Determination of twelve neonicotinoid pesticides in chili using an improved QuEChERS method with UPLC-Q-TOF/MS.

In this study, a QuEChERS method based on citrate was developed and utilized for the analysis of twelve neonicotinoid pesticides in fresh red chilies, fresh green chilies, and dried chilies, coupled with ultra-high performance liquid chromatography quadrupole time of flight mass spectrometry (UPLC-Q-TOF/MS). In the sample preparation, acetonitrile containing 1% formic acid was used as the extraction solvent. Anhydrous sodium sulfate replaced the traditional anhydrous magnesium sulfate for water removal, effectively eliminating the issues of salt caking. Graphitized carbon black, octadecyl silica, and primary secondary amine were used as cleaning agents. The method showed good sensitivity, with the limits of quantification below 0.03 mg/kg for fresh chilies and below 0.15 mg/kg for dried chilies. Values of matrix effects ranged from -19.5% to 8.4%, and the recovery was 86.9% - 105.2%. The analytical method provided an effective tool for the high throughput detection of neonicotinoid pesticide residues in multiple chili matrices.

Inhibitory effects of chlorophyll pigments on the bioaccessibility of ß-carotene: Influence of chlorophyll structure and oil matrix.

Chlorophylls and ß-carotene are fat-soluble phytochemicals in daily diets, while their bioaccessibility interaction remains unknown. Eight dietary chlorophylls and their derivatives (chlorophyll a, chlorophyll b, pheophytin a, pheophytin b, chlorophyllide a, chlorophyllide b, pheophorbide a, pheophorbide b) were combined with ß-carotene in six different oil matrices (corn oil, coconut oil, medium-chain triglycerides, peanut oil, olive oil and fish oil) and were subjected to in vitro digestion. Generally, chlorophylls significantly decreased ß-carotene bioaccessibility by competitive incorporation into micelles. Dephytylated chlorophylls had a greater inhibitory effect on the micellarization and bioaccessibility of ß-carotene compared to phytylated chlorophylls. In their co-digestion system, olive oil group exhibited the smallest particle size and biggest zeta potential in both digesta and micelles. For chlorophylls, the phytol group and their levels are key factors, which was also buttressed by the mice model where additional supplementation of pheophorbide a significantly hindered the accumulation of ß-carotene and retinoids compounds.

Prevalence and influencing factors of post-traumatic stress disorder among Chinese healthcare workers during the COVID-19 epidemic: a systematic review and meta-analysis.

Background: Post-traumatic stress disorder is an important psychological problem affecting the physical mental health of Chinese healthcare workers during the COVID-19 pandemic. Aims: To estimate the prevalence and influencing factors of post-traumatic stress disorder (PTSD) among Chinese healthcare workers during COVID-19. Methods: Search of Chinese and English literature in PubMed, EMbase, Web of Science, Medline, Elsevier, SpringerLink, China Biomedical Literature Database, CNKI, Wan-fang, and CQVIP for the period from December 2019 to August 2023. Stata 14.0 software was used for data analysis. The methodological quality of each study was scored, and data were extracted from the published reports. Pooled prevalence was estimated using the Random-effects model. Publication bias was evaluated using Egger's test and Begg's test. Results: Twenty-one studies included 11841 Chinese healthcare workers in this review. First, the overall prevalence of Post-traumatic stress disorder among Chinese healthcare workers during the COVID-19 epidemic was 29.2% (95% CI: 20.7% to 33.7%). Twelve factors included in the meta-analysis were found to be protective against PTSD among Chinese healthcare workers: female, nurse, married, front-line work, less work experience, family or friend diagnosed with COVID-19, history of chronic disease and fear of COVID-19. Conversely, outside Hubei, higher education, social support and psychological resilience are protective factors. Conclusion: These recent findings increase our understanding of the psychological status of Chinese healthcare workers and encourage that long-term monitoring and long-term interventions should be implemented to improve the mental health of Chinese healthcare workers in the aftermath of the COVID-19.

Changes in toxicity after mixing imidacloprid and cadmium: enhanced, diminished, or both? From a perspective of oxidative stress, lipid metabolism, and amino acid metabolism in mice.

Imidacloprid (IMI) and cadmium (Cd) are pollutants of concern in the environment. Although investigations about their combined toxicity to organisms such as earthworms, aquatic worms, Daphnia magna, and zebrafish have been carried out, their combined toxicity to mammals remains unknow. In this study, twenty-four 8-week-old mice were arbitrarily separated into 4 groups: CK (control group), IMI (15 mg/kg bw/day, 1/10 LD50), Cd (15 mg/kg bw/day, 1/10 LD50), and IMI + Cd (15 mg/kg bw/day IMI + 15 mg/kg bw/d Cd) and the combined toxic effects of IMI and Cd were examined with biochemical (oxidative stress testing) and omics approaches (metabolomics and lipidomics). The results revealed changes in each treatment group in terms of oxidative stress, abnormalities in lipid metabolism, and disturbances in amino acid metabolism. Co-administration had antagonistic effects on MDA accumulation and lipid metabolism disorders while acting synergistically on changes in SOD and GSH-Px activities. It is worth noting that after analysis, the changes caused by mixed administration in vivo were closer to those caused by IMI administration alone. This study provides new insights into the combined toxicity of neonicotinoids and heavy metals, which is helpful for relevant environmental governance and further investigations about their impacts on human health and the environment.

Dominant influence of plants on soil microbial carbon cycling functions during natural restoration of degraded karst vegetation.

The impacts of natural restoration projects on soil microbial carbon (C) cycling functions have not been well recognized despite their wide implementation in the degraded karst areas of southwest China. In this study, metagenomic sequencing assays were conducted on functional genes and microorganisms related to soil C-cycling at three natural restoration stages (shrubbery, TG; secondary forest, SG; old-growth forest, OG) in the southeast of Guizhou Province, China. The aims were to investigate the changes in microbial potentials responsible for soil C cycling and the underlying driving forces. The natural restoration resulted in vegetation establishment at all three restoration stages, rendering alterations of soil microbial C cycle functions as indicated by metagenomic gene assays. When TG was restored into OG, the number and diversity of genes and microorganisms involved in soil C cycling remained unchanged, but their composition underwent significant shifts. Specifically, microbial potentials for soil C decomposition exhibited an increase driven by the collaborative efforts of plants and soils, while microbial potentials for soil C biosynthesis displayed an initial upswing followed by a subsequent decline which was primarily influenced by plants alone. In comparison to soil nutrients, it was determined that plant diversities served as the primary driving factor for the alterations in microbial carbon cycle potentials. Soil microbial communities involved in C cycling were predominantly attributed to Proteobacteria (31.87%-40.25%) and Actinobacteria (11.29%-26.07%), although their contributions varied across the three restoration stages. The natural restoration of degraded karst vegetation thus influences soil microbial C cycle functions by enhancing C decomposition potentials and displaying a nuanced pattern of biosynthesis potentials, primarily influenced by above-ground plants. These results provide valuable new insights into the regulation of soil C cycling during the restoration of degraded karst vegetation from genetic and microbial perspectives.

Cobalt Species-Loaded MOFs as Chemiluminescent Catalysts for Monitoring Carbendazim.

The application of active metal-based nanoscale catalysts as signal enhancers for chemiluminescent immunoassay (CLIA) is restricted by poor thermodynamic stability and ease of aggregation. For the present exploration, zirconium-based MOFs UiO-66-NH2 were adopted as supports to load cobalt species by an impregnation-reduction approach. Cobalt species were uniformly distributed in the framework architecture of the MOF materials. The prepared cobalt-loaded MOF hybrids, noted as UiO-66-NH2/Co, display superior chemiluminescence (CL) catalytic activity owing to the introduction of cobalt catalytic centers. The CL catalytic capability of UiO-66-NH2/Co hybrids is about 18 times of that of free cobalt ions at the same cobalt amount. The results of mechanism exploration manifest that the hybrids are capable of accelerating the decay of hydrogen peroxide and promoting the yield of reactive oxygen species. Based on their remarkable CL catalytic capability, a CLIA approach was proposed to monitor carbendazim by adopting the hybrids as signal probes, which showed the merits of high sensitivity and satisfactory selectivity. Carbendazim was quantitated within a concentration range of 0.05 to 60 ng mL-1, with a detection limit of 19.8 pg mL-1. The results for monitoring spiked samples verify the acceptable practicality of the proposed CLIA approach.

Composite Finite-Time Resilient Control for Cyber-Physical Systems Subject to Actuator Attacks.

Cyber-physical systems (CPSs) seamlessly integrate communication, computing, and control, thus exhibiting tight coupling of their cyber space with the physical world and human intervention. Forming the basis of future smart services, they play an important role in the era of Industry 4.0. However, CPSs also suffer from increasing cyber attacks due to their connections to the Internet. This article investigates resilient control for a class of CPSs subject to actuator attacks, which intentionally manipulate control commands from controllers to actuators. In our study, the supertwisting sliding-mode algorithm is adopted to construct a finite-time converging extended state observer (ESO) for estimating the state and uncertainty of the system in the presence of actuator attacks. Then, for the attacked system, a finite-time converging resilient controller is designed based on the proposed ESO. It integrates global fast terminal sliding-mode and prescribed performance control. Finally, an industrial CPS, permanent magnet synchronous motor control system, is investigated to demonstrate the effectiveness of the composite resilient control strategy presented in this article.

Adsorption Properties for La(III), Ce(III), and Y(III) with Poly(6-acryloylamino-hexyl hydroxamic acid) Resin.

Using polyacrylic resin followed by the substitution reaction with 6-aminohexyl hydroxamic acid, poly(6-acryloylamino-hexyl hydroxamic acid) resin (PAMHA) was successfully synthesized. PAMHA, a spherical resin with the particle size of 0.4 mm, is a novel polyamide hydroxamic acid chelating resin containing acylamino and hydroxamic acid functional groups. A series of influences (pH, contact time, temperature, and the initial concentrations of rare earth ions) were investigated to determine the adsorption properties. The adsorption capacity for La(III), Ce(III), and Y(III) ions were 1.030, 0.962, and 1.450 mmol·g-1, respectively. Thermodynamic and kinetic studies were also carried out to show that the uptake of rare earth ions onto PAMHA fitted well the pseudo-second-order model and Langmuir isotherm, and the adsorption process was spontaneous endothermic. In addition, desorption of rare earth ions was achieved by using 2 mol·L-1 HNO3 and desorption efficiencies for La(III), Ce(III), and Y(III) ions were 98.4, 99.1, and 98.8%, respectively. Properties of PAMHA resin were characterized by scanning electron microscope (SEM), Fourier transform infrared spectrometry (FTIR), and X-ray photoelectron spectrometer (XPS). The results showed that there was coordination between the rare earth ions with PAMHA and rare metal ions were chemically adsorbed on the surface of the PAMHA.

A screening method of oil-soluble synthetic dyes in chilli products based on multi-wavelength chromatographic fingerprints comparison.

A multi-wavelength HPLC fingerprint comparison method was proposed for the screening of oil-soluble synthetic dyes in chilli products. The screening was based on the fingerprint differences of normal unadulterated chilli sample with tested chilli samples. The samples were extracted with acetone and fingerprinted by HPLC under four visible light wavelengths (450 nm, 490 nm, 520 nm, and 620 nm). It was found that the fingerprints of different chilli product samples had a relatively fixed number of peaks and stable retention time. When 16 kinds of known synthetic dyes were used as model analytes to assess the screening efficiency, 14 of them could be screened using fingerprint comparison method, with LOD of 0.40-2.41 mg/kg. The new screening method was simple and had the possibility of finding existence of the adulterated dyes which could not be identified using known standard analytes as control.

Adulteration and cultivation region identification of American ginseng using HPLC coupled with multivariate analysis.

American ginseng (Panax quinquefolius) is originally grown in North America. Due to price difference and supply shortage, American ginseng recently has been cultivated in northern China. Further, in the market, some Asian ginsengs are labeled as American ginseng. In this study, forty-three American ginseng samples cultivated in the USA, Canada or China were collected and 14 ginseng saponins were determined using HPLC. HPLC coupled with hierarchical cluster analysis and principal component analysis was developed to identify the species. Subsequently, an HPLC-linear discriminant analysis was established to discriminate cultivation regions of American ginseng. This method was successfully applied to identify the sources of 6 commercial American ginseng samples. Two of them were identified as Asian ginseng, while 4 others were identified as American ginseng, which were cultivated in the USA (3) and China (1). Our newly developed method can be used to identify American ginseng with different cultivation regions.

Self-assembly of low dimensional nanostructures and materials via supramolecular interactions at interfaces.

Low dimensional inorganic-organic heterostructure nanomaterials with multiple different functional components attaching at interface have drawn considerable attention over the last decades, due to their excellent optical and electronic properties in comparison with their individual components. Supramolecular self-assembly of disordered building blocks has played an essential role in constructing well-defined functionalized structures. Solid-liquid interfaces are known as ideal platforms in the self-assembly process, thus providing a series of novel and attractive strategies to construct low dimensional inorganic-organic heterostructure nanomaterials with different sizes and shapes. In this review, we summarized low dimensional inorganic-organic heterostructure nanomaterials on the basis of self-assembly that is driven by synergistically metal-ligand coordination and other intermolecular interactions. Both stepwise self-assembly on the inorganic (or organic) solid surface and self-assembly of inorganic-organic building block through hydrogen bond, metal-ligand coordination interaction, π-π stacking, hydrophobic interaction, and covalently bonding were discussed.

A smart porphyrin cage for recognizing azide anions.

A smart porphyrin cage that can recognize azide anions by the changes of (1)H NMR spectra was synthesized by CuAAC "click" reaction in high yield.

Ion-specific self-assembly of low-dimension aggregate structures of conjugated polymer at two-phase interface.

A novel and facile approach to manipulate the morphology of Cu(2+)-ion-specific assembly of conjugated polymer by coordinative interaction at an oil-water two-phase interface is present. The application of increasing importance is the use of π-conjugated polymers as receptors, exploiting their ability to selectively form complexes, which can obviously change the optical properties in solution and induce the formation of varied solid nano/microstructures. By this method, microtubes are formed through self-rolling of a strained ionic bilayer film at the oil/water interface.

A dual sensor of fluorescent and colorimetric for the rapid detection of lead.

This study demonstrated a simple and reliable method to rapidly detect Pb(2+) in aqueous solution, exploiting gold nanoparticles as a lead ion probe; the results indicated that the dual channels sensor showed high selectivity and sensitivity for Pb(2+) as low as ppm levels in aqueous environment.

Synthesis of a [2]rotaxane incorporating a "magic sulfur ring" by the thiol-ene click reaction.

The mild and highly efficient thiol-ene click reaction has been used to construct a rotaxane incorporating dibenzo-24-crown-8 (DB24C8) and a dibenzylammonium-derived thread in high yield under the irradiation of UV light. A rotaxane containing a disulfide linkage in the macrocycle was also synthesized by the thiol-ene click reaction. It has been demonstrated that the formation of the [2]rotaxane with the disulfide bond in the macrocycle occurs by a mechanism that is different to the threading-followed-by-stoppering process. The successful construction of a rotaxane directly from its constituent components, the macrocycle containing a disulfide linkage and the dibenzylammonium hexafluorophosphate salt, suggests that the space within the macrocycle incorporating the disulfide linkage is smaller than the phenyl unit and a plausible reaction mechanism has been proposed as follows: A small amount of the initiator forms two radicals upon the absorption of UV irradiation; the radicals act as a "key" to "unlock" the disulfide bond in the macrocycle. The resulting crown ether like moiety in the macrocycle is clipped around the ammonium ion center in the dumb-bell-shaped compound. The [2]rotaxane is generated upon recombination of the disulfide linkage.

Organic crystallizable solvent served as template for constructing well-ordered PPE films.

Tuning the solidification of the crystallizable solvent naphthalene, well-patterned conjugated polymer poly(phenyleneethynylene) (PPE) films with well-defined nanostructures of 0D nanodots, 1D lamellas, and 2D texture nanostructures have been prepared by several strategies. The nanostructures have been characterized and the formation mechanisms for the morphologies have been discussed.

Constructing hybrid films of conjugated oligomers and gold nanoparticles for efficient photoelectronic properties.

Hybrid films of conjugated oligomers and gold nanoparticles have been fabricated by a coordination approach on the surface of gold nanoparticles. This method facilitates mild linkage of the oligomer/nanoparticle layers in ambient conditions, which provides a general route for preparation of organic/inorganic interlayer superstructures. Characterization of the as-obtained hybrid film has been carried out by UV-vis absorption, fluorescence spectroscopy, and atomic force microscopy (AFM). The hybrid film exhibits dramatic changes in both optical and photovoltaic properties upon encapsulation of fullerene. A photoelectrical application is presented by taking electrochemical measurements of the self-assembled film. The results reveal potential technological uses in photovoltaic devices.

An unusual addition reaction for constructing a novel pH-controlled fluorescence switch.

A pH-controlled fluorescence switch based on a core-substituted naphthalenediimide compound (NDI-DBU) was constructed. The novel pentacyclic compound (NDI-DBU) was derived from naphthalenediimide (NDI) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in only one synthetic operation, catalysized by CuI.

Construction and photophysical properties of organic-inorganic nanonetworks based on oligo(phenylenevinylene) and functionalized gold nanoparticles.

Novel organic-inorganic nanonetworks of oligo(phenylenevinylene) (OPV) and gold nanoparticles (GNPs) have been synthesized by the amine-based epoxide ring-opening reaction. The resulting OPV-GNPs nanocomposites exhibit homogeneous and well-defined interfaces between the organic ligands and the inorganic nanoparticles, thereby promoting efficient electronic interfacial interaction between the two constituents. The functionalized gold nanoparticles serve as chemical reagents for the construction of nanohybrids, while the epoxide-terminated OPV acts as linkage between gold nanoparticles. The new architecture provides a facile methodology for fabrication of novel organic-inorganic nanohybrids under relatively mild conditions, which facilitates further applications of hybrid materials.

Synthesis of a fluorescent polymer bearing covalently linked thienylene moieties and rhodamine for efficient sensing.

A novel conjugated polymer (RB-PPETE) of poly[p-(phenylene ethynylene)-alt-(thienylene ethynylene)] (PPETE) bearing covalently linked thienylene rings and Rhodamine B units has been synthesized and successfully used to detect metal ions. The Rhodamine B exists as a lactone, which is colorless and non-fluorescent. Hg(2+) ions can induce the Rhodamine group to form a ring-opened state. The fluorescence resonance energy transfer (FRET) was demonstrated in the polymer, and in the presence of Hg(2+) ions the excitation energy along the backbone of the conjugated polymer is transferred to the energy acceptor (Rhodamine B), which leads to a visual color change of the solution from slight yellow to orange. Meanwhile, this new system shows outstanding Hg(2+) -selective FRET off-on type fluoroionophoric properties among the representative metal ions in tetrahydrofuran.