Kiwada H | Faculty Of Pharmaceutical Sciences University Of Tokushima

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著作論文

Studies on the Uptake Mechanism of Liposomes by Perfused Rat Liver. I. : An Investigation of Effluent Profiles with Perfusate Containing No Blood Component
Application of Synthetic Alkyl Glycoside Vesicles as Drug Carriers. III. : Plasma Components Affecting Stability of the Vesicles
Application of Synthetic Liposomes Based on Acyl Amino Acids or Acyl Peptides as Drug Carriers. I. Their Preparation and Transport of Glutathione into the Liver(Pharmaceutical)
Studies on the Uptake Mechanism of Liposomes by Perfused Rat Liver. II. : An Indispensable Factor for Liver Uptake in Serum(Pharmaceutical)
Feasibility of Magnetic Liposomes as a Targeting Device for Drugs
Effects of Dose and Vesicle Size on the Pharmacokinetics of Liposomes
Uptake of Liposomes Surface-Modified with Glycyrrhizin by Primary Cultured Rat Hepatocytes
Targeting of Liposomes Surface-Modified with Glycyrrhizin to the Liver. I. Preparation and Biological Disposition
Effect of Cetylmannoside Modification on the Alternative Complement Pathway Activation by Liposomes in Rat Serum
Tissue Distribution and Pharmacokinetic Evaluation of the Targeting Efficiency of Synthetic Alkyl Glycoside Vesicles
Application of Synthetic Alkyl Glycoside Vesicles as Drug Carriers. I. Preparation and Physical Properties
Correlations between in Vivo and in Vitro Dissolution Rates of (α-Bromoisovaleryl) urea Polymorphs
Pharmacokinetic Study on the Polymorphs of (α-Bromoisovaleryl) urea in the Rat
The Determination of (α-Bromoisovaleryl) urea in Plasma and the Bioavailabilities of Its Polymorphic Forms in the Rat
The Dissolution Properties and Physico-chemical Properties of Polymorphic Forms of (α-Bromoisovaleryl) urea
The Preparation and Properties of a New Polymorphic Form of (α-Bromoisovaleryl) urea
The Pharmacokinetic Study on the Fate of 8-Hydroxyquinoline in Rat
A New Numerical Calculation Method for Deconvolution in Linear Compartment Analysis of Pharmacokinetics
Effect of Vesicle Size on in Vivo Release of Daunorubicin from Hydrogenated Egg Phosphatidylcholine-Based Liposomes into Blood Circulation

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