The
2019 coronavirus outbreak (COVID-19) is affecting over 210
countries and territories, and it is spreading mainly by respiratory
droplets. The use of disposable surgical masks is common for patients,
doctors, and even the general public in highly risky areas. However,
the current surgical masks cannot self-sterilize in order to reuse
or be recycled for other applications. The resulting high economic
and environmental costs are further damaging societies worldwide.
Herein, we reported a unique method for functionalizing commercially
available surgical masks with outstanding self-cleaning and photothermal
properties. A dual-mode laser-induced forward transfer method was
developed for depositing few-layer graphene onto low-melting temperature
nonwoven masks. Superhydrophobic states were observed on the treated
masks’ surfaces, which can cause the incoming aqueous droplets
to bounce off. Under sunlight illumination, the surface temperature
of the functional mask can quickly increase to over 80 °C, making
the masks reusable after sunlight sterilization. In addition, this
graphene-coated mask can be recycled directly for use in solar-driven
desalination with outstanding salt-rejection performance for long-term
use. These roll-to-roll production-line-compatible masks can provide
us with better protection against this severe virus. The environment
can also benefit from the direct recycling of these masks, which can
be used for desalinating seawater.
The COVID-19 pandemic is endangering the world due to the spread of respiration droplets with viruses. Medical workers and frontline staff need to wear respirators to protect themselves from breathing in the virus-containing respiration droplets. The most frequently used state-of-the-art respirators are of N95 standard; however, they lack selfdecontamination capabilities. In addition, the viruses and bacteria can accumulate on the respirator surfaces, possessing high risks to the wearers over long-term usage. Photothermal decontamination is a contactless, fast, low-cost, and widely available method, capable of decontaminating the respirators. Herein, we report a plasmonic photothermal and superhydrophobic coating on N95 respirators, possessing significantly better protection than existing personal protection equipment. The plasmonic heating can raise the surface temperature to over 80 °C for this type of respirator within 1 min of sunlight illumination. The superhydrophobic features prohibit respiration droplets from accumulating on the respirator surfaces. The presence of the silver nanoparticles can provide additional protection via the silver ion's disinfection toward microbes. These synergistic features of the composite coatings provide the N95 respirator with better protection and can inspire experts from interdisciplinary fields to develop better personal protection equipment to fight the COVID-19 pandemic.
zMicroRNAs (miRNAs) are endogenously expressed small noncoding RNAs that regulate approximately one-third of human genes at post-transcription level. Previous studies have shown that miRNAs were implicated in many cellular processes and participated in the progress of various tumors including hepatocellular carcinoma (HCC). Among all miRNAs, the let-7 family is well recognized to play pivotal roles in tumorigenesis by functioning as potential growth suppressor. In the present study, we aimed to investigate the role of let-7 family, particularly the hsa-let-7g, in the molecular pathogenesis of HCC. By use of MTT, qPCR, Western blotting and 2-dimensional electrophoresis (2-DE), over-expression of hsa-let-7g was found to inhibit the proliferation of HCC cell line via negative and positive regulations of c-Myc and p16 INK4A , respectively. The expression of hsalet-7g was noted to be markedly lowered in the HepG2, Hep3B and Huh7 cells, yet higher in the Bel-7404 HCC cell line. Proliferation of HCC cell line was significantly inhibited after the transfection of hsa-let-7g mimics, while hsa-let-7g inhibitor transfection exerted an opposite effect. Concurrently, the mRNA and protein levels of c-Myc were found significantly decreased in HepG2 cells after transfection of hsa-let-7g mimics, but obviously increased in Bel-7404 cells after transfection of hsa-let-7g inhibitor. As revealed by 2-DE, a significant upregulation of p16 INK4A was revealed after the gain-of-function study using hsa-let-7g. Therefore, we suggest that hsa-let-7g may act as a tumor suppressor gene that inhibits HCC cell proliferation by downregulating the oncogene, c-Myc, and upregulating the tumor suppressor gene, p16 INK4A .
Super-tough and highly squeezable hydrogel by a one-step polymerization shows ultra extendability and healability and leads to a shape-memory absorbent fiber.
Four experiments compared the extinction of responding to a continuously reinforced (CRf) conditioned stimulus (CS) consistently reinforced on every trial, with extinction of responding to a partially reinforced (PRf) CS that had been inconsistently reinforced. To equate the acquisition of responding between the two CSs, the average duration of the CRf CS was extended so that it scheduled the same overall rate of reinforcement per unit time as the PRf CS. Experiment 1 used a within-subjects design to compare the rates of extinction for a 10-s PRf CS reinforced on 33% of trials versus a 30-s CRf CS. Experiment 2 made the same comparison but using a between-subjects design. Experiment 3 compared extinction in a group trained with a 10-s PRf CS reinforced on 20% of trials and a group trained with a 50s CRf CS. Experiment 4 compared the rates of extinction following two partial reinforcement schedules, a 10-s PRf CS reinforced on 33% of trial versus a 20-s CRf CS reinforced on 66% of trials. In each experiment, responding took longer to extinguish for the CS that scheduled a lower per-trial probability of reinforcement. Modelling of individual extinction curves using Weibull functions indicated that the latency to initiate extinction was directly related to the per-trial probability of reinforcement learned during acquisition. For example, compared to training with a CRf CS, rats reinforced on 33% of trials took approximately three times as many trials to initiate extinction, and rats reinforced on 20% of trials took five times as many trials to initiate extinction. These results provide support for trial-based accounts of extinction (e.g. Capaldi, 1967), whereby rats learn about the expected number of trials per reinforcer, and extinction depends on the number of expected reinforcers that have been omitted rather than on the number of extinction trials per se.
Pavlovian conditioning is sensitive to the temporal relationship between the conditioned stimulus (CS) and the unconditioned stimulus (US). This has motivated models that describe learning as a process that continuously updates associative strength during the trial or specifically encodes the CS-US interval. These models predict that extinction of responding is also continuous, such that response loss is proportional to the cumulative duration of exposure to the CS without the US. We review evidence showing that this prediction is incorrect, and that extinction is trial-based rather than time-based. We also present two experiments that test the importance of trials versus time on the Partial Reinforcement Extinction Effect (PREE), in which responding extinguishes more slowly for a CS that was inconsistently reinforced with the US than for a consistently reinforced one. We show that increasing the number of extinction trials of the partially reinforced CS, relative to the consistently reinforced CS, overcomes the PREE. However, increasing the duration of extinction trials by the same amount does not overcome the PREE. We conclude that animals learn about the likelihood of the US per trial during conditioning, and learn trial-by-trial about the absence of the US during extinction. Moreover, what they learn about the likelihood of the US during conditioning affects how sensitive they are to the absence of the US during extinction.
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