Distinctive hydrodynamic properties and ecological responses of multi-thread rivers under different degrees of multiplicity in the Upper Yellow River.

Alluvial rivers that exhibit multi-thread patterns are common in nature and can be the dominant channel morphology in large rivers. However, their ecological properties in response to diverse and dynamic channel morphology has gained limited attention and remained poorly understood. In this study, we adopted an eco-hydraulic model by integrating a hydrodynamic, a sediment-transport, and a habitat-suitability model to assess habitat quality for fish species (Schizopygopsis pylzovi and Platypharodon extremus) in three anabranching reaches with each exhibiting a distinct anabranching morphology in the Upper Yellow River, eastern Qinghai-Tibet Plateau. Based on the hydrologic data and actual channel morphology, we modeled the hydrodynamic and sediment-transport conditions for a period spanning ten years, and simulated habitat conditions under a potentially changing environment with different flow magnitudes and frequencies. The results indicated that the average flow velocity in the low and mid-order anabranching reaches is higher than that in the high-order, complex anabranching reaches. Meanwhile, the bedload transport rate was higher in the high and mid-order anabranching reaches than that in the low-order anabranching reach, demonstrating a greater transport efficiency of multi-thread systems with a greater multiplicity. Consequently, the habitat suitability shows a deteriorating trend over the ten-year modeling period and Schizopygopsis pylzovi shows better habitat status than Platypharodon extremus. The flow magnitudes and frequency also have a significant impact on the distribution of high habitat suitability index among the different river patterns in Upper Yellow River. This study can provide valuable information to optimize ecological outcomes and provide valuable insights for future dam operation strategies and consideration efforts aimed at preserving and restoring riverine ecosystems.

Multifunctional protocatechuic acid-polyacrylic acid hydrogel adhesives for wound dressings.

Multifunctional hydrogel adhesives are highly desirable in wound healing applications, yet their preparation often requires complex material system design to achieve. Herein, a straightforward one-pot two-step polymerization method is developed to prepare adhesive hydrogels for wound dressing based on protocatechuic acid (PCA), polyacrylic acid (PAA), and polyamidoamine-epichlorohydrin (PAE), where PCA provides the catechol groups for strong adhesion, PAA serves as the primary polymer matrix, and PAE acts as a bridge connecting PCA and PAA. This design results in a PAA-PAE-PCA hydrogel having a remarkable instant 90-degree peeling interfacial toughness of 431 J m-2 on porcine skin, which is further amplified to 615 J m-2 after 30 minutes. The hydrogel also possesses the desired features for wound dressing, such as self-healing, antioxidant, anti-UV and antibacterial properties, good cytocompatibility, strong adhesion in use and weak adhesion on removal, as well as reversible and wet adhesion. Finally, in vivo data reveal that the PAA-PAE-PCA hydrogels can significantly accelerate wound healing, as evidenced by a noticeable reduction in the wound area and a diminished inflammatory response. Collectively, these results endorse the obtained multifunctional hydrogel as a promising candidate for wound healing and related fields.

Regulation of Hard Segment Cluster Structures for High-performance Poly(urethane-urea) Elastomers.

Elastomers are widely used in daily life; however, the preparation of degradable and recyclable elastomers with high strength, high toughness, and excellent crack resistance remains a challenging task. In this report, a polycaprolactone-based poly(urethane-urea) elastomer is presented with excellent mechanical properties by optimizing the arrangement of hard segment clusters. It is found that long alkyl chains of the chain extenders lead to small and evenly distributed hard segment clusters, which is beneficial for improving mechanical properties. Together with the multiple hydrogen bond structure and stress-induced crystallization, the obtained elastomer exhibits a high strength of 63.3 MPa, an excellent toughness of 431 MJ m-3 and an outstanding fracture energy of 489 kJ m-2, while maintaining good recyclability and degradability. It is believed that the obtained elastomer holds great promise in various application fields and it contributes to the development of a sustainable society.

Fracture-Resistant Stretchable Materials: An Overview from Methodology to Applications.

Stretchable materials, such as gels and elastomers, are attractive materials in diverse applications. Their versatile fabrication platforms enable the creation of materials with various physiochemical properties and geometries. However, the mechanical performance of traditional stretchable materials is often hindered by the deficiencies in their energy dissipation system, leading to lower fracture resistance and impeding their broader range of applications. Therefore, the synthesis of fracture-resistant stretchable materials has attracted great interest. This review comprehensively summarizes key design considerations for constructing fracture-resistant stretchable materials, examines their synthesis strategies to achieve elevated fracture energy, and highlights recent advancements in their potential applications.

Tough, Recyclable, and Degradable Elastomers for Potential Biomedical Applications.

Elastomers have many industrial, medical and commercial applications, however, their huge demand raises an important question of how to dispose of the out-of-service elastomers. Ideal elastomers that are concurrently tough, recyclable, and degradable are in urgent need, but their preparation remains a rigorous challenge. Herein, a polycaprolactone (PCL) based polyurethane elastomer is designed and prepared to meet this demand. Owing to the presence of dynamic coordination bond and the occurrence of strain-induced crystallization, the obtained elastomer exhibits a high toughness of ≈372 MJ m-3 and an unprecedented fracture energy of ≈646 kJ m-2 , which is much higher than natural rubber (≈50 MJ m-3 for toughness and ≈10 kJ m-2 for fracture energy). In addition, the elastomer can be recycled at least three times using solvent without losing its mechanical properties and can be degraded by lipase in ≈2 months. Finally, biological experiments demonstrate that the elastomer possesses good biocompatibility and can facilitate wound healing in mice when used as sutures. It is believed that the obtained elastomer meets the requirements for next-generation elastomers and is expected to be used in emerging fields such as biomedicine, flexible electronics, robotics and beyond.

Stretchable Hydrogels with Low Hysteresis and High Fracture Toughness for Flexible Electronics.

Stretchable materials, especially hydrogels, are emerging in various fields recently. Many applications demand low hysteresis and high fracture toughness of the materials to be used under dynamic mechanical loads. Herein, the authors report a hydrogel with high fracture toughness and low hysteresis through using a strong metal coordination bond and relatively high crosslinking density. This design allows the sacrificial bond to remain intact under normal operation, while fracturing to dissipate mechanical energy in the fracture zone to prevent propagation of the cracks. The obtained hydrogel exhibits a low hysteresis (≈1.5%) and a high fracture toughness (≈2,164 J m-2 ). Moreover, the hydrogel possesses a high fatigue threshold of ≈141 J m-2 and a reasonable conductivity. This study provides a worth-adopted approach to synthesize hydrogels with low hysteresis and high fracture toughness.

Functionalized starch as a novel eco-friendly vulcanization accelerator enhancing mechanical properties of natural rubber.

A novel eco-friendly vulcanization accelerator, starch supported sodium isobutyl xanthate (SSX) has been synthesized firstly. The modification of starch using sodium isobutyl xanthate (SIBX) has improved the thermal stability significantly, and the vulcanization process of natural rubber (NR) could be accelerated by SSX at 145 ℃ accordingly. More importantly, SSX can be dispersed into NR matrix uniformly along with the strong interfacial interaction between SSX and NR, as evidenced by the constrained rubber chains around SSX surface. In addition, mechanical properties of the obtained NR have been enhanced remarkably, showing a 22.4 % increase in tensile strength when compared with traditional vulcanization accelerator. Laying on the fact that a novel vulcanization accelerator has been fabricated successfully using SIBX functionalized starch, new strategies for the preparation of green vulcanization accelerators and the functional application of biopolymers can be provided.

FGF8 promotes cell proliferation and resistance to EGFR inhibitors via upregulation of EGFR in human hepatocellular carcinoma cells.

Fibroblast growth factor 8 (FGF8), a member of the fibroblast growth factor (FGF) family, is upregulated in several human cancers, including HCC (HCC). Previous studies have demonstrated that FGF8 increased cell growth and invasion of tumor cells. In the present study we investigated whether FGF8 is involved in the cell proliferation and resistance to several drugs in human HCC cells. We stably overexpressed FGF8 by lentiviral transfection. In addition, we also added recombinant FGF8 instead of stably overexpressing FGF8 in human HCC cells. Stable overexpression of FGF8 or exogenous recombinant FGF8 resulted in significantly enhanced cell proliferation in human HCC cells. With the use of CellTiter-Glo assay for the determination of cell viability, we found that FGF8 increased the resistance to epidermal growth factor receptor (EGFR) inhibitors in human HCC cells. Additionally, the expression of EGFR was also upregulated by stably overexpressing FGF8 or exogenous recombinant FGF8. Yes-associated protein 1 (YAP1) was reported to upregulate the expression of EGFR. Moreover, we also found that FGF8 increased the expression of YAP1 and knockdown of YAP1 eliminated the upregulation of EGFR and the resistance to EGFR inhibition induced by FGF8. Our study provides evidence that FGF8 plays an important role in the resistance to EGFR inhibition of human HCC cells.