Cancer-Associated Fibroblasts Promote Lymphatic Metastasis in Cholangiocarcinoma via the PDGF-BB/PDGFR-ß Mediated Paracrine Signaling Network.

Patients with cholangiocarcinoma (CCA) with lymph node metastasis (LNM) have the worst prognosis, even after complete resection; however, the underlying mechanism remains unclear. Here, we established CAF-derived PDGF-BB as a regulator of LMN in CCA. Proteomics analysis revealed upregulation of PDGF-BB in CAFs derived from patients with CCA with LMN (LN+CAFs). Clinically, the expression of CAF-PDGF-BB correlated with poor prognosis and increased LMN in patients with CCA, while CAF-secreted PDGF-BB enhanced lymphatic endothelial cell (LEC)-mediated lymphangiogenesis and promoted the trans-LEC migration ability of tumor cells. Co-injection of LN+CAFs and cancer cells increased tumor growth and LMN in vivo. Mechanistically, CAF-derived PDGF-BB activated its receptor PDGFR-ß and its downstream ERK1/2-JNK signaling pathways in LECs to promote lymphoangiogenesis, while it also upregulated the PDGFR-ß-GSK-P65-mediated tumor cell migration. Finally, targeting PDGF-BB/PDGFR-ß or the GSK-P65 signaling axis prohibited CAF-mediated popliteal lymphatic metastasis (PLM) in vivo. Overall, our findings revealed that CAFs promote tumor growth and LMN via a paracrine network, identifying a promising therapeutic target for patients with advanced CCA.

Meta-Analysis of Hematological Biomarkers as Reliable Indicators of Soft Tissue Sarcoma Prognosis.

Background: Several recent studies have reported the reliable prognostic effect of hematological biomarkers in various tumors. Yet, the prognostic value of these hematological markers in soft tissue sarcoma (STS) remains inconclusive. Thus, the aim of this meta-analysis was to check the effect of hematological markers on the prognosis of STS. Methods: We systematically searched for relevant papers published before October 2019 in the PubMed and EMBASE databases. Overall survival (OS) and disease-specific survival (DSS) were the primary outcome, whereas disease-free survival was the secondary outcome. A thorough study of hazard ratios (HR) and 95% of confidence intervals (CIs) was done for determining the prognostic significance. Results: We performed 23 studies that comprised of 4,480 patients with STS. The results revealed that higher neutrophil-to-lymphocyte ratio (NLR), C-reactive protein (CRP), and platelet-to-lymphocyte ratio (PLR) were associated with poor OS/DFS (HR = 2.08/1.72, for NLR; HR = 1.92/1.75, for CRP, and HR = 1.86/1.61, for PLR). In contrast, a low lymphocyte-to-monocyte ratio (LMR) was relate to worse OS/DFS (HR = 2.01/1.90, for LMR). Moreover, pooled analysis illustrated that elevated NLR and CRP represents poor DSS, with HRs of 1.46 and 2.06, respectively. In addition, combined analysis revealed that higher Glasgow prognostic score (GPS) was linked to an adverse OS/DSS (HR = 2.35/2.77). Conclusion: Our meta-analysis suggested that hematological markers (NLR, CRP, PLR, LMR, and GPS) are one of the important prognostic indicators for patients affected by high-grade STS and patients with the STS being located in the extremity.

In Situ Construction of Ag/TiO2/g-C3N4 Heterojunction Nanocomposite Based on Hierarchical Co-Assembly with Sustainable Hydrogen Evolution.

The construction of heterojunctions provides a promising strategy to improve photocatalytic hydrogen evolution. However, how to fabricate a nanoscale TiO2/g-C3N4 heterostructure and hinder the aggregation of bulk g-C3N4 using simple methods remains a challenge. In this work, we use a simple in situ construction method to design a heterojunction model based on molecular self-assembly, which uses a small molecule matrix for self-integration, including coordination donors (AgNO3), inorganic titanium source (Ti(SO4)2) and g-C3N4 precursor (melamine). The self-assembled porous g-C3N4 nanotube can hamper carrier aggregation and it provides numerous catalytic active sites, mainly via the coordination of Ag+ ions. Meanwhile, the TiO2 NPs are easily mineralized on the nanotube template in dispersive distribution to form a heterostructure via an N-Ti bond of protonation, which contributes to shortening the interfacial carrier transport, resulting in enhanced electron-hole pairs separation. Originating from all of the above synergistic effects, the obtained Ag/TiO2/g-C3N4 heterogenous photocatalysts exhibit an enhanced H2 evolution rate with excellent sustainability 20.6-fold-over pure g-C3N4. Our report provides a feasible and simple strategy to fabricate a nanoscale heterojunction incorporating g-C3N4, and has great potential in environmental protection and water splitting.

Facile Preparation and Highly Efficient Catalytic Performances of Pd-Cu Bimetallic Catalyst Synthesized via Seed-Mediated Method.

With the rapid development of industry, the problem of environmental pollution has become increasingly prominent. Exploring and preparing green, efficient, and low cost catalysts has become the key challenge for scientists. However, some conventional preparation methods are limited by conditions, such as cumbersome operation, high energy consumption, and high pollution. Here, a simple and efficient seed-mediated method was designed and proposed to synthesize a highly efficient bimetallic catalyst for catalyzing nitro compounds. A Pd-Cu bimetallic composite (BCM) can be prepared by synthesizing the original seed crystal of precious metal palladium, then growing the mature nanocrystalline palladium and supporting the transition metal copper. Importantly, after eight consecutive catalytic cycles, the conversion of the catalyzed 2-NA was 84%, while the conversion of the catalyzed 4-NP was still 72%. And the catalytic first order rates of 2-NA and 4-NP constants were 0.015 s-1, and 0.069 s-1, respectively. Therefore, current research of nanocomposites catalyst showed great significance for serious environmental pollution problems and the protection of living environment, providing a new idea for the preparation of new bimetallic catalytic materials.

Facile preparation of a self-assembled Artemia cyst shell-TiO2-MoS2 porous composite structure with highly efficient catalytic reduction of nitro compounds for wastewater treatment.

The catalytic reduction of nitro compounds is currently a hot research area, how to efficiently and stably degrade such toxic and harmful substances has become the research goal of many researchers. In this work, an Artemia cyst shell (ACS)-TiO2-MoS2 ternary porous structure was proposed and prepared as a catalyst for the reduction of 2-nitroaniline (2-NA) and 4-nitrophenol (4-NP). The ACS has a large number of porous structures, exhibits a good binding ability with TiO2 and MoS2, and provides a large number of active sites for the catalytic reduction process. The obtained composite material has a good reduction effect on 4-NP and 2-NA, with a good stability and recyclability, which is obviously higher than the reduction effect of ACS-TiO2 and MoS2 under the same conditions. This work provides ideas for the design of porous catalytic materials.

Facile Preparation and Enhanced Catalytic Properties of Self-Assembled Pd Nanoparticle-Loaded Nanocomposite Films Synthesized via the Electrospun Approach.

In recent years, people pay more attention to environmental pollution and the treatment of sewage has become the focus of recent research. Palladium nanoparticles have good catalytic properties but are easy to agglomerate. Therefore, we used the electrospinning technology to prepare a uniform composite nanofiber film based on polyacrylic acid (PAA) and polyvinyl alcohol (PVA), which demonstrated that they are good carriers of palladium nanoparticles to make the nanoparticles well dispersed. Furthermore, carbon nanotubes (CNTs) were added to increase the specific surface area of the composite nanofiber film and improve its mechanical properties. The successfully synthesized PAA/PVA/CNT-COOH@palladium nanoparticle (PdNP) composite fiber films were characterized by scanning electron microscopy, transmission electron microscopy, and thermogravimetry analysis. p-Nitrophenol and 2-nitroaniline were utilized as typical pollutants to further evaluate the catalytic performance of PAA/PVA/CNT-COOH@PdNP composite fiber films. The PAA/PVA/CNT-COOH@PdNP composite fiber films exhibited enhanced catalytic performance and could be reused for eight consecutive cycles. This work provided new clues for the preparation and application of composite electrospun film materials.

Self-Assembled Naphthylidene-Containing Schiff Base Anchored Polystyrene Nanocomposites Targeted for Selective Cu(II) Ion Removal from Wastewater.

Self-assembled composite adsorbents that combine the controllability of self-assembly with a mild operation process are promising for removal of heavy metal ions in wastewater. The design and preparation of functionalized composite adsorbent materials with multiple-site adsorption ability remain the most attractive in effectively removing heavy metal ions. Inspired by the macroporous structure of charged polystyrene (PS) resin and chelation of Schiff bases with heavy metal ions, smart composite adsorbents are constructed based on the combination and synergistic effect of multiple hydrophobic, π-π stacking, and electrostatic noncovalent interactions between polystyrene resin and naphthylidene-containing Schiff base (NSB). The resulting hybrid nanomaterials (PS-NSB) have uniform porous structures and well-defined and multiple target sites. These properties promote diffusion of the target ion, increase the binding site, and enhance the removal efficacy. This study offers a new strategy to harness a self-assembled Schiff base with integrated flexibility and multifunctions to enhance target metal ion specific binding and removal effects, highlighting opportunities to develop smart composite adsorbents.

Highly Efficient Catalytic Performances of Nitro Compounds and Morin via Self-Assembled MXene-Pd Nanocomposites Synthesized through Self-Reduction Strategy.

With development of the society, the problem of environmental pollution is becoming more and more serious. There is the urgent need to develop a new type of sustainable green material for degradable pollutants. However, the conventional preparation method is limited by conditions such as cumbersome operation, high energy consumption, and high pollution. Here, a simple method named self-reduction has been proposed, to synthesize highly efficient catalytic nitro compounds and morin self-assembled MXene-Pd nanocomposites. Palladium nanoparticles were grown in situ on MXene nanosheets to form MXene@PdNPs. MXene@PdNPs composites with different reaction times were prepared by adjusting the reduction reaction time. In particular, MXene@PdNPs20 exhibited a high catalytic effect on 4-NP and 2-NA, and the first-order rate constants of the catalysis were 0.180 s-1 and 0.089 s-1, respectively. It should be noted that after eight consecutive catalytic cycles, the conversion to catalyze 4-NP was still greater than 94%, and the conversion to catalyze 2-NA was still greater than 91.8%. Therefore, the research of self-assembled MXene@PdNPs nanocomposites has important potential value for environmental management and sustainable development of human health, and provides new clues for the future research of MXene-based new catalyst materials.

Facile preparation of self-assembled hydrogels constructed from poly-cyclodextrin and poly-adamantane as highly selective adsorbents for wastewater treatment.

Self-assembled hydrogel materials constructed from cyclodextrin polymer (P-CD)/adamantane-modified poly acrylic acid (PAA-Ad) were designed and prepared via host-guest interactions. It was observed that the prepared supramolecular hydrogels had an interconnected three-dimensional porous network. In addition, the obtained hydrogels showed a recovery performance and it was confirmed that the host-guest interactions between ß-cyclodextrin and adamantane were the main driving force for the formation of the hydrogels. The mechanical properties of the hydrogels could be adjusted by varying the concentrations of PAA-Ad. In particular, the prepared supramolecular hydrogels exhibited superior performances in water purification. The results demonstrated that the hydrogels possessed different mechanisms in the adsorption of the four typical poisonous organic dye molecules used, including bisphenol A (BPA), 4-aminoazobenzene (N-Azo), methylene blue (MB), and rhodamine B (RhB). The hydrogels mainly adsorbed N-Azo by host-guest interaction and adsorbed BPA by host-guest interaction and hydrogen bond synergy. They also adsorbed MB and RhB by hydrogen bonding and electrostatic interaction.

A facile preparation method for new two-component supramolecular hydrogels and their performances in adsorption, catalysis, and stimuli-response.

In this study, we prepared a novel multifunctional two-component supramolecular hydrogel (T-G hydrogel) via two organic molecules in ethanol/water mixed solvents. In addition, we prepared gold nanoparticle/T-G (AuNPs/T-G) composite hydrogels using T-G hydrogel as a template for stabilizing AuNPs by adding HAuCl4 and NaBH4 during the heating and cooling process of T-G hydrogels. The morphology and microstructure of the as-prepared hydrogels were characterized using SEM, TEM, XRD, and FT-IR. The hydrogels prepared by solutions that contained different ethanol/water volume ratios exhibited different microstructures, such as sheets, strips, and rods. The obtained T-G hydrogels exhibited a sensitive response to pH changes in the process of sol-gel transformation and showed good adsorption properties for model organic dyes. In the presence of NaBH4, the obtained AuNP/T-G composite hydrogels exhibited the excellent catalytic performance for 4-nitrophenol (4-NP) degradation. Thus, the current research provides new clues in developing new multifunctional two-component supramolecular gel materials and exhibits potential applications for wastewater treatment.

Experimental Investigations on Fluorescence Excitation and Depletion of Carbon Dots.

Carbon dots (CDs) can be readily synthesized and utilized as attractive fluorescent probes for a variety of applications. In this study, we have synthesized CDs using a previously published method and characterized their photo-physical properties. The resultant CDs possess prominent photo-stability and short emission wavelength in the violet region. Our study reveals that CDs, with weak photo-bleaching, enable them to be employed to achieve high spatial resolution in stimulated emission depletion (STED) microscopy. The depletion efficiency can reach 60%. More importantly, the shorter excitation wavelength of CDs contributes to further improvement of resolution for STED microscopy. An excellent candidate for fluorophores, these CDs have potential to be used in super-resolution imaging for STED microscopy.

Fluorescent pH sensor based on Ag@SiO2 core-shell nanoparticle.

We have demonstrated a novel method for the preparation of a fluorescence-based pH sensor by combining the plasmon resonance band of Ag core and pH sensitive dye (HPTS). A thickness-variable silica shell is placed between Ag core and HPTS dye to achieve the maximum fluorescence enhancement. At the shell thickness of 8 nm, the fluorescence intensity increases 4 and 9 times when the sensor is excited at 405 and 455 nm, respectively. At the same time, the fluorescence intensity shows a good sensitivity toward pH value in the range of 5-9, and the ratio of emission intensity at 513 nm excited at 455 nm to that excited at 405 nm versus the pH value in the range of 5-9 is determined. It is believed that the present pH sensor has the potential for determining pH real time in the biological sample.

[Preliminary study on normal aerification of paranasal sinuses in children].

OBJECTIVE: To explore the normal aerification of paranasal sinuses in Chinese children with magnetic resonance imaging. METHODS: Two hundred and eighty Chinese children aged from 17 days to 14 years without any symptoms related to sinusitis were statistically analyzed in MRI features, including counting the number of paranasal sinus pneumatization and the maximum axial and sagittal area of the left maxillary. RESULTS: The pneumatization rate of maxillary sinus was 85% in children aged from 0 to 1 years. Until 3 years the pneumatization rate of maxillary sinus was 95% and there was no significant difference in boys and girls (χ(2) = 0.741, P = 0.389). The pneumatization rate of maxillary sinus reached 100% after 4 years old. The pneumatization rate of ethmoid sinus was 100% in this study. The pneumatization rate of sphenoid sinus was 0 within 1 year old, 49% within 4 years old and 100% after 7 years old. There was no significant difference in boys and girls on the pneumatization rate of sphenoid sinus (χ(2) = 2.452, P = 0.117). The pneumatization rate of frontal sinus was 0 within 5 years old, 62% within 9 years old and 95% after 10 years old. There was no significant difference in boys and girls on the pneumatization rate of frontal sinus (χ(2) = 0.124, P = 0.724). The axial and sagittal maximum area of maxillary sinus was (689.28 ± 221.79) and (659.76 ± 263.31) mm(2) in girls and (668.13 ± 206.38) and (638.60 ± 207.67) mm(2) in boys. The differences were significant (t = -19.78, P < 0.001; t = -19.89, P < 0.001). CONCLUSION: The study of the development and normal aerification of paranasal sinuses of children can help radiologist make correct diagnosis of paranasal sinuses in children.

Efficient near-infrared emission from neodymium by broadband sensitization of bismuth in zeolites.

Nd-Bi codoped zeolites were prepared by an ion-exchange process, and the optical properties were investigated by photoluminescence (PL) and PL excitation spectra, and decay time measurements. The results show that the NIR emission of Nd(3+) ions is significantly enhanced by the introduction of bismuth in codoped samples, and the lifetime reaches 246 µs. It is also observed that NIR-active Bi acts as a sensitizer of Nd(3+) ions. The energy transfer efficiency is also estimated. The peculiar optical properties make Nd-Bi codoped zeolites promising for potential application in biological probes.

Near-infrared photoluminescence and Raman characterization of bismuth-embedded sodalite nanocrystals.

Ultrabroadband near-IR (NIR) emission has been realized in bismuth-embedded sodalite nanocrystals. Steady-state and time-resolved photoluminescence and Raman results suggest that Bi(+) active centers contribute to the NIR emission. This study demonstrates that sodalite nanocrystals can serve as excellent hosts for bismuth NIR active centers, thus paving the way for their wide applications in nanophotonics.

Efficient near-infrared luminescence and energy transfer in erbium/bismuth codoped zeolites.

We have shown that tunable and highly efficient broadband near-IR (NIR) luminescence can be realized in erbium/bismuth codoped zeolites. The emission covers the ranges of 930-1450nm and 1450-1630nm. The intensity ratio of the two bands can be tuned by adjusting the concentration of erbium and the excitation wavelength. Steady-state and time-resolved photoluminescence (PL), and PL excitation measurements indicate that two kinds of emitters coexist in the pores of zeolites, and that NIR active bismuth simultaneously acts as a sensitizer of erbium. The present results demonstrate an important rational strategy for the design of a tunable NIR-emitting zeolite-based nanosystem.

Significantly enhanced superbroadband near infrared emission in bismuth/aluminum doped high-silica zeolite derived nanoparticles.

Significantly enhanced superbroadband near infrared emission has been realized in bismuth/aluminum doped high-silica zeolite derived nanoparticles. The emission intensity can be easily tailored by the introduction of aluminum. The luminescence lifetime can reach up to 695 micros. The results reveal that the existence of charge imbalance environment caused by [AlOV(4/2)](-) units in host materials is requisite to the formation of infrared-active Bi(+). The finding presents a feasible route to design high-efficient bismuth activated infrared luminescent nanoparticles. These bismuth doped nanoparticles may find applications as superbroadband near infrared nano optical sources.