Size Of Iron Oxide Nanoparticles Research Articles

Investigating the toxic effects induced by iron oxide nanoparticles on neuroblastoma cell line: an integrative study combining cytotoxic, genotoxic and proteomic tools

Nanomaterials have gained much attention for their use and benefit in several fields. Iron Oxide Nanoparticles (IONPs) have been used in Biomedicine as contrast agents for imaging cancer cells. However, several studies reported the potential toxicity of those nanoparticles in different models, especially in cells. Therefore, in our present study, we investigated the effects of IONPs on the SH-SY5Y neuroblastoma cell line. We carried out cytotoxic and genotoxic studies to evaluate the phenotypic effects, and proteomic investigation to evaluate the molecular effects and the mechanisms by which this kind of NPs could induce toxicity. Our results showed that the use of three different sizes of IONPs (14, 22 and 30 nm) induced cell detachment, cell morphological changes, size, and concentration-dependent IONP internalization and cell mortality. IONPs induced slight genotoxic damage assayed by modified comet assay without affecting cell cycle, mitochondrial function, membrane integrity, intracellular calcium level, and without inducing ROS generation. All the studies were performed to compare also the effects of IONPs to the ferric iron by incubating cells with equivalent concentration of FeCl3. In all tests, the NPs exhibited more toxicity than the ferric iron. The proteomic analysis followed by gene ontology and pathway analysis evidenced the effects of IONPs on cytoskeleton, cell apoptosis, and cancer development. Our findings provided more information about IONP effects on human cells and especially on cancer cell line.

Genotoxic Assessment of Different Sizes of Iron Oxide Nanoparticles and Ionic Iron in Earthworm (Eisenia hortensis) Coelomocytes by Comet Assay and Micronucleus Test.

The current study was designed to evaluate genotoxicity of different sizes of iron oxide nanoparticles (IONPs) and ionic iron using coelomocytes of the earthworms Eisenia hortensis. Earthworms were exposed to different series of IONPs and ionic iron concentrations to find the respective LC50 of the chosen chemicals. LC50 for < 50, <100nm and the ionic iron of IONPs were 500, 200, 250µg/mL respectively. Concentrations of LC50/2 (250, 100, 125µg/mL for < 50, <100nm and the ionic iron respectively) and LC50 for 48 h were used to perform the comet assay and micronucleus test. Statistically significant (p < 0.05) increase in DNA and chromosomal damage was observed for all sizes of IONPs and ionic iron. In the comet assay system, the greatest genotoxicity was observed in the treatments with < 100nm IONPs, whereas the greatest numbers of micronuclei and binucleate cells were observed in the treatments with ionic iron. It was concluded that different types of nanoparticles (i.e. sizes, shapes) may have different genotoxic potencies in different assays with E. hortensis earthworms.

Cytotoxicity assay of plant-mediated synthesized iron oxide nanoparticles using Juglans regia green husk extract

Synthesis of iron oxide nanoparticles has attracted increasing interest due to their importance in biomedical and technological applications. To investigate the ability of Juglans regia (J. regia) green husk extract in iron oxide nanoparticles size control, they were synthesized through co-precipitation method with J. regia extract and without it. For both tests, other experimental conditions were same. According to High-resolution transmission electron microscopy, the mean diameter and standard deviation of iron oxide nanoparticles and J. regia/iron oxide nanoparticles synthesized using co-precipitation method were 12.60 ± 2.87 and 5.77 ± 1.66 nm respectively. These results showed that J. regia/iron oxide nanoparticles synthesized using extract have a smaller size than nanoparticles fabricated by co-precipitation method; moreover, green husk extract plays the main role as size control. The obtained results of Powder X-ray diffraction (PXRD), High resolution transmission electron microscopy (HR-TEM), Field emission scanning electron microscopy (FESEM), and Energy dispersive X-ray (EDX) are in good agreement with each other and confirm the high purity of fabricated magnetic nanoparticles using J. regia extract. Vibrating sample magnetometer (VSM) revealed that the J. regia/iron oxide nanoparticles due to their proper magnetic properties have high saturation magnetization and low coercivity. According to FTIR spectrum, the J. regia would be coated on the iron oxide nanoparticles surface in a successful manner. The non-toxic effect of J. regia/iron oxide nanoparticles concentration below 1000 µg/ml was observed in the studies of in vitro cytotoxicity on normal and cancerous cell lines, respectively. The dose-dependent toxicity made it a suitable candidate for various medical applications.

Evaluation of antibacterial activity and toxic metal removal of chemically synthesized magnetic iron oxide titanium coated nanoparticles and application in bacterial treatment

ABSTRACTCo-precipitation method was used for preparation of two types of iron oxide nanoparticles coated by titanium dioxide according to divalent salts used. The average size of iron oxide nanoparticles coated by titanium dioxide measured by particle size analyzer, ranged approximately between 20 nm and 100 nm with mean particle size of 60 nm. Characterization of the prepared nanoparticles was done by X-ray diffraction analysis and scanning electron microscope indicating the sole existence of inverse cubic spinel phase of magnetic iron oxide nanoparticles. Further, the antibacterial activity of two prepared iron oxide nanoparticles was evaluated against four pathogenic bacteria where both preparations showed promising antibacterial activities against Gram positive and Gram negative strains which offers a potential application in pharmaceutical and biomedical industries. The antibacterial activity showed high reduction percent after 30 min by 150 μg mL−1 of nanoparticles prepared. Also, high reduction percent was achieved for removal of iron and manganese ions from polluted water and good effect on decreasing chemical oxygen demand and biochemical oxygen demand concentrations with decreased percent of total nitrogen concentration.

Formation of iron oxide nanoparticles for the photooxidation of water: Alteration of finite size effects from ferrihydrite to hematite

Iron oxide nanoparticles represent a promising low-cost environmentally-friendly material for multiple applications. Especially hematite (α-Fe2O3) nanoparticles demonstrate great possibilities in energy storage and photoelectrochemistry. A hydrothermal one-pot synthesis can be used to synthesise hematite nanoparticles. Here, the particle formation, nucleation and growth of iron oxide nanoparticles using a FeCl3 precursor over time is monitored. The formation of 6-line ferrihydrite seeds of 2–8 nm which grow with reaction time and form clusters followed by a phase transition to ~15 nm hematite particles can be observed with ex situ X-ray diffraction (XRD), transmission electron microscopy (TEM), Raman and UV/Vis spectroscopy. These particles grow with reaction time leading to 40 nm particles after 6 hours. The changes in plasmon and electron transition patterns, observed upon particle transition and growth lead to the possibility of tuning the photoelectrochemical properties. Catalytic activity of the hematite nanoparticles can be proven with visible light irradiation and the use of silver nitrate as scavenger material. The generation of elementary silver is dependent on the particle size of iron oxide nanoparticles while only slight changes can be observed in the oxygen generation. Low-cost nanoscale hematite, offers a range of future applications for artificial photosynthesis.

Iron Oxide Nanoparticles Derived from Mill Scale Waste as Potential Scavenging Agent in Dye Wastewater Treatment for Batik Industry

In this work, iron oxide were derived from millscale has been used as a potential scavenging agent in wastewater treatment due to its high adsorption capacity and its shorter sedimentation time during wastewater treatment. Iron oxide obtained from the magnetic separation technique was subjected to high energy ball milling (HEBM) at different milling time to produce different size of nanoparticles of iron oxide. X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM) and Scanning Trasmission Electron microscopy (STEM) were performed to study the morphological properties of the iron oxide nanoparticles. After HEBM, iron oxide nanoparticles was modified with Hexadecyltrimethylammonium Bromide (CTAB) to study the adsorption possibility of iron oxide nanoparticle modified with CTAB (Iron oxide– CTAB nanoparticles) in dye wastewater. The variation effect of particle size of derived Iron oxide– CTAB were studied. Permanent magnet was used to separate iron oxide nanoparticles from the solution. The clear part of the solution (treated wastewater) was filtered out and adsorption efficiency of Iron oxide– CTAB nanoparticles was measured using UV – Visible spectroscopy. Efficiency adsorption of iron oxide nanoparticles modified with CTAB greatly achieved above 99 % and the size of iron oxide nanoparticles affected its performance in dye wastewater treatment.

Effect of iron oxide nanoparticle size on electromagnetic properties of composite nanofibers

Electrically conductive and magnetically permeable carbon nanofiber-based composites were developed using the electrospinning with subsequent heat treatment. The composite nanofiber contains a variable composition of magnetite nanoparticles with two different size regimes, ranging from superparamagnetic (10–20 nm) to ferromagnetic (20–30 nm). The composite nanofibers are then characterized using Scanning/Transmission Electron Microscopy, X-Ray Diffractometry, Raman Spectroscopy, four-point probe, and a Superconducting Quantum Interference Device. Electromagnetic Interference Shielding Effectiveness of pristine carbon nanofibers as well as electromagnetic composite nanofibers are examined in the X-band frequency region. Higher degree of graphitization, electrical conductivity, and magnetic strength are obtained for nanocomposites containing larger magnetite nanoparticles (20–30 nm). A transition from superpartamagnetic to ferromagnetic characteristics is observed during nanocomposite processing. Electromagnetic Interference Shielding Effectiveness of as high as 68 dB (in the working frequency of 10.4 GHz) is observed for composite nanofibers fabricated with larger magnetite nanoparticles carbonized at 900℃.

Genotoxic evaluation of different sizes of iron oxide nanoparticles and ionic form by SMART, Allium and comet assay

In this study, the genotoxic potential of <50 nm, <100 nm iron oxide (Fe2O3) nanoparticles (IONPs) and ionic form were investigated using the wing somatic mutation and recombination test (SMART) and Allium and comet assays. In the SMART assay, different concentrations (1, 2, 5 and 10 mM) of NPs and ionic forms were fed to transheterozygous larvae of Drosophila melanogaster. No significant genotoxic effect was observed in <100 nm NPs and ionic form, while <50 nm IONPs showed genotoxicity at 1 and 10 mM concentrations. Allium cepa root meristems were exposed to five concentrations (0.001, 0.01, 0.1, 1 and 10 mM) of <50 nm and ionic forms for 4 h and three concentrations (2.5, 5 and 10 mM) for <100 nm of IONPs for 24 and 96 h. There was a statistically significant effect at 96 h at all concentrations of <100 nm IONPs. Similarly, <50 nm of IONPs and ionic forms also showed a statistically significant effect on mitotic index frequencies for all concentrations at 4 h. There was a dose-dependent increase in chromosomal abnormalities for IONPs and ionic form. Comet assay results showed time- and concentration-dependent increases in <100 nm NPs. There was a concentration-dependent increase in <50 nm NPs and ionic form ( p < 0.05). Consequently, the <50 nm of Fe2O3 was found toxic compared to 100 nm Fe2O3 and ionic form.

Effect of solvents on morphology, magnetic and dielectric properties of (α-Fe2O3@SiO2) core-shell nanoparticles.

Present work describes the formation of α-Fe2O3@SiO2 core shell structure by systematic layer by layer deposition of silica shell on core iron oxide nanoparticles prepared via various solvents. Sol-gel method has been used to synthesize magnetic core and the dielectric shell. The average crystallite size of iron oxide nanoparticles was calculated ∼20 nm by X-ray diffraction pattern. Morphological study by scanning electron microscopy revealed that the core-shell nanoparticles were spherical in shape and the average size of nanoparticles increased by varying solvent from methanol to ethanol to isopropanol due to different chemical structure and nature of the solvents. It was also observed that the particles prepared by solvent ethanol were more regular and homogeneous as compared to other solvents. Magnetic measurements showed the weak ferromagnetic behaviour of both core α-Fe2O3 and silica-coated iron oxide nanoparticles which remained same irrespective of the solvent chosen. However, magnetization showed dependency on the types of solvent chosen due to the variation in shell thickness. At room temperature, dielectric constant and dielectric loss of silica nanoparticles for all the solvents showed decrement with the increment in frequency. Decrement in the value of dielectric constant and increment in dielectric loss was observed for silica coated iron oxide nanoparticles in comparison of pure silica, due to the presence of metallic core. Homogeneous and regular silica layer prepared by using ethanol as a solvent could serve as protecting layer to shield the magnetic behaviour of iron oxide nanoparticles as well as to provide better thermal insulation over pure α-Fe2O3 nanoparticles.

Adsorption Kinetics and Evaluation Study of Iron Oxide Nanoparticles Impregnated in Polyurethane Matrix for Water Filtration Application

A polyurethane (PU) foam composite, loaded with iron oxide nanoparticles (IONPs), was developed for arsenic removal from drinking water at low concentrations. The effect of various synthesis parameters such as the size of IONPs and the foam shape, on the performance of the adsorbents in removing arsenic was investigated. To examine the surface adsorption of arsenic species, Energy Dispersive X-ray Microscopy (EDX) was utilized. Mercury Porosimetry was used to analyze the porosity and density of the PU-IONPs nanocomposites. Atomic Absorption Spectrometry (AAS) was conducted to measure the arsenic concentration in the treated solutions. Kinetic models were applied to determine the mechanisms which control the adsorption process. A pseudo-second-order model was found to be the best fit model for the adsorption data. Experimental results revealed that decreasing the size of IONPs from 50 - 100 nm to 15 - 20 nm yields a higher removal capacity. In addition, granular adsorbents exhibit higher removal capacity compared to cubical shaped adsorbents in the order of 20% - 100%.

Effect of precursor concentration on size evolution of iron oxide nanoparticles

Changing the precursor concentration to tune the iron-oxide nanoparticle size alters the surfactant/precursor ratio and leads to the observation of two size regimes.

From iron coordination compounds to metal oxide nanoparticles.

Various types, shapes and sizes of iron oxide nanoparticles were obtained depending on the nature of the precursor, preparation method and reaction conditions. The mixed valence trinuclear iron acetate, [Fe2IIIFeIIO(CH3COO)6(H2O)3]·2H2O (FeAc1), μ3-oxo trinuclear iron(III) acetate, [Fe3O(CH3COO)6(H2O)3]NO3∙4H2O (FeAc2), iron furoate, [Fe3O(C4H3OCOO)6(CH3OH)3]NO3∙2CH3OH (FeF), iron chromium furoate, FeCr2O(C4H3OCOO)6(CH3OH)3]NO3∙2CH3OH (FeCrF), and an iron complex with an original macromolecular ligand (FePAZ) were used as precursors for the corresponding oxide nanoparticles. Five series of nanoparticle samples were prepared employing either a classical thermal pathway (i.e., thermal decomposition in solution, solvothermal method, dry thermal decomposition/calcination) or using a nonconventional energy source (i.e., microwave or ultrasonic treatment) to convert precursors into iron oxides. The resulting materials were structurally characterized by wide-angle X-ray diffraction and Fourier transform infrared, Raman, energy-dispersive X-ray, and X-ray fluorescence spectroscopies, as well as thermogravimetric analysis. The morphology was characterized by transmission electron microscopy, atomic force microscopy and dynamic light scattering. The parameters were varied within each route to fine tune the size and shape of the formed nanoparticles.

Particle size and type effects on heat transfer enhancement of Ferro-nanofluids in a pulsating heat pipe

The present study evaluated the effect of γ (gamma) and α (alpha) Fe2O3/Kerosene nanofluids for a closed loop pulsating heat pipe under the magnetic field. The nanoparticles had a size ranged from 10nm to 30nm. The heat transfer rate and the temperature distribution of the heat pipe were examined with and without the magnetic field. Likewise, the Fe2O3 base nanofluids were exposed to a magnetic field to measure the vapor temperature at the center of the pulsating heat pipe directly. The results showed that both heat transfer coefficient and thermal performance of the pulsating heat pipe are enhanced by the addition of Fe2O3 nanoparticles, especially when the magnetic field is present. The increased input heat flux rises the heat transfer coefficient of the condenser and the evaporator. Lower evaporator heat transfer coefficient and higher temperature difference between condenser and evaporator were seen because of α-Fe2O3 nanoparticles as compared to γ-Fe2O3 nanoparticles. Among six nanoparticles investigated in this research, the optimum type and size of Iron oxide nanoparticles under similar conditions for attaining the best heat transfer performance was 20nm γ-Fe2O3 nanoparticles.

Effect of coating thickness of iron oxide nanoparticles on their relaxivity in the MRI.

Iron oxide nanoparticles have found prevalent applications in various fields including drug delivery, cell separation and as contrast agents. Super paramagnetic iron oxide (SPIO) nanoparticles allow researchers and clinicians to enhance the tissue contrast of an area of interest by increasing the relaxation rate of water. In this study, we evaluate the dependency of hydrodynamic size of iron oxide nanoparticles coated with Polyethylene glycol (PEG) on their relativities with 3 Tesla clinical MRI. We used three groups of nanoparticles with nominal sizes 20, 50 and 100 nm with a core size of 8.86 nm, 8.69 nm and 10.4 nm that they were covered with PEG 300 and 600 Da. A clinical magnetic resonance scanner determines the T1 and T2 relaxation times for various concentrations of PEG-coated nanoparticles. The size measurement by photon correlation spectroscopy showed the hydrodynamic sizes of MNPs with nominal 20, 50 and 100 nm with 70, 82 and 116 nm for particles with PEG 600 coating and 74, 93 and 100 nm for particles with PEG 300 coating, respectively. We foud that the relaxivity decreased with increasing overall particle size (via coating thickness). Magnetic resonance imaging showed that by increasing the size of the nanoparticles, r2/r1 increases linearly. According to the data obtained from this study it can be concluded that increments in coating thickness have more influence on relaxivities compared to the changes in core size of magnetic nanoparticles.

The biocompatibility evaluation of iron oxide nanoparticles synthesized by a one pot process for intravenous iron supply

This paper reports a new synthesis method to control the size of iron oxide nanoparticles (IONs) by adding sodium citrate during fabrication to obtain sodium citrate-modified iron oxide nanoparticles (SCIONs).

Diosgenin Functionalized Iron Oxide Nanoparticles as Novel Nanomaterial Against Breast Cancer.

Iron oxide nanoparticles (IONPs) have gained immense importance recently as drug nanocarriers due to easy multifunctionalization, simultaneous targeting, imaging and cancer hyperthermia. Herein, we report a novel nanomedicine comprising of IONPs core functionalized with a potent anticancer bioactive principle, diosgenin from medicinal plant Dioscorea bulbifera via citric acid linker molecule. IONPs were synthesized by reverse co-precipitation and characterized using field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM) and dynamic light scattering (DLS). Diosgenin functionalization was confirmed using fourier transform infrared spectroscopy (FTIR) and biochemical methods. Synthesized IONPs, citrate linked IONPs (IONPs-CA), diosgenin functionalized IONPs (IONPs-D) along with free citric acid and diosgenin were checked for anticancer activity against MCF7 breast cancer cells by MTT assay, wound migration assay, confocal microscopy and protein expression by western blotting. Size of IONPs, IONPs-CA and IONPs-D gradually increased ranging from 12 to 21 nm as confirmed by FESEM and HRTEM. Signature peaks of diosgenin at 2914, 1166 and 1444 cm-1 IONPs-D, revealed in FTIR indicated the presence of functionalized diosgenin. IONPs-D exhibited 51.08 ± 0.37% antiproliferative activity against MCF7 cells, which was found to be superior to free citric acid (17.71 ± 0.58%) and diosgenin (33.31 ± 0.37%). Treatment with IONPs-D exhibited reduced wound migration upto 40.83 ± 2.91% compared to bare IONPs (89.03 ± 2.58%) and IONPs-CA (50.35 ± 0.48%). IONPs-D and diosgenin exhibited apoptosis induction, confirmed by Alexa Fluor 488 annexin V/PI double-stained cells indicating extensive cell membrane damage coupled with PI influx leading to nuclear staining in treated cells. IONPs-D mediated selective PARP cleavage strongly rationalized it as superior apoptotic inducers. Based on these findings, IONPs-D can be considered as first diosgenin functionalized novel magnetic nanomedicine with antiproliferative, migration inhibiting and apoptosis inducing properties against breast cancer.

Microwave Assisted Synthesis of Ferrite Nanoparticles: Effect of Reaction Temperature on Particle Size and Magnetic Properties.

The preparation of ferrite magnetic nanoparticles of different particle sizes by controlling the reaction temperature using microwave assisted synthesis is reported. The iron oxide nanoparticles synthesized at two different temperatures viz., 45 and 85 °C were characterized using techniques such as X-ray diffraction (XRD), small angle X-ray scattering (SAXS), vibrating sample magnetometry (VSM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). The average size of iron oxide nanoparticles synthesized at 45 and 85 °C is found to be 10 and 13.8 nm, respectively, and the nanoparticles exhibited superparamagantic behavior at room temperature. The saturation magnetization values of nanoparticles synthesized at 45 and 85 °C were found to be 67 and 72 emu/g, respectively. The increase in particle size and saturation magnetization values with increase in incubation temperature is attributed to a decrease in supersaturation at elevated temperature. The Curie temperature was found to be 561 and 566 0C for the iron oxide nanoparticles synthesized at 45 and 85 °C, respectively. The FTIR spectrum of the iron oxide nanoparticles synthesized at different temperatures exhibited the characteristic peaks that corresponded to the stretching of bonds between octahedral and tetrahedral metal ions to oxide ions. Our results showed that the ferrite nanoparticle size can be varied by controlling the reaction temperature inside a microwave reactor.

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Thermo-stable carbon nanotube-TiO2 nanocompsite as electron highways in dye-sensitized solar cell produced by bio-nano-process

We produced a thermostable TiO2-(anatase)-coated multi-walled-carbon-nanotube (MWNT) nanocomposite for use in dye-sensitized solar cells (DSSCs) using biological supuramolecules as catalysts. We synthesized two different sizes of iron oxide nanoparticles (NPs) and arrayed the NPs on a silicon substrate utilizing two kinds of genetically modified cage-shaped proteins with silicon-binding peptide aptamers on their outer surfaces. Chemical vapor deposition (CVD) with the vapor–liquid-solid phase (VLS) method was applied to the substrate, and thermostable MWNTs with a diameter of 6 ± 1 nm were produced. Using a genetically modified cage-shaped protein with carbon-nanomaterials binding and Ti-mineralizing peptides as a catalyst, we were able to mineralize a titanium compound around the surface of the MWNT. The products were sintered, and thin TiO2-layer-coated MWNTs nanocomoposites were successfully produced. Addition of a 0.2 wt% TiO2-coated MWNT nanocomposite to a DSSC photoelectrode improved current density by 11% and decreased electric resistance by 20% compared to MWNT-free reference DSSCs. These results indicate that a nanoscale TiO2-layer-coated thermostable MWNT structure produced by our mutant proteins works as a superior electron transfer highway within TiO2 photoelectrodes.

Composition and Oxidation State of Cobalt and Nickel-Iron Oxide Colloidal Nanoparticles in Liquid Phase

The magnetic nanoparticles of cobalt-and nickel-iron oxide have been extensive interest due to their superparamagnetic properties and their potential applications in many fields. The iron, cobalt and nickel can stay in many oxidation states and are easily oxidized especially in ambient air therefore the composition and oxidation states of these oxides can be unintentionally modified. Usually, the composition and oxidation states in these magnetic nanoparticles are determined by various experimental techniques required a sample in solid phase. This may lead the nanoparticles to directly contact with air and change the state. In this study, the magnetic nanoparticles in colloidal phase with concentration of 24mg/ml, derived from co-precipitation process, were directly injected to liquid cell for X-ray absorption near-edge structure (XANES) measurement. The iron-, cobalt-or nickel-iron oxide nanoparticles were prepared by dissolving CoCl2/FeCl3 or NiCl2/FeCl3, respectively, in deionized water with various atomic ratios. The average iron oxide nanoparticle size obtained by dynamic light scattering is about 4.2 nm with polydispersity of 0.987. Spherical shape with some stabilizer layer was observed by transmission electron microscope. The iron content in various composition nanoparticles was estimated in liquid phase by the ratio between the Fe edge peak and Co or Ni edge peak. The oxidation states of metal ions were also derived from the linear fitting of standard compounds at particular oxidation states. The shifts of peak positions were examined to indicate the variation of oxidation state as well.