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Katarzyna Niemirowicz,1,2 Izabela Swiecicka,3 Agnieszka Z Wilczewska,4 Iwona Misztalewska,4 Beata Kalska-Szostko,4 Kamil Bienias,2 Robert Bucki,1,5,6 Halina Car21Department of Microbiological and Nanobiomedical Engineering, 2Department of Experimental Pharmacology, Medical University of Bialystok, 3Department of Microbiology, 4Institute of Chemistry, University of Bialystok, Bialystok, 5Faculty of Health Sciences, Jan Kochanowski University, Kielce, Poland; 6Institute for Medicine and Engineering, University of Pennsylvania, Philadelphia, PA, USAAbstract: Superparamagnetic iron oxide nanoparticles (SPIONs) and their derivatives (aminosilane and gold-coated) have been widely investigated in numerous medical applications, including their potential to act as antibacterial drug carriers that may penetrate into bacteria cells and biofilm mass. Pseudomonas aeruginosa is a frequent cause of infection in hospitalized patients, and significant numbers of currently isolated clinical strains are resistant to standard antibiotic therapy. Here we describe the impact of three types of SPIONs on the growth of P. aeruginosa during long-term bacterial culture. Their size, structure, and physicochemical properties were determined using transmission electron microscopy, X-ray diffraction analysis, and Fourier transform infrared spectroscopy. We observed significant inhibition of P. aeruginosa growth in bacterial cultures continued over 96 hours in the presence of gold-functionalized nanoparticles (Fe3O4@Au). At the 48-hour time point, growth of P. aeruginosa, as assessed by the number of colonies grown from treated samples, showed the highest inhibition (decreased by 40%). These data provide strong evidence that Fe3O4@Au can dramatically reduce growth of P. aeruginosa and provide a platform for further study of the antibacterial activity of this nanomaterial.Keywords: antibacterial activity, Pseudomonas aeruginosa, superparamagnetic nanoparticles, iron oxides, gold-coated nanoparticles

The influence of the surface modification on the magnetism of 4–14 nm sized core and core/shell gallium ferrites obtained by different preparation methods (Massart's and thermal decomposition from acetylacetonates) was studied. The physical properties of GaxFe3-xO4 were investigated in a wide range of Ga admixtures 0 ≤ x ≤ 1.5. Ga ions location at 8a or/and 16d positions of a spinel structure depends on the synthesis method and has a pronounced effect on the superparamagnetic properties of nanoparticles. Magnetization and Mössbauer experiments show the dominant superparamagnetic contribution for the nanoparticles with x > 0.8 with the blocking temperature TB significantly below 200 K. Surface-modified nanoferrites disclosed spontaneous magnetization that does not exceed 60 emu/g. [ABSTRACT FROM AUTHOR]

• Reorientation of magnetic moments as a consequence of elemental composition is seen. • Reorientation of magnetic moments as a consequence of elemental ordering is observed. • Difference between layered and alloyed nanowires is discussed. Anomalous deposition of multi-element nanowires continuously interests scientists to study such a system. In this paper, two types of magnetic nanowires were electrodeposited: multilayered and alloy-like. Fe-Co and Fe-Ni nanowires with various relative molar ratio were prepared by DC electrodeposition in aluminum oxide matrix, with a mean pore diameter of 140 ± 20 nm. The nanostructures were investigated in two states: released and within the matrix, using the following techniques: Scanning Electron Microscopy, Energy Dispersive X-ray spectroscopy, X-ray diffraction, Infrared, and Mössbauer spectroscopy. The Scanning Electron Microscopy showed that the length of Fe-(Co, Ni) nanowires is of the order of 3 µm and the diameter determined by the pores of the anodic aluminum oxide templates. The X-ray diffraction and Mössbauer spectroscopy also showed that the fabrication method allows for the obtainment of both multilayered as well as alloyed nanowires with tunable magnetic properties which depend on both the elements' relative ratio and its ordering. The magnetic texture observed by Mössbauer measurements demonstrated the almost random distribution of magnetic moments of iron in the studied samples which are rather unusual in layered systems. [ABSTRACT FROM AUTHOR]

We have succeeded in synthesizing orthorhombic Ga(1_X)Fe(1+X)03 (-0.05 ≤ x ≤ 0.5), hexagonal GayFe(2-y)O3 (0 ≤ y ≤1.8) and cubic Ga(1+Z)Fe(2-Z)04 (--0.1 ≤ z ≤ 0.8) nanograins of gallium ferrites using conventional precursors and an organic environment of Pechini scenario under atmosphericpressure conditions (SG method). Phase composition and homogeneity were analyzed using X-ray diffraction. Small angle neutron scattering disclosed ellipsoidal particle shapes of gallium iron oxides (GFO) crystallizing in orthorhombic (o-GFO) and hexagonal (h-GFO) symmetry and parallelepiped shapes of Ga(1+y)Fe(2-y)O4 (c-GFO) grains. Despite local agglomeration among the magnetic grains, the scanning electron microscopy and transmission electron microscopy images point to faced-elliptical shapes. The Mössbauer spectroscopy with magnetization measurements was carried out in the temperature range of 5-295 K. The analysis of gallium ferrites magnetism demonstrates that iron atoms locate with various probabilities in crystallography positions and the spontaneous magnetization preserves up to room temperature (RT). [ABSTRACT FROM AUTHOR]

The effects of the external magnetic field presence on the electrocrystallization of Fe/Ni alloy have been investigated. It is reported that the magnetic field superposed perpendicular to the electrode surface has an influence on the Fe/Ni alloy growth. It is found that the Fe content increases over the entire Fe/Ni solution deposition and the layer morphology strongly depends on the bath composition. Samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray, X-ray fluorescence. [ABSTRACT FROM AUTHOR]

The magnetic nanoparticles with core diameter 10 nm were modified by poly-L-lysine to bind antibody for cancer cell detection. Prepared biocompatible magnetic fluid (MFPLL) was characterized by dynamic light scattering method to obtain the particle size distribution. The microstructure of the MNPs and MFPLL samples were studied by transmission electron microscopy, X-ray diffraction and Mössbauer spectroscopy. Magnetic properties of the samples were measured by SQUID magnetometer and superparamagnetic behaviour of the samples was confirmed. [ABSTRACT FROM AUTHOR]

Highlights: [•] Stability of magnetite nanoparticles in environmental solutions was tested. [•] The most aggressive model solutions were determined to be citric acid, acetic acid and white wine. [•] The chosen model solutions dissolve magnetic core (acids) or modifies mostly particle surface (wine). [ABSTRACT FROM AUTHOR]

The magneto-optical properties of 14-nm CoAg core-shell nanoparticles ( x=0.7, 0.8, and 0.35) deposited on different substrates are investigated at room temperature in the photon-energy range from 0.8 to 4.8 eV. Particles with low Ag content show spectra very similar to pure Co nanoparticles while particles with high Ag content have totally different features, where the Ag plasma edge dominates the spectra. The spectral features of the polar Kerr rotation depend on particle composition. The ageing process and development of an oxide layer influence the particles' core-shell structures and magnetization curves. Co-rich particles exhibit lower resistance to the oxidation process as compared to Ag-rich ones. The quality of the nanoparticles was checked by transmission electron microscopy in respect of time scale. [ABSTRACT FROM AUTHOR]

Abstract: The iron nanowires were obtained by DC electrochemical method in nanoporous anodic alumina templates (AAO). For stability tests these materials were placed in different solutions: white wine, citric acid, 0.9% NaCl, distilled water and ethanol for a 1–3week time period. The results of such treatment (solubility or possible changes on the surface) of the Fe nanowires were measured by IR (infrared spectroscopy), ASA (atomic absorption spectroscopy), TEM (transmission electron microscopy), XRD (X-ray diffraction) and DSC (differential scanning calorimetry) methods. [Copyright &y& Elsevier]

Abstract: In the present study Fe3O4 magnetic nanoparticles were synthesized by coprecipitation of Fe2+ and Fe3+ from chlorides. In the next step magnetite–gold core–shell nanoparticles were synthesized from HAuCl4 using an ethanol as a reducing agent. Finally, magnetic nanoparticles were functionalized by hexadecanethiol. The immobilization of biological molecules (trypsin and glucose oxidase) to the thiol-modified and unmodified magnetite–gold nanoparticles surface was tested. The resulting nanoparticles were characterized by infrared spectroscopy, differential scanning calorimetry, Mössbauer spectroscopy and transmission electron microscopy. [Copyright &y& Elsevier]

Magnetic nanowires of Fe, Fe-Co, and Fe-Ni alloy and layered structure were prepared by electrochemical alternating current (AC) deposition method. The morphology of the nanowires in and without the matrix was studied by energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), and X-ray diffraction (XRD), respectively. The wires either show strong dependence on the combination of elements deposition (alloy or layered) or chemical composition (Co or Ni). The magnetic properties of the nanostructures were determined on the basis of Mössbauer spectroscopy (MS).

The hyperfine fields and atomic ordering in Ni1−xFexMnGe (x = 0.1, 0.2, 0.3) alloys were investigated using X-ray diffraction and Mössbauer spectroscopy at room temperature. The X-ray diffraction measurements show that the samples with x = 0.2, 0.3 crystallized in the hexagonal Ni2In-type of structure, whereas in the sample with x = 0.1, the coexistence of two phases, Ni2In- and orthorhombic TiNiSi-type of structures, were found. The Mössbauer spectra measured with x = 0.2, 0.3 show three doublets with different values of isomer shift (IS) and quadrupole splitting (QS) related to three different local surroundings of Fe atoms in the hexagonal Ni2In-type structure. It was shown that Fe atoms in the hexagonal Ni2In-type structure of as-cast Ni1−xFexMnGe alloys are preferentially located in Ni sites and small amount of Fe is located in Mn and probably in Ge sites. The spectrum for x = 0.1 shows the doublets in the central part of spectrum and a broad sextet. The doublets originate from the Fe atoms in the paramagnetic state of hexagonal Ni2In-type structure, whereas the sextet results from the Fe atoms in orthorhombic TiNiSi-type structure.

The ferrite magnetic nanoparticles with core-shell structures were obtained in two step preparation process. The Mössbauer spectra obtained for particles of pure maghemite or magnetite and two layered core-shell one the magnetite on maghemite and maghemite on magnetite are very different from each other. The presented results show that interparticle and intraparticle interaction plays important role in overall magnetic properties as well. [ABSTRACT FROM AUTHOR]

[Display omitted] • The influence of synthetic procedure on nanoparticles growth was tested. • The influence of dopant concentration on nanoparticles growth was established. • The correlation between particles growth condition and magnetic properties was achieved. The studies presented in this paper show the results of synthesis and physicochemical characterization of modified ferrite nanoparticles, which can be described by the general formula M x Fe 3-x O 4 (where x = 0.15 or 0.45) doped with Al3+, Cr3+, Cu2+ and Zn2+ ions. The nanoparticles were obtained through procedures using either water or organic environment. The aim of this study was to determine the influence of synthetic routine and doping on the quality of the obtained structure, morphology and magnetic properties of nanoparticles. Additionally, doping concentration of selected elements is a crucial influence on the crystallinity and magnetic properties of the obtained nanoparticles. Doped nanoparticles were synthesized by two chemical methods: co-precipitation of iron chlorides in a basic solution and thermal decomposition of iron(III) acetylacetonate in an organic high-boiling solvent. Obtained nanoparticles were characterized by transmission electron microscopy, energy dispersive X-ray, X-ray diffraction, porosimetry, infrared spectroscopy and Mössbauer spectroscopy. [ABSTRACT FROM AUTHOR]