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Atsushi Shoji

Researcher at Tokyo University of Pharmacy and Life Sciences

Publications -  42
Citations -  449

Atsushi Shoji is an academic researcher from Tokyo University of Pharmacy and Life Sciences. The author has contributed to research in topics: Chemistry & Lipid bilayer. The author has an hindex of 10, co-authored 35 publications receiving 371 citations. Previous affiliations of Atsushi Shoji include Nihon University & University of Tokyo.

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Analytical separation of tea catechins and food-related polyphenols by high-speed counter-current chromatography

TL;DR: High-speed counter-current chromatography (HSCCC) using the type-J coil planet centrifuge was applied to compositional analysis of tea catechins and separation of other food-related polyphenols, providing useful information about the hydrophobic diversity of these bioactivepolyphenols present in various types of teas and food products.
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Retention behavior of oligomeric proanthocyanidins in hydrophilic interaction chromatography

TL;DR: Data reveal that two effects, i.e. hydrogen bonding between the carbamoyl terminal on the column and the hydroxyl group of solute oligomer and hydrophilicity based on the high-order structure of oligomeric PAs, corporately contribute to the separation, but the hydrogen bonding effect is predominant in the authors' HILIC separation mode.
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Determination of Log Po/w for Catechins and Their Isomers, Oligomers, and Other Organic Compounds by Stationary Phase Controlled High‐Speed Countercurrent Chromatography

TL;DR: The stationary phase volume in the CCC column was effectively controlled under hydrodynamic equilibrium system, and the linear relationship (correlation coefficient value, r=0.993) was observed between log P o/w values obtained by the shake-flask method and those values by the HSCCC method as mentioned in this paper.
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High-throughput determination of octanol/water partition coefficients using a shake-flask method and novel two-phase solvent system

TL;DR: Log D values for highly polar compounds for which no log D values have been reported, such as amino acids, peptides, proteins, nucleosides, and nucleotides, can be estimated indirectly from the narrow range of log K(AN) values determined using the present method.
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A Fluorinated Carbanionic Substituent for Improving Water Solubility and Lipophilicity of Fluorescent Dyes.

TL;DR: This work clearly demonstrates that the fluorinated, highly stabilised carbanionic substituent is a new option for controlling the macroscopic property of chemical materials.