Consideration of Human Factors in a Design of Fire-rescue Window

Fire-rescue window is a NPD (new product development) project that aims to increase the successful rate of fire rescue. The concept attempts being used in residential buildings and public constructions. The project places greater emphasis on providing a safe space for sufferers such as elder people, children and disables. It intended to insulate people from a fire through easy operations and to enhance safety and usability. After several tests, it is proofed that the product appears to be an effective and creative solution in fire rescue. Human factors knowledge has been considered over the NPD process at both physical (anthropometric) and psychological (cognitive) levels. Based on background research and application of new material & technology, the concept learned from mechanism principle and assimilated into understanding of environment/system design, Kansei engineering and material technology. Driven by user centred design, the design conducted various research methods in terms of observation, recording and analysis. Sufferers’ data and information have been discovered/ collected, in particular disables. This helps to determine a proper route of escaping. A prototype of concept simulated the window’s covetable structure and function, as well as testified the rationality of special usage. The fire-rescue window is named as - ‘Harbour’, which won the gold medal of ‘Janus Design Award 2016’ in France. ‘Harbour’ has been recognized as one of the successful solutions in the field of fire rescue. It also passed the ergonomic evaluation and is expected to satisfy various rescue requirements precisely and efficiently

Polylysine-immobilized affinity nylon membrane used for bilirubin adsorption

Microporous polyamide membranes were activated by epibromohydrin and subsequently bound with hydroxyethylcellulose (HEC) to amplify reactive groups. Then polylysine (PLL) as ligand was also immobilized onto the nylon membranes by epibromohydrin activation. Such PLL-HEC affinity membranes are used to adsorb bilirubin from the phosphate buffer solutions. The adsorption mechanism of bilirubin and the effects of temperature and ionic strength on adsorption were investigated by batch experiments. These membranes were also set in stack and used to adsorb bilirubin. The results showed that the quicker adsorption equilibrium was attained and these membranes exhibited high binding affinity capacities for bilirubin

Cosmology from HI galaxy surveys with the SKA

The Square Kilometer Array (SKA) has the potential to produce galaxy redshift surveys which will be competitive with other state of the art cosmological experiments in the next decade. In this chapter we summarise what capabilities the first and the second phases of the SKA will be able to achieve in its current state of design. We summarise the different cosmological experiments which are outlined in further detail in other chapters of this Science Book. The SKA will be able to produce competitive Baryonic Oscillation (BAOs) measurements in both its phases. The first phase of the SKA will provide similar measurements as optical and IR experiments with completely different systematic effects whereas the second phase being transformational in terms of its statistical power. The SKA will produce very accurate Redshift Space Distortions (RSD) measurements, being superior to other experiments at lower redshifts, due to the large number of galaxies. Cross correlations of the galaxy redshift data from the SKA with radio continuum surveys and optical surveys will provide extremely good calibration of photometric redshifts as well as extremely good bounds on modifications of gravity. Basing on a Principle Component Analysis (PCA) approach, we find that the SKA will be able to provide competitive constraints on dark energy and modified gravity models. Due to the large area covered the SKA it will be a transformational experiment in measuring physics from the largest scales such as non-Gaussian signals from $\textrm{f}_{\textrm{nl}}$. Finally, the SKA might produce the first real time measurement of the redshift drift. The SKA will be a transformational machine for cosmology as it grows from an early Phase 1 to its full power

Synergy between the Large Synoptic Survey Telescope and the Square Kilometre Array

We provide an overview of the science benefits of combining information from the Square Kilometre Array (SKA) and the Large Synoptic Survey Telescope (LSST). We first summarise the capabilities and timeline of the LSST and overview its science goals. We then discuss the science questions in common between the two projects, and how they can be best addressed by combining the data from both telescopes. We describe how weak gravitational lensing and galaxy clustering studies with LSST and SKA can provide improved constraints on the causes of the cosmological acceleration. We summarise the benefits to galaxy evolution studies of combining deep optical multi-band imaging with radio observations. Finally, we discuss the excellent match between one of the most unique features of the LSST, its temporal cadence in the optical waveband, and the time resolution of the SKA

A Versatile Route for the Synthesis of Nickel Oxide Nanostructures Without Organics at Low Temperature

Nickel oxide nanoparticles and nanoflowers have been synthesized by a soft reaction of nickel powder and water without organics at 100 °C. The mechanism for the formation of nanostructures is briefly described in accordance with decomposition of metal with water giving out hydrogen. The structure, morphology, and the crystalline phase of resulting nanostructures have been characterized by various techniques. Compared with other methods, the present method is simple, fast, economical, template-free, and without organics. In addition, the approach is nontoxic without producing hazardous waste and could be expanded to provide a general and convenient strategy for the synthesis of nanostructures to other functional nanomaterials

Current knowledge, challenges and innovations in developmental pharmacology: A combined conect4children Expert Group and European Society for Developmental, Perinatal and Paediatric Pharmacology White Paper

Developmental pharmacology describes the impact of maturation on drug disposition (pharmacokinetics, PK) and drug effects (pharmacodynamics, PD) throughout the paediatric age range. This paper, written by a multidisciplinary group of experts, summarizes current knowledge, and provides suggestions to pharmaceutical companies, regulatory agencies and academicians on how to incorporate the latest knowledge regarding developmental pharmacology and innovative techniques into neonatal and paediatric drug development. Biological aspects of drug absorption, distribution, metabolism and excretion (ADME) throughout development are summarized. Although this area made enormous progress during the last two decades, remaining knowledge gaps were identified. Minimal risk and burden designs allow for optimally informative but minimally invasive PK sampling, while concomitant profiling of drug metabolites may provide additional insight in the unique PK behavior in children. Furthermore, developmental PD needs to be considered during drug development, which is illustrated by disease- and/or target organ-specific examples. Identifying and testing PD targets and effects in special populations, and application of age- and/or population-specific assessment tools are discussed. Drug development plans also need to incorporate innovative techniques like preclinical models to study therapeutic strategies, and shift from sequential enrollment of subgroups, to more rational designs. To stimulate appropriate research plans, illustrations of specific PK/PD-related as well as drug safety-related challenges during drug development are provided. The suggestions made in this joint paper of the Innovative Medicines Initiative conect4children Expert group on Developmental Pharmacology and the European Society for Developmental, Perinatal and Paediatric Pharmacology, should facilitate all those involved in drug development

A Novel Xenograft Model in Zebrafish for High-Resolution Investigating Dynamics of Neovascularization in Tumors

Tumor neovascularization is a highly complex process including multiple steps. Understanding this process, especially the initial stage, has been limited by the difficulties of real-time visualizing the neovascularization embedded in tumor tissues in living animal models. In the present study, we have established a xenograft model in zebrafish by implanting mammalian tumor cells into the perivitelline space of 48 hours old Tg(Flk1:EGFP) transgenic zebrafish embryos. With this model, we dynamically visualized the process of tumor neovascularization, with unprecedented high-resolution, including new sprouts from the host vessels and the origination from VEGFR2+ individual endothelial cells. Moreover, we quantified their contributions during the formation of vascular network in tumor. Real-time observations revealed that angiogenic sprouts in tumors preferred to connect each other to form endothelial loops, and more and more endothelial loops accumulated into the irregular and chaotic vascular network. The over-expression of VEGF165 in tumor cells significantly affected the vascularization in xenografts, not only the number and size of neo-vessels but the abnormalities of tumor vascular architecture. The specific inhibitor of VEGFR2, SU5416, significantly inhibited the vascularization and the growth of melanoma xenografts, but had little affects to normal vessels in zebrafish. Thus, this zebrafish/tumor xenograft model not only provides a unique window to investigate the earliest events of tumoral neoangiogenesis, but is sensitive to be used as an experimental platform to rapidly and visually evaluate functions of angiogenic-related genes. Finally, it also offers an efficient and cost-effective means for the rapid evaluation of anti-angiogenic chemicals

DNA microarray revealed and RNAi plants confirmed key genes conferring low Cd accumulation in barley grains

List of genes down-regulated in both W6nk2 and Zhenong8 after 15 days exposure to 5 ΟM Cd. (DOC 130 kb

Association between serum keptin concentrations and insulin resistance: A population-based study from China

BACKGROUND Insulin resistance contributes to the cardio-metabolic risk. The effect of leptin in obese and overweight population on insulin resistance was seldom reported. METHODS A total of 1234 subjects (572 men and 662 women) aged ≥18 y was sampled by the procedure. Adiposity measures included BMI, waist circumference, hip circumference, WHR, upper arm circumference, triceps skinfold and body fat percentage. Serum leptin concentrations were measured by an ELISA method. The homeostasis model (HOMA-IR) was applied to estimate insulin resistance. RESULTS In men, BMI was the variable which was most strongly correlated with leptin, whereas triceps skinfold was most sensitive for women. More importantly, serum leptin levels among insulin resistant subjects were almost double compared to the subjects who had normal insulin sensitivity at the same level of adiposity in both men and women, after controlling for potential confounders. In addition, HOMA-IR increased significantly across leptin quintiles after adjustment for age, BMI, total energy intake, physical activity and smoking status in both men and women (p for trend <0.0001). CONCLUSIONS There was a significant association between HOMA-IR and serum leptin concentrations in Chinese men and women, independently of adiposity levels. This may suggest that serum leptin concentration is an important predictor of insulin resistance and other metabolic risks irrespective of obesity levels. Furthermore, leptin levels may be used to identify the cardio-metabolic risk in obese and overweight population.Hui Zuo, Zumin Shi, Baojun Yuan, Yue Dai, Gaolin Wu, Akhtar Hussai