ACE2-based capacitance sensor for rapid native SARS-CoV-2 detection in biological fluids and its correlation with real-time PCR.

The spread of the SARS-CoV-2 and its increasing threat to human health worldwide have necessitated the development of new technological tools to combat the virus. Particular emphasis is given to the development of diagnostic methods that monitor the spread of the virus rapidly and effectively. In this study, we report the development and testing of an antibody-free biosensor, based on the immobilization of ACE2 protein on the surface of gold interdigitated electrode. When the sensor was used in laboratory conditions for targeting the virus' structural spike protein, it showed a limit of detection [LOD] of 750 pg/µL/mm2. Thereafter, the response of the sensor to swab and saliva samples from hospitalized patients was examined. The virus presence in the samples was confirmed by electrical effective capacitance measurements executed on the biosensor, and correlated with real-time PCR results. We verified that the biosensor can distinguish samples that are positive for the virus from those that are negative in a total of 7 positive and 16 negative samples. In addition, the biosensor can be used for semi-quantitative measurement, since its measurements are divided into 3 areas, the negative samples, the weakly positive and the positive samples. Reproducibility of the experiments was demonstrated with at least 3 replicates and stability was tested by keeping the sensor standby for 7 days at 4 °C before repeating the experiment. This work presents a biosensor that can be used as a fast-screening test at point of care detection of SARS-CoV-2 since it needs less than 2 min to provide results and is of simple operation.

Experimental and first-principles characterization of functionalized magnetic nanoparticles.

Magnetic iron oxide nanoparticles synthesized by coprecipitation and thermal decomposition yield largely monodisperse size distributions. The diameters of the coprecipitated particles measured by X-ray diffraction and transmission electron microscopy are between approximately 9 and 15 nm, whereas the diameters of thermally decomposed particles are in the range of 8 to 10 nm. Coprecipitated particles are indexed as magnetite-rich and thermally decomposed particles as maghemite-rich; however, both methods produce a mixture of magnetite and maghemite. Fourier transform IR spectra reveal that the nanoparticles are coated with at least two layers of oleic acid (OA) surfactant. The inner layer is postulated to be chemically adsorbed on the nanoparticle surface whereas the rest of the OA is physically adsorbed, as indicated by carboxyl O-H stretching modes above 3400 cm(-1). Differential thermal analysis (DTA) results indicate a double-stepped weight loss process, the lower-temperature step of which is assigned to condensation due to physically adsorbed or low-energy bonded OA moieties. Density functional calculations of Fe-O clusters, the inverse spinel cell, and isolated OA, as well as OA in bidentate linkage with ferrous and ferric atoms, suggest that the higher-temperature DTA stage could be further broken down into two regions: one in which condensation is due ferrous/ferrous- and/or ferrous/ferric-OA and the other due to condensation from ferrous/ferric- and ferric/ferric-OA complexes. The latter appear to form bonds with the OA carbonyl group of energy up to fivefold that of the bond formed by the ferrous/ferrous pairs. Molecular orbital populations indicate that such increased stability of the ferric/ferric pair is due to the contribution of the low-lying Fe(3+) t(2g) states into four bonding orbitals between -0.623 and -0.410 a.u.

Identification and quantification of microstructures formed during nanocrystallization of amorphous (Fe, Co)-Nb-(Si, B) systems.

The effect of addition of Si and variation of the Fe/Co ratio on the evolution of the nanostructure was studied in a modification of the Fe-Nb-B system. The entire system (Fe, Co)(73)Nb(7)(Si, B)(20) was prepared in an amorphous state by rapid quenching using the planar flow casting method over a wide range of Fe/Co atomic ratios, ranging from 0 to 1. Nanocrystallization was investigated by evolution of the electrical resistivity with time and temperature. The microstructural analysis was performed using transmission electron microscopy as well as electron and X-ray diffraction. The results from microscopy observations were used to determine the distribution of grain size, which in these alloys attain very small dimensions of approximately 5-8 nm. New algorithms of microscope image analysis were used for grain size determination, crucial for quantifying the microprocesses controlling nucleation and growth from the amorphous rapidly quenched phase.

Pecularities of nanocrystal formation in rapidly quenched (FeCo)MoCuB amorphous alloys.

The effect of the substitution of Fe by Co on the enhancement of glass-forming ability limits and subsequent nanocrystallization was studied in a rapidly quenched amorphous system (Fe(x)Co(y))(79)Mo(8)Cu(1)B(12) for y/x ranging from 0 to 1. The effect of Cu on nanocrystallization was investigated by comparison with Cu-free amorphous Fe(80)Mo(8)B(12). Systems partially crystallized at the surface layer were prepared for y/x = 0 using different quenching conditions. The effect of heat treatment of master alloys used for ribbon casting was also assessed. The microstructure and surface/bulk crystallization effects were analysed using transmission electron microscopy and electron and X-ray diffraction in relation to the expected enhancement of high-temperature soft magnetic properties, drastically reduced grain sizes (approximately 5 nm) and Co content. Unusual surface phenomena were observed, indicating the origin of possible nucleation sites for preferential crystallization in samples with low Co content.