Influence of Controlled Dipolar Interaction for Polymer-Coated Gd-Doped Magnetite Nanoparticles toward Magnetic Hyperthermia Application.

To maximize heat release from immobilized nanoparticles (NPs), a detailed understanding of the controlled dipolar interaction is essential for challenging magnetic hyperthermia (MH) therapies. To design optimal MH experiments, it is necessary to precisely determine magnetic states impacted by the inevitable concurrence of magnetic interactions under a common experimental form. In this work, we describe how the presence of dipolar interaction significantly alters the heating mechanism of host materials when NPs are embedded in them for MH applications. The concentration of the NPs and the intensity of their interaction can profoundly impact the amplitude and shape of the heating curves of the host material. The heating capability of interacting NPs might be enhanced or diminished, depending on their concentration within the host material. We propose chitosan- and dextran-coated Gd-doped Fe3O4 NPs directing dipole interactions effective for the linear regime to enlighten the pragmatic trends. The outcomes of our study may have substantial implications for cancer therapy and could inspire novel approaches for maximizing the effectiveness of MH.

An exhaustive scrutiny to amplify the heating prospects by devising a core@shell nanostructure for constructive magnetic hyperthermia applications.

An interfacial integration at the nanoscale domain through a core@shell (CS) nanostructure has constructively unbarred a wide dimension to researchers on biomedical applications, especially for magnetic fluid hyperthermia. Lately, the interconnection of the exchange bias effect (EBE) through the interface coupling to the magnetic heating efficiency has uttered its utmost prominence for researchers. Here, we delineate the ascendency of the heating ability through a coalescing assembly of mixed ferrite Co0.5Zn0.5 Fe2O4 (CZ) and soft magnetic material Fe3O4 (F), by devising a network of CoZnFe2O4@Fe3O4 (CZF) CS nanostructure. A hefty interface activity with validation of the EBE phenomenon is divulged through magnetic scrutiny for the CS sample. The magnetic nanoparticles heating response to applied magnetic field and frequency is discerned at three distinct fields, where the outcome prevailed to inflated specific loss power for CS CZF in distinction to bare F and CZ samples for all the assessments. Remarkably; a lofty intrinsic loss parameter is also perceived for the CS sample recorded to about 5.36 nHm2 g-1; which is another eccentric outcome that significantly labels the CS CZF sample as a potentially high heating competence agent. This comprehension accords to a finer perspective to meliorate the theranostic environment for hyperthermia applications.

A temperature-dependent switching of the exchange bias effect from negative to positive under a fixed intermediate cooling field.

An interfacial coupling origin of the exchange bias effect (EBE) is a novel phenomenon due to its technological and fundamental importance. We have carefully synthesized an Fe3O4@NiO (FO@N) core@shell (CS) nanostructure using a co-precipitation method, and the CS nanostructure formation was evident from the HRTEM analysis. The magnetic measurement study endorses unique characteristics on the temperature-dependent EBE switching from negative to the positive axis under a fixed cooling field. To the best of our knowledge, this unique characteristic behavior at a fixed cooling field has not been reported, particularly for the ferro/ferrimagnetic@antiferromagnetic FiM@AFM CS nanostructure. The switching is attributed to a formation of ferromagnetic (negative) or antiferromagnetic (positive) coupling arrangement at the magnetically disordered interface of two materials.

A comparative investigation of normal and inverted exchange bias effect for magnetic fluid hyperthermia applications.

Exchange bias (EB) of magnetic nanoparticles (MNPs) in the nanoscale regime has been extensively studied by researchers, which have opened up a novel approach in tuning the magnetic anisotropy properties of magnetic nanoparticles (MNPs) in prospective application of biomedical research such as magnetic hyperthermia. In this work, we report a comparative study on the effect of magnetic EB of normal and inverted core@shell (CS) nanostructures and its influence on the heating efficiency by synthesizing Antiferromagnetic (AFM) NiO (N) and Ferrimagnetic (FiM) Fe3O4 (F). The formation of CS structures for both systems is clearly authenticated by XRD and HRTEM analyses. The magnetic properties were extensively studied by Vibrating Sample Magnetometer (VSM). We reported that the inverted CS NiO@Fe3O4 (NF) MNPs have shown a greater EB owing to higher uncompensated spins at the interface of the AFM, in comparison to the normal CS Fe3O4@NiO (FN) MNPs. Both the CS systems have shown higher SAR values in comparison to the single-phased F owing to the EB coupling at the interface. However, the higher surface anisotropy of F shell with more EB field for NF enhanced the SAR value as compared to FN system. The EB coupling is hindered at higher concentrations of NF MNPs because of the enhanced dipolar interactions (agglomeration of nanoparticles). Both the CS systems reach to the hyperthermia temperature within 10 min. The cyto-compatibility analysis resulted in the excellent cell viability (> 75%) for 3 days in the presence of the synthesized NPs upto 1 mg/ml. These observations endorsed the suitability of CS nanoassemblies for magnetic fluid hyperthermia applications.