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Cells are attractive as carriers that can help to enhance control over the biodistribution of polymer nanomedicines. Cell Cycle inhibitor One strategy to use cells as carriers is based on the cell surface immobilization of the nanoparticle cargo. While a range of strategies can be used to immobilize nanoparticles on cell surfaces, only limited effort has been made to investigate the effect of these surface modification chemistries on cell viability and functional properties. This study has explored seven different approaches for the immobilization of poly(lactic acid) (PLA) nanoparticles on the surface of two different T lymphocyte cell lines. The cell lines used were human Jurkat T cells and CD4+ TEM cells. The latter cells possess blood-brain barrier (BBB) migratory properties and are attractive for the development of cell-based delivery systems to the central nervous system (CNS). PLA nanoparticles were immobilized either via covalent active ester-amine, azide-alkyne cycloaddition, and thiol-maleimide coupling, or via noncovaligating and understanding the impact of nanoparticle-cell surface conjugation chemistries on the viability and properties of cells is important to further improve the design of cell-based nanoparticle delivery systems. The results of this study present a first step in this direction and provide first guidelines for the surface modification of T cells, in particular in view of their possible use for drug delivery to the CNS.A tremella-like Mo and N codoped graphitic nanosheet array supported on activated carbon (Mo2C-MoC/AC-N) is prepared via in situ carbonization of nitrogen-rich cobalt phthalocyanine nanoparticulates anchored on activated carbon as a high-performance anode for potassium-ion batteries. The nanosheets about 5 nm thick are uniformly distributed on the surface of activated carbon for fast K-ion intercalation, and the abundant micropores in activated carbon provide additional adsorption sites of potassium ions, forming a three-dimensional architecture for potassium storage. The 3.9 atom % Mo in Mo2C-MoC/AC-N is in the form of Mo2C and MoC flakes (around 11) attached to the graphitic nanosheets. X-ray diffraction (XRD) analysis revealed that the reaction with Mo2C (forming K2C) happens mainly at 0.8-0.4 V, while the reaction with MoC (forming K2C) occurs primarily at 0.4-0.01 V. The N doping (9.6 atom %) causes an interlayer spacing expansion of 0.3 Å in the graphitic nanosheets, beneficial to the potassium-ion insertion reaction to form KC8 at 0.4-0.01 V. The Mo2C-MoC/AC-N anode exhibits a capacity of 457.5 mA h g-1 at a current density of 0.05 A g-1 and an excellent capacity of 144.4 mA h g-1 at a high current of 5 A g-1 with a capacity loss rate of 0.49‰ per cycle.The rapid development of soft electronics has revitalized the research of conducting elastomers. However, the design of conducting elastomers having high stretchability and good transparency still remains a considerable challenge. In this study, we develop a highly transparent, stretchable, and conducting ionoelastomer based on a poly(ionic liquid) in which cations are fixed to a stretchable elastomeric network and counter anions are mobile. The ionoelastomer solves the dilemma of simultaneous transparency and stretchability in the design of traditional conducting elastomers, possessing good transparency (96%) with an extraordinarily high stretchability, up to a limiting strain of 1460%. Moreover, this novel material is completely nonvolatile and nonhygroscopic, endowing the ionoelastomer with highly stable thermal, environmental, electrochemical, and mechanoelectrical properties. An underwater sensor based on the ionoelastomer is developed with good performance in an aqueous environment. Also, a transparent dielectric elastomer actuator (DEA) is demonstrated using the ionoelastomer. It is believed that the ionoelastomer would pave the way to develop exceptional conducting elastomers toward next-generation soft electronics.Compared with conventional transparent conductive indium tin oxide (ITO) films, poly(3,4-ethylenedioxythiophene)poly (styrenesulfonic acid) (PEDOTPSS) as a conductive polymer material has been diffusely applied in organic optoelectronic devices. However, its optoelectrical properties need to be further improved. Therefore, a simple and universal approach with introducing ITO nanoparticles (NPs) was proposed to improve the optoelectrical properties of PEDOTPSS thin films. The results show that the vertical conductivity (σDC⊥) and average transmittance (from 300 to 1200 nm) of PEDOTPSS films were enhanced about 26.8 and 6.3%, respectively. Crystalline silicon (c-Si)/organic heterojunction solar cells (HSCs) with PEDOTPSS/ITO NP hybrid films were fabricated and performances led to further improvement. The spatial distributions of relative electrical field intensity and the carrier generation rate of the HSCs under the standard AM 1.5 G condition were simulated, which were in good agreement with the experimental conclusions.Neural stem cells (NPCs) efficiently communicate in an intercellular manner to govern specific cell fate decisions during the developmental process despite withstanding the fluctuating cellular environment. How these fluctuations from diverse origins functionally affect the precise cell fate decision making remains elusive. By taking a stochastic mathematical modeling approach, we unravel that the transcriptional variability arising within an NPC population due to intermittent cell cycle events significantly influences the neuron to NPC ratio during development. Our model proficiently quantifies the impact of different sources of heterogeneities in maintaining an exact neuron to NPC ratio and predicts plausible experimental ways to fine-tune the development of NPCs. In the future, these modeling insights may lead to better therapeutic avenues to regenerate neurons from NPCs.Most of the current electrocatalysts for the methanol oxidation reaction are precious group metals such as Pt, Pd, and Ru. However, their use is limited due to their high cost, scarcity, and issues with carbon monoxide poisoning. We developed a simple method to prepare a nickel foam (NF)-based monolith electrode with a NiO nanosheet array structure as an efficient electrocatalyst toward the oxidation of methanol to produce formate. By a simple ultrasonic acid treatment and air oxidation at room temperature, an inert NF was converted to NiO/NF as a catalytically active electrode due to the uniform NiO nanosheet array that was rapidly formed on the surface of NiO/NF. In alkaline electrolytes containing methanol, the as-prepared NiO/NF catalysts exhibited a lower methanol oxidation reaction (MOR) potential of +1.53 V vs RHE at 100 mA cm-2 compared to that of inert NF samples. The difference in potentials between the EMOR and the EOER at that current density was found to be 280 mV, indicating that methanol oxidation occurred at lower potentials as compared to the oxygen evolution reaction (OER).
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