永井恒司 | Research Center Taisho Pharmaceutical Co. Ltd.

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著作論文

Evaluation of New Paty-Type Implantable Devices Consisting of Poly(ε-caprolactone/δ-valerolactone) and Estracyt or Estramustine
Comparative Bioavailability Study of Acetaminophen Solutions Used in Hospital Formulary
Preparation and Evaluation of Free Oxygen Absorber in Pharmaceutical Preparations
Pharmacokinetic Characteristics and Antitumor Activity of the N-Succinyl-chitosan-Mitomycin C Conjugate and the Carboxymethyl-chitin-Mitomycin C Conjugate
Synthesis and Drug-Release Characteristics of the Conjugates of Mitomycin C with N-Succinyl-chitosan and Carboxymethyl-chitin
Accelerated Degradation of Non-steroid Anti-inflammatory Drugs at Carbon Black/Water Interface
In Vitro pH-Dependent Drug Release from N^4-(4-Carboxybutyryl)-1-β-D-arabinofuranosylcytosine and Its Conjugate with Poly-L-lysine or Decylenediamine-dextran T70
Novel Preparation of Decylenediamine-dextran T70 and Inhibitory Activity toward Dihydrofolate Reductase of Decylenediamine-dextran T70-Methotrexate Conjugate(Pharmaceutical)
Preparation of Dextran T70-Methotrexate Conjugate and Dextran T70-Mycophenolic Acid Conjugate, and in Vitro Effect of Dextran T70-Methotrexate on Dihydrofolate Reductase
Particle Size Distribution Affects the Human Bioavailability of Phenytoin
Dissolution and Bioavailability of Phenytoin in Phenytoin-Polyvinylpyrrolidone-Sodium Deoxycholate Coprecipitate
Particle Size Dependency of Dissolution Rate and Human Bioavailability of Phenytoin in Powders and Phenytoin-Polyethylene Glycol Solid Dispersions
Sustained-Release Formulation of Buformin Hydrochloride
Analysis of Factors affecting Dissolution of Digoxin from Tablets
Physicochemical Properties and Stability in the Acidic Solution of a New Macrolide Antibiotic, Clarithromycin, in Comparison with Erthyomycin
Development of a Tablet Excipient from Bagasse(Pharmaceutical)
Kinetic Approach to Determine the Generation Rate of Available Surface Area during the Dissolution Process
Effect of Compression Pressure and Formulation on the Available Surface Area of Flufenamic Acid in Tablets
Influence of Wetting Factors on the Dissolution Behavior of Flufenamic Acid
Dissolution Profiles of Nalidixic Acid Powders Having Weibull Particle Size Distribution
Prediction of Available Surface Area of Powdered Particles of Flufenamic Acid in Tablets
Kinetics of Hydrolysis of Oxazolam in Aqueous Solution
Properties of Cyclodextrin Polymer as a Tabletting Aid
The Acid-Base Equilibrium Reaction of Benzodiazepinooxazoles
Absorption of Salicylic Acid through the Oral Mucous Membrane of Hamster Cheek Pouch
Permeation of Drug through a Model Membrane consisting of Millipore Filter with Oil
Complexes of Polyethylene Oxide with Guanidine Hydrochloride and with Phenobarbital. Preliminary Structural Studies by Differential Scanning Calorimetry, Polarized Infrared Spectroscopy and X-Ray Fiber Photography

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