4 research outputs found
Highly Cross-Linked and Biocompatible Polyphosphazene-Coated Superparamagnetic Fe<sub>3</sub>O<sub>4</sub> Nanoparticles for Magnetic Resonance Imaging
Highly
cross-linked and biocompatible poly(cyclotriphosphazene-<i>co</i>-4,4′-sulfonyldiphenol) (PZS) were used to directly
coat hydrophilic superparamagnetic Fe<sub>3</sub>O<sub>4</sub> nanoparticles
by a facile but effective one-pot polycondensation. The obtained core–shell
Fe<sub>3</sub>O<sub>4</sub>@PZS nanohybrids were characterized by
transmission electron microscopy (TEM), scanning electron microscopy
(SEM), Fourier-transform infrared (FTIR) and X-ray diffraction spectra.
Interesting, the size and T<sub>2</sub> relaxivity of Fe<sub>3</sub>O<sub>4</sub>@PZS increased with increasing the mass ratio of Fe<sub>3</sub>O<sub>4</sub> to PZS. All these nanohybrids could be internalized
by HeLa cells but show negligible cytotoxicity. The PZS layer slowly
degraded into less dangerous forms such as 4,4′-sulfonyldiphenol,
phosphate and ammonia at neutral or acid atmosphere. Considering their
excellent water dispersibility, colloidal and chemical stability,
magnetic manipulation, and magnetic resonance imaging (MRI) properties,
Fe<sub>3</sub>O<sub>4</sub>@PZS nanohybrids have great potential in
MRI diagnosis of cancer
Facile Synthesis of Superparamagnetic Fe<sub>3</sub>O<sub>4</sub>@polyphosphazene@Au Shells for Magnetic Resonance Imaging and Photothermal Therapy
Multifunctional nanoparticles were
prepared by directly welding superparamagnetic Fe<sub>3</sub>O<sub>4</sub> nanoparticles and Au shells together with highly cross-linked
polyphosphazene as “glue” in a facile but effective
way. The as-prepared particles can simultaneously take advantages
of both magnetization of Fe<sub>3</sub>O<sub>4</sub> core for magnetic
resonance imaging diagnosis and strong near-infrared absorption of
Au nanoshell for photothermal therapy
Golden Single-Walled Carbon Nanotubes Prepared Using Double Layer Polysaccharides Bridge for Photothermal Therapy
Golden single-walled carbon nanotubes
(SWNTs) were prepared by growing gold nanoparticles onto the bilayer
polysaccharide functionalized SWNTs. The layer-by-layer self-assembly
of sodium alginate and chitosan on SWNTs provided an ideal surface
with high density of active metal-binding groups such as amino and
carboxylic acid groups, and then an approach of seed growth was adopted
to facilitate the formation of gold nanoparticles coated SWNTs. The
resulting golden SWNT hybrids have good water dispersibility and biocompatibility
and tend to enter cancer cells. Interestingly, they have an enhanced
NIR absorption and effectively transfer NIR laser into heat. The material
can quickly cause localized hyperthermia, resulting in rapid cell
death, and therefore appears to act as a highly effective photothermal
converter for cancer ablation
Dual-Responsive Controlled Drug Delivery Based on Ionically Assembled Nanoparticles
Ionically assembled nanoparticles (INPs) have been formed
from
poly(ionic liquid-<i>co</i>-<i>N</i>-isopropylacrylamide)
with deoxycholic acid through electrostatic interaction. The structure
and properties of the INPs were investigated by using <sup>1</sup>H NMR, Fourier transform infrared (FTIR), transmission electron microscopy
(TEM), dynamic light scattering (DLS), and so on. Due to pH-responsive
deoxycholic acid (p<i>K</i><sub>a</sub> = 6.2) and thermo
responsive <i>N</i>-isopropylacrylamide included in the
ionic complex, the INPs exhibit highly pH and thermal dual-responsive
properties. The potential practical applications as drug delivery
carriers were demonstrated using doxorubicin (DOX) as a model drug.
With a lower pH (pH 5.2) and higher temperature (above 37 °C),
structural collapse of the INPs occurred as well as release of DOX
owing to protonated DA departure from the INPs and a lower LCST (lower
critical solution temperature) at the pathological conditions. The
result shows that 80% of DOX molecules were released from INPs within
48 h at pH 5.2, 43 °C, but only 30% of the drug was released
within 48 h at 37 °C and pH 7.4. Moreover, drug-loaded INPs exhibit
an inhibitory effect on cell growth