宮崎正三 | 東日本学園大学薬学部

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概要

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著作論文

ラットにおけるジソピラミドの腎排泄(第1報)
直腸の組織透過性におよぼす薬物の影響(第1報)スルファグアニジンの直腸透過性におよぼす製剤添加物の影響
112 漿膜露出胃癌治療の工夫 : 抗癌剤腹腔内投与に関して(第32回日本消化器外科学会総会)
胃癌患者におけるCyclophosphamideの血漿中および組織中濃度
Interaction of Drugs with Bile Components. II. Effect of Bile on the Absorption of Indomethacin and Phenylbutazone in Rats
Effect of Antacids on the Dissolution Behavior of Tetracycline and Methacycline
Interaction of Drugs with Bile Components. I. Effects of Bile Salts on the Dissolution Behavior of Indomethacin and Phenylbutazone
Solubility Characteristics of Weak Bases and Their Hydrochloride Salts in Hydrochloric Acid Solutions
Common Ion Effect of Chloride on the Dissolution Properties of Papaverine Hydrochloride
The Use of Chitin and Chitosan as Drug Carriers
Controlled Release of Prednisolone from Ethylene-Vinyl Acetate Copolymer Matrix
Dissolution Properties of Salt Forms of Berberine
Use of Fibrin Film as a Carrier for Drug Delivery : In Vitro Drug Permeabilities of Fibrin Film
Effect of Formulation Additives on the Dissolution Behavior of Tetracycline Antibiotics
Effect of Additives on the Polymorphic Transformation of Chlortetracycline Hydrochloride Crystals
Polymorphic Transformation of Chlortetracycline Hydrochloride Crystals Studied by Infrared Spectrophotometric Method
A Comparison of Solubility Characteristics of Free Bases and Hydrochloride Salts of Tetracycline Antibiotics in Hydrochloric Acid Solutions
Effect of Crystal Forms on the Dissolution Behavior and Bioavailability of Tetracycline, Chlortetracycline, and Oxytetracycline Bases
テトラサイクリンの数種の固相の物性と消化管吸収
Effect of Polymorphism on the Dissolution Behavior and Gastrointestinal Absorption of Chlortetracycline Hydrochloride
A Comparison of Bioavailability of Free Bases and Hydrochloride Salts of Chlortetracycline, Demethylchlortetracycline, and Methacycline

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