ABSTRACT
This study investigates the crystal structure, epitaxial relation, and magnetic properties in CoFe thin films deposited on a flexible mica substrate. The epitaxial growth of CoFe thin films was successfully achieved by DC magnetron sputtering, forming three CoFe(002) domains exhibiting four-fold symmetry on the mica substrate. A notable achievement of this work was the attainment of the highest anisotropic magnetoresistance (AMR) value reported to date on a flexible substrate. Additionally, it was observed that the magnetic characteristics of the CoFe films on the flexible mica substrate display reversibility upon strain release. More importantly, the AMR effect of epitaxial CoFe films on flexible mica shows lesser dependence on the crystalline orientation and remains the same under different bending states. These findings demonstrate the potential of utilizing CoFe films on flexible substrates to develop wearable magnetoresistance sensors with diverse applications.
ABSTRACT
Face recognition plays an essential role for the biometric authentication. Conventional lens-based imagery keeps the spatial fidelity with respect to the object, thus, leading to the privacy concerns. Based on the point spread function engineering, we employed a coded mask as the encryption scheme, which allows a readily noninterpretable representation on the sensor. A deep neural network computation was used to extract the features and further conduct the identification. The advantage of this data-driven approach lies in that it is neither necessary to correct the lens aberration nor revealing any facial conformity amid the image formation chain. To validate the proposed framework, we generated a dataset with practical photographing and data augmentation by a set of experimental parameters. The system has the capability to adapt a wide depth of field (DoF) (60-cm hyperfocal distance) and pose variation (0 to 45 deg). The 100% recognition accuracy on real-time measurement was achieved without the necessity of any physics priors, such as the encryption scheme.
Subject(s)
Biometric Identification , Facial Recognition , Algorithms , Biometric Identification/methods , Neural Networks, Computer , PrivacyABSTRACT
Nasogastric intubation is a common procedure in hospitals that causes adverse outcomes if performed incorrectly. There is currently insufficient guidance for patient positioning, which increases the success of nasogastric intubation at the bedside. Therefore, a systematic review with a meta-analysis was performed to determine the effectiveness of changing an unconscious adults' positions compared with the supine position to improve the correct placement of a nasogastric tube, intubation time, and complications. The Cochrane Library, MEDLINE, Embase, PubMed, and CINAHL databases were searched from inception to April 2019 for randomized controlled trials. The Cochrane Collaboration Risk of Bias tool was used to assess the quality of eligible studies. Cochrane Review Manager 5.3 software was used to analyze the data. A total of 288 articles were obtained in the literature search, 10 of which were included in the analysis. Most of the included trials were at low risk of bias. All postures were significantly effective, though neck flexion had the highest success rate (odds ratio = 4.87, 95% confidence interval [2.48, 9.57], Z = 4.6, p < .00001, I2 = 0%) for nasogastric intubation. In terms of the time required for the procedure, compared with the usual posture, although the total effects were significant ( MD =-10.33, 95% confidence interval [-15.38, -5.29], Z = 4.02, p < .00001, I2 = 98%), only neck flexion and lifting of the larynx reduced the time. The meta-analysis suggests that patient positioning improves the success rate of nasogastric intubation and increases safety. Finally, the authors developed a procedural instruction sheet to aid practitioners with nasogastric intubation.
Subject(s)
Intubation, Gastrointestinal , Adult , Humans , Intubation, Gastrointestinal/adverse effects , Intubation, Gastrointestinal/methodsABSTRACT
In this paper, we proposed a new technique to realize a high-quality three-dimensional (3D) display by using binary holograms. First, we applied a localized random down-sampling (LRDS) mask to down-sample the object function and generated a binary CGH by direct sign-thresholding. Subsequently, we devised the display by adaptive intensity accumulation (AIA). In AIA, multiple CGHs of the same object are generated. However, selective sampling points of the same scene are removed according to the reconstructed image of previous binary CGHs as the second and more binary CGHs are generated. Finally, these holograms are sequentially displayed on a fast spatial light modulator, a digital micromirror device (DMD). Thus, a high-quality 3D image is reconstructed without artifacts and speckle noise.
ABSTRACT
One neurotoxic mechanism of amyloid-beta peptide (Aß), the major component of senile plaques in the brains of Alzheimer's disease (AD) patients, is to trigger cell cycle reentry in fully differentiated neurons. However, the detailed underlying mechanisms remain unclear. Using Aß25-35-treated primary rat cortical neurons as the experimental system, in the present study we tested whether Aß-induced inhibitor of differentiation-1 (Id1)/hypoxia-inducible factor-1alpha (HIF-1α) and cyclin-dependent kinase-5 (CDK5) contribute to cell cycle reentry in fully differentiated post-mitotic neurons. We found that Id1-induced HIF-1α mediated Aß25-35-dependent expression of the cell cycle markers cyclin D1 and proliferating cell nuclear antigen (PCNA), both colocalized with microtubule-associated protein-2 (MAP-2) + cells, indicative of cell cycle reentry in the mature neurons. Aß25-35 also enhanced p35 cleavage to p25 without affecting CDK5 expression. The CDK5 inhibitor roscovitine and the siRNA targeting CDK5 both suppressed Aß25-35-dependent HIF-1α expression and cell cycle reentry. Intriguingly, Aß25-35-induced Id1 repressed p25 production while CDK5/p25 reciprocally inhibited Id1 expression, despite the observation that both Id1 and CDK5/p25 acted upstream of HIF-1α. These results demonstrated that both Id1/HIF-1 and CDK5/HIF-1 contribute to Aß-induced cell cycle reentry in post-mitotic neurons; furthermore, Id1 and CDK5/p25 reciprocally suppress expression of each other.
Subject(s)
Cell Cycle , Cyclin-Dependent Kinase 5/metabolism , Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Inhibitor of Differentiation Protein 1/metabolism , Neurons/metabolism , Amyloid beta-Peptides/pharmacology , Animals , Cells, Cultured , Cerebral Cortex/cytology , Cyclin D1/genetics , Cyclin D1/metabolism , Cyclin-Dependent Kinase 5/antagonists & inhibitors , Cyclin-Dependent Kinase 5/genetics , Hypoxia-Inducible Factor 1, alpha Subunit/genetics , Inhibitor of Differentiation Protein 1/genetics , Mitosis , Neurons/cytology , Neurons/drug effects , Peptide Fragments/pharmacology , Proliferating Cell Nuclear Antigen/genetics , Proliferating Cell Nuclear Antigen/metabolism , Protein Kinase Inhibitors/pharmacology , Rats , Rats, Sprague-Dawley , Roscovitine/pharmacologyABSTRACT
We present an alternative scheme for determining the frequencies of cesium (Cs) atom 6S-8S Doppler-free transitions. With the use of a single electro-optical crystal, we simultaneously narrow the laser linewidth, lock the laser frequency, and resolve a narrow spectrum point by point. The error budget for this scheme is presented, and we prove that the transition frequency obtained from the Cs cell at room temperature and with one-layer µ-metal shielding is already very near that for the condition of zero collision and zero magnetic field. We point out that a sophisticated linewidth measurement could be a good guidance for choosing a suitable Cs cell for better frequency accuracy.
ABSTRACT
Our continuing effort of searching bioactive substances from the Formosan soft coral Cladiella australis has led to the isolation of a bioactive substance austrasulfone (1), which possesses significant neuroprotective activities. A straightforward synthesis of 1 was achieved by a two-step reaction sequence. Dihydroaustrasulfone alcohol (3), the synthetic precursor of 1, not only exhibited in vitro anti-inflammatory activity, but also showed potent therapeutic ability in the treatment of neuropathic pain, atherosclerosis, and multiple sclerosis in rats.
Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Atherosclerosis/drug therapy , Butanones/pharmacology , Multiple Sclerosis/drug therapy , Neuroprotective Agents/pharmacology , Pain/drug therapy , Sulfones/pharmacology , Animals , Anthozoa , Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Butanones/chemical synthesis , Butanones/chemistry , Cell Proliferation/drug effects , Drug Evaluation, Preclinical , Female , Humans , Male , Mice , Molecular Structure , Neuroprotective Agents/chemical synthesis , Neuroprotective Agents/chemistry , Pain Measurement , Rats , Rats, Inbred Lew , Rats, Wistar , Sulfones/chemical synthesis , Sulfones/chemistryABSTRACT
The EtOAc extract of a Taiwanese soft coral, Caldiella australis, yielded four new eunicellin-based diterpenoids, australins A-D (1-4). The chemical structures of these metabolites were determined on the basis of extensive spectroscopic (including 1D and 2D NMR) analyses and by comparison of their NMR spectral data with those of related metabolites. Metabolite 2 was found to possess a moderate cytotoxic activity against selected breast and liver cancer cell lines.