Increasing effectiveness of cancer
therapeutics requires a multipronged
approach. Delivery of controlled hyperthermia in the ranges of 43
to 45 °C on site aided by superparamagnetic particles ensures
cell death via the apoptosis pathway.We demonstrated the use of iron-oxide
embedded hydroxyapatite (HAIO) superparamagnetic particles for delivery
of controlled hyperthermia and contrast enhancement in MRI. To determine
optimal hyperthermia delivery, we used 5 and 10 mg/mL concentrations
of HAIO on various magnetic fields in alternating magnetic field (AMF)
study. Time–temperature profile and specific loss power (SLP)
data revealed that HAIO delivered precisely controlled temperature
in contrast to superparamagnetic iron oxide nanoparticles (SPIONs).
Earlier studies had demonstrated that HAIO concentrations of 0.5 to
3 mg/mL are cytocompatible. Exposure of HeLa cells to HAIO at a concentration
of 2 mg/mL and applied field of 33.8 mT for a period of 30 min resulted
in apoptosis induction in 75% of population. Significant cellular
disruption was affirmed via FACS, ESEM and cLSM techniques. An aqueous
phantom study and in vitro cell culture study evaluation
indicated relaxivity of 50.92 mM–1 s–1 and good pixel intensity variation in MRI. The current study assesses
the potential of HAIO to deliver controlled hyperthermia and act as
a negative MRI contrast agent. Repeated experiments have confirmed
enhanced utility of the technique in the burgeoning field of theranostics.
Herein
we have reported a new magneto-fluorescent nanogel built
on photoluminescent comacromer [PEG-maleic acid-glycine], N,N-dimethyl aminoethylmethacrylate and
citrate-capped superparamagnetic iron oxide nanoparticles (SPION).
The nanogel was found to have core–shell morphology (SPION
core and PEG shell) with particle size around 80 nm. The cytocompatibility
of the synthesized nanogel was studied using MTT, live/dead assays,
and flow cytometry. The cellular uptake of the nanogel on cervical
cancer cell line Hela evaluated through Prussian blue staining and
fluorescence microscopy has revealed good cancer cell imaging capability.
Magnetic hyperthermia experiments have shown that the synthesized
nanogel caused the lysis of cancer cells. The fluorescence bioimaging
capability of the nanogel in the murine model has shown good near
IR imaging capability. Overall, the reported results suggest that
the magneto-fluorescent nanogel shows promising future potential for
cancer theranostic applications.
Surface modification of superparamagnetic Fe3O4 nanoparticles using polymers (polyaniline/polypyrrole) was done by radio frequency (r.f.) plasma polymerization technique and characterized by XRD, TEM, TG/DTA and VSM. Surface-passivated Fe3O4 nanoparticles with polymers were having spherical/rod-shaped structures with superparamagnetic properties. Broad visible photoluminescence emission bands were observed at 445 and 580 nm for polyaniline-coated Fe3O4 and at 488 nm for polypyrrole-coated Fe3O4. These samples exhibit good fluorescence emissions with L929 cellular assay and were non-toxic. Magnetic hyperthermia response of Fe3O4 and polymer (polyaniline/polypyrrole)-coated Fe3O4 was evaluated and all the samples exhibit hyperthermia activity in the range of 42–45 °C. Specific loss power (SLP) values of polyaniline and polypyrrole-coated Fe3O4 nanoparticles (5 and 10 mg/ml) exhibit a controlled heat generation with an increase in the magnetic field.
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