Iron Oxide Research Articles

Iron oxide nanoparticles alleviate salt-alkaline stress and improve growth by modulating antioxidant defense system in cherry tomato

ABSTRACT The integration of nanoparticles (NPs) into agriculture is altering traditional methods, enhancing productivity and sustainability. This study explores the application of iron oxide nanoparticles (FeONPs) to mitigate salt-alkaline stress in cherry tomatoes. We investigated FeONPs at three concentrations (FeONP25, FeONP50, FeONP100 mg/kg soil) in pot experiments under non-stress (NS) and salt-alkaline stress (SAS) conditions. SAS conditions decreased biomass and nutrients in untreated plants, a trend reversed by FeONPs. FeONPs treatments significantly boosted pigment levels under SAS, thereby increasing chlorophyll a (10.65–43.05%), chlorophyll b (7.19–41.33%), total chlorophyll (9.84–42.49%), and carotenoids (8.97–36.09%) compared to the control. FeONPs also reduced NPQ under stress, indicating enhanced photosynthetic efficiency. Oxidative stress markers (H2O2, O₂−, and MDA) were strongly induced in control plants but significantly declined with FeONPs treatments. Antioxidants and osmoregulatory substances significantly improved with FeONPs, thereby demonstrating their potential to alleviate SAS in cherry tomato plants.

Water-Dispersible, Magnetically Recyclable Heterogeneous Cobalt Catalyst for C-C and C-N Cross-Coupling Reactions in Aqueous Media.

A cobalt catalyst supported on an iron oxide core, denoted as γ-Fe2O3@PEG@THMAM-Co, has been prepared and characterized by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray mapping, thermogravimetry differential thermogravimetry, vibrating sample magnetometry, and inductively coupled plasma. Polyhydroxy end groups in the shell make the catalyst particles dispersible in water, allowing Hiyama, Suzuki, and C-N cross-coupling reactions of aryl iodides and bromides. The catalyst could be recovered by magnetic decantation and reused for at least five successive runs with a negligent decrease in its activity or changes in its morphology. Water as a solvent without requiring additives, surfactants, or organic co-solvents, as well as an abundant and low-cost cobalt catalyst combined with facile recovery, low leaching, and scalability, provides an environmentally and economically attractive alternative to established palladium-catalyzed C-C and C-N coupling reactions.

Sodium titanate nanostructured modified by green synthesis of iron oxide for highly efficient photodegradation of dye contaminants

Abstract In this study, sodium titanate (ST)/iron oxide (Fe2O3) was successfully prepared as a novel binary photocatalyst for the first time to enhance the photocatalytic activity. The prepared photocatalyst was used in the photodegradation of methylene blue (MB) dye under sunlight and a tungsten lamp. The green synthesis method using orange peel extract was employed to prepare Fe2O3, while the hydrothermal method was used to synthesize ST. To achieve optimal photocatalytic efficiency, the loading of Fe2O3 onto ST was carefully controlled. The average crystallite size of ST, Fe2O3, and ST@Fe2O3 (with a 1:1 wt% ratio) was 999.8, 81.9, and 104 nm, respectively, using the Williamson–Hall (W–H) model. Optical analysis revealed that ST@Fe2O3 had a smaller direct bandgap (2.54 eV) compared to ST@0.3 Fe2O3 (2.70 eV) and ST@0.5 Fe2O3 (3.24 eV). The photodegradation of MB was analyzed considering the weight of the photocatalyst, the irradiation time, and the dye concentration. In-depth explanations of stability and kinetic models were also provided. Remarkably, the ST@Fe2O3 photocatalyst demonstrated superior performance compared to the other evaluated photocatalysts, completely degrading MB dye within just 60 min of solar light exposure. Incorporating Fe2O3 into ST effectively reduces the recombination of photo-produced electron/hole (e/h) pairs and broadens the response range of the solar spectrum. Based on these findings, ST@Fe2O3 appears to have a promising future as a practical photocatalyst for degrading various dye pollutants in wastewater.

Unraveling the synthesis and assembly of gold-iron oxide hybrid nanoparticles

Assembling magnetic particles into an ordered superlattice is an attractive and cost-effective method to create magnetic responsive materials. Introducing noble metals into the magnetic iron-based nanoparticles (NPs) can further tailor the material properties. Such heterogeneous assemblies exhibit distinctive and tunable optical and magnetic properties. However, the growth and assembly of iron-based hybrid nanomaterials involve intricate trade-offs among various complex forces during wet chemical reactions. Consequently, their dynamic assembly mechanism remains unclear, making it challenging to achieve controllable heterogeneous assembly and self-assembly induced by intrinsic magnetic interactions. Here, we observed the heterogeneous assembly between gold (Au) and iron oxide (FeOx) domains, as well as the self-assembly of the Au-FeOx hetero-NPs into superlattices. The heterogeneous assembly between the FeOx component and Au seed NPs enables the control of hetero-NPs, encompassing core-shell, flower-shaped, to dimeric morphologies. Moreover, pure FeOx NPs and Au-FeOx hetero-NPs showed spontaneous self-assembly into hexagonal close-packed superstructures in the SAXS pattern, occurring after reaching 7.5 and 9.1 nm, respectively. These self-assembly processes are dominated by the magnetic dipolar interactions related to the critical size of the FeOx domains. This work sheds light on developing the next generation of magnetic-functional materials with hierarchical assembly.

Comparable Antibacterial Effects of Silver and Iron Oxide Nanoparticles on Urinary Calculi Obtained After Percutaneous Nephrolithotomy

Background: In recent years, science and industry have focused on preparing nanoparticles (NPs). Due to the resistance of bacteria to antibiotics, there is an overwhelming need to find effective antimicrobials with fewer side effects. Objectives: The aim of this study was to synthesize silver and iron oxide NPs and investigate their antimicrobial effects on bacteria isolated from urinary stones. Methods: Cases of urolithiasis from 45 patients with staghorn stones, extracted through percutaneous nephrolithotomy (PCNL), were included in the study. Urinary stone cultures were performed, and the isolation and identification of bacteria were done using standard microbiological techniques. Silver and iron oxide NPs were synthesized, and the minimum bactericidal concentration (MBC) and minimum inhibitory concentration (MIC) were evaluated for the isolates. Results: Seventeen (60.7%) out of 28 positive cultured cases of the isolated bacteria were gram-negative, and 11 (39.3%) were gram-positive. The most abundant isolated bacterium was Escherichia coli, with 13 cases (46.4%). The antibacterial effects of silver and iron oxide NPs revealed that the maximum inhibitory zone for Ag NPs at 1000 ppm was 23 mm, and for Fe3O4 NPs, it was 18.5 mm. The MIC was 180 µg/mL for Ag and 250 µg/mL for Fe3O4. The MBC was 228 µg/mL for Ag and 300 µg/mL for Fe3O4. Conclusions: Nanoparticles exhibited antibacterial effects on the bacteria studied in a concentration-dependent manner. Ag NPs showed a more pronounced bactericidal effect than Fe3O4 NPs. As a result, these two NPs demonstrated effective antibacterial activity against both gram-positive and gram-negative bacteria.

Sodium titanate nanostructured modified by green synthesis of iron oxide for highly efficient photodegradation of dye contaminants

Abstract In this study, sodium titanate (ST)/iron oxide (Fe2O3) was successfully prepared as a novel binary photocatalyst for the first time to enhance the photocatalytic activity. The prepared photocatalyst was used in the photodegradation of methylene blue (MB) dye under sunlight and a tungsten lamp. The green synthesis method using orange peel extract was employed to prepare Fe2O3, while the hydrothermal method was used to synthesize ST. To achieve optimal photocatalytic efficiency, the loading of Fe2O3 onto ST was carefully controlled. The average crystallite size of ST, Fe2O3, and ST@Fe2O3 (with a 1:1 wt% ratio) was 999.8, 81.9, and 104 nm, respectively, using the Williamson–Hall (W–H) model. Optical analysis revealed that ST@Fe2O3 had a smaller direct bandgap (2.54 eV) compared to ST@0.3 Fe2O3 (2.70 eV) and ST@0.5 Fe2O3 (3.24 eV). The photodegradation of MB was analyzed considering the weight of the photocatalyst, the irradiation time, and the dye concentration. In-depth explanations of stability and kinetic models were also provided. Remarkably, the ST@Fe2O3 photocatalyst demonstrated superior performance compared to the other evaluated photocatalysts, completely degrading MB dye within just 60 min of solar light exposure. Incorporating Fe2O3 into ST effectively reduces the recombination of photo-produced electron/hole (e/h) pairs and broadens the response range of the solar spectrum. Based on these findings, ST@Fe2O3 appears to have a promising future as a practical photocatalyst for degrading various dye pollutants in wastewater.

Comparable Antibacterial Effects of Silver and Iron Oxide Nanoparticles on Urinary Calculi Obtained After Percutaneous Nephrolithotomy

Background: In recent years, science and industry have focused on preparing nanoparticles (NPs). Due to the resistance of bacteria to antibiotics, there is an overwhelming need to find effective antimicrobials with fewer side effects. Objectives: The aim of this study was to synthesize silver and iron oxide NPs and investigate their antimicrobial effects on bacteria isolated from urinary stones. Methods: Cases of urolithiasis from 45 patients with staghorn stones, extracted through percutaneous nephrolithotomy (PCNL), were included in the study. Urinary stone cultures were performed, and the isolation and identification of bacteria were done using standard microbiological techniques. Silver and iron oxide NPs were synthesized, and the minimum bactericidal concentration (MBC) and minimum inhibitory concentration (MIC) were evaluated for the isolates. Results: Seventeen (60.7%) out of 28 positive cultured cases of the isolated bacteria were gram-negative, and 11 (39.3%) were gram-positive. The most abundant isolated bacterium was Escherichia coli, with 13 cases (46.4%). The antibacterial effects of silver and iron oxide NPs revealed that the maximum inhibitory zone for Ag NPs at 1000 ppm was 23 mm, and for Fe3O4 NPs, it was 18.5 mm. The MIC was 180 µg/mL for Ag and 250 µg/mL for Fe3O4. The MBC was 228 µg/mL for Ag and 300 µg/mL for Fe3O4. Conclusions: Nanoparticles exhibited antibacterial effects on the bacteria studied in a concentration-dependent manner. Ag NPs showed a more pronounced bactericidal effect than Fe3O4 NPs. As a result, these two NPs demonstrated effective antibacterial activity against both gram-positive and gram-negative bacteria.

Iron mineral type controls organic matter stability and priming in paddy soil under anaerobic conditions

Associations of iron (hydr)oxides (FeOx) with organic carbon are vital in regulating the stability of soil organic carbon (SOC). Like SOC, FeOx is chemically dynamic in soils, particularly under anaerobic conditions. However, previous research has not clarified how the stability of FeOx (goethite versus ferrihydrite) and the formation pathway of FeOx-OC associations (adsorption versus coprecipitation) affect the stability of FeOx-bound OC and, subsequently, the priming effect (PE) under anaerobic conditions. With an aim to bridge this gap, we incubated paddy soils for 80 d under anaerobic conditions after adding free 13C-glucose, ferrihydrite- or goethite-bound 13C-glucose formed by either adsorption or coprecipitation. Compared with the free glucose addition, the FeOx-bound glucose addition increased 13CO2 production by 8%–21% but reduced 13C–CH4 production by 7%–10%. Ferrihydrite-bound glucose was mineralised more than goethite-bound glucose; this is consistent with its lower crystallinity facilitating reduction and, thus, higher OC bioavailability. Glucose induced a negative priming effect (PE) for CO2 but a positive PE for CH4, whereas FeOx-bound glucose showed the opposite trend. This may be because FeOx-bound glucose provides an energy source and electron acceptor for Fe-reducing bacteria; this promotes the dissimilating reduction of iron and combines with an aggravated microbial P limitation resulting from the FeOx input. The crystallinity of FeOx affected the amount of primed CH4 rather than its formation pathway. In conclusion, the crystallinity of FeOx controls the stability of FeOx-OC associations and the PE of SOC decomposition under anaerobic conditions.

The careful selection of zwitterionic nanoparticle coating results in rapid and efficient cell labeling for imaging‐based cell tracking

AbstractThe increased clinical application of cell‐based therapies has resulted in a parallel increase in the need for non‐invasive imaging‐based approaches for cell tracking, often through labeling with nanoparticles. An ideal nanoparticle for such applications must be biologically compatible as well as readily internalized by cells to ensure adequate and stable cell loading. Surface coatings have been used to make nanoparticle trackers suitable for these purposes, but those currently employed tend to have cytotoxic effects. Zwitterionic ligands are known to be biocompatible and antifouling; however, head‐to‐head evaluation of specific zwitterionic ligands for cell loading has not yet been explored. Magnetic particle imaging (MPI) detects superparamagnetic iron oxide nanoparticles (SPIONs) using time‐varying magnetic fields. Because MPI can produce high‐contrast, real‐time images with no tissue depth limitation, it is an ideal candidate for in vivo cell tracking. In this work, we have conjugated hard (permanently charged) and soft (pKa‐dependently charged) biomimetic zwitterionic ligands to SPIONs and characterized how these ligands changed SPION physicochemical properties. We have evaluated cellular uptake and subcellular localization between zwitterions, how the improvement in cell uptake generated stronger MPI signal for smaller numbers of cells, and how these cells can be tracked in an animal model with greater sensitivity for longer periods of time. Our best‐performing surface coating afforded high cell loading within 4 h, with full signal retention in vivo over 7 days.

The careful selection of zwitterionic nanoparticle coating results in rapid and efficient cell labeling for imaging‐based cell tracking

AbstractThe increased clinical application of cell‐based therapies has resulted in a parallel increase in the need for non‐invasive imaging‐based approaches for cell tracking, often through labeling with nanoparticles. An ideal nanoparticle for such applications must be biologically compatible as well as readily internalized by cells to ensure adequate and stable cell loading. Surface coatings have been used to make nanoparticle trackers suitable for these purposes, but those currently employed tend to have cytotoxic effects. Zwitterionic ligands are known to be biocompatible and antifouling; however, head‐to‐head evaluation of specific zwitterionic ligands for cell loading has not yet been explored. Magnetic particle imaging (MPI) detects superparamagnetic iron oxide nanoparticles (SPIONs) using time‐varying magnetic fields. Because MPI can produce high‐contrast, real‐time images with no tissue depth limitation, it is an ideal candidate for in vivo cell tracking. In this work, we have conjugated hard (permanently charged) and soft (pKa‐dependently charged) biomimetic zwitterionic ligands to SPIONs and characterized how these ligands changed SPION physicochemical properties. We have evaluated cellular uptake and subcellular localization between zwitterions, how the improvement in cell uptake generated stronger MPI signal for smaller numbers of cells, and how these cells can be tracked in an animal model with greater sensitivity for longer periods of time. Our best‐performing surface coating afforded high cell loading within 4 h, with full signal retention in vivo over 7 days.

TiO2 and Reducing Gas: Intricate Relationships to Direct Reduction of Iron Oxide Pellets

AbstractIn response to the imperative for sustainable iron production with reduced CO2 emissions, this study delves into the intricate role of TiO2 in the direct reduction of iron oxide pellets. The TiO2-dependent reducibility of iron oxide pellets utilizing H2 and CO gas across varied temperatures and gas compositions is thoroughly investigated. Our findings unveil the nuanced nature of the TiO2 effect, underscored by its concentration-dependent behavior, revealing an optimal range between 1 and 1.5 pct TiO2, where a neutral or positive impact on reduction kinetics and diffusion coefficient is observed. Notably, the synergistic interplay of CO and H2 at 1000 °C emerges as particularly efficacious, suggesting complementary effects on the reduction process. The introduction of H2 into the reducing atmosphere regulated by CO not only extends the transition range but also markedly expedites the rate of reduction. Furthermore, our study highlights the temperature sensitivity of the TiO2 effect, with higher TiO2 content correlating with prolonged reduction time in a 100 pct H2 atmosphere at 900 °C. In a 100 pct H2 atmosphere, the non-contributory role of TiO2 stems from the water-gas shift reaction. Conversely, introducing H2 into a CO-controlled reducing atmosphere with TiO2 enhances the transition range and expedites the reduction rate. Additionally, our findings underscore the role of total iron content, revealing a direct correlation with the reduction process.

Novel magnetic iron oxide-dextran sulphate nanocomposites as potential anticoagulants: Investigating interactions with blood components and assessing cytotoxicity

Examining the critical role of anticoagulants in medical practice, particularly their central function in preventing abnormal blood clotting, is of the utmost importance. However, the study of interactions between blood proteins and alternative anticoagulant nano-surfaces is still understood poorly. In this study, novel approach involving direct functionalisation of magnetic iron oxide nanoparticles (MNPs) as carriers with sulphated dextran (s-dext) is presented, with the aim of evaluating the potential of magnetically-responsive MNPs@s-dext as anticoagulants. The physicochemical characterisation of the synthesised MNPs@s-dext includes crystal structure analysis, morphology study, surface and electrokinetic properties, thermogravimetric analysis and magnetic properties` evaluation, which confirms the successful preparation of the nanocomposite with sulfonate groups. The anticoagulant potential of MNPs@s-dext was investigated using a standardised activated partial thromboplastin time (APTT) test and a modified APTT test with a quartz crystal microbalance with dissipation (QCM-D) which confirmed the anticoagulant effect. Time-resolved solid-liquid interactions between the MNPs@s-dext and model blood proteins bovine serum albumin and fibrinogen were also investigated, to gain insight into their hemocompatibility, and revealed protein-repellence of MNPs@s-dext against blood proteins. The study also addressed comprehensive cytotoxicity studies of prepared nanocomposites, and provided valuable insights into potential applicability of MNPs@s-dext as a promising magnetic anticoagulant in biomedical contexts.

Smoke Suppression Properties of Fe2O3 on Intumescent Fire-Retardant Coatings of Styrene–Acrylic Emulsion

The intumescent flame-retardant coatings were prepared using ammonium polyphosphate (APP), pentaerythritol (PER), melamine (MEL), styrene–acrylic emulsion, and iron oxide yellow (FeOOH) as the base material. A cone calorimeter (CCT), smoke density meter (SDA), and scanning electron microscope (SEM) were employed to investigate the smoke suppression and flame retardancy of FeOOH in intumescent fire-retardant coatings. The thermal degradation performance of intumescent fireproofing coatings with varying FeOOH content was investigated through thermogravimetric analysis (TGA). The structure of the carbon slag in the CCT test was analyzed using a scanning electron microscope (SEM). The results of the cone calorimeter (CCT) experiments demonstrated that FeOOH significantly reduced the heat release rate (HRR), total heat release rate (THR), smoke production rate (SPR), and total smoke release rate (TSR) of the coating, while simultaneously increasing the carbon residue rate of the coating. The smoke density analysis (SDA) results demonstrate that adding FeOOH can effectively reduce smoke generation, regardless of whether a pilot flame is used. TGA results demonstrate that FeOOH can enhance the weight of coke residue at elevated temperatures. SEM results indicate that incorporating FeOOH resulted in a more compact coke residue. According to these findings, among all the samples, those containing 2 wt% FeOOH showed low levels of HRR, THR, SPR, and TSR and high levels of SOD, which proves that FeOOH can be used as a smoke inhibitor in flame-retardant coatings.

Effect of composition and processing conditions on the direct reduction of iron oxide pellets

In this paper, HSC software is used to estimate the effects of composition and processing conditions on the reduction behavior of iron oxide pellets, i.e., hematite (Fe2O3), magnetite (Fe3O4), wustite (FeO), pure iron (Fe), and iron carbide (Fe3C), in a wide temperature range from room temperature (RT) to 1000°C in the presence of H2 and CO mixtures. The reducibility of iron ores, in particular Fe2O3, Fe3O4, FeO, Fe is discussed. The choice of reducing agents CO and H2 is explained, with CO proving to be the more effective reducing agent at high temperatures from a thermodynamic point of view. However, the free Gibbs energy of iron reduction is lowest in the presence of a 100% H2 atmosphere. In addition, H2 reduces tortuosity and increases porosity by reducing it at cooler temperatures and promoting diffusion. In contrast, CO increases tortuosity and reduces initial porosity because it requires higher temperatures for effective reduction and causes structural changes. The presence of impurities other than iron oxides has been shown to impair the activity of reduced pure iron by acting as catalyst poisons or participating in competing reactions. CaO accelerates the reduction of FeO, which is due to the formation of calcium ferrite, but the effect decreases at higher temperatures. MgO can either promote or hinder reduction, depending on its concentration and its influence on pellet porosity. The presence of several non‑iron oxides has been shown to affect the overall direct reduction of iron ore pellets, resulting in a significant impact of the overall process.

Zinc isotope fractionation during coprecipitation with amorphous iron (hydr)oxides

Coprecipitation facilitates the incorporation of Zn into the lattice of Fe (hydr)oxide, which is a crucial mechanism causing low Zn bioavailability in widespread Zn-deficient soils. Zn isotopes are a potential indicator of the coprecipitation of Zn and Fe (hydr)oxides in soils. However, the Zn isotope fractionation caused by coprecipitation with amorphous Fe (hydr)oxides (e.g., ferrihydrite) and the impact of environmentally relevant conditions remain unknown. Here, the molecular mechanism and impact factor of Zn isotope fractionation during Zn2+-Fe3+ coprecipitation under natural soil conditions (including different pH values and initial Zn/Fe ratios) were investigated by combining isotope ratio measurements, extended X-ray absorption fine structure (EXAFS) analyses, and density functional theory (DFT) geometry optimization. The results show that aqueous Zn (Znaq) can be complexed on the ferrihydrite surface (Znads) with positive isotope fractionation (Δ66Znads–aq = 0.42 ± 0.09 ‰) or directly incorporated into the ferrihydrite lattice with slightly negative isotope fractionation (Δ66Znstru-aq = −0.08 ± 0.03 ‰). In addition, over time, the surface-complexed Zn can further transform to a layered structure on the surface but exhibits limited Zn isotope fractionation. According to Zn K-edge EXAFS, the Zn isotope fractionation of surface complexation and incorporation of Znaq are related to the decrease in the Zn–O bond strength in the order surface complexed Zn (RZn–O = 2.00 Å) > aqueous Zn (RZn–O = 2.08 Å) > directly incorporated Zn (RZn–O = 2.06–2.07 Å with slight distortion). The limited Zn isotope fractionation associated with the transformation of Znads is related to the reconfiguration of Znads during the nucleation of octahedral Zn layer structures. Furthermore, the primary process controlling Zn isotope fractionation is different under varying experimental conditions, leading to distinct Zn isotope fractionation between the bulk solid and solution during Zn–Fe coprecipitation. Low pH values (5.0–6.0) and initial Zn/Fe ratios (0.01–0.02) favor the direct precipitation of Znaq, resulting in slightly negative Zn isotope fractionation between the bulk solid and solution. In contrast, high pH values (7.0–7.5) and initial Zn/Fe ratios (0.1–0.2) favor surface complexation and the transformation of Znads, leading to heavy Zn isotope enrichment in the bulk solid. These findings offer novel insights into the primary mechanism through which Fe (hydr)oxides regulate Zn bioavailability in Zn-deficient soils and provide experimental evidence supporting the potential application of Zn isotopes as an indicator for comprehending the fate of Zn controlled by Fe (hydr)oxides in soils.

Influence of tartaric acid on the electron transfer between oxyanions and lepidocrocite

Iron oxide minerals control the environmental behavior of trace elements. However, the potential effects of electron transfer directions by iron oxides between organic acids and trace elements remain unclear. This study investigates the redox capacity of tartaric acid (TA) with chromate (Cr(Ⅵ)) or arsenate (As(V)) on lepidocrocite (Lep) from the perspective of electron transfer. The results demonstrated the configurations of TA (bidentate binuclear (BB)), As(V) (BB), and Cr(Ⅵ) (BB and protonated monodentate binuclear (HMB)) on Lep. Frontier molecular orbital calculations and X-ray photoelectron spectroscopy (XPS) binding energy shifts further indicated different electron transfer directions between TA and the oxyanions on Lep. The iron of Lep might act as electron acceptors when TA is adsorbed, whereas the iron and oxygen of Lep act as electron donors when As(V) is adsorbed. The iron of Lep might accept electrons from its oxygen and subsequently transfer these electrons to Cr(Ⅵ). Macroscopic validation experiments showed the reduction of Cr(VI), whereas no reduction of As(V). The XPS analysis showed a peak shift, with the possible formation of As–Fe–TA ternary complexes and electron transfer on Lep. These findings indicate that mineral interfacial electron transfer considerably influences the transport and transformation of oxyanions.

Iron oxide nanoparticles of Cystoseira sp. Sugar alcohol treat MRSA and thyroid gland cancer

PurposeMethicillin-resistant Staphylococcus aureus (MRSA) infections are emerging as a cause of suppurative thyroiditis. The resistance to several antibiotics and finding treatment has grown more difficult. Hence, the purpose of this study was to examine biosynthesized iron oxide nanostructures’ antimicrobial activity as well as their cytotoxicity on normal and thyroid cancer cells. MethodsBy using the sugar alcohols of Cystoseira sp., the authors synthesized the advanced biosynthesis of iron oxide nanoparticles (COINs). An agar-well diffusion method and a broth dilution method were used to investigate COINs’ antimicrobial activity against MRSA isolates. However, their cytotoxicity against normal and thyroid cancer cell lines was determined by the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. ResultsA GC–MS analysis of the dried Cystoseira sp. extract revealed a high percentage of D-mannitol, which is essential for the synthesis of spherical nanoparticles with a mean average size of 5.8 ± 0.8 nm. The COINs showed a higher inhibition zone (9–15 mm) for 66.6 % of MRSA isolates, and the MIC of COINs was 256 μg/ml. The cell wall of these bacteria inhabits the absorption of COINs. As a result, a large concentration of COINs is required to restrict bacterial growth. Moreover, COINs have cytotoxicity on thyroid cancer cell proliferation and normal thyroid cell lines at IC50s of 1.71 ± 0.1 and 25.9 ± 1.6 μg/ml, respectively. This can be due to the negative charge of sugar alcohols, which affect protein absorption and subsequent biological behaviors. ConclusionThe promising findings of this study are in favor of the creation of very small iron oxide nanostructures for therapy.

Degree of PEGylatation of Lumbricus terrestris Hemoglobin Improves Microcirculatory Blood Flow but Increases the Rate of Auto-Oxidation.

The demand for red blood cells (RBCs) is on the rise due to the increasing diagnosis of chronic diseases such as sickle cell anemia, malaria, and thalassemia. Despite many commercial attempts, there are no U.S. FDA-approved artificial RBCs for use in humans. Existing RBC substitutes have employed various strategies to transport oxygen, extend the circulation time, and reduce organ toxicity, but none have replicated the natural protective mechanisms of RBCs, which prevent hemoglobin (Hb) dimerization and heme iron oxidation. Lumbricus terrestris (earthworm) erythrocruorin (LtEc) is a naturally occurring extracellular hemoglobin (Hb) with promising attributes: large molecular diameter (30 nm), high molecular weight (3.6 MDa), low auto-oxidation rate, and limited nitric oxide-scavenging properties. These characteristics make LtEc an ideal candidate as an RBC substitute. However, LtEc has a significant drawback, its short circulatory half-life. To address this issue, we explored thiol-mediated surface PEGylation of LtEc (PEG-LtEc) at varying polyethylene glycol (PEG) surface coverages. Increasing PEG surface coverage beyond 40% destabilizes LtEc into smaller subunits that are 1/12th the size of LtEc. Therefore, we evaluated two PEG surface coverage options: PEG-LtEc-0.2 (20% PEGylation) and PEG-LtEc-1.0 (100% PEGylation). We conducted experiments using golden Syrian hamsters with dorsal window chambers and catheters to assess the efficacy of these solutions. We measured microvascular parameters, organ function, cerebral blood flow, circulation time, mean arterial pressure, heart rate, and blood gases and performed histology to screen for toxicity. Our findings indicate that both PEG-LtEc molecules offer significant benefits in restoring microvascular parameters, organ function, cerebral blood flow, and circulation time compared to LtEc alone. Notably, PEG-LtEc-1.0 showed superior microvascular perfusion, although it exhibited a higher rate of auto-oxidation compared to PEG-LtEc-0.2. These results underscore the advantages of PEGylation in terms of tissue perfusion and organ health while highlighting its limitations.

Advances in functionalization and conjugation mechanisms of dendrimers with iron oxide magnetic nanoparticles.

Iron oxide magnetic nanoparticles (MNPs) are crucial in various areas due to their unique magnetic properties. However, their practical use is often limited by instability and aggregation in aqueous solutions. This review explores the advanced technique of dendrimer functionalization to enhance MNP stability and expand their application potential. Dendrimers, with their symmetric and highly branched structure, effectively stabilize MNPs and provide tailored functional sites for specific applications. We summarize key synthetic modifications, focusing on the impacts of dendrimer size, surface chemistry, and the balance of chemical (e.g., coordination, anchoring) and physical (e.g., electrostatic, hydrophobic) interactions on nanocomposite properties. Current challenges such as dendrimer toxicity, control over dendrimer distribution on MNPs, and the need for biocompatibility are discussed, alongside potential solutions involving advanced characterization techniques. This review highlights significant opportunities in environmental, biomedical, and water treatment applications, stressing the necessity for ongoing research to fully leverage dendrimer-functionalized MNPs. Insights offered here aim to guide further development and application of these promising nanocomposites.

Antibody-Decorated Nanoplatform to Reprogram Macrophage and Block Immune Checkpoint LSECtin for Effective Cancer Immunotherapy.

Repolarizing tumor-associated macrophages (TAMs) into tumor-inhibiting M1 macrophages has been considered a promising strategy for enhanced cancer immunotherapy. However, several immunosuppressive ligands (e.g., LSECtin) can still be highly expressed on M1 macrophages, inducing unsatisfactory therapeutic outcomes. We herein developed an antibody-decorated nanoplatform composed of PEGylated iron oxide nanoparticles (IONPs) and LSECtin antibody conjugated onto the surface of IONPs via the hydrazone bond for enhanced cancer immunotherapy. After intravenous administration, the tumor microenvironment (TME) pH could trigger the hydrazone bond breakage and induce the disassociation of the nanoplatform into free LSECtin antibodies and IONPs. Consequently, the IONPs could repolarize TAMs into M1 macrophages to remodel immunosuppressive TME and provide an additional anticancer effect via secreting tumoricidal factors (e.g., interlukin-12). Meanwhile, the LSECtin antibody could further block the activity of LSECtin expressed on M1 macrophages and relieve its immunosuppressive effect on CD8+ T cells, ultimately leading to significant inhibition of tumor growth.