10 research outputs found

    Interfacial Shearing Behavior along Xanthan Gum Biopolymer-Treated Sand and Solid Interfaces and Its Meaning in Geotechnical Engineering Aspects

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    Recently, environment-friendly microbial biopolymer has been widely applied as a new construction material in geotechnical engineering practices including soil stabilization, slope protection, and ground injection. Biopolymer is known to exhibit substantial improvements in geotechnical properties, such as shear strength enhancement and hydraulic conductivity reduction, through the formation of direct ionic bonds with soil particles, especially clay particles. Moreover, the rheological characteristics (e.g., pseudoplasticity, shear-rate dependent thixotropy) of biopolymers render distinctive behaviors such as shear thinning and lubrication effect under a high strain condition, while recovering their viscosities and shear stiffnesses when they are at rest. To ensure the practical applicability of biopolymer-based soil treatment, it is important to understand the interfacial interaction (i.e., friction) between biopolymer-treated soil and adjoining structural members which can be constructed in a biopolymer-treated ground. Thus, in this paper, interfacial shearing behavior of biopolymer-treated soil along solid surfaces as well as internal shearing on biopolymer-soil matrix were explored via direct and interface shear test. Experimental results show a predominant effect of the soil moisture content on the interfacial shear behavior of biopolymer-treated soil which attributes to the rheology transition of biopolymer hydrogels. At low moisture content, condensed biopolymer biofilm mobilizes strong intergranular bonding, where the interfacial shear mainly depends on the physical condition along the surface including the asperity angle. In contrast, the biopolymer induced intergranular bonding weakens as moisture content increases, where most interfacial failures occur in biopolymer-treated soil itself, regardless of the interface condition. In short, this study provides an overall trend of the interfacial friction angle and adhesion variations of xanthan gum biopolymer-treated sand which could be referred when considering a subsequent structural member construction after a biopolymer-based ground improvement practice in field

    Global CO2 Emission-Related Geotechnical Engineering Hazards and the Mission for Sustainable Geotechnical Engineering

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    Global warming and climate change caused by greenhouse gas (GHG) emissions have rapidly increased the occurrence of abnormal climate events, and both the scale and frequency of geotechnical engineering hazards (GEHs) accordingly. In response, geotechnical engineers have a responsibility to provide countermeasures to mitigate GEHs through various ground improvement techniques. Thus, this study provides a comprehensive review of the possible correlation between GHG emissions and GEHs using statistical data, a review of ground improvement methods that have been studied to reduce the carbon footprint of geotechnical engineering, and a discussion of the direction in which geotechnical engineering should proceed in the future

    Producing highly effective extracellular vesicles using IBAR and talin F3 domain fusion

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    ABSTRACTExtracellular vesicles (EVs), transporting diverse cellular components, play a crucial role in intercellular communication in numerous physiological and pathological processes. EVs have also been recognized as a drug delivery platform for therapeutic purposes and cell-free regenerative medicine. While various approaches have focused on increasing EV production for efficient use therapeutic use of EVs, enhancing the quality of EVs, such as ensuring efficient uptake by their target cells, has not been widely explored. In this study, we linked a negative membrane curvature-forming inverse BAR (IBAR) domain with an integrin β tail-binding talin F3 domain to create the IBAR-F3 fusion protein. We observed that IBAR-F3 can trigger filopodia-like membrane protrusions and attract integrins to those protrusion-rich regions, when expressed in Chinese hamster ovary cells expressing integrin αIIbβ3. Surprisingly, the expression of IBAR-F3 also induced a robust production of EVs, which were then efficiently taken up by nearby cells in an integrin-dependent manner. Moreover, IBAR triggered integrin activation, presumably by inducing negative membrane curvature that likely disrupts the interaction between the integrin α and β transmembrane domain. Therefore, we suggest that IBAR-F3 should be utilized to promote both EV production and efficient uptake mediated by integrins. Furthermore, the negative curvature-inducing integrin activation suggests that integrins on EVs can be activated by the nanoscale change in the curvature of the EV without the need for conventional machinery to activate integrin inside the EVs

    Yo-Yo Inspired Triboelectric Nanogenerator

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    Recently, as the demand for sustainable and renewable energy to power a large number of small electronics and sensors has increased, various mechanical energy harvesters such as electromagnetic, piezoelectric, and triboelectric generators have been highlighted because they have no environmental constraints to generate electricity and function as sustainable power sources. Among these generators, triboelectric nanogenerators (TENGs), which produce electrical energy via triboelectrification and electrostatic induction, are a promising energy harvesting technology that can utilize existing materials or the structure of existing commercial products. Considering the vast number of independent portable electronics used today, the development of hand-driven TENGs is important. There is great demand for TENG considering both commercial product-inspired designs, which are the merit of TENG itself, and the hand-driven type. However, relevant studies are still lacking, and therefore further studies in these areas are required. In this study, we developed a novel triboelectric nanogenerator (Y-TENG) inspired by the Yo-Yo that can produce a sustainable electric output by hand motion input. One generator of Y-TENG produced a maximum VOC of 10 V and an ICC of 0.7 μA. Peak/root mean square (RMS) voltage output-based quantitative analysis for the optimized number of blades and dielectric material was performed. The proposed Y-TENG was able to continuously light up three light-emitting diodes (LEDs) while the Y-TENG moved up and down

    Genetically Encoded Sensor Cells for the Screening of Glucocorticoid Receptor (GR) Effectors in Herbal Extracts

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    Although in vitro sensors provide facile low-cost ways to screen for biologically active targets, their results may not accurately represent the molecular interactions in biological systems. Cell-based sensors have emerged as promising platforms to screen targets in biologically relevant environments. However, there are few examples where cell-based sensors have been practically applied for drug screening. Here, we used engineered cortisol-detecting sensor cells to screen for natural mimetics of cortisol. The sensor cells were designed to report the presence of a target through signal peptide activation and subsequent fluorescence signal translocation. The developed sensor cells were able to detect known biological targets from human-derived analytes as well as natural product extracts, such as deer antlers and ginseng. The multi-use capability and versatility to screen in different cellular environments were also demonstrated. The sensor cells were used to identify novel GR effectors from medicinal plant extracts. Our results suggest that decursin from dongquai had the GR effector function as a selective GR agonist (SEGRA), making it a potent drug candidate with anti-inflammatory activity. We demonstrated the superiority of cell-based sensing technology over in vitro screening, proving its potential for practical drug screening applications that leads to the function-based discovery of target molecules

    Rapid Screening of Glucocorticoid Receptor (GR) Effectors Using Cortisol-Detecting Sensor Cells

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    Cortisol, a stress hormone, plays key roles in mediating stress and anti-inflammatory responses. As abnormal cortisol levels can induce various adverse effects, screening cortisol and cortisol analogues is important for monitoring stress levels and for identifying drug candidates. A novel cell-based sensing system was adopted for rapid screening of cortisol and its functional analogues under complex cellular regulation. We used glucocorticoid receptor (GR) fused to a split intein which reconstituted with the counterpart to trigger conditional protein splicing (CPS) in the presence of targets. CPS generates functional signal peptides which promptly translocate the fluorescent cargo. The sensor cells exhibited exceptional performance in discriminating between the functional and structural analogues of cortisol with improved sensitivity. Essential oil extracts with stress relief activity were screened using the sensor cells to identify GR effectors. The sensor cells responded to peppermint oil, and L-limonene and L-menthol were identified as potential GR effectors from the major components of peppermint oil. Further analysis indicated L-limonene as a selective GR agonist (SEGRA) which is a potential anti-inflammatory agent as it attenuates proinflammatory responses without causing notable adverse effects of GR agonists

    Molecular origin of AuNPs-induced cytotoxicity and mechanistic study

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    Abstract Gold nanoparticles (AuNPs) with diverse physicochemical properties are reported to affect biological systems differently, but the relationship between the physicochemical properties of AuNPs and their biological effects is not clearly understood. Here, we aimed to elucidate the molecular origins of AuNP-induced cytotoxicity and their mechanisms, focusing on the surface charge and structural properties of modified AuNPs. We prepared a library of well-tailored AuNPs exhibiting various functional groups and surface charges. Through this work, we revealed that the direction or the magnitude of surface charge is not an exclusive factor that determines the cytotoxicity of AuNPs. We, instead, suggested that toxic AuNPs share a common structural characteristics of a hydrophobic moiety neighbouring the positive charge, which can induce lytic interaction with plasma membrane. Mechanistic study showed that the toxic AuNPs interfered with the formation of cytoskeletal structure to slow cell migration, inhibited DNA replication and caused DNA damage via oxidative stress to hinder cell proliferation. Gene expression analysis showed that the toxic AuNPs down-regulated genes associated with cell cycle processes. We discovered structural characteristics that define the cytotoxic AuNPs and suggested the mechanisms of their cytotoxicity. These findings will help us to understand and to predict the biological effects of modified AuNPs based on their physicochemical properties
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