ZnCdS Dotted with Highly Dispersed Pt Supported on SiO2 Nanospheres Promoting Photocatalytic Hydrogen Evolution

[EN] The efficiency of solar hydrogen evolution closely depends on the fast transfer of charge carriers and the effective use of visible light. In this work, a novel photocatalyst SiO2/ZnCdS/Pt was successfully prepared to solve these two problems. An artistic structure of the photocatalyst was constructed and ZnCdS was successfully wrapped on the surface of SiO2 spheres with uniform Pt nanoparticles (NPs) in a size of 4.1 +/- 0.7 nm highly dispersed on the ZnCdS shell through the self-assembly method. Pt NPs can absorb the scattered light in the near field of SiO2 spheres. With the synergistic effect of SiO2 spheres and small highly dispersed Pt NPs, the absorption of visible light was significantly promoted. Meanwhile, the electron-hole recombination was also effectively inhibited, thus improving the photocatalytic activity. The hydrogen production activity of the highly efficient photocatalyst was as high as 8.3 mmol g(-1) h(-1) under visible light (lambda > 420 nm). The photocatalytic activity of SiO2/ZnCdS/Pt was 2.9 times higher than that of the ZnCdS/Pt photocatalyst.This work was supported by the National Natural Science Foundation of China (21976111), Shandong Provincial Natural Science Foundation (ZR2019MB052), and Large Instrument Open Foundation of Shandong Normal University (KFJJ2019004; KFJJ2021006).Liu, K.; Peng, L.; Zhen, P.; Chen, L.; Song, S.; García Gómez, H.; Sun, C. (2021). ZnCdS Dotted with Highly Dispersed Pt Supported on SiO2 Nanospheres Promoting Photocatalytic Hydrogen Evolution. The Journal of Physical Chemistry C. 125(27):14656-14665. https://doi.org/10.1021/acs.jpcc.1c0353514656146651252

Single-cell ligand–receptor profiling reveals an immunotherapy-responsive subtype and prognostic signature in triple-negative breast cancer

BackgroundTriple-negative breast cancer (TNBC) is an aggressive form of cancer that lacks specific targeted therapies. Although ligand–receptor (LR) interactions play a crucial role in intercellular communication and contribute to tumor heterogeneity, their molecular details and potential as prognostic or predictive markers in TNBC have not been thoroughly investigated.MethodsWe analyzed single-cell RNA sequencing data to categorize TNBC into 12 subgroups and 10 distinct cell types. From this dataset, we identified LR pairs that exhibited significant intercellular crosstalk and evaluated their prognostic relevance in a METABRIC TNBC cohort (n = 298). Through consensus clustering of these LR pairs, two molecular subtypes were defined. Key LR genes were then selected using Lasso regression and stepwise multivariate analysis to build an LR-based prognostic scoring system (LR.score), which was validated using both the METABRIC and GSE58812 datasets (n = 107). Additionally, we performed siRNA-mediated knockdown of the CXCL9/CXCR3 axis in MDA-MB-231 cells, confirming the knockdown via RT-qPCR and Western blot. The functional impact was assessed through proliferation, colony formation, and wound healing assays.ResultsOne subtype (Clust1) demonstrated strong immune cell infiltration, higher immune scores, and enrichment in pathways such as epithelial–mesenchymal transition, angiogenesis, and KRAS signaling—indicative of a basal-like, immune-active phenotype. Among the LR pairs, the CXCL9–CXCR3 axis was identified as a key factor in immune cell recruitment and anti-tumor responses. Functionally, silencing the CXCL9/CXCR3 axis significantly diminished the proliferation, colony formation, and migratory capabilities of MDA-MB-231 cells. Moreover, a higher LR.score was correlated with poorer overall survival (HR = 1.69, 95% CI = 1.12–2.56, P < 0.05) and reduced response to immune checkpoint inhibitors (ICIs), while patients with lower LR.score showed increased sensitivity to ICIs, particularly in anti–PD-L1 cohorts.ConclusionThe LR.score serves as an independent prognostic factor and a reliable predictor of immunotherapy response in TNBC. Targeting crucial LR interactions, especially the CXCL9–CXCR3 axis, may enhance immunotherapeutic efficacy and refine prognostic evaluations, paving the way for improved treatment strategies in TNBC

Optimization of degradable temporary plugging material and experimental study on stability of temporary plugging layer

Temporary plugging technology is an important drilling technique for maintaining wellbore stability and resolving lost circulation problems. The key to its success lies in the use of materials that can form a tight and stable “temporary plugging layer” with certain pressure bearing capacity and a permeability close to zero in the loss channel near the wellbore. Experimental studies have been conducted to develop adhesion formulations for optimal temporary plugging materials, as the matching relationship between particle size and fracture width is critical [(0.5−1)/1]. By measuring the permeability of the temporary plugging layer under varying confining pressure with a soap foam flowmeter, researchers have been able to evaluate the effectiveness, degradation, and dosages of temporary plugging agents. It has been shown that a single-particle material, such as a walnut shell, has a smaller permeability than a hyperfine CaCO3 coated temporary plug layer. The latter, however, is less capable of bearing pressure. By combining different materials, such as walnut shells and hyperfine CaCO3 particles, the researchers were able to create a temporary plug layer that had the lowest permeability and did not change much at variable confining pressures. Its pressure-bearing capacity is strong and the temporary plug works well. Experiments have shown that a ratio of 2:1–3:1 of hyperfine CaCO3 and walnut shell particles work well for plugging a fracture system with particles of size 2–3 times the fracture width. It developed an evaluation method for temporary plugging agents, studied their plugging capability and degradation performance for reservoir conversion, and evaluated degradation performance after successful temporary plugging. The temporary plugging rate of the temporary plugging agent increased from 98.10% to 99.81%, and the maximum temporary plugging pressure is 50.39 MPa, which can be completely reduced at 150°C for 4 h, meeting the technical requirements of “dense temporary plugging, two-way pressure bearing” to some extent

The inhibitory effect of mesenchymal stem cell on blood–brain barrier disruption following intracerebral hemorrhage in rats: contribution of TSG-6

BACKGROUND: Mesenchymal stem cells (MSCs) are well known having beneficial effects on intracerebral hemorrhage (ICH) in previous studies. The therapeutic mechanisms are mainly to investigate proliferation, differentiation, and immunomodulation. However, few studies have used MSCs to treat blood–brain barrier (BBB) leakage after ICH. The influence of MSCs on the BBB and its related mechanisms were investigated when MSCs were transplanted into rat ICH model in this study. METHODS: Adult male Sprague–Dawley (SD) rats were randomly divided into sham-operated group, PBS-treated (ICH + PBS) group, and MSC-treated (ICH + MSC) group. ICH was induced by injection of IV collagenase into the rats’ brains. MSCs were transplanted intravenously into the rats 2 h after ICH induction in MSC-treated group. The following factors were compared: inflammation, apoptosis, behavioral changes, inducible nitric oxide synthase (iNOS), matrix metalloproteinase 9 (MMP-9), peroxynitrite (ONOO(−)), endothelial integrity, brain edema content, BBB leakage, TNF-α stimulated gene/protein 6 (TSG-6), and nuclear factor-κB (NF-κB) signaling pathway. RESULTS: In the ICH + MSC group, MSCs decreased the levels of proinflammatory cytokines and apoptosis, downregulated the density of microglia/macrophages and neutrophil infiltration at the ICH site, reduced the levels of iNOS and MMP-9, attenuated ONOO(−) formation, and increased the levels of zonula occludens-1 (ZO-1) and claudin-5. MSCs also improved the degree of brain edema and BBB leakage. The protective effect of MSCs on the BBB in ICH rats was possibly invoked by increased expression of TSG-6, which may have suppressed activation of the NF-κB signaling pathway. The levels of iNOS and ONOO(−), which played an important role in BBB disruption, decreased due to the inhibitory effects of TSG-6 on the NF-κB signaling pathway. CONCLUSIONS: Our results demonstrated that intravenous transplantation of MSCs decreased the levels of ONOO(−) and degree of BBB leakage and improved neurological recovery in a rat ICH model. This strategy may provide a new insight for future therapies that aim to prevent breakdown of the BBB in patients with ICH and eventually offer therapeutic options for ICH