Investigation of systemic immune-inflammation index, neutrophil/high-density lipoprotein ratio, lymphocyte/high-density lipoprotein ratio, and monocyte/high-density lipoprotein ratio as indicators of inflammation in patients with schizophrenia and bipolar disorder

BackgroundThe systemic immune-inflammation index (SII), system inflammation response index (SIRI), neutrophil/high-density lipoprotein (HDL) ratio (NHR), lymphocyte/HDL ratio (LHR), monocyte/HDL ratio (MHR), and platelet/HDL ratio (PHR) have been recently investigated as new markers for inflammation. The purpose of this research is to use large-scale clinical data to discuss and compare the predictive ability of the SII, SIRI, NHR, LHR, MHR, and PHR in patients with schizophrenia (SCZ) and bipolar disorder (BD), to investigate potential biomarkers.Materials and methodsIn this retrospective, naturalistic, cross-sectional study, we collected the hematological parameter data of 13,329 patients with SCZ, 4,061 patients with BD manic episodes (BD-M), and 1,944 patients with BD depressive episodes (BD-D), and 5,810 healthy subjects served as the healthy control (HC) group. The differences in the SII, SIRI, NHR, LHR, MHR, and PHR were analyzed, and a receiver operating characteristic (ROC) curve was used to analyze the diagnostic potential of these parameters.ResultsCompared with the HC group, the values of the SII, SIRI, NHR, LHR, MHR, and PHR and the levels of neutrophils, monocytes, and triglycerides (TG) were higher in SCZ and BD groups, and levels of platelets, cholesterol (CHO), HDL, low-density lipoprotein (LDL), and apoprotein B (Apo B) were lower in SCZ and BD groups. Compared to the BD group, the values of the SIRI, lymphocytes, monocytes, and HDL were lower and the values of the SII, NHR, PHR, and platelet were higher in the SCZ group. In contrast to the BD-D group, the values of the SII; SIRI; NHR; and MHR; and levels of neutrophils, monocytes, and platelets were higher in the BD-M group, and the levels of CHO, TG, LDL, and Apo B were lower in the BD-M group. The MHR and NHR were predictors for differentiating the SCZ group from the HC group; the SIRI, NHR, and MHR were predictors for differentiating the BD-M group from the HC group; and the MHR was a predictor for differentiating the BD-D group from the HC group. The combination model of the indicators improved diagnostic effectiveness.ConclusionOur study highlights the role of systemic inflammation in the pathophysiology of SCZ, BD-M, and BD-D, the association between inflammation and lipid metabolism, and these inflammation and lipid metabolism indicators showed different variation patterns in SCZ, BD-D, and BD-M

EG-Assisted Synthesis and Electrochemical Performance of Ultrathin Carbon-Coated LiMnPO 4

Ultrathin carbon-coated LiMnPO4 (ULMP/C) nanoplates were prepared through an ethylene glycol- (EG-) assisted pyrolysis method. Different from most of LiMnPO4/C works, the obtained ULMP/C possessed relatively small particle size (less than 50 nm in thickness) and preferable carbon coating (~1 nm in thickness, 2 wt.%). As a reference, LiMnPO4/C (LMP/C) composites were also fabricated via the traditional hydrothermal method. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), thermogravimetric analysis (TG), galvanostatic charge-discharge, and cyclic voltammetry (CV) were performed to characterize the crystalline phase, morphology, structure, carbon content, and electrochemical behaviors of samples. The electrochemical performance of bare and carbon-coated LiMnPO4 was evaluated as cathodes in lithium ion batteries. As a result, the obtained ULMP/C nanoplates demonstrated much higher reversible capacities (110.9 mAh g−1 after 50 cycles at 0.1 C) and rate performances than pure LMP and LMP/C composites. This facile and efficient EG-assisted pyrolysis method can enlighten us on exploiting advanced routes to modify active materials with ultrathin and homogeneous carbon layers

Catholic education Distinctive and inclusive

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Facile One-Step Dynamic Hydrothermal Synthesis of Spinel LiMn2O4/Carbon Nanotubes Composite as Cathode Material for Lithium-Ion Batteries

Nano-sized spinel LiMn2O4/carbon nanotubes (LMO/CNTs) composite is facilely synthesized via a one-step dynamic hydrothermal approach. The characterizations and electrochemical measurements reveal that LiMn2O4 particles with narrow size distribution are well dispersed with CNTs in the composite. The LMO/CNTs nanocomposite with 5 wt % CNTs displays a high specific discharge capacity of 114 mAh g−1 at 1C rate, and the retention rate after 180 cycles at room temperature reaches 94.5% in the potential window of 3.3 to 4.3 V vs. Li/Li+. Furthermore, the electrochemical performance of the composite with 5 wt % CNTs at elevated temperature (55 °C) is also impressive, 90% discharging capacity could be maintained after 100 cycles at 1C. Such excellent electrochemical performance of the final product is attributed to the content of CNTs added in the hydrothermal process and small particle size inherited from pretreated MnO2 precursor

Size-dependent capacitive behavior of homogeneous MnO nanoparticles on carbon cloth as electrodes for symmetric solid-state supercapacitors with high performance

As promising electrode materials for supercapacitors, manganese oxides still have big challenges such as the low material utilization and poor ionic/electronic conductivity. Reducing particle sizes through nanotechnology has been used to improve material conductivity and electrochemical active sites at materials/electrolyte interfaces. Nevertheless, the extremely small particle size may result in physical and/or chemical instability, mass loss and subsequent capacitance attenuation. Understanding this trade-off effect of electrode materials size with their electrochemical properties is critical to fabricate high-performance supercapacitors. In this work, we prepare homogenous and size-tunable MnO particles (with mean diameters of 80, 41, 20, 15 and 9 nm) on carbon cloth via a facile gel-like film assisted method. It is found that the medium-size nanoparticle (20 nm) displays the best performance instead of the smallest one. These observations are different from the traditional view about material size-property relationship. Instead this work provides a new insight referring to both the size-dependent solubility and ionic/electronic transport. Beneficial from the good flexibility and high conductivity/stability of carbon cloth, the optimized MnO/carbon cloth electrode demonstrates extraordinary performance in symmetric solid-state supercapacitors with energy densities of 86 and 70 Wh kg−1 at the power densities of 450 W kg−1 and 9 kW kg−1, respectively

Enlarging Surface/Bulk Ratios of NiO Nanoparticles toward High Utilization and Rate Capability for Supercapacitors

© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Reasonable design and delicate control of microstructures are critical to achieve high energy density of active materials for pseudocapacitors that seriously depend on usable reaction interface. This work shows the effect of ultrasmall particle size on enhancing utilization and rate performance of active materials. Three types of NiO nanocrystals with different sizes of 3.36, 6.24, and 7.18 nm in average diameter are uniformly distributed on mesoporous carbon nanosheets derived from corn straw piths. The nanosheets with 3.36 nm NiO particles present an extremely high NiO utilization of 93.4% (2404 F g−1 at 0.5 A g−1), which is 2–2.5-fold higher than materials with large sizes (6.24 and 7.18 nm). This enhancement is ascribed to more complete conversion and higher ionic/electronic conductivity from a preferable surface/bulk ratio of NiO. By coupling with commercial activated carbon, the asymmetric supercapacitors present high energy and power densities (28.53 Wh kg−1 at 375 W kg−1), with 78.3% capacitance retention after 10 000 cycles at 10 A g−1

Enlarging Surface/Bulk Ratios of NiO Nanoparticles toward High Utilization and Rate Capability for Supercapacitors

Reasonable design and delicate control of microstructures are critical to achieve high energy density of active materials for pseudocapacitors that seriously depend on usable reaction interface. This work shows the effect of ultrasmall particle size on enhancing utilization and rate performance of active materials. Three types of NiO nanocrystals with different sizes of 3.36, 6.24, and 7.18 nm in average diameter are uniformly distributed on mesoporous carbon nanosheets derived from corn straw piths. The nanosheets with 3.36 nm NiO particles present an extremely high NiO utilization of 93.4% (2404 F g−1 at 0.5 A g−1), which is 2–2.5-fold higher than materials with large sizes (6.24 and 7.18 nm). This enhancement is ascribed to more complete conversion and higher ionic/electronic conductivity from a preferable surface/bulk ratio of NiO. By coupling with commercial activated carbon, the asymmetric supercapacitors present high energy and power densities (28.53 Wh kg−1 at 375 W kg−1), with 78.3% capacitance retention after 10 000 cycles at 10 A g−1.</p

Multi-yolk–shell SnO₂/Co₃Sn₂@C Nanocubes with High Initial Coulombic Efficiency and Oxygen Reutilization for Lithium Storage

The challenging problems of SnO₂ anode material for lithium ion batteries are the poor electronic conductivity and the low oxygen reutilization due to the irreversibility of Li₂O generated in the initial discharge leading to a theoretical initial Coulombic efficiency (ICE) of only 52.4%. Different from these strategies, this work proposes a novel strategy to level up the oxygen reutilization in SnO₂ by introducing Co₃Sn₂ nanoalloys which can release Co atoms to reversibly react with Li₂O instead. According to this protocol, multi-yolk–shell SnO₂/Co₃Sn₂@C nanocubes are designed and successfully prepared using hollow CoSn­(OH)₆ nanocubes as precursors followed a hydrothermal carbon coating and calcination treatment. The unique multi-yolk–shell nanostructure offers adequate breathing space for the volumetric deformation during long-term cycling. Moreover, the removal of Li₂O allows a high electronic conductivity and resultant rate performance. As a result, the efficient reutilization of oxygen enables a high ICE of 71.7% and a reversible capacity of 1003 mA h g^–1 after 200 cycles at 100 mA g^–1. Cyclic voltammetry, cycling performance at different voltage windows, and X-ray photoelectron spectroscopy confirm the proposed mechanism. This strategy employing oxygen-poor metals or alloys provides a novel approach to enhance the oxygen reutilization in SnO₂ for higher reversibility