Abstract
Nanosponges were prepared from β-cyclodextrins as nanoporous materials for possible use as carriers for drug delivery. The structure of β-cyclodextrin-based nanosponges was principally investigated by FT-IR, DSC and RX analyses. Sizes, morphology and toxicity were also examined. The capacity of the nanosponges to incorporate molecules within their structure was evaluated using drugs with different structures and solubilities. The nanosponges were found capable of carrying both lipophilic and hydrophilic drugs and of improving the solubility of poorly water-soluble molecules.
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Acknowledgements
The authors thank Dr. Loredana Serpe for the cytotoxicity experiments, Prof. Dino Aquilano for the RX analysis and Sea-Marconi Technologies for their generous grant.
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Cavalli, R., Trotta, F. & Tumiatti, W. Cyclodextrin-based Nanosponges for Drug Delivery. J Incl Phenom Macrocycl Chem 56, 209–213 (2006). https://doi.org/10.1007/s10847-006-9085-2
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DOI: https://doi.org/10.1007/s10847-006-9085-2