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Title: NMR spectroscopic study of cyclodextrin inclusion complexes with A-007 prodrugs. Author: Sagiraju S, Jursic BS. Journal: Carbohydr Res; 2008 May 19; 343(7):1180-90. PubMed ID: 18384761. Abstract: One- and two-dimensional NMR spectroscopy was used to demonstrate the formation of inclusion cyclodextrin complexes with several A-007 prodrugs. These complexes are comprised from the encapsulation of the two phenol moieties of the A-007 prodrugs within the cyclodextrin cavity. Considering the size of the two phenol moieties of the A-007 prodrugs compared to the sizes of alpha-, beta-, and gamma-cyclodextrin cavities, we observed complementary binding of the A-007 prodrug with only beta-cyclodextrin, which was also demonstrated spectroscopically. The beta-cyclodextrin inclusion complexes increased the prodrug solubility and modified the prodrug half-life in water. Therefore, beta-cyclodextrin inclusion complexes can be used as an essential form of A-007 prodrug delivery.[Abstract] [Full Text] [Related] [New Search]