RÉSUMÉ
JOURNAL/nrgr/04.03/01300535-202501000-00031/figure1/v/2024-05-14T021156Z/r/image-tiff Early identification and treatment of stroke can greatly improve patient outcomes and quality of life. Although clinical tests such as the Cincinnati Pre-hospital Stroke Scale (CPSS) and the Face Arm Speech Test (FAST) are commonly used for stroke screening, accurate administration is dependent on specialized training. In this study, we proposed a novel multimodal deep learning approach, based on the FAST, for assessing suspected stroke patients exhibiting symptoms such as limb weakness, facial paresis, and speech disorders in acute settings. We collected a dataset comprising videos and audio recordings of emergency room patients performing designated limb movements, facial expressions, and speech tests based on the FAST. We compared the constructed deep learning model, which was designed to process multi-modal datasets, with six prior models that achieved good action classification performance, including the I3D, SlowFast, X3D, TPN, TimeSformer, and MViT. We found that the findings of our deep learning model had a higher clinical value compared with the other approaches. Moreover, the multi-modal model outperformed its single-module variants, highlighting the benefit of utilizing multiple types of patient data, such as action videos and speech audio. These results indicate that a multi-modal deep learning model combined with the FAST could greatly improve the accuracy and sensitivity of early stroke identification of stroke, thus providing a practical and powerful tool for assessing stroke patients in an emergency clinical setting.
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Transition metal chalcogenides as potential anodes for lithium-ion batteries have been widely investigated. For practical application, the drawbacks of low conductivity and volume expansion should be further overcome. Besides the two conventional methods of nanostructure design and the doping of carbon-based materials, the component hybridization of transition metal-based chalcogenides can effectively enhance the electrochemical performance owing to the synergetic effect. Hybridization could promote the advantages of each chalcogenide and suppress the disadvantages of each chalcogenide to some extent. In this review, we focus on the four different types of component hybridization and the excellent electrochemical performance that originated from hybridization. The exciting problems of hybridization and the possibility of studying structural hybridization were also discussed. The binary and ternary transition metal-based chalcogenides are more promising to be used as future anodes of lithium-ion batteries for their excellent electrochemical performance originating from the synergetic effect.
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Numerous experiments have revealed that fullerene (C60) and its derivatives can bind to proteins and affect their biological functions. In this study, we explored the interaction between fullerine and the ß2-adrenergic receptor (ß2AR). The MD simulation results show that fullerene binds with the extracellular loop 2 (ECL2) and intracellular loop 2 (ICL2) of ß2AR through hydrophobic interactions and π-π stacking interactions. In the C60_in1 trajectory, due to the π-π stacking interactions of fullerene molecules with PHE and PRO residues on ICL2, ICL2 completely flipped towards the fullerene direction and the fullerene moved slowly into the lipid membrane. When five fullerene molecules were placed on the extracellular side, they preferred to stack into a stable fullerene cluster (a deformed tetrahedral aggregate), and had almost no effect on the structure of ß2AR. The hydroxyl groups of fullerene derivatives (C60(OH)X, X represents the number of hydroxyl groups, X = 4, 8) can form strong hydrogen bonds with the ECL2, helix6, and helix7 of ß2AR. The hydroxyl groups firmly grasp the ß2AR receptor like several claws, blocking the binding entry of ligands. The simulation results show that fullerene and fullerene derivatives may have a significant effect on the local structure of ß2AR, especially the distortion of helix4, but bring about no great changes within the overall structure. It was found that C60 did not compete with ligands for binding sites, but blocked the ligands' entry into the pocket channel. All the above observations suggest that fullerene and its derivatives exhibit certain cytotoxicity.
Sujet(s)
Fullerènes , Sites de fixation , Fullerènes/composition chimique , Fullerènes/pharmacologie , Liaison hydrogène , Interactions hydrophobes et hydrophiles , Ligands , Récepteurs bêta-2 adrénergiques/composition chimiqueRÉSUMÉ
Cobalt oxides have been intensely explored as anodes of lithium-ion batteries to resolve the intrinsic disadvantages of low electrical conductivity and volume change. However, as a precursor of preparing cobalt oxides, Co(OH)2 has rarely been investigated as the anode material of lithium-ion batteries, perhaps because of the complexity of hydroxides. Hybridized Co(OH)2 nanomaterial structures were synthesized by the water bath method and exhibited high electrochemical performance. The initial discharge and charge capacities were 1703.2 and 1262.9 mAh/g at 200 mA/g, respectively. The reversible capacity was 1050 mAh/g after 150 cycles. The reversible capability was 1015 mAh/g at 800 mA/g and increased to 1630 mAh/g when driven back to 100 mA/g. The electrochemical reaction kinetics study shows that the lithium-ion diffusion-controlled contribution is dominant in the energy storage mechanism. The superior electrochemical performance could result from the water bath method and the hybridization of nanosheets and nanoparticles structures. These hybridized Co(OH)2 nanomaterial structures with high electrochemical performance are promising anodes for lithium-ion batteries.
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Due to the high theoretical capability, copper-based oxides were widely investigated. A facile water bath method was used to synthesis CuO nanowires and CuO/Cu2O/Cu nanocomposites. Owing to the synergetic effect, the CuO/Cu2O/Cu nanocomposites exhibit superior electrochemical performance compared to the CuO nanowires. The initial discharge and charge capacities are 2,660.4 mAh/g and 2,107.8 mAh/g, and the reversible capacity is 1,265.7 mAh/g after 200 cycles at 200 mA/g. Moreover, the reversible capacity is 1,180 mAh/g at 800 mA/g and 1,750 mAh/g when back to 100 mA/g, indicating the excellent rate capability. The CuO/Cu2O/Cu nanocomposites also exhibit relatively high electric conductivity and lithium-ion diffusion coefficient, especially after cycling. For the energy storage mechanism, the capacitive controlled mechanism is predominance at the high scan rates, which is consistent with the excellent rate capability. The outstanding electrochemical performance of the CuO/Cu2O/Cu nanocomposites indicates the potential application of copper-based oxides nanomaterials in future lithium-ion batteries.
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With the extension of the applications of sandwich panels with corrugated core, sound insulation performance has been a great concern for acoustic comfort design in many industrial fields. This paper presents a numerical and experimental study on the vibro-acoustic optimization of a finite size sandwich panel with corrugated core for maximizing the sound transmission loss. The numerical model is established by using the wave-based method, which shows a great improvement in the computational efficiency comparing to the finite element method. Constrained by the fundamental frequency and total mass, the optimization is performed by using a genetic algorithm in three different frequency bands. According to the optimization results, the frequency averaged sound transmission of the optimized models in the low, middle, and high-frequency ranges has increased, respectively, by 7.6 dB, 7.9 dB, and 11.7 dB compared to the baseline model. Benefiting from the vast number of the evolution samples, the correlation between the structural design parameters and the sound transmission characteristics is analyzed by introducing the coefficient of determination, which gives the variation of the importance of each design parameter in different frequency ranges. Finally, for validation purposes, a sound insulation test is conducted to validate the optimization results in the high-frequency range, which proves the feasibility of the optimization method in the practical engineering design of the sandwich panel.
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In order to solve the poor cycle stability and the pulverization of cobalt sulfides electrodes, a series of amorphous and crystalline cobalt sulfides were prepared by one-pot solvothermal synthesis through controlling the reaction temperatures. Compared to the crystalline cobalt sulfide electrodes, the amorphous cobalt sulfide electrodes exhibited superior electrochemical performance. The high initial discharge and charge capacities of 2,132 mAh/g and 1,443 mAh/g at 200 mA/g were obtained. The reversible capacity was 1,245 mAh/g after 200 cycles, which is much higher than the theoretical capacity. The specific capability was 815 mAh/g at 800 mA/g and increased to 1,047 mAh/g when back to 100 mA/g, indicating the excellent rate capability. The outstanding electrochemical performance of the amorphous cobalt sulfide electrodes could result from the unique characteristics of more defects, isotropic nature, and the absence of grain boundaries for amorphous nanostructures, indicating the potential application of amorphous cobalt sulfide as anodes for lithium-ion batteries.
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Nickel sulfide has been widely studied as an anode material for lithium-ion batteries due to its environmental friendliness, low cost, high conductivity, and high theoretical capacity. A simple hydrothermal method was used to prepare NiS nanospheres materials with the size in the range of 100-500 nm. The NiS nanospheres electrodes exhibited a high reversible capacity of 1402.3 mAh g-1 at 200 mA g-1 after 280 cycles and a strong rate capability of 814.8 mAh g-1 at 0.8 A g-1 and 1130.5 mAh g-1 when back to 0.1 A g-1. Excellent electrochemical properties and the simple preparation method of the NiS nanospheres make it possible to prepare NiS on a large scale as the anode of lithium-ion batteries.
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To observe the clinical effect of estrogenic drugs (Bazedoxifene) on bone targeting in the treatment of osteoporosis and explore its mechanism. METHODS: 112 patients with postmenopausal osteoporosis who received Bazedoxifene drugs in our hospital from January to December 2018 were collected as a study group, and 56 patients treated with calcium alone were collected as a control group. the risk of adverse events such as bone mineral density, osteoprotegerin (OPG), insulin-like growth factor (IGF), tumor necrosis factor (TNF-α), and fracture after treatment were analyzed before and after treatment. RESULTS: There was no significant difference in the mean lumbar positive position (L2-4) and right femoral neck bone density and OPG, IGF, TNF-α level between the two groups before treatment (P>0.05). The total effective rate of clinical treatment in the study group was 88.39%, the control group was 23.21%, the difference between the two groups was statistically significant (PË0.05). After treatment, the mean lumbar positive position (L2-4) and the right femoral neck bone density and OPG, IGF in the study group were higher than those in the control group, lower than those in the control group (P<0.05). the occurrence of adverse events such as fracture, spinal deformation and fatigue in the study group after 12 months of treatment was significantly lower than that in the control group (P<0.05), but there was no significant difference in the occurrence of hot flashes and venous thromboembolism between the two groups (P>0.05). CONCLUSION: Bazedoxifene is an effective drug for the treatment of postmenopausal osteoporosis. It can not only prevent the rapid loss of bone mass, effectively relieve the symptoms of menopause, but also improve bone density and reduce the risk of fracture.
Sujet(s)
Densité osseuse/effets des médicaments et des substances chimiques , Indoles/pharmacologie , Facteur de croissance IGF-I/métabolisme , Ostéoprotégérine/métabolisme , Facteur de nécrose tumorale alpha/métabolisme , Sujet âgé , Femelle , Fractures osseuses/physiopathologie , Humains , Vertèbres lombales/effets des médicaments et des substances chimiques , Vertèbres lombales/anatomopathologie , Adulte d'âge moyen , Orthèses , Ostéoprotégérine/sang , Facteur de nécrose tumorale alpha/sangRÉSUMÉ
Amyloid aggregation initiates from a slow nucleation process, where the association of monomers is unfavorable in energetics. In principle, the enthalpy change for aggregation should compensate the entropy loss as new monomers attach to formed oligomers. However, the classical force fields with fixed point charges failed to yield the correct enthalpy change due to the lack of electrostatic polarization effect on amyloid aggregation. In this work, we performed molecular dynamics simulation for the full-length human islet amyloid using the polarized protein-specific charges and calculated the electrostatic interaction energy for amyloid oligomers. The results of molecular dynamics simulation show that the aggregates simulated with polarized charges have larger enthalpy change than that with fixed charges. The large enthalpy change mainly originates from the electrostatic polarization, which makes a significant contribution to the cooperative effect of aggregation and facilitates the nucleation process of amyloids.