Abstract
The complex forming ability of a water-soluble ß-cyclodextrin epichlorohydrin polymer (CDPS) and its different molecular weight fractions was studied and compared with the complexing properties of ß-cyclodextrin (ßCD) and dimethyl-ßCD (DM-ßCD). CDPS was separated into two main fractions. CDPS and its fractions formed well soluble inclusion compounds with the studied drugs. The low molecular weight fraction formed rather stable complexes with small guest molecules, the high molecular weight fraction was found to be more efficient in binding larger substrates. Structural studies of furosemide-CD complexes were attempted by NMR spectroscopy.
Presented at the Fourth International Symposium on Inclusion Phenomena and the Third International Symposium on Cyclodextrins, Lancaster, U.K., 20–25 July 1986.
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© 1987 D. Reidel Publishing Company
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Szemán, J., Fenyvesi, E., Szejtli, J., Ueda, H., Machida, Y., Nagai, T. (1987). Water Soluble Cyclodextrin Polymers: Their Interaction with Drugs. In: Atwood, J.L., Davies, J.E.D. (eds) Inclusion Phenomena in Inorganic, Organic, and Organometallic Hosts. Advances in Inclusion Science, vol 4. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-3987-5_55
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DOI: https://doi.org/10.1007/978-94-009-3987-5_55
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