Hyperthermia of superparamagnetic nanoparticles driven
by Néel
relaxation in an alternating magnetic field (AMF) has been studied
in biomedical areas; however, Brownian motion, induced by another
magnetic relaxation mechanism, has not been explored extensively despite
its potential in intracellular mechanoresponsive applications. We
investigated whether superparamagnetic cage-shaped iron oxide nanoparticles
(IO-nanocages), previously demonstrated to carry payloads inside their
cavities for drug delivery, can generate Brownian motion by tuning
the nanoparticle size at 335 kHz AMF frequency. The motivation of
this work is to examine the magnetically driven Brownian motion for
the delivery of nanoparticles allowing escape from endosomes before
digestion in lysosomes and efficient delivery of siRNA cargoes to
the cytoplasm. Superconducting quantum interference device (SQUID)
measurements reveal the nanocage size dependence of Brownian relaxation,
and a magnetic Brownian motion of 20 nm IO-nanocages improved the
efficiency of siRNA delivery while endosomal membranes were observed
to be compromised to release IO-nanocages in AMFs during the delivery
process.