23 research outputs found

    A Sunlight-Degradable Autonomous Self-Healing Supramolecular Elastomer for Flexible Electronic Devices

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    Preparing an autonomous self-healing supramolecular elastomer with sunlight degradability is still a challenging task in related fields. In this work, we report a supramolecular elastomer by using the classic host–guest complexation of visible-light-photolabile picolinium-containing adamantanes (Ad) and β-cyclodextrin nanogels (β-CD). The as-synthesized elastomer possesses merits of high mechanical strength, excellent stretchability (>1500% strain), efficient self-healing (>85% at 60 min), ultrastability against electrolytes, and photodegradation properties, implying versatile applications in flexible and stretchable electronics. As proofs-of-concept, self-healable strain and pressure sensors using conductive elastomers are first fabricated, which feature exceptionally high sensitivity (e.g., 0.1% in capacitance at 0.2 kPa) and fast response to detect human body motions. A degradable and flexible supercapacitor is also fabricated using the conductive elastomer as the flexible matrix. Remarkably, both the elastomer and this supercapacitor can be degraded upon the exposure to sunlight irradiation in 48 h at very mild conditions. Therefore, it is anticipated that such a novel strategy and the as-prepared supramolecular elastomer can inspire further applications in the multidisciplinary fields of materials science, electronics, etc

    A Sunlight-Degradable Autonomous Self-Healing Supramolecular Elastomer for Flexible Electronic Devices

    No full text
    Preparing an autonomous self-healing supramolecular elastomer with sunlight degradability is still a challenging task in related fields. In this work, we report a supramolecular elastomer by using the classic host–guest complexation of visible-light-photolabile picolinium-containing adamantanes (Ad) and β-cyclodextrin nanogels (β-CD). The as-synthesized elastomer possesses merits of high mechanical strength, excellent stretchability (>1500% strain), efficient self-healing (>85% at 60 min), ultrastability against electrolytes, and photodegradation properties, implying versatile applications in flexible and stretchable electronics. As proofs-of-concept, self-healable strain and pressure sensors using conductive elastomers are first fabricated, which feature exceptionally high sensitivity (e.g., 0.1% in capacitance at 0.2 kPa) and fast response to detect human body motions. A degradable and flexible supercapacitor is also fabricated using the conductive elastomer as the flexible matrix. Remarkably, both the elastomer and this supercapacitor can be degraded upon the exposure to sunlight irradiation in 48 h at very mild conditions. Therefore, it is anticipated that such a novel strategy and the as-prepared supramolecular elastomer can inspire further applications in the multidisciplinary fields of materials science, electronics, etc

    Unexpected Temperature-Dependent Single Chain Mechanics of Poly(<i>N</i>-isopropyl-acrylamide) in Water

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    Poly­(<i>N</i>-isopropyl-acrylamide) (PNIPAM) is a paradigm thermally sensitive polymer, which has a lower critical solution temperature (LCST) of ∼32 °C in water. Herein by AFM-based single molecule force spectroscopy (SMFS), we measured the single chain elasticity of PNIPAM across the LCST in water. Below LCST, the force curves obtained at different temperatures have no remarkable difference; while above LCST, an unexpected temperature dependent elasticity is observed, mainly in the middle force regime. We found that 35 °C is a turning point of the variation: from 31 to 35 °C, the middle parts of the force curves drop gradually, whereas from 35 to 40 °C, the middle parts rise gradually. A possible mechanism for the unexpected temperature dependent mechanics is proposed. The single chain contraction against external force upon heating from 35 to 40 °C may cast new light on the design of molecular devices that convert thermal energy to mechanical work

    Down-Regulated Receptor Interacting Protein 140 Is Involved in Lipopolysaccharide-Preconditioning-Induced Inactivation of Kupffer Cells and Attenuation of Hepatic Ischemia Reperfusion Injury

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    <div><p>Background</p><p>Lipopolysaccharide (LPS) preconditioning is known to attenuate hepatic ischemia/reperfusion injury (I/RI); however, the precise mechanism remains unclear. This study investigated the role of receptor-interacting protein 140 (RIP140) on the protective effect of LPS preconditioning in hepatic I/RI involving Kupffer cells (KCs).</p><p>Methods</p><p>Sprague—Dawley rats underwent 70% hepatic ischemia for 90 minutes. LPS (100 μg/kg) was injected intraperitoneally 24 hours before ischemia. Hepatic injury was observed using serum and liver samples. The LPS/NF-κB (nuclear factor-κB) pathway and hepatic RIP140 expression in isolated KCs were investigated.</p><p>Results</p><p>LPS preconditioning significantly inhibited hepatic RIP140 expression, NF-κB activation, and serum proinflammatory cytokine expression after I/RI, with an observation of remarkably reduced serum enzyme levels and histopathologic scores. Our experiments showed that protection effects could be effectively induced in KCs by LPS preconditioning, but couldn’t when RIP140 was overexpressed in KCs. Conversely, even without LPS preconditioning, protective effects were found in KCs if RIP140 expression was suppressed with siRNA.</p><p>Conclusions</p><p>Down-regulated RIP140 is involved in LPS-induced inactivation of KCs and hepatic I/RI attenuation.</p></div

    Protein Crystallization-Mediated Self-Strengthening of High-Performance Printable Conducting Organohydrogels

    No full text
    Conductive polymers have many advanced applications, but there is still an important target in developing a general and straightforward strategy for printable, mechanically stable, and durable organohydrogels with typical conducting polymers of, for example, polypyrrole, polyaniline, or poly(3,4-ethylenedioxythiophene). Here we report a protein crystallization-mediated self-strengthening strategy to fabricate printable conducting organohydrogels with the combination of rational photochemistry design. Such organohydrogels are one-step prepared via rapidly and orthogonally controllable photopolymerizations of pyrroles and gelatin protein in tens of seconds. As-prepared conducting organohydrogels are patterned and printed to complicated structures via shadow-mask lithography and 3D extrusion technology. The mild photocatalytic system gives the transition metal carbide/nitride (MXene) component high stability during the oxidative preparation process and storage. Controlling water evaporation promotes gelatin crystallization in the as-prepared organohydrogels that significantly self-strengthens their mechanical property and stability in a broad temperature range and durability against continuous friction treatment without introducing guest functional materials. Also, these organohydrogels have commercially electromagnetic shielding, thermal conducting properties, and temperature- and light-responsibility. To further demonstrate the merits of this simple strategy and as-prepared organohydrogels, prism arrays, as proofs-of-concept, are printed and applied to make wearable triboelectric nanogenerators. This self-strengthening process and 3D-printability can greatly improve their voltage, charge, and current output performances compared to the undried and flat samples

    The influence of LPS preconditioning dose on hepatic ischemia/reperfusion injury.

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    <p>Animals subjected to 90 minutes of 70% hepatic ischemia, followed by 6 h reperfusion, then the hepatic I/RI was evaluated. <b>(A)</b> The H&E staining of the liver from sham group, LPS + I/RI group and I/RI group. <b>(B)</b> ALT serum level. <b>(C)</b> Suzuki’s pathological score (*, <i>P</i> < 0.01).</p

    The influence of LPS on RIP140 expression of KCs.

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    <p>The RIP140 knockdown and overexpression in KCs were assessed using RT-PCR and WB <b>(A)</b>. KC RIP140 expression was examined with RT-PCR, western blot <b>(B)</b>, and immunofluorescence assay <b>(C)</b> (<i>*</i>, <i>P</i> < 0.01).</p

    Synthetic Glycopolymers for Highly Efficient Differentiation of Embryonic Stem Cells into Neurons: Lipo- or Not?

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    To realize the potential application of embryonic stem cells (ESCs) for the treatment of neurodegenerative diseases, it is a prerequisite to develop an effective strategy for the neural differentiation of ESCs so as to obtain adequate amount of neurons. Considering the efficacy of glycosaminoglycans (GAG) and their disadvantages (e.g., structure heterogeneity and impurity), GAG-mimicking glycopolymers (designed polymers containing functional units similar to natural GAG) with or without phospholipid groups were synthesized in the present work and their ability to promote neural differentiation of mouse ESCs (mESCs) was investigated. It was found that the lipid-anchored GAG-mimicking glycopolymers (lipo-pSGF) retained on the membrane of mESCs rather than being internalized by cells after 1 h of incubation. Besides, lipo-pSGF showed better activity in promoting neural differentiation. The expression of the neural-specific maker β3-tubulin in lipo-pSGF-treated cells was ∼3.8- and ∼1.9-fold higher compared to natural heparin- and pSGF-treated cells at day 14. The likely mechanism involved in lipo-pSGF-mediated neural differentiation was further investigated by analyzing its effect on fibroblast growth factor 2 (FGF2)-mediated extracellular signal-regulated kinases 1 and 2 (ERK1/2) signaling pathway which is important for neural differentiation of ESCs. Lipo-pSGF was found to efficiently bind FGF2 and enhance the phosphorylation of ERK1/2, thus promoting neural differentiation. These findings demonstrated that engineering of cell surface glycan using our synthetic lipo-glycopolymer is a highly efficient approach for neural differentiation of ESCs and this strategy can be applied for the regulation of other cellular activities mediated by cell membrane receptors

    Protein Crystallization-Mediated Self-Strengthening of High-Performance Printable Conducting Organohydrogels

    No full text
    Conductive polymers have many advanced applications, but there is still an important target in developing a general and straightforward strategy for printable, mechanically stable, and durable organohydrogels with typical conducting polymers of, for example, polypyrrole, polyaniline, or poly(3,4-ethylenedioxythiophene). Here we report a protein crystallization-mediated self-strengthening strategy to fabricate printable conducting organohydrogels with the combination of rational photochemistry design. Such organohydrogels are one-step prepared via rapidly and orthogonally controllable photopolymerizations of pyrroles and gelatin protein in tens of seconds. As-prepared conducting organohydrogels are patterned and printed to complicated structures via shadow-mask lithography and 3D extrusion technology. The mild photocatalytic system gives the transition metal carbide/nitride (MXene) component high stability during the oxidative preparation process and storage. Controlling water evaporation promotes gelatin crystallization in the as-prepared organohydrogels that significantly self-strengthens their mechanical property and stability in a broad temperature range and durability against continuous friction treatment without introducing guest functional materials. Also, these organohydrogels have commercially electromagnetic shielding, thermal conducting properties, and temperature- and light-responsibility. To further demonstrate the merits of this simple strategy and as-prepared organohydrogels, prism arrays, as proofs-of-concept, are printed and applied to make wearable triboelectric nanogenerators. This self-strengthening process and 3D-printability can greatly improve their voltage, charge, and current output performances compared to the undried and flat samples

    The influence of LPS preconditioning on RIP140 expression and NF-κB signal transduction.

    No full text
    <p>Hepatic RIP140 expression in the rats from different groups was examined with immunohistochemical analysis <b>(A)</b>, RT-PCR <b>(B)</b>, and western blot <b>(C)</b>. Hepatic NF-κB activity <b>(D)</b>, and TNF-α, IL-1β, and IL-6 expression levels <b>(E)</b> were examined with ELISA and RT-PCR (*, <i>P</i> < 0.01).</p
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