Synthesis and biological evaluation of novel β-cyclodextrin-fluvastatin conjugates

Drugs that may regulate lipid metabolism and lower cholesterol, such as statins (drugs that reduce de novo cholesterol synthesis) or cyclodextrins (that promote cholesterol removal), are currently investigated as potential therapeutics for neuronal disorders like Alzheimer's and Niemann Pick type C disease. Fluvastatin is a member of the statin class widely used in preventing heart diseases as it lowers cholesterol and other lipids. beta-cyclodextrin derivatives can also act as cholesterol scavengers to promote cholesterol efflux from cells to extracellular acceptors. This context has inspired us to synthesize and characterize two new cyclodextrin-fluvastatin conjugates representing the first example of cyclodextrin conjugates of statins. We synthesized 3- and 6-functionalized beta-cyclodextrin with fluvastatin through an amide bond. We studied the stability, cytotoxicity and protective activity in cells of the new derivatives. We observed that the Fluvastatin cyclodextrin conjugates are stable in plasma and mouse brain homogenates. Moreover, we found that the fluvastain derivatives are well tolerated by cultured neuron cells, and they completely rescue from cell death induced by A beta oligomers. Overall, the fluvastain derivatives have potential as therapeutic agents in diseases related to cholesterol dyshomeostasis.

Automated summary

Researchers have synthesized and characterized two new cyclodextrin-fluvastatin conjugates, the first example of cyclodextrin conjugates of statins. Experimental results suggest that these conjugates are stable in cells and can protect cells to some extent from cell death induced by Aβ oligomers.