Synthesis of Efficient and Stable Tetrabutylammonium Copper Halides with Dual Emissions for Warm White Light-Emitting Diodes.

In order to achieve a high color-rendering index (CRI) and low correlated color temperature (CCT) indoor lighting, single-component phosphors with broad-band dual emission are in high demand for white-light-emitting diodes (WLEDs). However, phosphors with such fluorescent properties are rare at present. Herein, we report a facile solid-state chemical method for the synthesis of single-component phosphor with broad-band emission and a large Stokes shift that can meet the requirements of future white-light sources. These new tetrabutylammonium copper halides phosphors have excellent warm white emission characteristics, and their luminescence peaks are located at 494 and 654 nm. The optimized photoluminescence (PL) quantum yield can reach 93.7 %. The typical CIE coordinate of the as-fabricated WLED is at (0.3620, 0.3731) with a CRI of 89 and low CCT of 4516 K.

Resveratrol improves ovarian state by inhibiting apoptosis of granulosa cells.

AIM: Among the natural polyphenolic compounds, resveratrol (RES) is known for reducing the effects of declining reproductive power through resisting senility, anti-oxidant and anti-inflammatory, while the molecular mechanism of RES in human ovaries is unclear. We aimed to evaluate the most likely mechanisms of RES against apoptosis induced by H2O2 in human ovary granulosa cells. METHODS: Ovarian granulosa cells from infertile women (≤35 years old) were collected. Those patients defined as polycystic ovary syndrome (PCOS), poor ovarian responder (POR) and Endometriosis were excluded. Then they were randomly divided into control group, model group and the treatment group. Cellular apoptosis was analyzed by flow cytometer method. The related protein and mRNA expressions were detected by western blot and RT-PCR. RESULTS: Apoptosis rates of the treatment group containing RES with concentrations of 1 µM and 10 µM were significantly decreased (p < 0.001). Western blot results demonstrated that the proteins levels of transforming growth factor-ß (TGF-ß), Bax and Caspase 9 were decreased, and Bcl-2 was increased under RES treatment, while the protein levels of Caspase 8, Caspase 3, growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) expressed no significant difference. The results by RT-PCR of follicle and ovarian development related mRNA factors were consistent with that of western blot assay. CONCLUSION: In conclusion, the present study provides the evidence that RES may affects apoptotic factors to protect human ovarian state.

Reciprocal interaction between IK1 and If in biological pacemakers: A simulation study.

Pacemaking dysfunction (PD) may result in heart rhythm disorders, syncope or even death. Current treatment of PD using implanted electronic pacemakers has some limitations, such as finite battery life and the risk of repeated surgery. As such, the biological pacemaker has been proposed as a potential alternative to the electronic pacemaker for PD treatment. Experimentally and computationally, it has been shown that bio-engineered pacemaker cells can be generated from non-rhythmic ventricular myocytes (VMs) by knocking out genes related to the inward rectifier potassium channel current (IK1) or by overexpressing hyperpolarization-activated cyclic nucleotide gated channel genes responsible for the "funny" current (If). However, it is unclear if a bio-engineered pacemaker based on the modification of IK1- and If-related channels simultaneously would enhance the ability and stability of bio-engineered pacemaking action potentials. In this study, the possible mechanism(s) responsible for VMs to generate spontaneous pacemaking activity by regulating IK1 and If density were investigated by a computational approach. Our results showed that there was a reciprocal interaction between IK1 and If in ventricular pacemaker model. The effect of IK1 depression on generating ventricular pacemaker was mono-phasic while that of If augmentation was bi-phasic. A moderate increase of If promoted pacemaking activity but excessive increase of If resulted in a slowdown in the pacemaking rate and even an unstable pacemaking state. The dedicated interplay between IK1 and If in generating stable pacemaking and dysrhythmias was evaluated. Finally, a theoretical analysis in the IK1/If parameter space for generating pacemaking action potentials in different states was provided. In conclusion, to the best of our knowledge, this study provides a wide theoretical insight into understandings for generating stable and robust pacemaker cells from non-pacemaking VMs by the interplay of IK1 and If, which may be helpful in designing engineered biological pacemakers for application purposes.

Hyperspectral Estimation of Winter Wheat Leaf Area Index Based on Continuous Wavelet Transform and Fractional Order Differentiation.

Leaf area index (LAI) is highly related to crop growth, and the traditional LAI measurement methods are field destructive and unable to be acquired by large-scale, continuous, and real-time means. In this study, fractional order differential and continuous wavelet transform were used to process the canopy hyperspectral reflectance data of winter wheat, the fractional order differential spectral bands and wavelet energy coefficients with more sensitive to LAI changes were screened by correlation analysis, and the optimal subset regression and support vector machine were used to construct the LAI estimation models for different growth stages. The precision evaluation results showed that the LAI estimation models constructed by using wavelet energy coefficients combined with a support vector machine at the jointing stage, fractional order differential combined with support vector machine at the booting stage, and wavelet energy coefficients combined with optimal subset regression at the flowering and filling stages had the best prediction performance. Among these, both flowering and filling stages could be used as the best growth stages for LAI estimation with modeling and validation R2 of 0.87 and 0.71, 0.84 and 0.77, respectively. This study can provide technical reference for LAI estimation of crops based on remote sensing technology.

Wheat Ear Recognition Based on RetinaNet and Transfer Learning.

The number of wheat ears is an essential indicator for wheat production and yield estimation, but accurately obtaining wheat ears requires expensive manual cost and labor time. Meanwhile, the characteristics of wheat ears provide less information, and the color is consistent with the background, which can be challenging to obtain the number of wheat ears required. In this paper, the performance of Faster regions with convolutional neural networks (Faster R-CNN) and RetinaNet to predict the number of wheat ears for wheat at different growth stages under different conditions is investigated. The results show that using the Global WHEAT dataset for recognition, the RetinaNet method, and the Faster R-CNN method achieve an average accuracy of 0.82 and 0.72, with the RetinaNet method obtaining the highest recognition accuracy. Secondly, using the collected image data for recognition, the R2 of RetinaNet and Faster R-CNN after transfer learning is 0.9722 and 0.8702, respectively, indicating that the recognition accuracy of the RetinaNet method is higher on different data sets. We also tested wheat ears at both the filling and maturity stages; our proposed method has proven to be very robust (the R2 is above 90). This study provides technical support and a reference for automatic wheat ear recognition and yield estimation.

Luminescence Enhancement of CsMnBr3 Nanocrystals through Heterometallic Doping.

The absorption and photoluminescence (PL) of CsMnBr3 with Mn(II) in octahedral crystal fields are extremely weak due to a d-d forbidden transition. Herein, we introduce a facile and general synthetic procedure that can prepare undoped and heterometallic doped CsMnBr3 NCs at room temperature. Importantly, both PL and absorption of CsMnBr3 NCs were significantly improved after doping a small amount of Pb2+ (4.9%). The absolute photoluminescence quantum yield (PL QY) of Pb-doped CsMnBr3 NCs is up to 41.5%, 11-fold higher than undoped CsMnBr3 NCs (3.7%). The PL enhancement is attributed to the synergistic effects between [MnBr6]4- units and [PbBr6]4- units. Furthermore, we verified the similar synergistic effects between [MnBr6]4- units and [SbBr6]4- units in Sb-doped CsMnBr3 NCs. Our results highlight the potential of tailoring luminescence properties of manganese halides through heterometallic doping.

Ultra-small α-CsPbI3 perovskite quantum dots with stable, bright and pure red emission for Rec. 2020 display backlights.

The synthesis of α-CsPbI3 perovskite quantum dots (QDs) with pure red emission around 630 nm is in high demand for display backlight application. However, the phase transition of α-CsPbI3 to yellow non-emitting δ-CsPbI3 has been proven to be a great challenge for the classic colloidal synthesis route for perovskite QDs in octadecene (ODE). Herein, we report a novel colloidal synthesis route by replacing ODE with lauryl methacrylate (LMA) as the reaction solvent to improve the solubility of precursors, resulting in small sized α-CsPbI3 QDs with a diameter of only 4.2 nm, which are the smallest red PQDs reported so far. The corresponding CsPbI3 QD films exhibit a tunable photoluminescence (PL) emission peak in the bright pure red region of 627 to 638 nm. The CsPbI3 QD polymer composite films with PL emission at 630 nm exhibit a superior photoluminescence quantum yield (PLQY) and photostability to mixed halide CsPbBrI2 films under intense illumination. Perovskite light emitting diodes (LED) with the color gamut reaching 96% of the Rec. 2020 standard are achieved using these films. This study provides a high-performance pure red fluorescent material with a robust, low-cost, and reproducible colloidal chemistry that will pave the way for the adoption of perovskite QDs in display backlight application.

Solid-state synthesis of cesium manganese halide nanocrystals in glass with bright and broad red emission for white LEDs.

Recently, lead halide perovskite nanocrystals (NCs) have attracted extensive attention due to their unique optical properties. However, the toxicity of lead and the instability to moisture obstruct their further commercial development. Herein, a series of lead-free CsMnX3 (X = Cl, Br, and I) NCs embedded in glasses were synthesized by a high temperature solid-state chemistry method. These NCs embedded in glass can remain stable after soaking in water for 90 days. It is found that increasing the amount of cesium carbonate in the synthesis process can not only prevent the oxidation of Mn2+ to Mn3+ and promote the transparency of glass in the 450-700 nm region, but also significantly increase its photoluminescence quantum yield (PLQY) from 2.9% to 65.1%, which is the highest reported value of the red CsMnX3 NCs so far. Using CsMnBr3 NCs with a red emission peak at 649 nm and full-width-at-half-maximum (FWHM) of 130 nm as the red light source, a white light-emitting diode (LED) device with International Commission on illumination (CIE) coordinates of (0.33, 0.36) and a color rendering index (CRI) of 94 was obtained. These findings, together with future research, are likely to yield stable and bright lead-free NCs for the next generation of solid-state lighting.

Promoting the doping efficiency and photoluminescence quantum yield of Mn-doped perovskite nanocrystals via two-step hot-injection.

Manganese-doped perovskite nanocrystals (NCs) have been synthesized by a novel two-step hot-injection strategy with an unprecedented Mn doping efficiency of 48.5%, bright orange emission under ultraviolet light and X-ray excitation and a photoluminescence quantum yield of 84.4%, making them excellent luminescent materials.

In silico mechanisms of arsenic trioxide-induced cardiotoxicity.

It has been found that arsenic trioxide (ATO) is effective in treating acute promyelocytic leukemia (APL). However, long QT syndrome was reported in patients receiving therapy using ATO, which even led to sudden cardiac death. The underlying mechanisms of ATO-induced cardiotoxicity have been investigated in some biological experiments, showing that ATO affects human ether-à-go-go-related gene (hERG) channels, coding rapid delayed rectifier potassium current (I Kr ), as well as L-type calcium (I CaL ) channels. Nevertheless, the mechanism by which these channel reconstitutions induced the arrhythmia in ventricular tissue remains unsolved. In this study, a mathematical model was developed to simulate the effect of ATO on ventricular electrical excitation at cellular and tissue levels by considering ATO's effects on I Kr and I CaL . The ATO-dose-dependent pore block model was incorporated into the I Kr model, and the enhanced degree of ATO to I CaL was based on experimental data. Simulation results indicated that ATO extended the action potential duration of three types of ventricular myocytes (VMs), including endocardial cells (ENDO), midmyocardial cells (MCELL), and epicardial cells (EPI), and exacerbated the heterogeneity among them. ATO could also induce alternans in all three kinds of VMs. In a cable model of the intramural ventricular strand, the effects of ATO are reflected in a prolonged QT interval of simulated pseudo-ECG and a wide vulnerable window, thus increasing the possibility of spiral wave formation in ventricular tissue. In addition to showing that ATO prolonged QT, we revealed that the heterogeneity caused by ATO is also an essential hazard factor. Based on this, a pharmacological intervention of ATO toxicity by resveratrol was undertaken. This study provides a further understanding of ATO-induced cardiotoxicity, which may help to improve the treatment for APL patients.

Biological pacemaker: from biological experiments to computational simulation.

Pacemaking dysfunction has become a significant disease that may contribute to heart rhythm disorders, syncope, and even death. Up to now, the best way to treat it is to implant electronic pacemakers. However, these have many disadvantages such as limited battery life, infection, and fixed pacing rate. There is an urgent need for a biological pacemaker (bio-pacemaker). This is expected to replace electronic devices because of its low risk of complications and the ability to respond to emotion. Here we survey the contemporary development of the bio-pacemaker by both experimental and computational approaches. The former mainly includes gene therapy and cell therapy, whilst the latter involves the use of multi-scale computer models of the heart, ranging from the single cell to the tissue slice. Up to now, a bio-pacemaker has been successfully applied in big mammals, but it still has a long way from clinical uses for the treatment of human heart diseases. It is hoped that the use of the computational model of a bio-pacemaker may accelerate this process. Finally, we propose potential research directions for generating a bio-pacemaker based on cardiac computational modeling.

Role of If Density on Electrical Action Potential of Bio-engineered Cardiac Pacemaker: A Simulation Study.

Due to the inevitable drawbacks of the implantable electrical pacemaker, the biological pacemaker was believed to be an alternative therapy for heart failure. Previous experimental studies have shown that biological pacemaker could be produced by genetically manipulating non-pacemaking cardiac cells by suppressing the inward rectifier potassium current (IK1) and expressing the hyperpolarization- activated current (If). However, the role of If in such bio-engineered pacemaker is not clear. In this study, we simulated the action potential of biological pacemaker cells by manipulating If-IK1 parameters (i.e., inhibiting IK1 as well as incorporating If) to analyze possible mechanisms by which different If densities control pacemaking action potentials. Our simulation results showed different pacing mechanism between the bioengineered pacemaking cells with and without If. In addition, it was shown that a greater If density might result in a slower pacing frequency, and excessive of it might produce an early-afterdepolarizations-like action potential due to a sudden release of calcium from sarcoplasmic reticulum into the cytoplasm. This study indicated that when IK1 was significantly suppressed, incorporating If may not enhance the pacing ability of biological pacemaker, but lead to abnormal dynamics of intracellular ionic concentration, increasing risks of dysrhythmia in the heart.

Pharmacotherapeutic Effects of Quinidine on Short QT Syndrome by Using Purkinje-Ventricle Model: A Simulation Study.

AIMS: Short QT syndrome (SQTS) arises due to gene mutations leading to accelerated ventricular repolarization, and increased risk of cardiac arrhythmias and sudden cardiac death (SCD). The SQT1, SQT2 and SQT3 variants of the SQTS result from inherited gain-of-function mutations (e.g. N588K, V307L and D172N, respectively) to potassium channels. However, the effective management of SQTS remains a challenge, and is incompletely understood. In this study, computational modelling was used to investigate pharmacotherapeutic effects of selected class I drug quinidine on SQT1, SQT2 and SQT3 variants. METHODS AND RESULTS: The biophysically-detailed Stewart et al. model of Purkinje fibre cell action potentials and the ten Tusscher et al. model of ventricular cell action potentials were coupled together into a heterogeneous two-dimensional (2D) tissue model. Previously validated IKr, IKs and IK1 channel formulations for SQT1, SQT2 and SQT3 were incorporated in ventricular cell and tissue models. The channel-blocking effects of quinidine on ionic currents were modelled by using Hill coefficient and IC50 values from the literature. At the 10 µM concentration tested in this study, quinidine effectively prolonged the action potential duration (APD) under all the SQT1, SQT2 and SQT3 conditions. In 2D simulations, quinidine prolonged the ventricular repolarization process and prolonged the QT intervals under all SQTS variants conditions. CONCLUSIONS: Our findings provide a rational basis for the pursuit of pharmacotherapeutic agent quinidine in the treatment of all SQTS variants.

Computational Cardiac Modeling Reveals Mechanisms of Ventricular Arrhythmogenesis in Long QT Syndrome Type 8: CACNA1C R858H Mutation Linked to Ventricular Fibrillation.

Functional analysis of the L-type calcium channel has shown that the CACNA1C R858H mutation associated with severe QT interval prolongation may lead to ventricular fibrillation (VF). This study investigated multiple potential mechanisms by which the CACNA1C R858H mutation facilitates and perpetuates VF. The Ten Tusscher-Panfilov (TP06) human ventricular cell models incorporating the experimental data on the kinetic properties of L-type calcium channels were integrated into one-dimensional (1D) fiber, 2D sheet, and 3D ventricular models to investigate the pro-arrhythmic effects of CACNA1C mutations by quantifying changes in intracellular calcium handling, action potential profiles, action potential duration restitution (APDR) curves, dispersion of repolarization (DOR), QT interval and spiral wave dynamics. R858H "mutant" L-type calcium current (ICaL ) augmented sarcoplasmic reticulum calcium content, leading to the development of afterdepolarizations at the single cell level and focal activities at the tissue level. It also produced inhomogeneous APD prolongation, causing QT prolongation and repolarization dispersion amplification, rendering R858H "mutant" tissue more vulnerable to the induction of reentry compared with other conditions. In conclusion, altered ICaL due to the CACNA1C R858H mutation increases arrhythmia risk due to afterdepolarizations and increased tissue vulnerability to unidirectional conduction block. However, the observed reentry is not due to afterdepolarizations (not present in our model), but rather to a novel blocking mechanism.