Origin of non-linearity in phase solubility: solubilisation by cyclodextrin beyond stoichiometric complexation
Author:
Affiliation:
1. York Structural Biology Laboratory
2. Department of Chemistry
3. University of York
4. York YO10 5DD
5. UK
6. Division of Chemical Engineering
7. Graduate School of Engineering Science
8. Osaka University
9. Toyonaka
10. Japan
Abstract
The low solubility of drugs, which poses a serious problem in drug development, can in part be overcome by the use of cyclodextrins (CDs) and their derivatives.
Funder
Japan Society for the Promotion of Science
Ministry of Education, Culture, Sports, Science, and Technology
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2016/CP/C6CP01582D
Reference58 articles.
1. Strategies to Address Low Drug Solubility in Discovery and Development
2. Improvement in solubility and dissolution rate of flavonoids by complexation with β-cyclodextrin
3. Study of the solubility, antioxidant activity and structure of inclusion complex of vanillin with β-cyclodextrin
4. Solubility and stability of taxol: effects of buffers and cyclodextrins
5. Solubility Enhancement of Flavonols in the Inclusion Complex with Thioether-bridged Dimeric β-Cyclodextrins
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