Iron
oxide nanorods are considered to be very promising platforms
for biomedical applications, such as magnetic hyperthermia, magnetic
resonance imaging, or immunoassays based on magnetooptical effects.
However, their efficient colloidal stabilization is challenging, and
colloidal aggregation could lead to the total loss of their performance.
This work is focused on the synthesis and colloidal stabilization
of iron oxide nanorods of an average length and diameter, L × d = 31 × 6 nm, synthesized
by the hydrolysis of iron(III) salt, followed by reduction of the
obtained akaganeite to iron oxide in a microwave reactor. Synthesized
nanorods exhibited a weak ferrimagnetic behavior with remnant magnetization M
R ∼ 3 emu/g and saturation magnetization M
S ∼ 13 emu/g. The nanorods were dispersed
in water after adsorption on their surface of three different polymers:
linear bisphosphonate–poly(ethylene glycol) (PEG) molecules
(denoted as OPT), polymethacrylate backbone/PEG side chains comb polymer
(denoted as PCP; with PEG brushes both extended toward the solvent
and having molecular weight M
w ∼
3000 g/mol), and polyacrylic sodium salt (PAA; M
w ∼ 15000 g/mol). Experiments and theoretical evaluation
of the interaction potential show that increasing the polymer grafting
density on the nanorod surface as well as decreasing the concentration
of a nonadsorbed polymer improve the nanorod colloidal stability.
The best stability is obtained on an optimal range of weight ratio
of the added polymer to the nanorods between 0.5 and 1.6 mg/mg. A
higher grafting density reached with a OPT polymer with a bisphosphonate
terminal group (2–4 nm–2) allows much better
stability than using multiple adsorption with PCP (0.2–0.4
nm–2) or PAA. Even though the nanorods are still
subject to some aggregation (effective hydrodynamic diameter ∼60
nm, compared to their TEM size of L × d = 31 × 6 nm), significant progress toward understanding
their colloidal stability was achieved.