Search

Polyimide (PI) refers to a type of high-performance polymer containing imide rings in the main chain, which has been widely used in fields of aerospace, microelectronic and photonic devices, gas separation technology, and so on. However, traditional aromatic PIs are, in general, the inefficient fluorescence or even no fluorescence, due to the strong inter- and intramolecular charge transfer (CT) interactions causing unavoidable fluorescence quenching, which greatly restricts their applications as light-emitting functional layers in the fabrication of organic light-emitting diode (OLED) devices. As such, the development of fluorescent PIs with high fluorescence quantum efficiency for their application fields in the OLED is an important research direction in the near future. In this review, we provide a comprehensive overview of fluorescent PIs as well as the methods to improve the fluorescence quantum efficiency of PIs. It is anticipated that this review will serve as a valuable reference and offer guidance for the design and development of fluorescent PIs with high fluorescence quantum efficiency, ultimately fostering further progress in OLED research. [ABSTRACT FROM AUTHOR]

Using finite element simulation and single-variable experimental methods, this study analyzes the variations in the microstructure and hardness of a 304 stainless steel wire during Joule heating fused filament fabrication. The effects of current intensity, printing speed, and roller pressure on the macroscopic morphology, microstructure, and microhardness of a single-layer single-channel formation were investigated. The results indicate that when the current intensity is 400 A, the printing speed is 1000 mm/min, and the roller pressure is 0.3 N, the surface of the single-layer single-channel formation is smooth and exhibits optimal forming characteristics with a width-to-height ratio of 3.23, a dilution rate of 51.61%, and an average microhardness of 238.17 HV. As the current intensity increases, the microstructure in the fusion zone initially decreases in size and then increases; similarly, with the increase in printing speed, the microstructure in the fusion zone first decreases and then increases; as the roller pressure increases, the microstructure in the fusion zone initially increases in size and then decreases. The microhardness initially increases and then decreases with the increase in process parameters, resulting in uneven hardness distribution due to the variations in microstructure size. The optimal combination of process parameters achieves a balance between heat input, cooling rate, and growth rate, thereby achieving grain refinement and hardness improvement, ultimately enhancing the mechanical properties of the material. [ABSTRACT FROM AUTHOR]

Purpose: To study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC). Patients and Methods: The clinical characteristics together with LARS1 expression levels were obtained from the TCGA database. Immunohistochemistry confirmed LARS1 expression levels in paraneoplastic and tumor tissues. To investigate LARS1-related downstream molecules, a network of protein-protein interactions (PPIs) and the Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) were built. Furthermore, gene set enrichment analysis (GSEA) was used to analyze the pathways associated with LARS1 expression, whereas Single-sample GSEA (ssGSEA) was applied to perform an association study between immune infiltration and LARS1 gene expression. The TISCH Database and the TISIDB database were used to compare the difference of LARS1 expression in hepatocellular carcinoma and immunomodulators. Results: In comparison to that in normal tissues, the LARS1 expression level was elevated in tumor tissues. LARS1 expression exhibited substantial correlation with AFP, Histologic grade, pathologic stage, Residual tumor, and Vascular invasion in HCC. Higher LARS1 expression in HCC was linked to lower progression-free survival (PFS), disease-specific survival (DSS), and overall survival (OS). According to the GO/KEGG study, the important biological process (neutral lipid metabolic process), cellular component (triglyceride-rich plasma lipoprotein), molecular functions (lipase inhibitor activity), and KEGG pathway (cholesterol metabolism) could be a probable function mechanism in promoting HCC. Various pathways as per GSEA revealed that they were enriched in samples with elevated LARS1 expression. The expression level of LARS1 in malignant tumor cells after immunotherapy was significantly higher than that before immunotherapy. LARS1 was also remarkably linked to the infiltration level and the immunomodulators. Conclusion: LARS1 can be used as a biomarker of HCC, which is associated to immune infiltration of HCC. [ABSTRACT FROM AUTHOR]

An in situ gel separator based on an electrospun three-layer nanofibrous membrane (PSE11-Gel) is developed for high-performance lithium-organic batteries (LOBs). The highly efficient shuttle effect inhibition of organic cathode molecules or lithiated intermediates has been demonstrated for PSE11-Gel to realize high-capacity stable LOBs. [ABSTRACT FROM AUTHOR]

To change the situation of shape memory polymers (SMPs) that can only remember very few shapes and enable discretional morphing for practical application, the authors report a reversible stepless multiple SMP derived from ultrahigh molecular weight polyethylene (UHMWPE). As the crystals of semi‐crystalline polymers are assembled by those with slightly different melting temperatures, and each type of crystal can remember a single shape, the crystalline region of UHMWPE is allowed to remember plenty of temporary shapes after programming. Changing the temperature of the programmed polymer within the melting/crystallization temperature ranges would lead to releasing/recovery of the memorized temporary shapes. Accordingly, multiple shape memory effects can be easily realized without an elaborate design of material structure and training process in advance as before. The temperature‐dependent adjustability of the analog capacitor and soft lens with embedded programmed UHMWPE as actuators, characterized by the continuous/random/proportional responsivity, further reveals the utilization prospects of the controllable reversible stepless discretionary morphing effect. Moreover, the maximum work density of the programmed UHMWPE is found to be 210 kJ/m3, which is more than 10 times of piezoelectric ceramics, so that it can serve as a proof‐of‐concept mechanical driver for reversibly pumping of ethanediol‐droplet upon heating/cooling. [ABSTRACT FROM AUTHOR]

Hepatocellular carcinoma (HCC) constitutes a major global health threat due to the high incidence and mortality. Sorafenib is known as the first-line medication for advanced HCC; however, it only extends the limited benefit for HCC patients as the development of acquired resistance. Withaferin A exerts broad pharmaceutical applications in several cancers. However, its effects on HCC cell metastatic potential and sorafenib resistance remain elusive. Here, we corroborated that Withaferin A greatly restrained cell viability, invasion, vasculogenic mimicry (VM) formation, and VE-cadherin levels in HepG2 and SNU449 cells. Moreover, Withaferin A sensitized sorafenib (SR)-resistant HCC cells to sorafenib. In striking contrast to the parental cells, lower ferroptosis was observed in SR-resistant cells as the lower ROS, MDA, and higher intracellular GSH levels in SR-resistant cells. Of interest, Withaferin A enhanced ferroptosis in SR-resistant cells, which was reversed by ferroptosis antagonist liproxstation-1. Notably, Withaferin A elevated Keap1 expression to mitigate Nrf2 signaling activation-mediated epithelial to mesenchymal transition (EMT) and ferroptosis-related protein xCT expression. Importantly, blockage of the Keap1/Nrf2 signaling overturned Withaferin A-evoked ferroptosis and facilitated sorafenib resistance. In addition, knockdown of Keap1 antagonized the inhibitory efficacy of Withaferin A on HCC cell viability, invasion, and VM formation. Consequently, Withaferin A may attenuate the metastatic potential and sorafenib resistance by regulating Keap1/Nrf2-associated EMT and ferroptosis. Thus, Withaferin A may serve as a promising agent for HCC therapy, especially for advanced HCC. [ABSTRACT FROM AUTHOR]