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1. Multifunctional Superparamagnetic Copper Iron Oxide Nanoparticles for Synergistic Cancer Therapy via Magnetic Hyperthermia, Oxidative Stress and Immune Reprogramming

   https://doi.org/10.1002/adfm.202425286  

   Cai, Yuxin; Kang, Xuejia; Zhou, Lang; Wu, Shuai; Wang, Chuanyu; Wu, Siqi; Huang, Chunghui; Wang, Qi; Chang, Ya; Babu, R_Jayachandra; et al (March 2025, Advanced Functional Materials)

   Abstract Aggressive cancers, characterized by high metastatic potential and resistance to conventional therapies, present a significant challenge in oncology. Current treatments often fail to effectively target metastasis, recurrence, and the immunosuppressive tumor microenvironment, while causing significant off‐target toxicity. Here, superparamagnetic copper iron oxide nanoparticles (SCIONs) as a multifunctional platform that integrates magnetic hyperthermia therapy, immune modulation, and targeted chemotherapeutic delivery, aiming to provide a more comprehensive cancer treatment is presented. Specifically, SCIONs generate localized hyperthermia under an alternating magnetic field while delivering a copper‐based anticancer agent, resulting in a synergistic anticancer effect. The hyperthermia induced by SCIONs caused ER stress and ROS production, leading to significant tumor cell death, while the copper complex further enhanced oxidative stress, ferroptosis, and apoptosis. Beyond direct cytotoxicity, SCIONs disrupted the tumor microenvironment by inhibiting cancer‐associated fibroblasts, downregulating epithelial‐mesenchymal transition markers, and reducing cell migration and invasion, thereby limiting metastasis. Additionally, SCION‐based therapy reprogrammed the immune microenvironment by inducing immunogenic cell death and enhancing dendritic cell activation, resulting in increased CD8+ T cell infiltration and amplified antitumor immunity. This integrated approach targets primary and metastatic tumors while mitigating immunosuppression, offering a promising next‐generation therapy for combating cancer with enhanced efficacy and reduced side effects. 

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2. Characterization of carbon-coated core-shell iron nanoparticles annealed by oxygen and nitrogen

   https://doi.org/10.1063/9.0000845  

   Iglesias, Franco; Gonzalez, Cristian_Reynaga; Baughman, Jonah; Wonderling, Nichole; Shallenberger, Jeffrey; Khodagulyan, Armond; Bernal, Oscar_O; Kocharian, Armen_N (February 2024, AIP Advances)

   Nanocomposites consisting of nanoparticles of iron oxide (Fe3O4) and iron carbide (Fe3C) with a core-shell structure (Fe core, Fe3O4 and/or Fe3C shells) coated with additional graphite-like carbon layer dispersed in carbon matrix have been synthesized by solid-phase pyrolysis of iron-phthalocyanine (FePc) and iron-porphyrin (FePr) with a pyrolysis temperature of 900°C, and post-annealing conducted at temperatures ranging from 150°C to 550°C under controlled oxygen- and/or nitrogen-rich environments. A comprehensive analysis of the samples’ morphology, composition, structure, size, and magnetic characteristics was performed by utilizing scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-STEM) with elemental mapping, X-ray diffraction analysis (XRD), and magnetic measurements by utilizing vibrating sample magnetometry (VSM). The effect of the annealing process on magnetic performance and efficient control of the hysteresis loop and specific absorption rate (SAR) are discussed. 

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3. Influence of Hard/Soft Layer Ordering on Magnetization Reversal of Bimagnetic Nanoparticles: Implications for Biomedical/Theranostic Applications

   https://doi.org/10.1021/acsanm.3c00510  

   Kons, Corisa; Krycka, Kathryn L.; Robles, Joshua; Ntallis, Nikolaos; Pereiro, Manuel; Phan, Manh-Huong; Srikanth, Hariharan; Borchers, Julie A.; Arena, Darío A. (July 2023, ACS Applied Nano Materials)

   We investigate the spatial distribution of spin orientation in magnetic nanoparticles consisting of hard and soft magnetic layers. The nanoparticles are synthesized in a core–shell spherical morphology where the target stoichiometry of the magnetically hard, high anisotropy layer is CoFe2O4 (CFO), while the synthesis protocol of the lower anisotropy material is known to produce Fe3O4. The nanoparticles have a mean diameter of ∼9.2–9.6 nm and are synthesized as two variants: a conventional hard/soft core–shell structure with a CFO core/FO shell (CFO@FO) and the inverted structure FO core/CFO shell (FO@CFO). High-resolution electron microscopy confirms the coherent spinel structure across the core–shell boundary in both variants, while magnetometry indicates the nanoparticles are superparamagnetic at 300 K and develop a considerable anisotropy at reduced temperatures. Low-temperature M vs H loops suggest a multistep reversal process. Small angle neutron scattering (SANS) with full polarization analysis reveals a considerable alignment of the spins perpendicular to the field even at fields approaching saturation. The perpendicular magnetization is surprisingly correlated from one nanoparticle to the next, though the interaction is of limited range. More significantly, the SANS data reveal a pronounced difference in the reversal process of the magnetization parallel to the field for the two nanoparticle variants. For the CFO@FO nanoparticles, the core and shell magnetizations appear to track each other through the coercive region, while in the FO@CFO variant, the softer Fe3O4 core reverses before the higher anisotropy CoFe2O4 shell, consistent with expectations from mesoscale magnetic modeling. These results highlight the interplay between interfacial exchange coupling and anisotropy as a means to tune the composite properties of the nanoparticles for tailored applications including biomedical/theranostic uses. 

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4. Nitride‐Oxide‐Metal Heterostructure with Self‐Assembled Core–Shell Nanopillar Arrays: Effect of Ordering on Magneto‐Optical Properties

   https://doi.org/10.1002/smll.202007222  

   Wang, Xuejing; Jian, Jie; Wang, Haohan; Liu, Juncheng; Pachaury, Yash; Lu, Ping; Rutherford, Bethany X.; Gao, Xingyao; Xu, Xiaoshan; El‐Azab, Anter; et al (January 2021, Small)

   Abstract Magneto‐optical (MO) coupling incorporates photon‐induced change of magnetic polarization that can be adopted in ultrafast switching, optical isolators, mode convertors, and optical data storage components for advanced optical integrated circuits. However, integrating plasmonic, magnetic, and dielectric properties in one single material system poses challenges since one natural material can hardly possess all these functionalities. Here, co‐deposition of a three‐phase heterostructure composed of a durable conductive nitride matrix with embedded core–shell vertically aligned nanopillars, is demonstrated. The unique coupling between ferromagnetic NiO core and atomically sharp plasmonic Au shell enables strong MO activity out‐of‐plane at room temperature. Further, a template growth process is applied, which significantly enhances the ordering of the nanopillar array. The ordered nanostructure offers two schemes of spin polarization which result in stronger antisymmetry of Kerr rotation. The presented complex hybrid metamaterial platform with strong magnetic and optical anisotropies is promising for tunable and modulated all‐optical‐based nanodevices. 

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5. Synthesis of colloidal MnAs _x Sb _1−x nanoparticles: compositional inhomogeneity and magnetic consequences

   https://doi.org/10.1039/D1TC02479E  

   Hettiarachchi, Malsha A.; Su’a, Tepora; Abdelhamid, Ehab; Pokhrel, Shiva; Nadgorny, Boris; Brock, Stephanie L. (October 2021, Journal of Materials Chemistry C)

   The ternary manganese pnictide phases, MnAs 1− x Sb x , are of interest for magnetic refrigeration and waste heat recovery due to their magnetocaloric properties, maximized at the Curie temperature ( T C ), which varies from 580–240 K, depending on composition. Nanoparticles potentially enable application in microelectronics (cooling) or graded composites that can operate over a wide temperature range, but manganese pnictides are synthetically challenging to realize as discrete nanoparticles and their fundamental magnetic properties have not been extensively studied. Accordingly, colloidal synthesis methods were employed to target discrete MnAs x Sb 1− x nanoparticles ( x = 0.1–0.9) by arrested precipitation reactions of Mn 2 (CO) 10 with (C 6 H 5 ) 3 AsO and (C 6 H 5 ) 3 Sb in coordinating solvents. The MnAs x Sb 1− x particles are spherical in morphology with average diameters 10–13 nm (standard deviations <20% based on transmission electron microscopy analysis). X-Ray fluorescence spectroscopy measurements on ensembles showed that all phases had an excess of Sb relative to the targeted composition, whereas energy dispersive spectroscopic mapping data of single particles revealed that the nanoparticles are inhomogeneous, adopting a core–shell structure, with the amorphous shell rich in Mn and O (and sometimes Sb) while the crystalline core is rich in Mn, As, and Sb. Magnetization measurements of the nanoparticle ensemble demonstrated the presence of both ferromagnetic and paramagnetic phases. By combining the magnetization measurements with precision chemical mapping and simple modeling, we were able to unambiguously attribute ferromagnetism to the MnAs x Sb 1− x crystalline core, whereas paramagnetism was attributed to the amorphous shell. Magnetization measurements at variable temperatures were used to determine the superparamagnetic transition of the nanoparticles, although for some compositions and particle sizes the blocking temperature exceeded room temperature. Preliminary magnetic studies also revealed a conventional dependence between core size and coercivity, in spite of variable compositions of the nanoparticles, an unexpected result. 

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