In this study, we
present a thermoresponsive thin hydrogel
layer
based on poly(N-isopropylacrylamide), functionalized
with β-cyclodextrin groups (p(NIPA-βCD)), as a novel electrochemically
controlled release system. This thin hydrogel layer was synthesized
and simultaneously attached to the surface of a Au quartz crystal
microbalance (QCM) electrode using electrochemically induced free
radical polymerization. The process was induced and monitored using
cyclic voltammetry and a quartz crystal microbalance with dissipation
monitoring (QCM-D), respectively. The properties of the thin layer
were investigated by using QCM-D and scanning electron microscopy
(SEM). The incorporation of β-cyclodextrin moieties within the
polymer network allowed rhodamine B dye modified with ferrocene (RdFc),
serving as a model metallodrug, to accumulate in the p(NIPA-βCD)
layer through host–guest inclusion complex formation. The redox
properties of the electroactive p(NIPA-βCD/RdFc) layer and the
dissociation of the host–guest complex triggered by changes
in the oxidation state of the ferrocene groups were investigated.
It was found that oxidation of the ferrocene moieties led to the release
of RdFc. It was crucial to achieve precise control over the release
of RdFc by applying the appropriate electrochemical signal, specifically,
by applying the appropriate potential to the electrode. Importantly,
the electrochemically controlled RdFc release process was performed
at a temperature similar to that of the human body and monitored using
a spectrofluorimetric technique. The presented system appears to be
particularly suitable for transdermal delivery and delivery from intrabody
implants.