and Solubility of Noncrystalline Cephalexin
• Influence of Particle Size on Physicochemical Properties of Pharmaceutical Powders. V. On Fluidity of Sodium Borate and Boric Acid Powders. (2)
• Influence of Particle Size on Physicochemical Properties of Pharmaceutical Powders. I. On Fluidity of Sodium Borate and Boric Acid Powders. (1).
• Solubilization of Amobarbital by Mechanical Treatment in the Presence of Diluents
• A Decrease in Crystallinity of Amobarbital by Mechanical Treatment in the Presence of the Diluents
• The Effect of Crystal Hardness on Compaction Propensity
• The Effect of Particle Size on the Compaction Properties and Compaction Mechanism of Sulfadimethoxine and Sulfaphenazole
• Preparation of Phenylbutazone Polymorphs and Their Transformation in Solution
• Variation in the Molecular Weight Distribution of Polyvinylpyrrolidone by Ball-Milling
• Induction Period for a Decrease in Molecular Weight of Polyvinylpyrrolidone by Ball-Milling in Various Kinds of Atmosphere in the Presence of Organic and Inorganic Powders
• Solubilization of Water-Insoluble Organic Powders by Ball-Milling in the Presence of Polyvinylpyrrolidone
• Influence of Molecular Weight of Polyethylene Glycol on Interaction between Polyethylene Glycol and Iodine
• Influence of Operational Variables on Vibro-milling of Silica Sands
• Influence of Addition of Organic and Inorganic Powders on Degradation of Polyvinylprrolidone by Ball-Milling in Air
• Influence of Operational Variables on Ball-Milling of Sulfadimethoxine and White Alundum
• Influence of Physicochemical Properties on Ball-Milling of Pharmaceutical Powders
• Influence of Particle Size on Physicochemical Properties of Pharmaceutical Powders. IX. Fluidity of Binary Mixtures of Potato Starch
• Influence of Particle Size on Physicochemical Properties of Pharmaceutical Powders. VII. Fluidity and Packing Property of Binary Mixtures
• Influence of Particle Size on Physicochemical Properties of Pharmaceutical Powders. IV. On Packing of Pharmaceutical Powders. (2)
• Influence of Particle Size on Physicochemical Properties of Pharmaceutical Powders. II. On Packing of Sodium Borate and Boric Acid Powders.
• Dissolution of Slightly Soluble Drugs. VI. Effect of Particle Size of Sulfadimethoxine on the Oral Bioavailability
• Effect of Fasting on the Elimination of Barbital and Phenobarbital in Rabbits
• Interaction between Iodine and Polyvinylpyrrolidone or α-Pyrrolidone
• Complexation of Chlorpromazine with Adenosine and Its Phosphates
• Effect of Water on Rate of Charge-Transfer Reaction of Aniline with Chloranil
• Effect of Water on Charge-Transfer Complexations
• Solvent Effects on π-π Charge-Transfer Complexations
• Spectral Changes of Various Dyes by Bovine Serum Albumin and by Organic Solvents
• Spectroscopic Studies on Molecular Interactions. VI. Mechanism of Metachromasy of 2-(4'-Hydroxyphenylazo) benzoic Acid by Serum Albumin
• Spectroscopic Studies on Molecular Interactions. V. Charge-Transfer Property and Enzymatic Acetylation of Aniline Derivatives
• Adsorption of Solute from the Solutions. IV. Adsorption of Benzoic Acids on Graphite
• Adsorption of Solute from the Solutions. V. Adsorption Rate of Cyanocobalamin on Talc
• Spectroscopic Studies on Molecular Interactions. IV. Charge-Transfer Properties and Antibacterial Activity of Sulfonamides
• Spectroscopic Studies on Molecular Interactions. III. Improvement of the Benesi-Hildebrand Method for the Determination of Equilibrium Constants
• Spectroscopic Studies on Molecular Interactions. II. Complexation between Polyvinylpyrrolidone and Iodine
• Spectroscopic Studies on Molecular Interactions. I. Complexations between Caffeine and Benzoic Acids
• Adsorption of Solute from the Solutions. III. Repression of Adsorption of Cyanocobalamin on Talc by Polyvinylpyrrolidone
• Adsorption of Solute from the Solutions. II. Competitive Adsorption of Cyanocobalamin with Pyridoxine and Thiamine on Talc
• Dissolution of slightly Soluble Drugs. V. Effect of Particle Size on Gastrointestinal Drug Absorption and Its Relation to Solubility
• Dissolution of slightly Soluble Drugs. IV. Effect of Particle Size of Sulfonamides on in Vitro Dissolution Rate and in Vivo Absorption Rate, and Their Relation to Solubility
• Dissolution of slightly Soluble Drugs. III. Surface Condition of Powder Particles and Their Initial Dissolution Behavior
• Dissolution of Slightly Soluble Drugs. II. Effect of Particle Size on Dissolution Behavior in Sodium Lauryl Sulfate Solutions
• Dissolution of slightly Soluble Drugs. I. Influence of Particle Size on Dissolution Behavior

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