Abstract
A new strategy for design and development of a magnetic “smart” drug delivery system (DDS) based on β-cyclodextrin (β-CD) and poly(2-ethyl-2-oxazoline) (PEtOx) was reported. For this purpose, a β-CD-(I)7 was acetylated, and then EtOx monomer was grafted onto the acetylated β-CD-(I)7 through cationic ring-opening polymerization followed by simultaneous crosslinking with amine-end capped Fe3O4 nanoparticles (Fe3O4-NH2 NPs) and cystamine to produce a β-CD-g-(PEtOx)7/Fe3O4 as a reduction- and pH-responsive magnetic DDS. The developed magnetic nanohydrogel was loaded with doxorubicin hydrochloride (Dox), and its drug loading and encapsulation efficiencies, as well as its pH- and reduction-triggered drug release behaviors were investigated. The anticancer activity of the formulated β-CD-g-(PEtOx)7/Fe3O4-Dox was investigated against MCF7 cells. According to the results, the formulated β-CD-g-(PEtOx)7/Fe3O4-Dox can be considered as an efficient and “smart” DDS for cancer therapy and diagnosis due to its high drug loading value (∼ 74 %), slow and stimuli-triggered drug release behavior, and acceptable magnetic properties.
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