What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Enzyme
- Biochemistry
The scientist’s investigation covers issues in Cyclodextrin, Chromatography, Solubility, Biochemistry and Drug carrier.
His Cyclodextrin study incorporates themes from Dosage form, Combinatorial chemistry, Stereochemistry and Drug.
His biological study spans a wide range of topics, including Cyclodextrin Derivatives and 2 hydroxypropyl β cyclodextrin.
His Chromatography study integrates concerns from other disciplines, such as Oral administration, Pharmacology and Ion exchange.
His research integrates issues of Nuclear chemistry, Bioavailability, Aqueous solution and Dissolution in his study of Solubility.
His Biochemistry research is multidisciplinary, incorporating elements of Biophysics and Transfection.
His most cited work include:
- Cyclodextrin Drug Carrier Systems. (1797 citations)
- Pharmaceutical applications of cyclodextrins. III. Toxicological issues and safety evaluation (716 citations)
- Differential effects of α‐, β‐ and γ‐cyclodextrins on human erythrocytes (510 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Cyclodextrin, Chromatography, Solubility, Organic chemistry and Pharmacology.
The study incorporates disciplines such as Dosage form, Crystallography, Stereochemistry and Aqueous solution in addition to Cyclodextrin.
His studies deal with areas such as Drug carrier and Active ingredient as well as Dosage form.
The Moiety and Steric effects research he does as part of his general Stereochemistry study is frequently linked to other disciplines of science, such as Conjugate, therefore creating a link between diverse domains of science.
His study on Chromatography also encompasses disciplines like
- Bioavailability which intersects with area such as Oral administration, Absorption and Intestinal absorption,
- Drug which connect with Combinatorial chemistry.
His work in Solubility covers topics such as Dissolution which are related to areas like Nuclear chemistry and Absorption.
He most often published in these fields:
- Cyclodextrin (53.18%)
- Chromatography (24.17%)
- Solubility (20.36%)
What were the highlights of his more recent work (between 2009-2020)?
- Cyclodextrin (53.18%)
- Chromatography (24.17%)
- Nuclear chemistry (12.72%)
In recent papers he was focusing on the following fields of study:
Kaneto Uekama spends much of his time researching Cyclodextrin, Chromatography, Nuclear chemistry, Conjugate and Endocrinology.
The various areas that Kaneto Uekama examines in his Cyclodextrin study include Dosage form, Stereochemistry, Drug carrier, Aqueous solution and Solubility.
His Aqueous solution research is multidisciplinary, incorporating perspectives in Crystallography and Inclusion compound.
His study in Chromatography is interdisciplinary in nature, drawing from both Ether, Bioavailability, Famotidine and Active ingredient.
His Bioavailability study combines topics in areas such as Absorption and Beta-Cyclodextrins.
His work deals with themes such as Reactive oxygen species, Benzyl acetate and Dissolution, which intersect with Nuclear chemistry.
Between 2009 and 2020, his most popular works were:
- In Vitro and In Vivo gene delivery mediated by Lactosylated Dendrimer/α-Cyclodextrin Conjugates (G2) into Hepatocytes (73 citations)
- Inhibitory effect of 2-hydroxypropyl-beta-cyclodextrin on crystal-growth of nifedipine during storage: superior dissolution and oral bioavailability compared with polyvinylpyrrolidone K-30. (69 citations)
- In-vitro Evaluation of Biphenylyl Acetic Acid-β-Cyclodextrin Conjugates as Colon-targeting Prodrugs: Drug Release Behaviour in Rat Biological Media (51 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Enzyme
- Biochemistry
Cyclodextrin, Dosage form, Pharmacology, In vitro and Chromatography are his primary areas of study.
His Cyclodextrin research integrates issues from Pharmacokinetics, Drug carrier, Active ingredient and Solubility.
Kaneto Uekama combines subjects such as Nifedipine, Nuclear chemistry, Stereochemistry, Beta-Cyclodextrins and Azone with his study of Dosage form.
His Pharmacology study combines topics from a wide range of disciplines, such as Prostaglandin E1, Fatty alcohol and Hairless.
The concepts of his In vitro study are interwoven with issues in Dendrimer and Stability constants of complexes.
His research investigates the connection with Chromatography and areas like Famotidine which intersect with concerns in Chemical stability.
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