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Three new compounds (1‒3), including a phenylpropanoid (1), a bistetrahydrofuran lignin (2), and a lignan dimer (3), and seven known lignans (4‒10), were isolated from an EtOH extract of the aerial parts of Triadica rotundifolia. The structures of the new compounds were elucidated by comprehensive spectroscopic analyses. New compounds 1−3 were evaluated for their antineuroinflammatory and antioxidant activities. Research on the antineuroinflammatory activity suggested that compounds 2 and 3 had significant inhibitory effects on NO production in LPS-induced BV-2 cells, with the IC50 values of 15.7 and 5.8 μM, respectively. Meanwhile, compounds 2 and 3 exhibited better DPPH free radical scavenging activities with EC50 values of 2.0 and 4.3 μM, respectively, than the positive control vitamin C (EC50 = 14.3 μM).

Three new pairs of lignan enantiomers (1a/1b‒3a/3b) and two pairs of known lignan enantiomers (4a/4b and 5a/5b) were isolated from the stems of Mappianthus iodoides. The structures of the enantiomers were elucidated by comprehensive spectroscopic analyses. Their absolute configurations were assigned by single-crystal X-ray diffraction analysis as well as comparison of the experimental and calculated ECD spectra. The antineuroinflammatory activity research revealed that compounds 2a, 2b, 3a, 4a, and 5b could moderately inhibit NO production in LPS-induced BV-2 microglial cells with IC50 values ranging from 13.42 to 48.34 μM.

Chemotherapy resistance is a bottleneck for ovarian cancer treatment; therefore, revealing its regulatory mechanism is critical. In the present study, we found that prostate tumor overexpressed-1 (PTOV1) was upregulated significantly in ovarian cancer cells and tissues. Patients with high PTOV1 levels had a poor outcome. In addition, PTOV1 overexpression increased CDDP (cisplatin) resistance, while PTOV1 knockdown inhibited CDDP resistance, as determined using cell viability assays, apoptosis assays, and an animal model. Mechanistic analysis showed that PTOV1 increased nuclear factor kappa B (NF-κB) pathway activity, reflected by increased nuclear translocation of its p65 subunit and the phosphorylation of inhibitor of nuclear factor kappa-B kinase subunits alpha and beta, which are markers of NF-κB pathway activation. Inhibition of the NF-κB pathway in PTOV1-overexpressing ovarian cancer cells increased CDDP-induced apoptosis, suggesting that PTOV1 promoted chemotherapy resistance by activating the NF-κB pathway. In summary, we identified PTOV1 as a prognostic factor for patients with ovarian cancer. PTOV1 might be a target for inhibition of chemotherapy resistance., Graphical Abstract, Chemotherapy resistance is a bottleneck of ovarian cancer treatment. In this study, we found PTOV1 not only served as a prognostic factor for ovarian cancer patients but also was a novel target for inhibition of cisplatin resistance.

Nitrate (NO3-) is known to be actively involved in the processes of mineralization and heavy metal transformation; however, it is unclear whether and how it affects the bioavailability of antimony (Sb) in paddy soils and subsequent Sb accumulation in rice. Here, the effects of NO3- on Sb transformation in soil-rice system were investigated with pot experiments over the entire growth period. Results demonstrated that NO3- reduced Sb accumulation in brown rice by 15.6% compared to that in the control. After amendment with NO3-, the Sb content in rice plants increased initially and then gradually decreased (in roots by 46.1%). During the first 15 days, the soil pH increased, the oxidation of Sb(III) and sulfides was promoted, but the reduction of iron oxide minerals was inhibited, resulting in the release of adsorbed and organic-bound Sb from soil. The microbial arsenite-oxidizing marker gene aoxB played an important role in Sb(III) oxidation. From days 15 to 45, after NO3- was partially consumed, the soil pH decreased, and the reductive dissolution of Fe(III)-bearing minerals was enhanced; consequently, iron oxide-bound Sb was transformed into adsorbed and dissolved Sb species. After day 45, NO3- was completely reduced, Sb(V) was evidently reduced to Sb(III), and green rust was generated gradually. Thus, the available Sb decreased due to its enhanced affinity for iron oxides. Moreover, NO3- inhibited the reductive dissolution of iron minerals, which ultimately caused low Sb availability. Therefore, NO3- can chemically and biologically reduce the Sb availability in paddy soils and alleviate Sb accumulation in rice. This study provides a potential strategy for decreasing Sb accumulation in rice in the Sb-contaminated sites.

Motivated by novel graphyne-like carbon nanostructure C68-GY, spin-polarized DFT calculations with dispersion-correction were performed to investigate the hydrogen adsorption capacity of Li decorated C68-GY nanosheet. The binding energy between Li and C68-GY was larger than the cohesive energy of bulk metal, indicating Li atoms would prefer to separately attached on C68-GY. The ab initio molecular dynamics simulation has been performed to confirm the stability of Li/C complex. When five Li atoms decorated on C68-GY, 14H2 molecules were captured. The maximum hydrogen storage density was 8.04 wt% with an average hydrogen adsorption energy of −0.227 eV per H2. The positively charged Li atoms aroused electrostatic field and induced the polarization of H2. It was notable to observe strong hybridization between the main peak of H-1s orbitals with Li below Fermi level, which was responsible for the enhancement of hydrogen binding energy, indicating its potential application on hydrogen storage.

The hydrogen storage capacity of yttrium decorated graphyne nanotubes is calculated using spin polarized DFT method. The stabilities, electronic properties and the structures of Y attachment on graphyne tube are investigated. It is revealed that Y can be separately adsorbed on graphyne tube with the binding energy of 6.76 eV and the clustering of metal atoms is hindered. The geometry optimization shows that Y atoms decorated graphyne tube can capture 42H2 molecules through Dewar-Kubas like interaction and the polarization under the electrostatic potential formed by Y and graphyne tubes. The weight percent capacity is 5.71 wt%, with an average hydrogen adsorption energy of −0.153 eV per H2, indicating its potential application on hydrogen storage candidates.

Thiol-ene click reactions are more oxygen tolerant alternative to the conventional (meth)acrylate chemistry that is frequently used for the rapid production of photopolymerized networks with numerous desirable properties. To attain a high curing efficiency while maintaining the advantages of thiol-ene systems, a castor oil-based hyperbranched urethane acrylate was employed in this work as a primary oligomer for UV-curable coating formulation. Subsequently, a tetrathiol monomer (PETMP) was introduced into the coating formulation to obtain a thiol-ene system. The effects of PETMP loadings on the UV-curing kinetics and final polymer properties were systematically investigated. Consequently, thiol-ene based films with excellent flexibility and water resistance were obtained as a result of the high efficient thiol-ene photopolymerization. The double bond conversion of the thiol-ene system was found to increase with the addition of more PETMP. Impressively, with the incorporation of 5 wt% PETMP, the resultant UV-cured film had the best acid resistance and exhibited a double bond conversion of 93.6%, a pencil hardness of 6H, a water absorption of 0.76%. Additionally, all of the prepared films were completely transparent and possessed good microstructures. These thiol-ene based films may provide insight into the preparation of high-performance UV-curable coatings with excellent flexibility.

Lignin was used herein to prepare chemical grouting materials as replacements for petroleum-based epoxy precursors. Demethylation, phenolation, and hydroxymethylation were conducted and the products were characterized via FT-IR, 1H NMR, and GPC. A quantitative NMR method was used to study the precise changes in the functional group composition. Raw lignin (RL), demethylated lignin (DML), phenolated lignin (PHL), and hydroxymethylated lignin (HML) were respectively reacted with epichlorohydrin to synthesize various lignin epoxy resin (LEP), including raw lignin epoxy resin (RLEP), demethylated lignin epoxy resin (DMLEP), phenolated lignin epoxy resin (PHLEP), and hydroxymethylated lignin epoxy resin (HMLEP). With LEP as feedstocks, new grouting materials were prepared and the effects of the RLEP content and the LEP variants were investigated. The results demonstrated that the prepared lignin epoxy grouting resin had outstanding viscosity and mechanical properties with RLEP content up to 16%, and this performance greatly exceeded the industry standard. DMLEP, PHLEP, and HMLEP were able to provide better tensile properties, heat-resistance, chemical-resistance and curing performance compared with that achieved with RLEP. Overall, lignin has displayed great potential in replacing petroleum-based materials for the preparation of high-performance chemical grouting materials.

Fluoride removal from aqueous solution by adsorption using fly ash cenospheres (FAC) modified with paper mill lime mud (LM) as composite adsorbent had been investigated. The characterization of FAC and composite adsorbent were analyzed by Scanning electron spectroscope (SEM), Energy dispersive spectrometer (EDS), Brunauer emmett teller (BET) and Fourier transform infrared (FTIR), which demonstrated that the porous structure of composite adsorbent was obtained after surface modification. Adsorption of fluoride on modified fly ash cenospheres was fitted with pseudo-second-order model and Langmuir model. Response surface methodology (RSM) was employed to investigate the effects of F− concentration, pH, adsorbent dosage and temperature on the removal efficiency. Analysis of variance (ANOVA) was used to test the adequacy of the mathematical models. The Nonelectrostatic model of modified fly ash cenospheres adsorbing fluoride was built through the Generalized composite method, indicating that two inner-spherical complexes, ≡SF and ≡SOHF−, were formed in the adsorption process by means of the ligand exchange and surface complexation. Optimization of the adsorption conditions enabled the realization of the practical needs for fluoride contaminated water.

Selective oxidation of sulfides into sulfoxides or sulfones is an important transformation in organic synthesis. Activated carbon supported Nb-based catalysts were prepared by the impregnation method and then characterized by the XRD, TEM and XPS. The characterization results indicate Nb species is amorphous Nb2O5. The catalysts were applied for the catalytic oxidation of sulfides in aqueous phase with H2O2 as the oxidant. Sulfides could be converted into the corresponding sulfoxides or sulfones with high conversion and selectivity at room temperature. The recycling experiments showed the Nb2O5/AC catalysts exhibited good reusability. They could be recycled for 10 times without obvious loss of activity and selectivity.

Cross-linked sustained-release polycarboxylate superplasticizers (SPs) are superior alternative to the comb-type polycarboxylate SPs due to they offer both a high fluidity and a good retention effect for concrete slurry. In this context, a series of cross-linked polycarboxylate superplasticizers were synthesized using acrylic acid, methylallyl polyoxyethylene ether and four different cross-linkers containing ester groups, respectively. The key difference among these four cross-linkers is their molecular weights because they each possessed the different ethoxy content. The fluidity and fluidity retention tests, adsorption performance and scanning electron microscope tests showed that the cross-linked superplasticizers offered good dispersing effects and excellent slump performance. Excitingly, the maximum flow reached up to 394 mm at a water-cement ratio of 0.35 and this high fluidity could be simultaneously maintained for 2 h, which facilitated concrete transport over long distances, therefore improving the practical workability of concrete. Furthermore, it was found that the superplasticizers derived from cross-linkers with higher ethoxy group contents provided cement paste samples with improved fluidity. Evaluation of the hydration heat and setting time demonstrated that the cross-linked polycarboxylate superplasticizers could delay the hydration of cement and the final setting time had been extended by 4 h in comparation with blank samples. After 3, 7 and 28 d, the compressive strength of the cement mortar was improved with increases of molecular weight of the cross-linker in the cross-linked superplasticizers due to the elevation of ethoxy content.

A new chlorinated diphenyl ether, ethyl dichloroasterrate (1), and a new sesquilignan, mappilignan A (2), along with two known diphenyl ethers (3 and 4) and one known sesquilignan (5), were isolated from the stems of Mappianthus tomentosus. The structures of 1−5 were assigned by spectroscopic data analysis and by comparison with literature data. The absolute configuration of 2 was established using experimental and calculated ECD data. Compound 2 displayed inhibition of nitric oxide production in lipopolysaccharide (LPS)-induced BV-2 microglial cells, with IC50 value of 38.87 ± 2.27 μM.

Summary Background Identification of high-risk localised renal cell carcinoma is key for the selection of patients for adjuvant treatment who are at truly higher risk of reccurrence. We developed a classifier based on single-nucleotide polymorphisms (SNPs) to improve the predictive accuracy for renal cell carcinoma recurrence and investigated whether intratumour heterogeneity affected the precision of the classifier. Methods In this retrospective analysis and multicentre validation study, we used paraffin-embedded specimens from the training set of 227 patients from Sun Yat-sen University (Guangzhou, Guangdong, China) with localised clear cell renal cell carcinoma to examine 44 potential recurrence-associated SNPs, which were identified by exploratory bioinformatics analyses of a genome-wide association study from The Cancer Genome Atlas (TCGA) Kidney Renal Clear Cell Carcinoma (KIRC) dataset (n=114, 906 600 SNPs). We developed a six-SNP-based classifier by use of LASSO Cox regression, based on the association between SNP status and patients' recurrence-free survival. Intratumour heterogeneity was investigated from two other regions within the same tumours in the training set. The six-SNP-based classifier was validated in the internal testing set (n=226), the independent validation set (Chinese multicentre study; 428 patients treated between Jan 1, 2004 and Dec 31, 2012, at three hospitals in China), and TCGA set (441 retrospectively identified patients who underwent resection between 1998 and 2010 for localised clear cell renal cell carcinoma in the USA). The main outcome was recurrence-free survival; the secondary outcome was overall survival. Findings Although intratumour heterogeneity was found in 48 (23%) of 206 cases in the internal testing set with complete SNP information, the predictive accuracy of the six-SNP-based classifier was similar in the three different regions of the training set (areas under the curve [AUC] at 5 years: 0·749 [95% CI 0·660–0·826] in region 1, 0·734 [0·651–0·814] in region 2, and 0·736 [0·649–0·824] in region 3). The six-SNP-based classifier precisely predicted recurrence-free survival of patients in three validation sets (hazard ratio [HR] 5·32 [95% CI 2·81–10·07] in the internal testing set, 5·39 [3·38–8·59] in the independent validation set, and 4·62 [2·48–8·61] in the TCGA set; all p Interpretation Our six-SNP-based classifier could be a practical and reliable predictor that can complement the existing staging system for prediction of localised renal cell carcinoma recurrence after surgery, which might enable physicians to make more informed treatment decisions about adjuvant therapy. Intratumour heterogeneity does not seem to hamper the accuracy of the six-SNP-based classifier as a reliable predictor of recurrence. The classifier has the potential to guide treatment decisions for patients at differing risks of recurrence. Funding National Key Research and Development Program of China, National Natural Science Foundation of China, Guangdong Provincial Science and Technology Foundation of China, and Guangzhou Science and Technology Foundation of China.

A novel hydrolysable cationic monomer of quaternary ammonium dialkyl maleate was synthesized and subsequently copolymerized with acrylic acid and isobutenyl polyethylene glycol to successfully yield an amphoteric polycarboxylate superplasticizer (APC). The effects of the APC on cement particles were systematically investigated. The fluidity, fluidity retention and mechanical properties were measured to evaluate the performances of the APC and compared with those of a polycarboxylate superplasticizer (PCE). In addition, X-ray diffraction, thermogravimetric and scanning electron microscopy characterization were performed to investigate the influences of the APC on cement particles from microscopic level. Furthermore, the interactions of the APC with cement particles were also investigated via adsorption, hydration heat and zeta potential measurements. It was found that the introduction of a hydrolysable cationic monomer could improve the micro-structure and delay the hydration of cement. Moreover, the APC could increase the cement paste fluidity and fluidity retention.

Fluorescein has been found as an efficient visible-light-induced oxidase mimic and its catalytic performance is group-dependent. Herein, a facile colorimetric strategy for β-galactosidase (β-gal) was developed using fluorescein di β-D-galactopyranoside (FDG) as a probe based on the analyte induced change in oxidase mimicking activity of fluorescein derivatives. FDG doesn’t possess any visible-light-induced oxidase activity and can generate fluorescein and fluorescein mono β-D-galactopyranoside (FMG) in the presence of β-gal. The in situ generated fluorescein and FMG possess high oxidase-like activities under visible-light illumination and could catalyze the oxidation of 3, 3′, 5, 5′-tetramethylbenzidine (TMB) upon short irradiation by light-emitting diode (LED) lamp. Thus, the β-gal activity can be selectively detected in linear range from 0.10 to 12.9 μg mL−1 with a limit of detection (LOD) of 0.04 μg mL−1. We further integrated with the visual detection of α-fetoprotein antigen (AFP) based on the corresponding colorimetric signal induced by β-gal-linked colorimetric immunoassay, a LOD of 0.08 ng mL−1 could be achieved. Significantly, our proposed assay provides a facile sensing platform based on the change in enzyme mimicking activity induced by analytes. In addition, this optical method works without complex synthesis procedure and efficiently avoids participation of unstable H2O2 as an oxidant. Therefore, the present work not only shows the excellent assay performance in β-gal and tumor biomarker detection, but also opens up a new avenue for its application in practical optical sensing.

Six new lignans with various type of linkage between two C6-C3 fragments (1a, 1b, 2a, 2b, 3, 4), two new meroterpenoids (5, 6) and 24 known compounds (7–30) were isolated from an EtOH extract of the stems and leaves of Piper puberulum. The absolute configurations of enantiomers 1a and 1b were determined by single-crystal X-ray diffraction analysis, 2a and 2b were determined by comparing their calculated and experimental ECD spectra. Biogenetically, all the new lignans may come from the polymerization of two molecules of hydroxychavicol (30). In the anti-neuroinflammation activity assay, the IC50 values of fifteen compounds were lower than those of the positive control minocycline, and compound 1a showed good activity, but its enantiomer 1b showed no activity. Compound 1a have notable anti-neuroinflammatory activity, and can significantly decrease mRNA levels of proinflammatory cytokines (IL-1β, IL-6, TNF-α) in a dose-dependent manner.

Two new cadinane sesquiterpene glucosides (1, 2), two new phenylpropanoid glycosides (3, 4), and two new diterpenoid glucosides (5, 6), as well as 6 known compounds were isolated from the stems of Tinospora sinensis. The structures of these compounds were elucidated by extensive spectroscopic analysis and chemical methods. The absolute configuration of compound 1 was determined by timedependent density functional theory (TDDFT) electronic circular dichroism (ECD) calculations and in situ dimolybdenum CD method. All the isolated compounds except for compounds 7, 11 and 12 were evaluated for their anti-neuroinflammatory effect by inhibiting the nitric oxide (NO) production in lipopolysaccharide (LPS)-activated murine BV-2 microglial cells, and compound 4 showed anti-neuroinflammatory activity with IC50 values 42.90 μM in vitro assay.

Two previous undescribed cyclic pentapeptide-type compounds (1–2), with two known ones (3–4), were first isolated and purified from Clerodendrum japonicum (Thunb.) Sweet. Their structures were elucidated by extensive spectroscopic data (1D and 2D NMR) analysis. The absolute configurations of the two compounds were assigned using a combination of Marfey’s method and HPLC-MS analysis. All four compounds showed weak cytotoxicity against four human cancer cells lines (T24, A549, HepG2, MGC-803), with IC50 values ranging from 23.8 to 39.6 μM.

A novel waterborne polyurethane (WPU) resin with low gloss and micro-roughness was synthesized by the prepolymer and self-emulsification method. It was achieved by introducing multi-hydroxyl castor oil and reactive bisphenol A-type epoxy E-44 or E-51 resin to polyurethane prepolymer to form a cross-linking network structural waterborne polyurethane emulsion, which demonstrated the distinctive characteristic of the shear-thinning pseudoplastic fluid with a yield stress. The chemical structures and rough surface morphologies of the WPU films were characterized by FTIR-ATR, LCRS, AFM, SPMS and SEM, respectively. The specular gloss values at 20°, 60° and 85° incident angles were measured, and the values of different kinds of roughness parameters were obtained. The relationship between the gloss and the castor oil content was also discussed in detail. In general, this WPU resin endowed the film with micro-roughness, moderate hardness and good adhesive strength, making it very prospective in substitution for the traditional low gloss coatings.

Six previously undescribed oleanane-type triterpenoid saponins, fortunosides A–F, together with six known ones, were isolated from the aerial parts of Lysimachia fortunei Maxim. Their structures were established by spectroscopic data analyses (1D, 2D-NMR and HRESIMS) and chemical methods. All isolated triterpenoid saponins were evaluated for their cytotoxicity against four human liver cancer cell lines (SMMC-7721, Hep3B, HuH7, and SK-Hep-1). Three saponins with the aglycone protoprimulagenin A exhibited moderate cytotoxicity against all of the tested human cancer cell lines, with IC50 values ranging from 4.76 to 15.12 μM.

A series of low gloss waterborne polyurethane acrylate (WPUA) hybrid emulsions with different weight ratios of hard/soft monomers of acrylic monomers were synthesized successfully. Compared with the traditional low gloss coatings that achieve low gloss effects by adding a large number of pigments, fillers or both to roughen the surfaces, the low gloss effect of these WPUA emulsions was achieved through the formation of self-roughed surfaces during film formation with zero loading of extraneous dulling agent. Gloss levels could be as low as 3 units at 60° incident angle. The chemical structures of these WPUA films were characterized by nuclear magnetic resonance carbon spectroscopy ( 13 C NMR), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The rough surface topographies of these WPUA films were observed by scanning electron microscopy (SEM). The particle size distributions of these WPUA emulsions were analyzed by DLS measurement. The polymeric phase separation behaviors of these WPUA films were assessed by DSC analysis. In general, the WPUA emulsions that afforded films with good hardness, good adhesion strengths and excellent thermal stabilities, showed a great advantage in applications of low gloss aqueous coating.

Natural chalcopyrite (NCP) was used as a low-cost and efficient activator of peroxymonosulfate (PMS) to repair groundwater polluted by aged landfill leachate. The optimal remediation effect of polluted groundwater was achieved at pH 8, PMS concentration 25 mM and NCP dosage 10 g/L via response surface method. The excellent performance of NCP was mainly Fe3+/Fe2+ and Cu2+/Cu+ cycles promoted by sulfur species, which was investigated via XPS analysis. Furthermore, the transformation of SO4•─, •OH and O2•─ were clarified by quenching experiments and ESR. The conversion of organics was revealed by UV–vis spectra and three-dimensional fluorescence spectra. Moreover, the toxicity of polluted groundwater after remediation was significantly reduced through the growth of Chlorella pyrenoidosa. Finally, the flowing experiment using NCP/sand column showed that NCP could effectively activate PMS and thereby restore polluted groundwater.

Graphene is an important class of carbon-based materials that exhibits excellent thermal conductivity along its layers. In order to construct a 3D thermal transport material, herein, SiO2@C was successfully inserted into the reduced graphene oxide (rGO) layers to enhance its axial thermal transport performance via vacuum-assisted electrostatic self-assembly and pyrolysis processes. The formed rGO-SiO2@C composite exhibits an enhanced axial thermal conductivity of 6.65 W/(m*K) and an in-plane thermal conductivity of 36.54 W/(m*K). Moreover, it also displays good electromagnetic shielding properties, with the high total shielding effectiveness (SET) value of 45.59 dB, and an ultralow shielding effectiveness reflection (SER) value of 2.72 dB. Our work provides a simple method to construct a hybrid as a 3D conductive and thermal conductive network.

We herein reported a series of superplasticizers that were synthesized from the macro-monomer polyethylene glycol methacrylate and the monomers acrylic acid, sodium allyl sulfonate, or vinylphosphonic acid at different molar ratios. In order to explore the influence of COO-, SO32-, and PO32- on the performance of superplasticizers, fluidity tests and plastic viscosity tests were carried out to evaluate the dispersion performance of these polymers. Furthermore, the conformation of these superplasticizers in calcium hydroxide solution was analyzed via dynamic light scattering and Ca2+ concentration tests. The results showed that these superplasticizers exhibited the best dispersion effect when the molar ratio of COO-:SO32- and COO-:PO32- was 3:1. In addition, the calcium complexing capacity of the phosphonate groups was higher than that of the sulfonate ions, leading to the lower plastic viscosity of cement pastes containing the superplasticizer with COO-:PO32- at a ratio of 3:1. This study provides valuable information for the application in practical engineering.

Sixteen chebulic acid derivatives, including nine new (1–9) and seven known (10–16) ones, were isolated from an ethanol extract of the branches and leaves of Balakata baccata. The structures of the new compounds were elucidated by their UV, IR, HRESIMS, NMR, electronic circular dichroism (ECD) and single-crystal X-ray diffraction data. The effects of all the isolates on antineuroinflammatory and antioxidant activities were evaluated. Compared with the positive control minocycline (IC50 = 1.21 ± 0.71 μM), compounds 1–16 with IC50 values being greater than 50 μM, displayed almost no effects on the inhibition of NO production in LPS-induced BV-2 microglial cells, however, the results of antioxidant activity for compounds 1–16 showed significant DPPH-radical scavenging abilities with EC50 value ranging from 3.98 to 14.24 μM, while the EC50 value of positive control vitamin C was 14.31 μM. At last, the results of PCR (qRT-PCR) analysis showed that compound 1 could enhance the expression of antioxidases (HO-1, GCLC, and NQO1) at the mRNA levels.

Magnesium phosphate cement-fly ash (MPC-FA) has been synthesized as a new cutoff wall material to control lead pollution in groundwater. A series of experiments were conducted to investigate its properties including adsorption, mechanical performances, morphologies, microstructure and migration of Pb(Ⅱ) through the magnesium phosphate cement-fly ash cutoff walls. X-ray microcomputed tomography was used to get the microscale three-dimensional real geometry images of the cutoff walls. The internal structural parameters were analyzed through digital image processing technology. Lattice Boltzmann method (LBM) was employed to simulate the hydraulic conductivity and three-dimensional velocity fields distribution of cutoff walls. The optimized fly ash ratio (in mass) of cutoff walls was 40%, and the sodium dihydrogen phosphate/monopotassium phosphate molar ratio was 1:1. The compressive strength and flexural strength during 14 days were 23.2 MPa a nd 5.6 MPa, respectively. The laboratorial hydraulic conductivity of MPC-FA was 1.22 × 10−9 m/s and the theoretical maximum adsorption capacity was 467.87 mg/g. The pore-network model showed that the connected porosity of MPC-FA was 14.45%, and the most of the pores and throats in cutoff walls were microflow paths (radius ≤ 12 μm). The hydraulic conductivity simulated by LBM basically coincided with the measured results, and the velocity fields indicated that the flow paths were tortuous and complex. Under different breakthrough concentration standards, the penetration of Pb(Ⅱ) at initial concentration of 4000 mg/L through cutoff walls with thickness of 0.6 m, 1 m, 1.2 m, 1.5 m needed 8–10, 22–28, 31–41 and 49–64 years, respectively. The model obtained by Visual MODFLOW numerical simulation showed that the contaminant plume of Pb(Ⅱ) was controlled after 7400 days in the polluted site with MPC-FA cutoff walls, which supported that the MPC-FA met the requirements for good control of Pb(Ⅱ) in the lead-contaminated sites.

A peak aged (T6 heat treatment: 743 K /1.5 h + 393 K/24 h) Al-Zn-Mg-Cu alloy was subjected to compression tests at different strain rates from 1.0 × 10−3 s−1 to 5.0 × 103 s−1. The yield strength of the Al alloy is increasing with strain rates from 1.0 × 10−3 s−1 to 4.0 × 103 s−1and is decreasing with increasing strain rate from 4.0 × 103 s−1 to 5.0 × 103 s−1 showing strain rate sensitivity (SRS). A large number of Al3Zr, GP zones, η’, T (Al2Mg3Zn3) and S (Al2CuMg) precipitates are present in the Al alloy after compression at 1.0 × 10−3 s−1 and Al3Zr, η’, η, T and S phases are dominant after high strain rate compression from 3.5 × 103 s−1 to 5.0 × 103 s−1. The precipitates average size is increased after compression at 1.0 × 10−3 s−1. High strain rate compression leads to the growth of precipitates and overlapping. Coarse precipitates are mainly found along the grain boundaries and dislocations. The increasing SRS with increasing strain rates up to 4.0 × 103 s−1 owes to the growth of precipitates which are hindering dislocations motion and generating more dislocations. Increasing strain rates to 5.0 × 103 s−1, the coarse precipitates are no longer effective in pinning dislocations, leading to a decrease in yield strength and a negative SRS value.

Through inserting SiO2@Au into the reduced graphene oxide (rGO) layers, the rGO-SiO2@Au composites were prepared via the vacuum-assisted electrostatic self-assembly method. The obtained composites exhibit excellent electromagnetic interference (EMI) shielding effectiveness due to the successful construction of multi-nanocavities (spherical SiO2 cavities and layered air cavities between rGO), multi-reflection interfaces (rGO and Au shell) and continuous conductive network (rGO-Au-rGO). Among them, the total shielding effectiveness (SET) of the composites with 75.78 wt% SiO2 and 19.38 wt% rGO can reach 38.4 dB at 18 GHz. Thereinto, the shielding effectiveness absorption (SEA) is 36.4 dB, 1.3 and 13.5 times higher than that of rGO and SiO2@Au. And the shielding effectiveness reflection (SER) is always below 5 dB from 1 to 18 GHz, much lower than that of rGO (about 15 dB). Further studies found that the SEA values were enhanced at 12.6 GHz and 6.2 GHz due to the construction of cavities and location of Au nanoparticles between the rGO layers. This study provides a simple and mild method to prepare high-performance thin-layered materials with applications in the field of EMI absorption shielding.

A further phytochemical investigation of the aerial parts of Lysimachia foenum-graecum Hance led to the isolation of three new oleanane-type triterpenoid saponins, foegraecumosides L–N ( 1 – 3 ), along with one known saponin, 3- O - β - d -glucopyranosyl-(1 → 2)-α- l -arabinopyranosyl-cyclamiretin A ( 4 ). Their structures were elucidated by spectroscopic data analyses and chemical methods Compounds 1 − 4 were evaluated for their cytotoxicity against NCI-H460, MGC-803, HepG2, and T24 human cancer cell lines, and compound 4 showed moderate activity against all tested cell lines. Furthermore, the cytotoxicity of compound 4 was tested on drug-sensitive and drug-resistant lung cancer cell lines (A549 and A549/CDDP, respectively).

Objective Early allograft dysfunction (EAD) is frequent complication post-liver transplantation and is closely related to recipient's mortality and morbidity. We sought to develop a nomogram for predicting incidence of EAD. Methods Based on multivariate analysis of donor, recipient, and operation data of 199 liver transplants from deceased donors between 2013 and 2015, we identified 5 significant risk factors for EAD to build a nomogram. The model was subjected to prospective validation with a cohort of 42 patients who was recruited between January and June 2016. The predictive accuracy and discriminative ability were measured by area under the receiver operating characteristic curve (AUC). The agreement between nomogram prediction and actual observation was showed by the calibration curve. Results Incidence rate of EAD in the training set and validation cohort were 55.91% (104/199) and 54.76% (23/42), respectively. In the training set, according to the results of univariable and multivariable analysis, 5 independent risk factors including donor gender, donor serum gamma-glutamyl transpeptidase level, donor serum urea level, donor comorbidities (respiratory, cardiac, and renal dysfunction), and recipient Model for End-stage Liver Disease score were identified and assembled into the nomogram. The AUC of internal validation using bootstrap resampling and prospective validation using the external cohort of 42 patients was 0.74 and 0.60, respectively. The calibration curves for probability of EAD showed acceptable agreement between nomogram prediction and actual observation. According to the score table, the probability of EAD was under 30% when the total point tally was under 72. But when the total was up to 139, the risk of EAD increased to 60%. Conclusion We've established and validated a nomogram that can provide individual prediction of EAD for liver transplant recipients. The practical prognostic model may help clinicians to qualify the liver graft accurately, making a more reasonable allocation of organs.

In this study, novel macro porous Ni2+-imprinted chitosan foam adsorbents (F-IIP) were prepared using sodium bicarbonate and glycerine to obtain a porogen for adsorbing nickel ions from aqueous solutions. The use of the ion-imprinting technique for adsorbents preparation improved the nickel ion selectivity and adsorption capacity. We characterised the imprinted porous foam adsorbents in terms of the effects of the initial pH value, initial metal ion concentration, and contact time on the adsorption of nickel ions. The adsorption process was described best by Langmuir monolayer adsorption models, and the maximum adsorption capacity calculated from the Langmuir equation was 69.93mgg-1. The kinetic data could be fitted to a pseudo-second-order equation. Our analysis of selective adsorption demonstrated the excellent preference of the F-IIP foams for nickel ions compared with other coexisting metal ions. Furthermore, tests over five cycle runs suggested that the F-IIP foam adsorbents had good durability and efficiency.

Understanding the structure–property relationship of polyurethane (PU) binders is of critical importance in the construction engineering applications. A series of rapid room temperature-curable PU binders were prepared using polyoxypropylene glycol as the soft segments, along with polymethylene polyphenylene isocyanate and 4,4′-methylene-bis(2-chlorobenzenamine) as the hard segments. This work investigated the influence of the hard segment content (40 wt%, 45 wt%, and 50 wt%) and the soft segment molecular weight (1000 g/mol, 2000 g/mol, 3000 g/mol, and 4000 g/mol) on the microphase structure of the PU binders. Their influence on the compressive behaviors, flexural behaviors, impact strengths, and slant shear strengths of the PU-based polymer concretes was also investigated. Structural characterization revealed that increasing either the hard segment content or the larger soft segment molecular weight effectively enhanced hydrogen bonding as well as microphase separation. Our results also demonstrated that a higher hard segment content resulted in better mechanical performance and shorter pot life. In addition, the PU-based polymer concrete using 2000 g/mol polyoxypropylene glycol reached optimal mechanical performance when the hard segment was held constant. Hence, varying the hard segment content and soft segment length can be an effective method to adjust the engineering performance of PU-based polymer concrete.