Magnetite Magnetic Nanoparticles Research Articles

Sorption and concentration anionic azo dyes on nanomagnetite modified with cationic polyelectrolytes

Using the chemical coprecipitation method, magnetic magnetite nanoparticles (MNP) were synthesized, the surface of which was modified with biocompatible cationic polyelectrolytes polyethylenimine (PEI) and chitosan (Cht). The MNP were characterised by transmission microscopy and zeta potential measurements. The initial MNP have a shape close to spherical and an average size of (10±3) nm. Immobilization of polyelectrolyte on the surface of MNP led to the appearance of aggregates with an interconnected porous network (shell) around individual particles, with average sizes of (12±2) and (15±2) nm for Fe3O4@PEI and Fe3O4@Cht, accordingly. The influence of various experimental parameters, such as pH, extraction time, amount of sorbent and initial dye concentration on the adsorption and desorption of food azo dyes Allure Red AC (E129) and Brilliant Black BN (E151) was studied. It has been shown that under optimal conditions the degree of extraction of these dyes from aqueous solutions is 96-100%, the concentration coefficient is 2.7×103 and sorption capacity of 56 and 94 mg/g for Fe3O4@PEI and 46 and 69 mg/g on Fe3O4@ХТЗ for E129 and E151, respectively. A comparison of sorption isotherms and process kinetics showed that the Langmuir model and pseudo-first order are preferable for describing the sorption of dyes. In the acidic and neutral regions, electrostatic interactions are responsible for sorption, and in the alkaline region, hydrogen bonding and hydrophobic interactions also play a significant role. The proposed sorbents can be used both for the sorption and concentration of dyes in chemical analysis, and for the purification of wastewater from them. Nanomagnetite modified with polyethylenimine, which allows absorbing and concentrating dyes over a wide pH range of 6-9 is preferable for use.

Evaluation of Cr(VI) Removal from Tanning Effluents Using Magnetic Nanoparticles of Fe3O4 Synthesized with Olea europaea Bone Extract.

The tanning industry generates effluents with high chromium content, which require treatment prior to discharge into the sewage system. This article explores the use of magnetic magnetite nanoparticles (MNPs) to remove Cr(VI) from aqueous solutions, such as tanning effluents. The MNPs were synthesized by coprecipitation reaction using the Olea europaea extract as a reducing agent. Subsequently, they were characterized by dynamic light scattering spectroscopy (DLS), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). MNPs with irregular morphology and diameters ranging from 73.28 to 162.90 nm were obtained. Cr(VI) removal was performed using jar test methodology, and its efficiency was evaluated in the laboratory for different initial Cr(VI) (mg/L) concentration and nanoparticle (g/L) concentration. A kinetic study was developed and indicated that the equilibrium adsorption mechanism corresponds to a pseudo-second-order model. Furthermore, the isotherm analysis revealed that chromium adsorption best fits the Langmuir isotherm. Finally, Cr(VI) removal rates from 85% to 100% were achieved in tanning and retanning effluents.

Nonmonotonic magnetic field dependence of magnetization of self-assembled magnetite nanoparticles

We report a numerical study on the magnetization behavior of self-assembled magnetite magnetic nanoparticles (MNPs) with diameters of 10 and 14 nm magnetized at room temperature, based on molecular dynamics simulations. The results show that the nano-sheets or nano-chains, depending on the MNPs' diameter, are grown isotropically in the self-assembly process without a magnetic field, resulting in zero magnetization. The self-assembly also proceeds under a constant magnetic field. Interestingly, the magnetization of self-assembled MNPs is maximized under 0.05 T and monotonically decreases with further increasing magnetic field. Microscopically, the long nano-belts and nano-chains are favored, with the MNPs' arrangements and magnetic dipole orientations both aligning with the magnetic field direction under weak magnetic fields. On the contrary, under strong magnetic fields, small nano-sheets and short nano-chains with different magnetic dipole orientations are formed. The results are interpreted mainly due to the competition between magnetic dipole–dipole interaction and magnetic field, and a critical separation between MNPs, below which the internal interactions are predominant, is found to depend on MNPs' diameter and magnetic field strength. Therefore, the optimized magnetic field value can be exactly calculated, which provides a roadmap of critical research areas to enable the next generation of MNP-based materials synthesis.

An efficient magnetothermal actuation setup for fast heating/cooling cycles or long-term induction heating of different magnetic nanoparticle classes

Alternating magnetic fields (AMFs) in the ∼100 kHz frequency regime cause magnetic nanoparticles (MNPs) to dissipate heat to their nanoscale environment. This mechanism is beneficial for a variety of applications in biomedicine and nanotechnology, such as localized heating of cancer tissue, actuation of drug release, or inducing conformational changes of molecules. However, engineering electromagnetic resonant circuits which generate fields to efficiently heat MNPs over long time scales, remains a challenge. In addition, many applications require fast heating/cooling cycles over ΔT= 5 °C–10 °C to switch the sample between different states. Here, we present a home-built magnetothermal actuation setup maximized in its efficiency to deliver stable AMFs as well as to enable fast heating/cooling cycles of MNP samples. The setup satisfies various demands, such as an elaborate cooling system to control heating of the circuit components as well as of the sample due to inductive losses. Fast cycles of remote sample heating/cooling (up to ±15 °C min−1) as well as long-term induction heating were monitored via contact-free thermal image recording at sub-mm resolution. Next to characterizing the improved hyperthermia setup, we demonstrate its applicability to heat different types of MNPs: ‘nanoflower’-shaped multicore iron oxide nanoparticles, core shell magnetite MNPs, as well as magnetosomes from magnetotactic bacteria (Magnetospirillum gryphiswaldense). MNPs are directly compared in their structure, surface charge, magnetic properties as well as heating response. Our work provides practical guidelines for AMF engineering and the monitoring of MNP heating for biomedical or nano-/biotechnological applications.

A threefold increase in SAR performance for magnetic hyperthermia by compositional tuning in zinc-substituted iron oxide superparamagnetic nanoparticles with superior biocompatibility

In this work, we report a ultrahigh specific absorption rate (SAR) performance in Zn-substituted magnetite superparamagnetic (SPM) nanoparticles (NPs) for potential application in magnetic hyperthermia (MHT)-based cancer treatment. Although MHT shows promise in cancer therapy, challenges such as low heating performance, agglomeration of magnetic nanoparticles (MNPs) in blood veins, cytotoxicity, and hemocompatibility have hindered clinical uses. To overcome these challenges, we adopted a reverse-micelles based coprecipitation synthesis approach to prevent MNPs agglomeration and optimized the substitution of Zn ions in magnetite to enhance heating performance. Calorimetric measurements showed SAR values of 118 W/g and 181 W/g for magnetite NPs using the initial slope method (ISM) and Box Lucas method (BLM), respectively. Through our compositional optimizations, we achieved a significant increase in SAR value by consciously substituting Zn2+ ions in the magnetite lattice. Specifically, we obtained SAR values of 325 W/g and 579 W/g (>300% increase) for Zn0.3Fe2.7O4 MNPs using ISM and BLM, respectively. This enhancement can be attributed to improved saturation magnetization (174–257 kA/m) and magneto-crystalline anisotropy (12–24 kJ/m3). The increase in saturation magnetization in the magnetite MNPs can be explained by the higher magnetic moment resulting from increased Zn concentration up to ZnxFe3-xO4(x = 0.3), strengthening the JAB interaction. However, further increases in Zn concentration lead to a decrease in saturation magnetization due to non-collinearity, as described by the Yafet-Kittle model. Our optimized MNPs exhibit improved heating performance, enabling the use of lower MNPs concentrations for cancer treatment, reducing potential toxicity effects. Biocompatibility investigations demonstrated a low hemolysis rate (<5%) in a hemolysis assay with red blood cells and high cytocompatibility (>92% cell viability) in MTT assays for all compositions, confirming their potential suitability for clinical applications. This study offers a promising approach to enhance SAR performance, addressing MHT-based cancer treatment challenges, and improving clinical suitability.

Composite magnetic 3D-printing filament fabrication protocol opens new perspectives in magnetic hyperthermia

Three-dimensional (3D) printing technology has emerged as a promising tool for meticulously fabricated scaffolds with high precision and accuracy, resulting in intricately detailed biomimetic 3D structures. Producing magnetic scaffolds with the aid of additive processes, known as 3D printing, reveals multitude and state-of-the-art areas of application such as tissue engineering, bone repair and regeneration, drug delivery and magnetic hyperthermia. A crucial first step is the development of innovative polymeric composite magnetic materials. The current work presents a fabrication protocol of 3D printed polymer-bonded magnets using the Fused Deposition Modeling 3D printing method. Polymer-bonded magnets are defined as composites with permanent-magnet powder embedded in a polymer binder matrix. By using a low-cost mixing extruder, four (4) different filament types of 1.75 mm were fabricated using commercial magnetite magnetic nanoparticles mixed with a pure polylactic acid powder (PLA) and a ferromagnetic PLA (Iron particles included) filaments. The powder mixture of the basic filaments was compounded mixed with the nanoparticles (NPs), and extruded to fabricate the 3D printing filament, which is subsequently characterized structurally and magnetically before the printing process. Magnetic polymer scaffolds are finally printed using composite filaments of different concentration in magnetite. Our results demonstrate that the heating efficiency (expressed in W g−1) of the 3D printed magnetic polymer scaffolds (ranging from 2 to 5.5 W g−1 at magnetic field intensity of 30 mT and field frequency of 365 kHz) can be tuned by choosing either a magnetic or a non-magnetic filament mixed with an amount of magnetite NPs in different concentrations of 10 or 20 wt%. Our work opens up new perspectives for future research, such as the fabrication of complex structures with suitable ferromagnetic custom-made filaments adjusting the mixing of different filaments for the construction of scaffolds aimed at improving the accuracy of magnetic hyperthermia treatment.

Polyethylenimine–Silica–Magnetic Nanoparticle Composites for Efficient Extraction of Dissolved Copper from Aqueous Solutions and Multiphase Mixtures

Design of micro/nanoadsorbents developed for effective copper extraction should consider methods of their retrieval from relevant copper-rich environments, which are commonly complex multiphase mixtures, such as slurries of polluted soils and sediments, copper minerals including low-grade ores, and industrial and mining wastes. This work reports integration of copper-chelating polyethylenimine (PEI) with a robust silica network and highly magnetic magnetite nanoparticles, resulting in magnetic PEI–silica nanocomposite microparticles that enable efficient binding of copper ions in both aqueous solutions and complex, multiphase mixtures with subsequent retrieval using magnetic force. Produced via simple emulsion templating, these nanocomposite particles can withstand highly acidic conditions and multiple copper extraction cycles, without loss of efficiency after five consecutive cycles of copper extraction. PEI–silica–magnetic nanoparticles composites effectively bind all copper ions leached into an aqueous phase and allow their rapid magnetically induced separation from aqueous solutions and mixtures of both coarse and fine solid particles, demonstrating promising results for progress toward more sustainable copper extraction techniques.

Study of magnetic iron oxide nanoparticles coated with silicon oxide by ferromagnetic method

Magnetic nanoparticles of magnetite with a size of ~8 nm synthesized with a different type of coating were studied by ferromagnetic resonance in the temperature range from 7 to 300 K. The features of the experimental temperature dependences of the parameters of the ferromagnetic resonance curve (the magnitude of the resonant field, line width and intensity) and their approximation allowed us to estimate the values of characteristic temperatures. Firstly, the value of the Vervey temperature and the dependence of its value on the type of coating were determined. Secondly, the temperature of transition of nanoparticles to the superparamagnetic state (blocking temperature) and the temperature range within which the magnetic structure of the outer shell of the magnetic nanoparticle is in the spin glass state are established Keywords: iron oxide nanoparticles, ferromagnetic resonance, superparamagnetism, blocking temperature.

Исследование магнитных наночастиц оксида железа, покрытых оксидом кремния, методом ферромагнитного резонанса

Magnetic nanoparticles of magnetite with a size of ~8 nm synthesized with a different type of coating were studied by ferromagnetic resonance in the temperature range from 7 to 300 K. The features of the experimental temperature dependences of the parameters of the ferromagnetic resonance curve (the magnitude of the resonant field, line width and intensity) and their approximation allowed us to estimate the values of characteristic temperatures. Firstly, the value of the Vervey temperature and the dependence of its value on the type of coating were determined. Secondly, the temperature of transition of nanoparticles to the superparamagnetic state (blocking temperature) and the temperature range within which the magnetic structure of the outer shell of the magnetic nanoparticle is in the spin glass state are established

Synthesis of magnetic nanoparticles with covalently bonded polyacrylic acid for use as forward osmosis draw agents

Multicoated magnetite magnetic nanoparticles (MNP) with polyacrylic acid as a terminal hydrophilic ligand showed reproducibility of the composite particles when used as a draw solution. The tight covalent bond allows MNPs to maintain their osmotic potential after filtration.

Cation oxidation states and magnetic properties of MnxFe3−xO4 magnetic nanoparticles

10-nm MnxFe3−xO4 (x = 0, 0.3, 0.7) magnetic nanoparticles (MNPs) with single cubic structure were prepared by thermal decomposition method. The magnetic properties and cation oxidation state of MnxFe3−xO4 MNPs were investigated. Integrated analysis of X-ray diffraction indicates that Mn doping induces lattice expansion. Electron energy-loss spectroscopy results show that the fraction of Mn2+ and Mn3+ is 0.5:0.5 in Mn0.3Fe2.7O4 MNPs, and 2:1 in Mn0.7Fe2.3O4 MNPs. The saturation magnetization of Mn0.3Fe2.7O4 MNPs remain unchanged compared to magnetite MNPs, while the saturation magnetization of Mn0.7Fe2.3O4 MNPs decrease significantly. The reduction of magnetization is due to the lattice distortion, which weakens the superexchange interaction between B-site cations. Raising the ratio of Mn2+ and avoiding lattice distortion are beneficial to improve the magnetic properties of manganese ferrite. Further in vitro experiments show that Mn0.3Fe2.7O4 @SiO2 MNPs have good magnetic hyperthermia properties.

Atomic Force Manipulation of Single Magnetic Nanoparticles for Spin-Based Electronics.

Magnetic nanoparticles (MNPs) are instrumental for fabrication of tailored nanomagnetic structures, especially where top-down lithographic patterning is not feasible. Here, we demonstrate precise and controllable manipulation of individual magnetite MNPs using the tip of an atomic force microscope. We verify our approach by placing a single MNP with a diameter of 50 nm on top of a 100 nm Hall bar fabricated in a quasi-two-dimensional electron gas (q2DEG) at the oxide interface between LaAlO3 and SrTiO3 (LAO/STO). A hysteresis loop due to the magnetic hysteresis properties of the magnetite MNPs was observed in the Hall resistance. Further, the effective coercivity of the Hall resistance hysteresis loop could be changed upon field cooling at different angles of the cooling field with respect to the measuring field. The effect is associated with the alignment of the MNP magnetic moment along the easy axis closest to the external field direction across the Verwey transition in magnetite. Our results can facilitate experimental realization of magnetic proximity devices using single MNPs and two-dimensional materials for spin-based nanoelectronics.

Effect of an oscillating magnetic field in polymeric columns with magnetic nanoparticles

Magnetite magnetic nanoparticles (MNP) exhibit superparamagnetic behavior, which gives them important properties such as low coercive field, easy superficial modification and acceptable magnetization levels. This makes them useful in separation techniques. However, few studies have experimented with the interactions of MNP with magnetic fields. Therefore, the aim of this research was to study the influence of an oscillating magnetic field (OMF) on polymeric monolithic columns with vinylated magnetic nanoparticles (VMNP) for capillary liquid chromatography (cLC). For this purpose, MNP were synthesized by coprecipitation of iron salts. The preparation of polymeric monolithic columns was performed by copolymerization and aggregation of VMNP. Taking advantage of the magnetic properties of MNP, the influence of parameters such as resonance frequency, intensity and exposure time of a OMF applied to the synthesized columns was studied. As a result, a better separation of a sample according to the measured parameters was obtained, so that a column resolution (Rs) of 1.35 was achieved. The morphological properties of the columns were evaluated by scanning electron microscopy (SEM). The results of the chromatographic properties revealed that the best separation of the alkylbenzenes sample occurs under conditions of 5.5 kHz and 10 min of exposure in the OMF. This study constitutes a first application in chromatographic separation techniques for future research in nanotechnology.

How do artificial bacteria behave in magnetized nanofluid with variable thermal conductivity: application of tumor reduction and cancer cells destruction

PurposeThe study aims to determine an efficiency of external magnetic field on the bacteria surrounded by thousands of magnetic magnetite nanoparticles. The interstitial nanoliquid in which an artificial bacteria swims in biological cell is utilized with variable thermal conductivity. Two dimensions unsteady motion of second grade fluid are considered. The stretching wall is taken as a curved surface pattern.Design/methodology/approachThe mathematical results have been obtained by Chebyshev pseudospectral method.FindingsThe impact of the various governing parameters is described by numerical tables and diagrams. It is proven that the pure blood velocity curves are higher when compared with the magnetite/blood. It is demonstrated from clinical disease that dangerous tumors show diminished blood flow. This study concludes that the blood velocity profile increases by increasing the values of fluid parameters. This implies that the medication conveyance therapy lessens the tumor volume and helps in annihilating malignancy cells. The blood temperature distribution raises as the magnetite nanoparticles concentration increases. Consequently, the physical properties of the blood can be enhanced by immersing the magnetite nanoparticles. Further, the present outcomes cleared the thermal conductivity as, a variable function of the temperature, has an important role to enhance the heat transfer rate.Originality/valueTo the best of authors’ knowledge, this study is reported for the first time.

The Fine-Tuned Release of Antioxidant from Superparamagnetic Nanocarriers under the Combination of Stationary and Alternating Magnetic Fields.

Superparamagnetic magnetite nanoparticles (MNPs) with excellent biocompatibility and negligible toxicity were prepared by solvothermal method and stabilized by widely used and biocompatible polymer poly(ethylene glycol) PEG-4000 Da. The unique properties of the synthesized MNPs enable them to host the unstable and water-insoluble quercetin as well as deliver and localize quercetin directly to the desired site. The chemical and physical properties were validated by X-ray powder diffraction (XRPD), field emission scanning electron microscopy (FE–SEM), atomic force microscopy (AFM), superconducting quantum interference device (SQUID) magnetometer, FTIR spectroscopy and dynamic light scattering (DLS). The kinetics of in vitro quercetin release from MNPs followed by UV/VIS spectroscopy was controlled by employing combined stationary and alternating magnetic fields. The obtained results have shown an increased response of quercetin from superparamagnetic MNPs under a lower stationary magnetic field and s higher frequency of alternating magnetic field. The achieved findings suggested that we designed promising targeted quercetin delivery with fine-tuning drug release from magnetic MNPs.

Magnetosomes and Magnetosome Mimics: Preparation, Cancer Cell Uptake and Functionalization for Future Cancer Therapies.

Magnetic magnetite nanoparticles (MNP) are heralded as model vehicles for nanomedicine, particularly cancer therapeutics. However, there are many methods of synthesizing different sized and coated MNP, which may affect their performance as nanomedicines. Magnetosomes are naturally occurring, lipid-coated MNP that exhibit exceptional hyperthermic heating, but their properties, cancer cell uptake and toxicity have yet to be compared to other MNP. Magnetosomes can be mimicked by coating MNP in either amphiphilic oleic acid or silica. In this study, magnetosomes are directly compared to control MNP, biomimetic oleic acid and silica coated MNP of varying sizes. MNP are characterized and compared with respect to size, magnetism, and surface properties. Small (8 ± 1.6 nm) and larger (32 ± 9.9 nm) MNP are produced by two different methods and coated with either silica or oleic acid, increasing the size and the size dispersity of the MNP. The coated larger MNP are comparable in size (49 ± 12.5 nm and 61 ± 18.2 nm) to magnetosomes (46 ± 11.8 nm) making good magnetosome mimics. All MNP are assessed and compared for cancer cell uptake in MDA-MB-231 cells and importantly, all are readily taken up with minimal toxic effect. Silica coated MNP show the most uptake with greater than 60% cell uptake at the highest concentration, and magnetosomes showing the least with less than 40% at the highest concentration, while size does not have a significant effect on uptake. Finally, surface functionalization is demonstrated for magnetosomes and silica coated MNP using biotinylation and EDC-NHS, respectively, to conjugate fluorescent probes. The modified particles are visualized in MDA-MB-231 cells and demonstrate how both naturally biosynthesized magnetosomes and biomimetic silica coated MNP can be functionalized and readily up taken by cancer cells for realization as nanomedical vehicles.

Effective Elimination and Biodegradation of Polycyclic Aromatic Hydrocarbons from Seawater through the Formation of Magnetic Microfibres.

Supramolecular aggregates formed between polycyclic aromatic hydrocarbons and either naphthalene or perylene-derived diimides have been anchored in magnetite magnetic nanoparticles. The high affinity and stability of these aggregates allow them to capture and confine these extremely carcinogenic contaminants in a reduced space. In some cases, the high cohesion of these aggregates leads to the formation of magnetic microfibres of several microns in length, which can be isolated from the solution by the direct action of a magnet. Here we show a practical application of bioremediation aimed at the environmental decontamination of naphthalene, a very profuse contaminant, based on the uptake, sequestration, and acceleration of the biodegradation of the formed supramolecular aggregate, by the direct action of a bacterium of the lineage Roseobacter (biocompatible with nanostructured receptors and very widespread in marine environments) without providing more toxicity to the environment.

Mechanistic study on boron adsorption and isotopic separation with magnetic magnetite nanoparticles

Good boron removal and isotopic separation behavior was observed on magnetic magnetite nanoparticles (MMNs) in a previous study, but the mechanism of boron adsorption and isotopic separation remains unclear. Here, experimental studies accompanied by quantum chemistry calculations were implemented for the first time to reveal the nature of boron adsorption and isotopic separation on MMN. First, the fitted peaks of Fe2p of MMN by X-ray photoelectron spectrometry (XPS) before and after adsorption showed decrease in Fe(II)/Fe(III) ratio, which validated the formation of Fe–O–B interaction. Fe–O–B bond was also observed through fitted peaks of O1s and dihydroxy complexation where MMNs prefer to adsorb [B(OH)4]−(H3BO3) at pH pHzpc) identified by the ratio of integrated peaks. ATR-FTIR revealed the hydroxyl moiety as the main adsorptive group. The selectivity of MMN toward [B(OH)4]− at pH pHzpc was figured out by calculating the ratio between the integrated areas of B–O bands at different pH values. As a result, the trend of adsorption capacity as well as the isotopic separation factor with pH was well illustrated. The concluded adsorption mechanism from the experiment was further verified with the simulated adsorption energies (ΔE) and isotopic separation factors (S) calculated by DFT quantum simulation.

Influencia de un campo magnético oscilante en columnas poliméricas con nanopartículas magnéticas (ARTÍCULO RETRACTADO)

ARTÍCULO RETRACTADO Las nanopartículas magnéticas de magnetita (MNP) presentan comportamiento superparamagnético, lo que les confiere propiedades importantes como bajo campo coercitivo, fácil modificación superficial y niveles de magnetización aceptables. Esto las hace útiles en técnicas de separación. Sin embargo, pocos estudios han experimentado con las interacciones de las MNP con campos magnéticos. Por tanto, el objetivo de esta investigación fue estudiar la influencia de un campo magnético oscilante (CMO) en columnas monolíticas poliméricas con nanopartículas magnéticas vinilizadas (VMNP) para cromatografía líquida capilar (cLC). Para ello, se sintetizaron MNP mediante coprecipitación de sales de hierro. La preparación de las columnas monolíticas poliméricas se realizó por copolimerización y la agregación de VMNP. Aprovechando las propiedades magnéticas de las MNP, se estudió la influencia de los parámetros como frecuencia de resonancia, intensidad y tiempo de exposición de un CMO, aplicado a las columnas sintetizadas. Como resultado se obtuvo una mejor separación de una muestra según los parámetros medidos, de modo que se logró una resolución de la columna (Rs) de 1,35. Las propiedades morfológicas de las columnas fueron evaluadas mediante microscopía electrónica de barrido (SEM). Los resultados de las propiedades cromatográficas revelaron que la mejor separación de la muestra de alquilbencenos se da en condiciones de 5,5 kHz y 10 min de exposición en el CMO. Este estudio constituye una primera aplicación en técnicas de separación cromatográficas para futuras investigaciones en nanotecnología.

Simple Sonochemical Method to Optimize the Heating Efficiency of Magnetic Nanoparticles for Magnetic Fluid Hyperthermia.

We developed a fast, single-step sonochemical strategy for the green manufacturing of magnetite (Fe3O4) magnetic nanoparticles (MNPs), using iron sulfate (FeSO4) as the sole source of iron and sodium hydroxide (Na(OH)) as the reducing agent in an aqueous medium. The designed methodology reduces the environmental impact of toxic chemical compounds and minimizes the infrastructure requirements and reaction times down to minutes. The Na(OH) concentration has been varied to optimize the final size and magnetic properties of the MNPs and to minimize the amount of corrosive byproducts of the reaction. The change in the starting FeSO4 concentration (from 5.4 to 43.1 mM) changed the particle sizes from (20 ± 3) to (58 ± 8) nm. These magnetite MNPs are promising for biomedical applications due to their negative surface charge, good heating properties (≈324 ± 2 W/g), and low cytotoxic effects. These results indicate the potential of this controlled, easy, and rapid ultrasonic irradiation method to prepare nanomaterials with enhanced properties and good potential for use as magnetic hyperthermia agents.