小田切優樹 | Faculty of Pharmaceutical Science, Kumamoto University

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著作論文

Evaluation of Quinaldine Red as a Fluorescent Probe for Studies of Drug-α_1-Acid Glycoprotein Interaction
Characterization of Drug Binding Sites on α_1-Acid Glycoprotein
Characterization of Binding Sites for Sulfadimethoxine and Its Major Metaboite, N^4-Acetylsulfadimethoxine, on Human and Rabbit Serum Albumin
Analysis of Interfacial Transfer and Absorption Behavior of Drugs Following Dissolution from β-Cyclodextrin Complexes
ALLEVIATION OF PROCHLORPERAZINE-INDUCED PRIMARY IRRITATION OF SKIN BY CYCLODEXTRIN COMPLEXATION
Inclusion Mode of Flurbiprofen with β-Cyclodextrin and Heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, and Improvements of Some Pharmaceutical Properties of Flurbiprofen by Complexation
Characterization of High Affinity Binding Sites of Non-steroidal Anti-inflammatory Drugs with Respect to Site-Specific Probes on Human Serum Albumin
Contribution of N^4-Acetylsulfadimethoxine to the Interaction of Sulfadimethoxine with Ketoprofen in Rabbits(Pharmaceutical)
Characterization of Region Ic in Site I on Human Serum Albumin. Microenvironmental Analysis Using Fluorescence Spectroscopy
Mechanism of Inhibition of Carbonyl Reductase from Rabbit Kidney by Phenylbutazone
Influence of Aging on Acetohexamide Reductase Activities in Liver Microsomes and Cytosol of Male Rats
Kinetics of Befunolol Reductase from Rabbit Liver
Purification and Characterization of Befunolol Reductase from Rabbit Liver
Further Studies on Reductive Metabolism of Acetohexamide in Heart
Effect of pH Small Inorganic Ions on Binding of Sulfadimethoxine and Sulfaphenazole to Human Serum Albumin Measured by Circular Dichroism
Study on the Binding of Dicumarol to α_1-Acid Glycoprotein Using Circular Dichroism Spectroscopy
7-Alkylaminocoumarin-4-acetic Acids as Fluorescent Probe for Studies of Drug-Binding Sites on Human Serum Albumin
Interaction of the Fluorescent Probe 7-Anilino-4-methylcoumarin-3-acetic Acid with α-Globulin
Interaction between Methacycline and Human Serum Albumin
X-RAY CRYSTALLOGRAPHIC DETERMINATION OF THE ABSOLUTE CONFIGURATION OF (+) FLURBIPROFEN UTILIZING β-CYCLODEXTRIN COMPLEXATION
CRYSTAL AND MOLECULAR STRUCTURE OF 2 : 2 (±) FLURBIPROFEN-β-CYCLODEXTRIN COMPLEX
Effect of Oral Multiple-Dose Administration of Anti-inflammatory Flurbiprofen Chimera Drug on Gastric Lesion, Other Toxicities and Disposition Kinetics
Enhancement of Oral Bioavailability of Spironolactone by β- and γ-Cyclodextrin Complexations
Determination of Barnidipine in Human Serum and Dog Plasma by HPLC with Electrochemical Detection
Improvement of Dissolution Characteristics and Chemical Stability of Prostaglandin E_1 by γ-Cyclodextrin Complexation
Controlled-Release Preparation of Indomethacin Using Calcium Alginate Gel
Preparation and Evaluation of a Controlled-Release Formulation of Nifedipine Using Alginate Gel Beads
Stereoselective Disposition of Pranoprofen, a Nonsteroidal Antiinflammatory Drug, in Rabbits
Electrochemical Oxidation of Chlorpromazine-Cyclodextrin Inclusion Complex
Studies on Metabolic Reduction of Befunolol in Rabbit Liver and Kidney
Characterization of Binding Site of Uremic Toxins on Human Serum Albumin
Evaluation of Low-Molecular Gelatin as a Pharmaceutical Additive for Rapidly Absorbed Oral Dosage Formulation
Effect of Simultaneous Administration of Drugs on Absorption and Excretion. XVIII. Differential Effects of Oral and Rectal Administration of Chloral Hydrate on the Gastrointestinal Absorption of Sulfisoxazole in Rabbits
Effects of β- and γ-Cyclodextrins on Release of Betamethasone from Ointment Bases
Syntheses and Properties of 3-Hydroxy-4,6-dimethylpyrrolo [3,2-d] pyrimidine-5,7 (4H, 6H)-dione (9-Hydroxy-9-deazatheophylline) Derivatives
New Fluorescence Probes for Drug-Albumin Intereaction Studies
Inclusion Complexation of Barbiturates with β-Cyclodextrin in Aqueous Solution. I. Spectroscopic Study on the Mode of Interaction
Enhancement of Dissolution Rates of Several Drugs by Low-Molecular Chitosan and Alginate
METABOLIC REDUCTION OF ACETOHEXAMIDE BY RABBIT TISSUES
Enhancement of the Dissolution Rates of Poorly Water-Soluble Drugs by Water-Soluble Gelatin
In Vitro and in Situ Models for the Prediction of in Vivo Absorption Behavior of Sulfonamides Following Dissolution
Effects of Cyclodextrins on the Hydrolysis of Prostacyclin and Its Methyl Ester in Aqueous Solution
Interaction of Barbituric Acid Derivatives with Chloral Hydrate

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