The Influence of Drugs on the Physical Stability of Fatty Suppositories
スポンサーリンク
概要
- 論文の詳細を見る
To examine the influence of drugs on the physicochemical stability of semisynthetic fatty suppositories, model suppositories containing various kinds of drugs were prepared with Witepsol H-15 and storage experiments were performed. It was shown that the stability of pharmaceutical properties was largely dependent on the solubility of drugs in the fatty vehicle (S_o). That is, the rate of polymorphic transition of the vehicle measured by X-ray diffraction was accelerated by lipid-soluble drugs but was not much affected by lipid-insoluble drugs. The melting points measured by DTA generally decreased with inrreasing S_o, but they all increased by about 2 or 3℃ during storage. The softening time decreased with increasing S_o. The release properties measured at 37℃ were dependent on the solubility of the drugs in the dissolution fluid (S_w) initially but became dependent on S_o during storage. This phenomenon is discussed on the basis of the transportion mechanism of drugs in the lipid phase.
- 社団法人日本薬学会の論文
- 1982-03-25
著者
-
鮫島 政義
Product Formulation Research Laboratory Tanabe Seiyaku Co. Ltd.
-
小林 征雄
Pharmaceutics Research Laboratory, Tanabe Seiyaku Co., Ltd.,
-
吉野 廣祐
Pharmaceutics Research Laboratory Tanabe Seiyaku Co. Ltd.
-
吉野 広祐
田辺製薬
-
吉野 廣祐
Products Formulation Research Laboratory, Tanabe Seiyaku Co., Ltd.,
-
小林 征雄
Product Formulation Research Laboratory, Tanabe Seiyaku Co., Ltd.
-
小林 征雄
Pharmaceutics Research Laboratory Tanabe Seiyaku Co. Ltd.
関連論文
- Enhancement of Bioavailability of Dopamine via Nasal Route in Beagle Dogs
- Gastric Emptying Rate of Drug Preparations. III. Effects of Size of Enteric Micro-Capsules with Mean Diameters Ranging from 0.1 to 1.1 mm in Man
- Bioavailability of Sugar-Coated Tablets of Thiamine Disulfide in Humans. II. : Correlation with Bioavailability in Beagle Dogs
- Bioavailability of Sugar-Coated Tablets of Thiamine Disulfide in Humans. I. : Effect of Gastric Acidity and in Vivo-in Vitro Correlation
- Factors Effecting Spherical Granulation of Drugs by Tumbling Granulation Method
- Estimation of Polymorphic Transition Degree of Pharmaceutical Raw Materials
- Porosity-Controlled Ethylcellulose Film Coating. V. Mechanism of Drug Release from Beads Coated with Porous Ethylcellulose Film
- Porosity-Controlled Ethylcellulose Film Coating. IV. Evaluation of Mechanical Strength of Porous Ethylcellulose Film
- Porosity-Controlled Ethylcellulose Film Coating. III. Application of Porous Ethylcellulose Film Coating to Capsule-Type Controlled Release Preparation of Theophylline
- Porosity-Controlled Ethylcellulose Film Coating. I.Formation of Porous Ethylcellulose Film in the Casting Process and Factors Affecting Film-Density
- Influence of Compression Force on Consolidation Behavior and Drug Release Property of Wax Matrix Tablets
- Influence of Internal Structure on Kinetics of Drug Release from Wax Matrix Tablets
- Influence of Tabletting Speed on Compactibility and Compressibility of Two Direct Compressible Powders under High Speed Compression
- Influence of Fatty Acid Composition on the Properties and Polymorphic Transition of Fatty Suppository Bases
- Influence of the Liquid Phase Coexisting in Fatty Suppository Bases on the Polymorphic Transition Rate
- The Influence of Drugs on the Physical Stability of Fatty Suppositories
- Polymorphic Transition Rate of Semisynthetic Fatty Suppository Bases
- Laser Diffraction Estimation of Particle Size Distribution of Slightly Water-Soluble Drugs Coexisting with Additives : Application to Solid Dosage Forms
- Absorption of Diltiazem in Beagle Dog from Pulsatile Release Tablet
- Design and Preparation of Pulsatile Release Tablet as a New Oral Drug Delivery System
- Effect of Plasticizer on Microencapsulation with Enteric Polymer by Surface Neutralization Method
- Microencapsulation of Benzoic Acid Derivatives Using an Enteric Polymer by Surface Neutralization Method and Derivation of an Empirical Equation for Predicting Film Formation
- Effect of Polymer Species on Microencapsulation be a Surface Neutralization Method
- Microencapsulation of a Slightly Soluble Drug by Surface Neutralization Method Using an Enteric Polymer
- Studies on Dissolution Mechanism of Drugs from Ethylcellulose Microcapsules(Pharmaceutical)
- Effect of Powder Addition to Carboxyvinylpolymer Hydrogel on Viscoelasticity
- Influence of Powder Addition to Macrogol Ointment Japanese Pharmacopeia on the Pheological Properties
- Powder-Filled Semisolids : Influence of Powder Addition to Vaseline on the Rheological Properties
- Evaluation of the Rheological Properties of Various Kinds of Carboxyvinylpolymer Gels
- A New Method for Preparation of Enteric-Coated Microcapsules from Aqueous Medium(Pharmaceutical)
- Studies on Microcapsules. IV. : Influence of Properties of Drugs on Microencapsulation and Dissolution Behavior
- Studies on Microcapsules. III. Influence of Molecular Weight of Polyisobutylene in the Microencapsulation of Ascorbic Acid
- Application of Nonlinear Viscoelastic Analysis by the Oscillation Method to Some Pharmaceutical Ointments in the Japanese Pharmacopeia
- Studies on Microcapsules. II. Influence of Molecular Weight of Ethylcellulose in the Microencapsulation of Ascorbic Acid
- Studies on Microcapsules. I. Role and Effect of Coacervation-inducing Agents in the Microencapsulation of Ascorbic Acid by a Phase Separation Method