Fe3 O4 Research Articles

Response of mixed bacterial culture towards dibenzothiophene desulfurization under the influence of surfactants and microscopically (SEM and TEM) characterized magnetic Fe3 O4 nanoparticles.

Excessive emission of sulfur dioxides from the combustion of coal and other fossil fuels for thermal and industrial purposes has been associated with serious environmental hazards. Biodesulfisation (BDS) can be an effective approach for reducing the impact of toxic gases to its inbuilt operational feasibility under ambient environmental conditions. In the present research, two strategies for BDS of a standard organosulfur compound such as dibenzothiophene (DBT) were investigated under laboratory conditions. In the first treatment, the role of different surfactants such as Tween-20, Tween-80, SDS, and EDTA on the desulfurization of DBT was investigated by the application of bacterial consortium IQMJ-5. In the second treatment, Iron oxidenanoparticles were synthesized and immobilized on the surface of bacteria cells. Shake flask experiments were conducted with immobilized cells, surfactant amended immobilized cells, and control or noncoated cells. Among different surfactant treatments, Tween-80 was found to be the most effective surfactant, showing maximum desulfurization activity at a concentration of 5g/L. The transmission electron microscopy and X-ray diffraction analysis indicated that produced nanoparticles were spherical in shape with a size of about 46 nm and had a stoichiometric ratio of 55.85% and 44.15% between O and Fe, respectively. The nanoparticle treatment enhanced the DBT desulfurization process up to 11.37% as compared to the control, specifically when immobilized cells were used. Therefore, it was concluded that nanoparticles treatments with immobilization of the bacterial cells enhanced the desulfurization rate of DBT under ambient reaction conditions and provide a sustainable alternative for commercial coal BDS.

Magnetic Composite Rapidly Treats Staphylococcus aureus-Infected Osteomyelitis through Microwave Strengthened Thermal Effects and Reactive Oxygen Species.

It is difficult to effectively treat bacterial osteomyelitis using photothermal therapy or photodynamic therapy due to poor penetration of light. Here, a microwave (MW)-excited magnetic composite of molybdenum disulfide (MoS2 ) / iron oxide (Fe3 O4 ) is reported for the treatment of bacteria-infected osteomyelitis. In in vitro and in vivo experiments, MoS2 /Fe3 O4 is shown to effectively eradicate bacteria-infected mouse tibia osteomyelitis, due to MW thermal enhancement and reactive oxygen species (ROS) (1 O2 and ·O2 - ) production under MW radiation. In addition, the mechanism of MW heat generation is proposed by MW network vector analysis. By the density functional theory and finite element method, the ROS generation mechanism is proposed. The synergy or conductive network between dielectric MoS2 and magnetic Fe3 O4 can reach both enhancement of the dielectric and magnetic attenuation capability. In addition, abundant interfaces are generated to enhance the attenuation of electromagnetic waves by MoS2 and Fe3 O4, introducing multiple reflections and interfacial polarization. Therefore, MoS2 /Fe3 O4 has excellent MW absorption ability based on the synergy or conductive network between MoS2 and magnetic Fe3 O4 as well as multiple dielectric reflections and interfacial polarization.

Fe 3 O 4 Nanoparticles Enhanced Amorphous Ferric Silicate/Reduced Graphene Oxide for High‐Performance Lithium‐Ion Storage

Ferric silicate (FS) has been explored as a potential lithium ion batteries candidate for its environment benign, low cost, rich reserves, and high capacity. Despite these advantages, poor electronic conductivity and large volume variation obstruct its practical utilization. To improve its electrochemical performance, a unique hybrid structure with Fe3O4@ferric silicate nanosheets anchored on the reduced graphene oxide ([email protected]/RGO) is fabricated. The disordered amorphous nanosheet structure of FS not only shortens the transferred length for lithium ions but also facilities the Li+ diffusion and can effectively keep the structure integrity. RGO substrate ameliorates the electronic conductivity and slackens the strain upon cycling. Fe3O4 (FO) nanoparticles embedded in FS further boost the electronic conductivity and the lithium storage capability. The synergistic effects bestow the composite superior electrochemical properties. [email protected]/RGO shows high reversible capacity of 1113 mA h g−1 at 0.2 A g−1, an excellent rate performance of 681 mA h g−1 at 2 A g−1, and a splendid cycling stability with a capacity of 859 mA h g−1 at 1 A g−1 after 800 cycles.

Mo-Incorporated Magnetite Fe3 O4 Featuring Cationic Vacancies Enabling Fast Lithium Intercalation for Batteries.

Transition metal oxides (TMOs) as high-capacity electrodes have several drawbacks owing to their inherent poor electronic conductivity and structural instability during the multi-electron conversion reaction process. In this study, the authorsuse an intrinsic high-valent cation substitution approach to stabilize cation-deficient magnetite (Fe3 O4 ) and overcome the abovementioned issues. Herein, 5 at% of Mo4+ -ions are incorporated into the spinel structure to substitute octahedral Fe3+ -ions, featuring ≈1.7 at% cationic vacancies in the octahedral sites. This defective Fe2.93 ▫0.017 Mo0.053 O4 electrode shows significant improvements in the mitigation of capacity fade and the promotion of rate performance as compared to the pristine Fe3 O4 . Furthermore, physical-electrochemical analyses and theoretical calculations are performed to investigate the underlying mechanisms. In Fe2.93 ▫0.017 Mo0.053 O4 , the cationic vacancies provide active sites for storing Li+ and vacancy-mediated Li+ migration paths with lower energy barriers. The enlarged lattice and improved electronic conductivity induced by larger doped-Mo4+ yield this defective oxide capable of fast lithium intercalation. This is confirmed by a combined characterization including electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT) and density functional theory (DFT) calculation. This study provides a valuable strategy of vacancy-mediated reaction to intrinsically modulate the defective structure in TMOs for high-performance lithium-ion batteries.

A Dual Sensing Platform for Human Exhaled Breath Enabled by Fe-MIL-101-NH2 Metal-Organic Frameworks and its Derived Co/Ni/Fe Trimetallic Oxides.

Limited by the insufficient active sites and the interference from breath humidity, designing reliable gas sensing materials with high activity and moisture resistance remains a challenge to analyze human exhaled breath for the translational application of medical diagnostics. Herein, the dual sensing and cooperative diagnosis is achieved by utilizing metal-organic frameworks (MOFs) and its derivative. The Fe-MIL-101-NH2 serves as the quartz crystal microbalance humidity sensing layer, which exhibits high selectivity and rapid response time (16 s/15 s) to water vapor. Then, the Co2+ and Ni2+ cations are further co-doped into Fe-MIL-101-NH2 host to obtain the derived Co/Ni/Fe trimetallic oxides (CoNiFe-MOS-n). The chemiresistive CoNiFe-MOS-n sensor displays the high sensitivity (560) and good selectivity to acetone, together with a lower original resistance compared with Fe2 O3 and NiFe2 O4 . Moreover, as a proof-of-concept application, synergistic integration of Fe-MIL-101-NH2 and derived CoNiFe-MOS-n is carried out. The Fe-MIL-101-NH2 is applied as moisture sorbent materials, which realize a sensitivity compensation of CoNiFe-MOS-n sensors for the detection of acetone (biomarker gas of diabetes). The findings provide an insight for effective utilization of MOFs and the derived materials to achieve a trace gas detection in exhaled breath analysis.

Biohybrid Response Microparticles Decorated with Trained-MSCs for Acute Liver Failure Recovery.

Microcarrier-based mesenchymal stem cells (MSCs) delivery have attracted increasing attention in acute liver failure (ALF) therapy, while there is still room for improvement in terms of improving cell loading efficiency, enhancing anti-inflammatory features, and controlling cell release. Here, novel lipopolysaccharide (LPS)-composited magnetic-thermal responsive inverse opal particles (MIOPs) are presented for the delivery of MSCs. The MIOPs are composed of a chitosan inverse opal skeleton filled with a hydrogel containing LPS, poly(N-isopropylacrylamide), and Fe3 O4 nanoparticles. Benefitting from the biocompatible chitosan component and the huge specific surface area, the resultant MIOPs can capture MSCs in a nondestructive way. Furthermore, LPS can be released from the MIOPs under the stimulation of an alternating magnetic field, by which the MSCs are activated to gain the feature of "trained immunity." Moreover, this process can be monitored in real-time by the structural color change of the MIOPs. With that, the MSCs-laden MIOPs are employed in rats with ALF, and they exhibit obvious anti-inflammatory and therapeutic efficacy superior to untrained MSCs. These performances make the MIOPs a distinctive cell delivery platform for clinical tissue recovery applications.

Magnetic Alignment for Plasmonic Control of Gold Nanorods Coated with Iron Oxide Nanoparticles.

Plasmonic nanoparticles that can be manipulated with magnetic fields are of interest for advanced optical applications, diagnostics, imaging, and therapy. Alignment of gold nanorods yields strong polarization-dependent extinction, and use of magnetic fields is appealing because they act through space and can be quickly switched. In this work, cationic polyethyleneimine-functionalized superparamagnetic Fe3 O4 nanoparticles (NPs) are deposited on the surface of anionic gold nanorods coated with bovine serum albumin. The magnetic gold nanorods (MagGNRs) obtained through mixing maintain the distinct optical properties of plasmonic gold nanorods that are minimally perturbed by the magnetic overcoating. Magnetic alignment of the MagGNRs arising from magnetic dipolar interactions on the anisotropic gold nanorod core is comprehensively characterized, including structural characterization and enhancement (suppression) of the longitudinal surface plasmon resonance and suppression (enhancement) of the transverse surface plasmon resonance for light polarized parallel (orthogonal) to the magnetic field. The MagGNRs can also be driven in rotating magnetic fields to rotate at frequencies of at least 17Hz. For suitably large gold nanorods (148nm long) and Fe3 O4 NPs (13.4nm diameter), significant alignment is possible even in modest (<500Oe) magnetic fields. An analytical model provides a unified understanding of the magnetic alignment of MagGNRs.

Liquid Processing of Interfacially Grown Iron-Oxide Flowers into 2D-Platelets Yields Lithium-Ion Battery Anodes with Capacities of Twice the Theoretical Value.

Iron oxide (Fe2 O3 )is an abundant and potentially low-cost material for fabricating lithium-ion battery anodes. Here, the growth of α-Fe2 O3 nano-flowers at an electrified liquid-liquid interface is demonstrated. Sonication is used to convert these flowers into quasi-2D platelets with lateral sizes in the range of hundreds of nanometers and thicknesses in the range of tens of nanometers. These nanoplatelets can be combined with carbon nanotubes to form porous, conductive composites which can be used as electrodes in lithium-ion batteries. Using a standard activation process, these anodes display good cycling stability, reasonable rate performance and low-rate capacities approaching 1500 mAh g-1 , consistent with the current state-of-the-art for Fe2 O3 . However, by using an extended activation process, it is found that the morphology of these composites can be significantly changed, rendering the iron oxide amorphous and significantly increasing the porosity and internal surface area. These morphological changes yield anodes with very good cycling stability and low-rate capacity exceeding 2000 mAh g-1 , which is competitive with the best anode materials in the literature. However, the data implies that, after activation, the iron oxide displays a reduced solid-state lithium-ion diffusion coefficient resulting in somewhat degraded rate performance.

Rapid and Multimaterial 4D Printing of Shape-Morphing Micromachines for Narrow Micronetworks Traversing.

Micromachines with high environmental adaptability have the potential to deliver targeted drugs in complex biological networks, such as digestive, neural, and vascular networks. However, the low processing efficiency and single processing material of current 4D printing methods often limit the development and application of shape-morphing micromachines (SMMs). Here, two 4D printing strategies are proposed to fabricate SMMs with pH-responsive hydrogels for complex micro-networks traversing. On the one hand, the 3Dvortex light single exposure technique can rapidly fabricate a tubular SMM with controllable size and geometry within 0.1 s. On the other hand, the asymmetric multimaterial direct laser writing (DLW)method is used to fabricate SMMs with designable 3D structures composed of hydrogel and platinum nanoparticles (Pt NPs). Based on the presence of ferroferric oxide (Fe3 O4 ) and Pt NPs in the SMMs, efficient magnetic, bubble, and hybrid propulsion modes are achieved. Finally, it is demonstrated that the spatial shape conversion capabilities of these SMMs can be used for narrow micronetworks traversing, which will find potential applications in targeted cargo delivery in microcapillaries.

Geochemical Investigation of Cassiterite at Bisichi Kara II and Kuru-Jentar, Plateau State, Nigeria Using X-Ray Fluorescence Analysis (XRF)

Background: Artisanal Mining of Cassiterite at Bisichi (Kara II) and Kuru-Jentar is a very tedious activity that is carried out by artisanal miners. It involves the use of primitive tools like digger, spade, shovel and to mention afew. Most of the artisanal mining activity in the study area is done with no prior knowledge about the geochemical constituent of the mineral deposit in the area but in order to solve the above stated problem, a geochemical analysis was conducted on the obtained samples of cassiterite from the study area and a geologic map of the mining pit was digitized using Ilwis 3.1 academic and Surfer 12. Result: A random sampling method was used to obtain ten (10) samples of cassiterite from the various visited pit at the study area with each weighing 10g. A laboratory analysis was also conducted using X-ray Fluorescence (XRF) analysis which shows that samples from Pit 1 to Pit 5 in the mine site at Kuru-Jentar has 44.45% - 44.9% of Tin (Sn) and 7.86% - 9.00% of Iron (II) oxide (Fe2O3) while samples from Pit 5 to Pit 10 in the mine site at Bisichi (Kara II) has 28.2% - 32.2 % of Tin (Sn) and 15.57% - 16.67% of Iron II oxide (Fe2 O3 ). Conclusively, an understanding of the geochemical constituent of a mineral deposit within a given study area would help increase the knowledge of miners and also attract interested investors.

Periplasmic Bacterial Biomineralization of Copper Sulfide Nanoparticles.

Metal sulfides are a common group of extracellular bacterial biominerals. However, only a few cases of intracellular biomineralization are reported in this group, mostly limited to greigite (Fe3S4) in magnetotactic bacteria. Here, a previously unknown periplasmic biomineralization of copper sulfide produced by the magnetotactic bacterium Desulfamplus magnetovallimortis strain BW‐1, a species known to mineralize greigite (Fe3S4) and magnetite (Fe3O4) in the cytoplasm is reported. BW‐1 produces hundreds of spherical nanoparticles, composed of 1–2 nm substructures of a poorly crystalline hexagonal copper sulfide structure that remains in a thermodynamically unstable state. The particles appear to be surrounded by an organic matrix as found from staining and electron microscopy inspection. Differential proteomics suggests that periplasmic proteins, such as a DegP‐like protein and a heavy metal‐binding protein, could be involved in this biomineralization process. The unexpected periplasmic formation of copper sulfide nanoparticles in BW‐1 reveals previously unknown possibilities for intracellular biomineralization that involves intriguing biological control and holds promise for biological metal recovery in times of copper shortage.

Cycloacceleration of Reactive Oxygen Species Generation Based on Exceedingly Small Magnetic Iron Oxide Nanoparticles for Tumor Ferroptosis Therapy.

Because of the insufficiency of hydrogen peroxide, the relatively low rate of Fenton reaction, and the active glutathione (GSH) peroxidase 4 (GPX4) in tumor cells, it is difficult to achieve a desirable efficacy of ferroptosis therapy (FT) for tumors based on nanomaterials. Inspired by the concept of "cyclotron" in physics, in this study, a new concept of cycloacceleration of reactive oxygen species (ROS) generation in tumor cells to realize high-performance FT of tumors is proposed. Typically, a magnetic resonance imaging (MRI) contrast agent of dotted core-shell Fe3 O4 /Gd2 O3 hybrid nanoparticles (FGNPs) is prepared based on exceedingly small magnetic iron oxide nanoparticles (ES-MIONs). Sorafenib (SFN) is loaded and poly(ethylene glycol) methyl ether-poly(propylene sulfide)-NH2 (mPEG-PPS-NH2 ) is grafted on the surface of FGNP to generate SA-SFN-FGNP via self-assembly. The results of in vitro and in vivo demonstrate SA-SFN-FGNP can work with the acidic tumor microenvironment and endosomal conditions, Fenton reaction and system XC - , and generate cyclic reactions in tumor cells, resulting in specific cycloacceleration of ROS generation for high-performance FT of tumors. The very high longitudinal relaxivity (r1 , 33.43 mM-1 s-1 , 3.0 T) makes sure that the SA-SFN-FGNP can be used for MRI-guided FT of tumors.

Improvement in desulfurization of dibenzothiophene and dibenzothiophene sulfone by Paenibacillus strains using immobilization or nanoparticle coating.

Biodesulfurization of fossil fuels is a promising technology for deep desulfurization. Previously, we have shown that Paenibacillus strains 32O-W and 32O-Y can desulfurize dibenzothiophene (DBT) and DBT sulfone (DBTS) effectively. In this work, improvements in DBT and DBTS desulfurization by these strains were investigated through immobilization and nanoparticle coating of cells. Paenibacillus strains 32O-W and 32O-Y immobilized in alginate gel beads or coated with Fe3 O4 magnetite nanoparticles were grown at various concentrations (0.1-2 mmol l-1 ) of DBT or DBTS for 96 h. The production of 2-hydroxybiphenyl (2-HBP) from the 4S pathway biotransformation of DBT or DBTS was measured. The highest amounts of 2-HBP production occurred at concentrations of 0.1 and 0.5 mmol l-1 . Compared to planktonic cultures maximum 2-HBP production increased by 54% for DBT and 90% for DBTS desulfurization with immobilized strains, and 44% for DBT and 66% for DBTS desulfurization by nanoparticle-coated strains. Nanoparticle-coated and immobilized cells may be of use in efforts to increase the efficiency of biodesulfurization. Alginate immobilization or nanoparticle coating of bacterial cells may be useful approaches for the enhancement of biodesulfurization for eventual use on an industrial scale.

Programmable Anisotropic Hydrogels with Localized Photothermal/Magnetic Responsive Properties.

Programmable smart materials that can respond locally to specific stimuli hold great potential for many applications, but controllable fabrication of these materials remains challenging. This work reports the development of novel programmable anisotropic materials with both magnetic and photothermal stimuli‐responsiveness, which are fabricated by anchoring thermosensitive poly(N‐isopropyl acrylamide) (PNIPAm) and magnetic Fe3O4 nanoparticles on the surface of MoS2 nanosheets. Further embedding PNIPAm‐MoS2/Fe3O4 into 3D‐printed hydrogel cubes results in stimuli‐responsive building blocks, and the magnetic field can precisely control their orientation and near‐infrared (NIR) light absorbing property. Particularly, the variation of the orientation of MoS2/Fe3O4 block results in obvious changes of their photothermal efficiency and optical property. By exploiting the anisotropy of MoS2/Fe3O4 and their NIR light responsiveness, thermally‐induced phase transitions in individual 3D printed hydrogel building block can be locally controlled for magnetic field‐assisted programming a quick response (QR) code. Alternatively, fluorescent QR code with high contrast and security level can be achieved by photothermal‐induced release of fluorescent dyes. These 3D printed magnetically programmed hydrogels hold great potential for application in information storage, intelligent materials, and precise therapy.

Confinement Effects in Dynamics of Ionic Liquids with Polymer-Grafted Nanoparticles.

Ionic liquid mixed with poly(methyl methacrylate)-grafted Fe3 O4 nanoparticle aggregates at low particle concentrations was found to exhibit different dynamics and ionic conductivity than that of pure ionic liquid in our previous studies. In this work, we report on the quasi-elastic neutron scattering results of ionic liquid containing polymer-grafted Fe3 O4 nanoparticles at higher particle concentrations. The diffusivity of imidazolium (HMIM+ ) cations of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (HMIM-TFSI) in the presence of poly(methyl methacrylate)-grafted Fe3 O4 nanoparticles is discussed through the confinement. Analysis of the elastic incoherent structure factor revealed that the confinement radius decreased with the addition of grafted particles in HMIM-TFSI/solvent mixture. We propose the confinement that is induced by the high concentration of grafted particles shrinks the HMIM-TFSI restricted volume. We further conjecture that this enhanced diffusivity occurs as a result of the local ordering of cations within aggregates of poly(methyl methacrylate)-grafted Fe3 O4 nanoparticles.

Sol–Gel Synthesis and Photocatalytic Activity of Graphene Oxide/ZnFe2O4-Based Composite Photocatalysts

ZnO (ZO), Fe2O3 (FO), and graphene oxide (GO)/ZO/FO/ZnFe2O4 (ZFO) composite photocatalysts have been synthesized successfully via a simple sol–gel method and low-temperature technology. The phase structure and microstructural analysis confirmed that the GO/ZO/FO/ZFO magnetic separation photocatalyst is composed of GO, hexagonal ZnO, rhombohedral Fe2O3, and spinel ZnFe2O4 without any other impurities. The GO/ZO/FO/ZFO composite photocatalysts have a high visible light optical absorption coefficient and photocatalytic activity for degrading dyes, refractory pollutants, and antibiotics. The degradation percentages of methyl orange, tetrabromobisphenol A, and oxytetracycline hydrochloride by the GO/ZO/FO/ZFO magnetic separation photocatalyst were 98% for 180 min, 99% for 150 min, and 85% for 180 min, respectively. The special synthesis path leads to the formation of a special heterojunction between GO, ZnO, Fe2O3, and ZnFe2O4, which does not change the optical band gap value of the main lattice Fe2O3, and enhances the surface defects of the GO/ZO/FO/ZFO magnetic separation photocatalyst, resulting in high charge carrier transfer and separation efficiency of the catalyst and then enhanced the photocatalytic activity of the GO/ZO/FO/ZFO magnetic separation photocatalyst.

Microtexture analysis of copper-doped iron oxide thin films prepared by air pneumatic spray.

The stereometric and fractal concepts are crucial tools to analyse, to verify, to report 3-D microtexture of thin film surfaces on the nanometre scale and thereby to generate useful topographic characteristics for better understanding and steering them toward further improvements and rational use in modern applications. At first, the present work aimed to prepare hematite α-Fe2 O3 thin films with (0, 2, 4, 6 and 8 wt%) of Cu doping by using the air pneumatic spray method. Subsequently, the obtained pure α-Fe2 O3 and Cu-doped α-Fe2 O3 thin films were characterised by XRD device, which determines their polycrystalline nature with the rhombohedral hematite structure. Analysis by UV-VIS absorption showed that the transmittance of the thin films is extinct in the wavelength from approximately 500 to 800 nm, revealing that the films have good optical absorbance in the visible region. The obtained bandgap values varied between 2.23 and 2.21 eV. At second stage, the stereometric and fractal analysis are applied on 3-D image data of pure α- Fe2 O3 and Cu-doped α-Fe2 O3 thin films, which in prior generated using AFM device. Accordingly, the obtained statistical parameters such as surface roughness, density distribution of peaks, depths etc. were used to understand the influence of Cu doping on the 3D microtexture of pure α- Fe2 O3 and Cu-doped α- Fe2 O3 thin film surfaces.

Defective Fe3O4‐x Few‐Atom Clusters Anchored on Nitrogen‐Doped Carbon as Efficient Oxygen Reduction Electrocatalysts for High‐Performance Zinc–Air Batteries

It remains a challenge to develop cost-effective, high-performance oxygen electrocatalysts for rechargeable metal-air batteries. Herein, zinc-mediated zeolitic imidazolate frameworks are exploited as the template and nitrogen and carbon sources, onto which is deposited a Fe3 O4 layer by plasma-enhanced atomic layer deposition. Controlled pyrolysis at 1000°C leads to the formation of high density of Fe3 O4- x few-atom clusters with abundant oxygen vacancies deposited on an N-doped graphitic carbon framework. The resulting nanocomposite (Fe3 O4- x /NC-1000) exhibits a markedly enhanced electrocatalytic performance toward oxygen reduction reaction in alkaline media, with a remarkable half-wave potential of +0.930V versus reversible hydrogen electrode, long-term stability, and strong tolerance against methanol poisoning, in comparison to samples prepared at other temperatures and even commercial Pt/C. Notably, with Fe3 O4- x /NC-1000 as the cathode catalyst, a zinc-air battery delivers a high power density of 158mW cm-2 and excellent durability at 5mA cm-2 with stable 2000 charge-discharge cycles over 600 h. This is ascribed to the ready accessibility of the Fe3 O4- x catalytic active sites, and enhanced electrical conductivity, oxygen adsorption, and electron-transfer kinetics by surface oxygen vacancies. Further contributions may arise from the highly conductive and stable N-doped graphitic carbon frameworks.

Milk protein hydrolysates obtained with immobilized alcalase and neutrase on magnetite nanoparticles: Characterization and antigenicity study.

Enzymatic hydrolysis is the most commonly used method to reduce the antigenicity of milk protein, but free protease is unstable and difficult to recycle after application. In this study, alcalase and neutrase were selected for immobilization on the modified magnetic Fe3 O4 nanoparticles. The reusability of the immobilized enzyme was 68.23% of the total starting activity after 5 recycling batches. The optimal hydrolysis conditions were an enzyme to substrate ratio of 6000 U/g and reaction at 50℃ and pH 8.5 for 3 h. Under these conditions, 22.76% hydrolysis of hydrolysate was achieved, and the antigenicity reduction rates of β-lactoglobulin and casein were 21.34% and 30.89%, respectively. In addition, 82.75% of the hydrolysate had a molecular weight less than 1kDa, and free amino acids represented 13.65% of the sample. This result showed that the hydrolysis with immobilized enzyme was similar to that with free enzyme and the immobilized enzyme could be applied to produce hypoallergenic hydrolysate. PRACTICAL APPLICATION: Reduces milk protein allergenicity.

Magnetic-Powered Janus Cell Robots Loaded with Oncolytic Adenovirus for Active and Targeted Virotherapy of Bladder Cancer.

A unique robotic medical platform is designed by utilizing cell robots as the active "Trojan horse" of oncolytic adenovirus (OA), capable of tumor-selective binding and killing. The OA-loaded cell robots are fabricated by entirely modifying OA-infected 293T cells with cyclic arginine-glycine-aspartic acid tripeptide (cRGD) to specifically bind with bladder cancer cells, followed by asymmetric immobilization of Fe3 O4 nanoparticles (NPs) on the cell surface. OA can replicate in host cells and induce cytolysis to release the virus progeny to the surrounding tumor sites for sustainable infection and oncolysis. The asymmetric coating of magnetic NPs bestows the cell robots with effective movement in various media and wireless manipulation with directional migration in a microfluidic device and bladder mold under magnetic control, further enabling steerable movement and prolonged retention of cell robots in the mouse bladder. The biorecognition of cRGD and robust, controllable propulsion of cell robots work synergistically to greatly enhance their tissue penetration and anticancer efficacy in the 3D cancer spheroid and orthotopic mouse bladder tumor model. Overall, this study integrates cell-based microrobots with virotherapy to generate an attractive robotic system with tumor specificity, expanding the operation scope of cell robots in biomedical community.