Application of the Solid Dispersion Method to the Controlled Release of Medicine. VIII. Medicine Release and Viscosity of the Hydrogel of a Water-Soluble Polymer in a Three-Component Solid Dispersion System
スポンサーリンク
概要
- 論文の詳細を見る
Solid dispersions were prepared with a highly water-soluble medicine (oxprenolol hydrochloride (OXP)), water-insoluble ethylcellulose (EC) and four grades of water-soluble hydroxypropylcellulose (HPC) having different molecular weights. The effects of the composition ratio within the range of 5% of HPC and of the viscosity of HPC hydrogels on the release of OXP were studied. The bulk viscosity of HPC hydrogels was evaluated from the relationship between shear rate and shear stress. The microscopic viscosity was evaluated by the spin probe method of the electron spin resonance (ESR) technique.The release rate of OXP decreased with increasing HPC composition ratio and became almost constant at the HPC composition ratio of 3% and more. This result suggests that the release of OXP will occur through its diffusion into the swollen HPC gel phase formed in a solid dispersion at the HPC composition ratio of 3% and more. The bulk viscosity of HPC hydrogels markedly increased with increasing molecular weight of HPC, but there was little noticeable change in release rate and activation energy for the diffusion of OXP. This result can be explained by the fact that the microscopic viscosity was hardly affected by the molecular weight of HPC, suggesting that the resistance to diffusion of OXP into the swollen HPC gel phase in the solid dispersion was almost the same regardless of the moleclar weight of HPC.
- 公益社団法人日本薬学会の論文
- 1995-09-15
著者
-
湯浅 宏
東京薬科大学
-
金谷 芳雄
東京薬科大学
-
湯淺 宏
東京薬科大学 薬
-
湯浅 宏
東京薬科大学薬学部
-
湯浅 宏
Laboratory of Medical & Pharmaceutical Technology, School of Pharmacy, Tokyo University of Pharmacy
-
金谷 芳雄
Laboratory of Medical & Pharmaceutical Technology, School of Pharmacy, Tokyo University of Pharmacy
-
湯浅 宏
東京薬科大学 薬学部 製剤設計学教室
-
大石 勝敏
Nihon Pharmaceutical Industry Co., Ltd.,
-
Kanaya Yoshio
Laboratory Of Medical & Pharmaceutical Technology School Of Pharmacy Tokyo University Of Pharmac
-
Kanaya Yoshio
Tokyo College Of Pharmacy
-
尾関 哲也
Laboratory of Medical & Pharmaceutical Technology, School of Pharmacy, Tokyo University of Pharmacy
-
尾関 哲也
東京薬科大学薬学部製剤設計学教室
-
大石 勝敏
Nihon Pharmaceutical Industry Co. Ltd.
関連論文
- 2液混合型スプレードライヤーを用いたナノ粒子含有マイクロ粒子の調製 (特集 総合技術としてのドラッグデリバリーシステムの最前線)
- 散剤予製機による分包精度と粉体物性との関連性
- Studies on Improvement of Pharmaceutical Preparations Prescribed in Hospitals. III. : Prevention of Fading by Use of Solid Dispersion System of Ointment Containing Methylrosaniline Chloride
- 乳酸カルシウムならびにアルギン酸ナトリウムをコーティングした顆粒からの不溶性ゲル形成を応用した楽物放出制御^1
- P-59 子宮腺筋症及び深部内膜症治療を目的としたダナゾール膣錠の製剤設計
- 微量粉体試料における圧縮性評価
- 溶融造粒法を用いた抗癌剤TAT-59錠の安定化におけるポリエチレングリコールの分子量の影響^1
- 顆粒の準静的, 動的圧縮で得た錠剤の性状と圧縮プロセス
- 流動層コーティングにおける凝集抑制に関する研究(第4報)陽イオン添加における粒子凝集抑制
- グミ製剤の保存安定性
- グミ製剤からのアセトアミノフェンの放出性
- ゼラチンを用いたグミ製剤の調製
- Studies on Dissolution Tests for Soft Gelatin Capsules by the Rotating Dialysis Cell (RDC) Method. VI. Preparation and Evaluation of Ibuprofen Soft Gelatin Capsule
- 光および BHT 共存下における錠剤の変色
- コンドロイチン硫酸ナトリウムを用いた溶媒置換法による難溶性薬物の溶解性の向上
- Studies on the Granulation Process of Granules for Tableting with a High Speed Mixer. II. Influence of Particle Size of Active Substance on Granulation
- Effects of Compression Pressure on Physical and Chemical Stability of Tablets Containing an Anticancer Drug TAT-59
- Studies on the Granulation Process of Granules for Tableting with a High Speed Mixer. I. Physical Properties of Granules for Tableting
- Studies on Whisker Growth in Solid Preparations. VI. Whisker Growth in Mixtures Composed of Aspirin and Porous Glass Powder
- Effects of Water Content on Physical and Chemical Stability of Tablets Containing an Anticancer Drug TAT-59
- Studies on Internal Structure of Tablets. II. Effect of the Critical Disintegrator Amount on the Internal Structure of Tablets(Pharmaceutical)
- Studies on Whisker Growth on the Tablet Surface. III. : Mechanism of Whisker Growth on Aspirin Tablet and Its Effect on the Mechanical Strength of the Tablet
- Studies on Anisotropy of Compressed Powders. III. Effects of Different Granulation Methods on Anisotropy, Pore Size and Crushing Strength of Tablets
- 小児向け剤形の開発に関する研究(第7報)グミ製剤における墓剤成分の結晶析出抑制
- 小児向け剤形の開発に関する研究(第6報) : グミ製剤の基剤変色抑制による保存安定性の向上
- ゲル形成を応用したコーティング顆粒からのテオフィリンの放出制御
- 新規4流体ノズルスプレードライ法による粉末吸入剤用粒子の調製
- 圧力スイング造粒法による粉末吸入剤用2成分複合顆粒の調製と肺内in vitro吸入特性の評価
- Maltosyl-β-cyclodextrin ならびに sulphobutylether-β-cyclodextrin による pranlukast hydrate の包接挙動の解析、消化管吸収性に及ぼす影響
- 酸処理ビール酵母細胞壁の新規結合剤への応用
- 圧力スイング造粒法による粉末吸入剤用顆粒の造粒の可能性ならびに薬物粒子送達性
- 乳酸カルシウム, アルギン酸ナトリウムならびにカーボポールのゲル形成を応用した顆粒からの薬物放出制御
- 粉末吸入剤のための粒子設計に関する研究(第10報)Carrier-DPIにおける薬物粒子送達性に及ぼす担体乳糖表面での薬物粒子付着占有率の影響
- 粉末吸入剤のための粒子設計に関する研究(第11報)圧力スイング造粒法による粉末吸入剤用複合顆粒の調製ならびに粒子送達性
- 酵母分画物 (AYC)の製剤化への応用(第9報)崩壊機能を併せ持つ結合剤ならびに口腔内速崩壊錠への応用
- 粘膜付着性の放出制御型フィルムからのリドカインの放出
- 薬学教育用の教育映画・ビデオ・スライド等
- 経肺投与ナノ粒子製剤の設計
- 脳腫瘍に対するがん抑制ペプチドp53p-Antを用いた治療効果
- ナノ粒子含有マイクロスフェアの設計と経肺投与製剤への応用
- ナノ薬物粒子含有マイクロスフェアによる経肺投与DDS
- Application of the Solid Dispersion Method to Controlled Release of Medicine. I. Controlled Release of Water Soluble Medicine by Using Solid Dispersion
- Studies on Development of Dosage Forms for Pediatric Use (V) Oral Mucosal Irritation Study of Gummi Drugs in Hamster Cheek Pouch
- Studies on Development of Dosage Form for Pediatric Use (No.4) Time Courses of Plasma Concentration of Acetaminophen after Oral Administration of Gummi Drug and Powder Preparation in Dogs
- Studies on the Granulation Process of Granules for Tableting with a High Speed Mixer. III. Analysis of the Compression Process
- Application of Calcium Silicate for Medicinal Preparation. I. Solid Preparation Adsorbing an Oily Medicine to Calcium Silicate
- Melting Granulation by Addition of Polyethyleneglycol for Stabilization of TAT-59
- Effects of Grinding and Tableting on Physicochemical Stability of an Anticancer Drug, TAT-59
- Formation of Water-Insoluble Gel in Dry-Coated Tablets for the Controlled Release of Theophylline
- Application of Gel Formation for Taste Masking
- 口腔粘膜への適用を目的にしたフィルム状製剤の開発
- Studies on Internal Structure of Tablets. VI. Stress Dispersion in Tablets by Excipients
- Application of the Solid Dispersion Method to the Controlled Release of Medicine. VIII. Medicine Release and Viscosity of the Hydrogel of a Water-Soluble Polymer in a Three-Component Solid Dispersion System
- Application of the Solid Dispersion Method to the Controlled Release of Medicine. VII. Release Mechanism of a Highly Water-Soluble Medicine from Solid Dispersion with Different Molecular Weights of Polymer
- Studies on Production of Higher Functional Pharmaceutical Preparations by Using Various Additives. III. Application of Hollow Glass Beads for Intragastric Floating Granules
- Studies on the Development of Intragastric Floating and Sustained Release Preparation. I. Application of Calcium Silicate as a Floating Carrier
- Studies on Internal Structure of Tablets. III. : Manufacturing of Tablets Containing Microcapsules
- Applicaiotn of the Solid Dispersion Method to the Controlled Release of Medicine. VI. Release Mechanism of a Slightly Water Soluble Medicine and Interaction between Flurbiprofen and Hydroxypropyl Cellulose in Solid Dispersion
- Application of the Solid Dispersion Method to the Controlled Release of Medicine. V. Suppression Mechanism of the Medicine Release Rate in the Three-Component Solid Dispersion System
- Application of the Solid Dispersion Method to Controlled Release of Medicine. II. Sustained Release Tablet Using Solid Dispersion Granule and the Medicine Release Mechanism
- Application of the Solid Dispersion Method to the Controlled Release of Medicine. IV. Precise Control of the Release Rate of a Water Soluble Medicine by Using the Solid Dispersion Method Applying the Difference in the Molecular Weight of a Polymer
- Application of the Solid Dispersion Method to the Controlled Release of Medicine. III. Control of the Release Rate of Slightly Water Soluble Medicine from Solid Dispersion Granules