PubMed · 16711394
[Interactions in solution between cyclodextrins and statins].
Abstract
Cyclodextrins (CDs) are cyclic oligosaccharides, capable of forming inclusion complexes with hydrophobic molecules in aqueous solution and therefore, of improving the bioavailability of many drugs. They are biocompatible with living cells and do not cause toxic side effects. In this study, interactions in aqueous solutions between chemically different CDs and lovastatin and simvastatin, respectively, were investigated. It was found that the solubility of both statins can be considerably increased by the CD derivatives. The influence of the chemical structure of CD and of the temperature and pH on the solubility of the statin derivatives is described. Possible ways of increasing the solubility of these cholesterol-lowering drugs and their utilization in practice are also outlined.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
András Süle, Lajos Szente, Ferenc Csempesz. 2005. [Interactions in solution between cyclodextrins and statins].. https://pubmed.ncbi.nlm.nih.gov/16711394/
Cite the original work for its findings. Save a collection to share your selection of sources.