Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules
スポンサーリンク
概要
- 論文の詳細を見る
The release properties of phenyipropanolamine hydrochloride (PPA) from ethylcellulose (EC, ethylcellulose 10 cps (EC#10) and/or 100 cps (EC#100)) matrix granules prepared by the extrusion granulation method were examined. The release process could be divided into two parts, and was well analyzed by applying square-root time law and cube root law equations, respectively. The validity of the treatments was confirmed by the fitness of the simulation curve with the measured curve. At the initial stage, PPA was released from the gel layer of swollen EC in the matrix granules. At the second stage, the drug existing below the gel layer dissolved, and was released through the gel layer. Also, the time and release ratio at the connection point of the simulation curves was examined to determine the validity of the analysis. Comparing the release properties of PPA from the two types of EC matrix granules, EC#I00 showed more effective sustained release than EC#10. On the other hand, changes in the release property of the EC#10 matrix granule were relatively more clear than that of the EC#100 matrix granule. Thus, it was supposed that EC#10 is more available for controlled and sustained release formulations than EC#100.
- 公益社団法人日本薬学会の論文
- 2002-11-01
著者
-
Fujii R
Pharmaceutical Discovery Research Division Takeda Chemical Industries Ltd.
-
SUNADA Hisakazu
Faculty of Pharmacy, Meijo University
-
FUKUI Atsuko
Ryukakusan Co., Ltd.
-
FUJII Ryuta
Ryukakusan Co., Ltd.
-
YONEZAWA Yorinobu
Faculty of Pharmacy, Meijo University
-
Fujii R
Ryukakusan Co. Ltd.
-
Fukui Atsuko
Ryukakusan Co. Ltd.
-
Yonezawa Y
Faculty Of Pharmacy Meijo University
-
Yonezawa Yorinobu
Faculty Of Pharmaceutical Sciences Meijio University
-
Sunada H
Faculty Of Pharmacy Meijo University
-
Sunada Hisakazu
Fac. Of Pharmacy Meijo Univ.
-
Sunada Hisakazu
Faculty Of Pharmacy Meijo University
関連論文
- Preparation of Rapidly Disintegrating Tablets Containing Itraconazole Solid Dispersions
- Rapidly Disintegrating Tablets Prepared by a Surface-Modifying Method : Comparison of Disintegrants
- Effect of Several Cellulosic Binders on Particle Size Distribution of Granules Prepared by a High-Speed Mixer
- Synthesis of New Peptides, Apelin and Galanin-Like Peptide, by a Combination of Recombinant DNA Technology and Chemical Cleavage Reaction
- Synthesis of New Peptides with Prolactin-releasing Activity by a Combination of Recombinant DNA Technology and a Cysteine-specific Cyanylation Reaction
- Identification of Prolactin-Releasing Peptide
- Synthesis of New Peptides with Prolactin-releasing Activity by a Combination of Recombinant DNA Technology and a Cysteine-specific Cyanylation Reaction
- Identification of Neuromedin U Receptors
- 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
- ENHANCEMENT OF LYMPHATIC TRANSPORT OF 1-(2-TETRAHYDROFURYL)-5-FLUOROURACIL BY POLYACRYLIC ACID AQUEOUS GEL AND EMULSION TYPE SUPPOSITORIES IN RATS
- 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