Molecular
adsorption to the nanoparticle surface may switch the
colloidal interactions from repulsive to attractive and promote nanoparticle
agglomeration. If the nanoparticles are magnetic, then their agglomerates
exhibit a much stronger response to external magnetic fields than
individual nanoparticles. Coupling between adsorption, agglomeration,
and magnetism allows a synergy between the high specific area of nanoparticles
(∼100 m2/g) and their easy guidance or separation
by magnetic fields. This yet poorly explored concept is believed to
overcome severe restrictions for several biomedical applications of
magnetic nanoparticles related to their poor magnetic remote control.
In this paper, we test this concept using curcumin (CUR) binding (adsorption)
to β-cyclodextrin (βCD)-coated iron oxide nanoparticles
(IONP). CUR adsorption is governed by host–guest hydrophobic
interactions with βCD through the formation of 1:1 and, possibly,
2:1 βCD:CUR inclusion complexes on the IONP surface. A 2:1 stoichiometry
is supposed to promote IONP primary agglomeration, facilitating the
formation of the secondary needle-like agglomerates under external
magnetic fields and their magneto-microfluidic separation. The efficiency
of these field-induced processes increases with CUR concentration
and βCD surface density, while their relatively short timescale
(<5 min) is compatible with magnetic drug delivery application.