Supramolecular magnetolipogels: a co-assembly strategy for on-demand drug release

Abstract

In this work, magnetic liposomes, both solid and aqueous, were loaded with a model drug and combined with dehydropeptide-based hydrogels. The encapsulated drug distributed between hydrogel fibres and magnetoliposomes lipid bilayer, which was demonstrated to be independent of the magnetoliposome’s nanoarchitecture, resulting in an attenuated drug release from the magnetolipogels compared to hydrogels.