21,333 research outputs found

    Soft x-ray resonant magneto-optical Kerr effect as a depth-sensitive probe of magnetic heterogeneity: Its application to resolve helical spin structures using linear p polarization

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    We have calculated the soft x-ray resonant Kerr intensities as a function of the incident grazing angle of linearly p-polarized waves from the model spin structures, where the chirality (handedness) of the spin spirals (twist in depth) in a magnetic layer and the periodicity of a unit spiral are designed to vary. Variations in the chirality and the periodicity lead to noticeable changes in the Kerr intensity versus the grazing angle, which is due not only to a large sensitivity of the Kerr intensity of the linear p polarization to both the magnitude and direction of the transverse components of magnetizations, but also to a large dependence of the depth sensitivity on the grazing angle at the resonance regions. The measurement and analysis of the specular Kerr intensity are relatively straightforward in determining the inhomogeneous spin structures in depth, compared to those of the Kerr rotation and ellipticity. This is proven to be a convenient and useful probe to determine the handedness of spin spiral structures, as well as to resolve the detailed magnetic heterostructures in depth in ultrathin-layered films.open4

    Magnetoresistive biosensors with on-chip pulsed excitation and magnetic correlated double sampling.

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    Giant magnetoresistive (GMR) sensors have been shown to be among the most sensitive biosensors reported. While high-density and scalable sensor arrays are desirable for achieving multiplex detection, scalability remains challenging because of long data acquisition time using conventional readout methods. In this paper, we present a scalable magnetoresistive biosensor array with an on-chip magnetic field generator and a high-speed data acquisition method. The on-chip field generators enable magnetic correlated double sampling (MCDS) and global chopper stabilization to suppress 1/f noise and offset. A measurement with the proposed system takes only 20 ms, approximately 50× faster than conventional frequency domain analysis. A corresponding time domain temperature correction technique is also presented and shown to be able to remove temperature dependence from the measured signal without extra measurements or reference sensors. Measurements demonstrate detection of magnetic nanoparticles (MNPs) at a signal level as low as 6.92 ppm. The small form factor enables the proposed platform to be portable as well as having high sensitivity and rapid readout, desirable features for next generation diagnostic systems, especially in point-of-care (POC) settings

    HOXA10 controls osteoblastogenesis by directly activating bone regulatory and phenotypic genes

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    HOXA10 is necessary for embryonic patterning of skeletal elements, but its function in bone formation beyond this early developmental stage is unknown. Here we show that HOXA10 contributes to osteogenic lineage determination through activation of Runx2 and directly regulates osteoblastic phenotypic genes. In response to bone morphogenic protein BMP2, Hoxa10 is rapidly induced and functions to activate the Runx2 transcription factor essential for bone formation. A functional element with the Hox core motif was characterized for the bone-related Runx2 P1 promoter. HOXA10 also activates other osteogenic genes, including the alkaline phosphatase, osteocalcin, and bone sialoprotein genes, and temporally associates with these target gene promoters during stages of osteoblast differentiation prior to the recruitment of RUNX2. Exogenous expression and small interfering RNA knockdown studies establish that HOXA10 mediates chromatin hyperacetylation and trimethyl histone K4 (H3K4) methylation of these genes, correlating to active transcription. HOXA10 therefore contributes to early expression of osteogenic genes through chromatin remodeling. Importantly, HOXA10 can induce osteoblast genes in Runx2 null cells, providing evidence for a direct role in mediating osteoblast differentiation independent of RUNX2. We propose that HOXA10 activates RUNX2 in mesenchymal cells, contributing to the onset of osteogenesis, and that HOXA10 subsequently supports bone formation by direct regulation of osteoblast phenotypic genes. <br/

    Neural cell responses to wear debris from metal-on-metal total disc replacements

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    PURPOSE: Total disc replacements, comprising all-metal articulations, are compromised by wear and particle production. Metallic wear debris and ions trigger a range of biological responses including inflammation, genotoxicity, cytotoxicity, hypersensitivity and pseudotumour formation, therefore we hypothesise that, due to proximity to the spinal cord, glial cells may be adversely affected. METHODS: Clinically relevant cobalt chrome (CoCr) and stainless steel (SS) wear particles were generated using a six-station pin-on-plate wear simulator. The effects of metallic particles (0.5-50 μm3 debris per cell) and metal ions on glial cell viability, cellular activity (glial fibrillary acidic protein (GFAP) expression) and DNA integrity were investigated in 2D and 3D culture using live/dead, immunocytochemistry and a comet assay, respectively. RESULTS: CoCr wear particles and ions caused significant reductions in glial cell viability in both 2D and 3D culture systems. Stainless steel particles did not affect glial cell viability or astrocyte activation. In contrast, ions released from SS caused significant reductions in glial cell viability, an effect that was especially noticeable when astrocytes were cultured in isolation without microglia. DNA damage was observed in both cell types and with both biomaterials tested. CoCr wear particles had a dose-dependent effect on astrocyte activation, measured through expression of GFAP. CONCLUSIONS: The results from this study suggest that microglia influence the effects that metal particles have on astrocytes, that SS ions and particles play a role in the adverse effects observed and that SS is a less toxic biomaterial than CoCr alloy for use in spinal devices. These slides can be retrieved under Electronic Supplementary Material

    Soft x-ray resonant magneto-optical Kerr effect as a depth-sensitive probe of magnetic heterogeneity: A simulation approach

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    We report a noticeable depth sensitivity of soft x-ray resonant magneto-optical Kerr effect able to resolve depth-varying magnetic heterostructures in ultrathin multilayer films. For various models of depth-varying magnetization orientations in an ultrathin Co layer of realistic complex layered structures, we have calculated the Kerr rotation, ellipticity, intensity spectra versus grazing incidence angle ??, and their hysteresis loops at different values of ?? for various photon energies ?? 's near the Co resonance regions. It is found from the simulation results that the Kerr effect has a much improved depth sensitivity and that its sensitivity varies remarkably with ?? and ?? in the vicinity of the resonance regions. These properties originate from a rich variety of wave interference effects superimposed with noticeable features of the refractive and absorptive optical effects near the resonance regions. Consequently, these allow us to resolve depth-varying magnetizations and their reversals varying with depth in a single magnetic layer and allow us to distinguish interface magnetism from the bulk properties in multilayer films. In this paper, the depth sensitivity of the Kerr effect with an atomic-scale resolution is demonstrated and discussed in details in several manners with the help of model simulations for various depth-varying spin configurations.open9

    Obtaining strong ferromagnetism in diluted Gd-doped ZnO thin films through controlled Gd-defect complexes

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    We demonstrate the fabrication of reproducible long-range ferromagnetism (FM) in highly crystalline Gdx Zn 1−xO thin films by controlling the defects. Films are grown on lattice-matched substrates by pulsed laser deposition at low oxygen pressures (≤25 mTorr) and low Gd concentrations (x ≤ 0.009). These films feature strong FM (10 μB per Gd atom) at room temperature. While films deposited at higher oxygen pressure do not exhibit FM, FM is recovered by post-annealing these films under vacuum. These findings reveal the contribution of oxygen deficiency defects to the long-range FM. We demonstrate the possible FM mechanisms, which are confirmed by density functional theory study, and show that Gd dopants are essential for establishing FM that is induced by intrinsic defects in these films
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