Polymeric electronic materials have enabled soft and stretchable electronics. However, the lack of a universal micro/nanofabrication method for skin-like and elastic circuits results in low device density and limited parallel signal recording and processing ability relative to silicon-based devices. We present a monolithic optical microlithographic process that directly micropatterns a set of elastic electronic materials by sequential ultraviolet light–triggered solubility modulation. We fabricated transistors with channel lengths of 2 micrometers at a density of 42,000 transistors per square centimeter. We fabricated elastic circuits including an XOR gate and a half adder, both of which are essential components for an arithmetic logic unit. Our process offers a route to realize wafer-level fabrication of complex, high-density, and multilayered elastic circuits with performance rivaling that of their rigid counterparts.

Chiral assemblies of plasmonic nanoparticles are known for strong circular dichroism but not for high optical asymmetry, which is limited by the unfavorable combination of electrical and magnetic field components compounded by strong scattering. Here we show that these limitations can be overcome by long-range organization of nanoparticles similar to liquid crystals found in helical assemblies of gold nanorods with human islet amyloid polypeptide. Strong polarization-dependent spectral shift and reduced scattering of energy states with antiparallel orientation of dipoles activated in assembled helices increase optical asymmetry g-factors by more than 4600 times. The liquid crystal-like color variations and nanorods-accelerated fibrillation enable drug screening in complex biological media. Improvement of long-range order also provides structural guidance for the design of materials with high optical asymmetry.

Accurate prediction of the absolute or relative protein−ligand binding affinity is one of the major tasks in computer-aided drug design projects, especially in the stage of lead optimization. In principle, the alchemical free energy (AFE) methods such as thermodynamic integration (TI) or free-energy perturbation (FEP) can fulfill this task, but in practice, a lot of hurdles prevent them from being routinely applied in daily drug design projects, such as the demanding computing resources, slow computing processes, unavailable or inaccurate force field parameters, and difficult and unfriendly setting up and post-analysis procedures. In this study, we have exploited practical protocols of applying the CPU (central processing unit)-TI and newly developed GPU (graphic processing unit)-TI modules and other tools in the AMBER software package, combined with ff14SB/GAFF1.8 force fields, to conduct efficient and accurate AFE calculations on protein−ligand binding free energies. We have tested 134 protein−ligand complexes in total for four target proteins (BACE, CDK2, MCL1, and PTP1B) and obtained overall comparable performance with the commercial Schrodinger FEP+ program (Wang et al.

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Single wall carbon nanotube (SWNT) based thermo‐sensitive hydrogel (SWNT‐GEL) is reported, which provides an injectable drug delivery system as well as a medium for photothermal transduction. SWNT‐hydrogel alone appears to be nontoxic on gastric cancer cells (BGC‐823 cell line) but leads to cell death with NIR radiation through a hyperthermia proapoptosis mechanism. By incorporating hyperthermia therapy and controlled in situ doxorubicin (DOX) release, DOX‐loaded SWNT‐hydrogel with NIR radiation proves higher tumor suppression rate on mice xenograft gastric tumor models compared to free DOX without detectable organ toxicity. The developed system demonstrates improved efficacy of chemotherapeutic drugs which overcomes systemic adverse reactions and presents immense potential for gastric cancer treatment.

Chiral molecules are widely prevalent in nature and biological systems, and artificial chiral nanoparticles have drawn enormous interest owing to their unique optical and physical properties. However, nanoparticles with chiral morphologies and their potential role in biology have been rarely explored. Herein, we report a seed-mediated synthesis of enantiomorphic Au nanooctopods (NOPs) and their chiralmorphology dependence of cellular uptake. With a high yield (∼80%), the chiral NOPs possess eight uniform arms that bend from 〈111〉 to 〈100〉 directions, like a propeller structure. The chiral NOPs synthesized with L-or D-glutathione (GSH) have opposite handedness, resulting in opposite circular dichroism signals, which is consistent with finite-difference time-domain simulations. D-GSH NOPs demonstrate greater than 30% (ca. 15%) enhanced cellular uptake in GL261 and bEnd.3 cells compared with L-GSH NOPs (racemic NOPs). Moreover, D-GSH NOPs modified with poly(ethylene glycol) or L-GSH are also preferred by the cells, proving the chiral-morphology dependence of cellular uptake. Our study develops the exploration of the chiral-specific interaction in biological systems, providing potential applications for drug delivery, biosensing, and tumor detection.

To achieve ultralow-emission (ULE) standards, wet electrostatic precipitators (WESP) installed downstream from wet flue gas desulfurization (WFGD) have been widely used in Chinese coal-fired power plants (CFPPs). We conducted a comprehensive field test study at four 300 MW level ULE CFPPs, to explore the impact of wet clean processing (WFGD and WESP) on emission characteristics of three size fractions of particulate matter (PM: PM 2.5 , PM 10−2.5 , and PM >10 ) and their ionic compositions. All these CFPPs are installed with limestone-based/magnesium-based WFGD and followed by WESP as the end control device. Our results indicate that particle size distribution, mass concentration of PM, and ionic compositions in flue gas change significantly after passing WFGD and WESP. PM mass concentrations through WFGD are significantly affected by the relative strength between desulfur slurry scouring and flue gas carrying effects. Concentrations of ions in PM increase greatly after passing WFGD; especially, SO 4 2− in PM 2.5 , PM 10−2.5 , and PM >10 increase on average by about 1.4, 3.9, and 8.3 times, respectively. However, WESP before the stack can effectively reduce final PM emissions and their major ionic compositions. Furthermore, emission factors (kg/(t of coal)) of PM for different combinations of air pollution control devices are presented and discussed.

CCR9+ T cells have an increased potential to be activated and therefore may mediate strong antitumor responses. Here, we found, however, that CCL25, the only chemokine for CCR9+ cells, is not expressed in human or murine triple-negative breast cancers (TNBCs), raising a hypothesis that intratumoral delivery of CCL25 may enhance antitumor immunotherapy in TNBCs. We first determined whether this approach can enhance CD47-targeted immunotherapy using a tumor acidity–responsive nanoparticle delivery system (NP-siCD47/CCL25) to sequentially release CCL25 protein and CD47 small interfering RNA in tumor. NP-siCD47/CCL25 significantly increased infiltration of CCR9+CD8+ T cells and down-regulated CD47 expression in tumor, resulting in inhibition of tumor growth and metastasis through a T cell–dependent immunity. Furthermore, the antitumor effect of NP-siCD47/CCL25 was synergistically enhanced when used in combination with programmed cell death protein–1/programmed death ligand-1 blockades. This study offers a strategy to enhance immunotherapy by promoting CCR9+CD8+ T cell tumor infiltration.