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Repairing high-load connective tissues, such as ligaments, by surgically implanting artificial grafts after injury is challenging because they lack biointegration with host bones for stable interfaces. Herein, a high-performance helical composite fiber (HCF) ligament by wrapping aligned carbon nanotube (CNT) sheets around polyester fibers is proposed. Anterior cruciate ligament (ACL) reconstruction surgery shows that HCF grafts could induce effective bone regeneration, thus allowing the narrowing of bone tunnel defects. Such repair of the bone tunnel is in strong contrast to the tunnel enlargement of more than 50% for commercial artificial ligaments made from bare polyester fibers. Rats reconstructed with this HCF ligament show normal jumping, walking, and running without limping. This work allows bone regeneration in vivo through a one-step surgery without seeding cells or transforming growth factors, thereby opening an avenue for high-performance artificial tissues.
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Reconstrução do Ligamento Cruzado Anterior , Nanotubos de Carbono , Animais , Ratos , Ligamento Cruzado Anterior/transplante , PoliésteresRESUMO
Flexible batteries based on gel electrolytes with high safety are promising power solutions for wearable electronics but suffer from vulnerable electrode-electrolyte interfaces especially upon complex deformations, leading to irreversible capacity loss or even battery collapse. Here, a supramolecular sol-gel transition electrolyte (SGTE) that can dynamically accommodate deformations and repair electrode-electrolyte interfaces through its controllable rewetting at low temperatures is designed. Mediated by the micellization of polypropylene oxide blocks in Pluronic and host-guest interactions between α-cyclodextrin (α-CD) and polyethylene oxide blocks, the high ionic conductivity and compatibility with various salts of SGTE afford resettable electrode-electrolyte interfaces and thus constructions of a series of highly durable, flexible aqueous zinc batteries. The design of this novel gel electrolyte provides new insights for the development of flexible batteries.
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Biomedical polymers have been extensively developed for promising applications in a lot of biomedical fields, such as therapeutic medicine delivery, disease detection and diagnosis, biosensing, regenerative medicine, and disease treatment. In this review, we summarize the most recent advances in the synthesis and application of biomedical polymers, and discuss the comprehensive understanding of their property-function relationship for corresponding biomedical applications. In particular, a few burgeoning bioactive polymers, such as peptide/biomembrane/microorganism/cell-based biomedical polymers, are also introduced and highlighted as the emerging biomaterials for cancer precision therapy. Furthermore, the foreseeable challenges and outlook of the development of more efficient, healthier and safer biomedical polymers are discussed. We wish this systemic and comprehensive review on highlighting frontier progress of biomedical polymers could inspire and promote new breakthrough in fundamental research and clinical translation.
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The electrochemical conversion of carbon dioxide (CO2 ) to carbon monoxide (CO) is a favorable approach to reduce CO2 emission while converting excess sustainable energy to important chemical feedstocks. At high current density (>100â mA cm-2 ), low energy efficiency (EE) and unaffordable cell cost limit the industrial application of conventional CO2 electrolyzers. Thus, a crucial and urgent task is to design a new type of CO2 electrolyzer that can work efficiently at high current density. Here we report a polymer-supported liquid layer (PSL) electrolyzer using polypropylene non-woven fabric as a separator between anode and cathode. Ag based cathode was fed with humid CO2 and potassium hydroxide was fed to earth-abundant NiFe-based anode. In this configuration, the PSL provided high-pH condition for the cathode reaction and reduced the cell resistance, achieving a high full cell EE over 66 % at 100â mA cm-2 .
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Among all CO2 electroreduction products, methane (CH4) and ethylene (C2H4) are two typical and valuable hydrocarbon products which are formed in two different pathways: hydrogenation and dimerization reactions of the same CO intermediate. Theoretical studies show that the adsorption configurations of CO intermediate determine the reaction pathways towards CH4/C2H4. However, it is challenging to experimentally control the CO adsorption configurations at the catalyst surface, and thus the hydrocarbon selectivity is still limited. Herein, we seek to synthesize two well-defined copper nanocatalysts with controllable surface structures. The two model catalysts exhibit a high hydrocarbon selectivity toward either CH4 (83%) or C2H4 (93%) under identical reduction conditions. Scanning transmission electron microscopy and X-ray absorption spectroscopy characterizations reveal the low-coordination Cu0 sites and local Cu0/Cu+ sites of the two catalysts, respectively. CO-temperature programed desorption, in-situ attenuated total reflection Fourier transform infrared spectroscopy and density functional theory studies unveil that the bridge-adsorbed CO (COB) on the low-coordination Cu0 sites is apt to be hydrogenated to CH4, whereas the bridge-adsorbed CO plus linear-adsorbed CO (COB + COL) on the local Cu0/Cu+ sites are apt to be coupled to C2H4. Our findings pave a new way to design catalysts with controllable CO adsorption configurations for high hydrocarbon product selectivity.
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Mechanical mismatches between implanted electronics and biological tissues can lead to inaccurate readings and long-term tissue damage. Here, we show that functionalized multi-walled carbon nanotubes twisted into helical fibre bundles that mimic the hierarchical structure of muscle can monitor multiple disease biomarkers in vivo. The flexible fibre bundles are injectable, have a low bending stiffness and display ultralow stress under compression. As proof-of-concept evidence of the sensing capabilities of these fibre bundles, we show that the fibre bundles enable the spatially resolved and real-time monitoring of H2O2 when implanted in tumours in mice, and that they can be integrated with a wireless transmission system on an adhesive skin patch to monitor calcium ions and glucose in the venous blood of cats for 28 d. The versatility of the helical fibre bundles as chemically functionalized electrochemical sensors makes them suitable for multiple sensing applications in biomedicine and healthcare.
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Técnicas Biossensoriais/instrumentação , Técnicas Biossensoriais/métodos , Diabetes Mellitus Tipo 1/metabolismo , Técnicas Eletroquímicas/instrumentação , Técnicas Eletroquímicas/métodos , Nanotubos de Carbono , Neoplasias/metabolismo , Animais , Materiais Biocompatíveis , Biomarcadores/metabolismo , Biomarcadores Tumorais/metabolismo , Gatos , Diabetes Mellitus Tipo 1/diagnóstico , Feminino , Peróxido de Hidrogênio/análise , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Nus , Monitorização Fisiológica , Nanotubos de Carbono/ultraestrutura , Neoplasias/diagnósticoRESUMO
Flexible strain sensors have attracted extensive attention in electronic skins and health monitoring systems. To date, it remains a great challenge for the development of a multifunctional strain sensor with simultaneous ultralow detection limit, broad sensing range, and high repeatability. In this paper, we report a new carbon nanotube/flexible fiber-shaped strain sensor. The fiber substrate has a novel microstructure where a highly elastic rubber fiber core is tightly wound by a continuous spring-like polypropylene fiber as the shell. Our sensor offers combined sensing performances of ultralow detection limit of 0.01% strain, wide sensing range of 200% strain, and high repeatability of 20â¯000 cycles by designing double-leveled helical gaps. This strain sensor shows a rapid response time of 70 ms under both stretching and releasing. In addition, it is available for a variety of other deformations such as bending and torsion. Due to the unique fiber structure, it can extend the torsion detection range to 1000 rad m-1. On the basis of the superior sensing performances, our sensor demonstrates to efficiently work for both subtle physiological activities and vigorous human motions. This work provides a general and effective strategy for designing smart wearable devices with high performance.
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Dispositivos Eletrônicos Vestíveis , Limite de Detecção , Nanotubos de Carbono/química , Polipropilenos/químicaRESUMO
Solar radiation, especially ultraviolet (UV) light, is a major hazard for most skin-related cancers. The growing needs for wearable health monitoring systems call for a high-performance real-time UV sensor to prevent skin diseases caused by excess UV exposure. To this end, here a novel self-powered p-CuZnS/n-TiO2 UV photodetector (PD) with high performance is successfully developed (responsivity of 2.54 mA W-1 at 0 V toward 300 nm). Moreover, by effectively replacing the Ti foil with a thin Ti wire for the anodization process, the conventional planar rigid device is artfully turned into a fiber-shaped flexible and wearable one. The fiber-shaped device shows an outstanding responsivity of 640 A W-1 , external quantum efficiency of 2.3 × 105 %, and photocurrent of ≈4 mA at 3 V, exceeding those of most current UV PDs. Its ultrahigh photocurrent enables it to be easily integrated with commercial electronics to function as a real-time monitor system. Thus, the first real-time wearable UV radiation sensor that reads out ambient UV power density and transmits data to smart phones via wifi is demonstrated. This work not only presents a promising wearable health monitor, but also provides a general strategy for designing and fabricating smart wearable electronic devices.
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Monitoramento de Radiação/instrumentação , Raios Ultravioleta , Desenho de Equipamento , Humanos , Nanocompostos/química , Processos Fotoquímicos , Energia Solar , Luz Solar , Titânio/química , Dispositivos Eletrônicos VestíveisRESUMO
Herein, we develop a novel method for designing electrochemical biosensors with both current and potential signal outputs for the simultaneous determination of two species in a living system. Oxygen (O2 ) and pH, simple and very important species, are employed as model molecules. By designing and synthesizing a new molecule, Hemin-aminoferrocene (Hemin-Fc), we create a single electrochemical biosensor for simultaneous detection and ratiometric quantification of O2 and pH in the brain. The reduction peak current of the hemin group increases with the concentration of O2 from 1.3 to 200.6â µm. Meanwhile, the peak potential positively shifts with decreasing pH from 8.0 to 5.5, resulting in the simultaneous determination of O2 and pH. The Fc group can serve as an internal reference for ratiometric biosensing because its current and potential signals remain almost constant with variations of O2 and pH. The developed biosensor has high temporal and spatial resolutions, as well as remarkable selectivity and accuracy, and is successfully applied in the real-time quantification of O2 and pH in the brain upon ischemia, as well as in tumor during cancer therapy.
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Técnicas Biossensoriais , Encéfalo/metabolismo , Técnicas Eletroquímicas , Isquemia/metabolismo , Neoplasias/tratamento farmacológico , Oxigênio/análise , Antineoplásicos/química , Antineoplásicos/uso terapêutico , Técnicas Biossensoriais/instrumentação , Técnicas Eletroquímicas/instrumentação , Desenho de Equipamento , Humanos , Concentração de Íons de Hidrogênio , Neoplasias/diagnóstico , Neoplasias/metabolismo , Oxigênio/metabolismoRESUMO
Owing to the high theoretical energy density of metal-air batteries, the aluminum-air battery has been proposed as a promising long-term power supply for electronics. However, the available energy density from the aluminum-air battery is far from that anticipated and is limited by current electrode materials. Herein we described the creation of a new family of all-solid-state fiber-shaped aluminum-air batteries with a specific capacity of 935â mAh g(-1) and an energy density of 1168â Wh kg(-1) . The synthesis of an electrode composed of cross-stacked aligned carbon-nanotube/silver-nanoparticle sheets contributes to the remarkable electrochemical performance. The fiber shape also provides the aluminum-air batteries with unique advantages; for example, they are flexible and stretchable and can be woven into a variety of textiles for large-scale applications.