257 research outputs found

    Geotemporal Twitter Demographics

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    The study and application of demographic data are widespread in both industry and academia, with applications ranging from demographic profiling to supply and demand modelling. Yet, while there exist numerous applications, in recent years demographics has seen few major developments. This may in part reflect continuing dependence on traditional population data, such as the UK Census of Population. Given these limitations, there is an increased interest in the potential of new forms of data such as are collected from online social networks or by utilities companies. Here, we demonstrate how, given sufficient consideration, Twitter data may be employed as an effective source of population insight

    Estimating the Prevalence of Shared Accommodation across the UK from Big Data

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    This paper introduces a new means of measuring the proportion of shared accommodation within UK neighbourhoods using linked administrative and consumer data. An address-level multi-person household indicator (MHI) was produced for individual years spanning 1997 to 2016. Crucially, this new indicator enables fine-grained spatial analysis of trends in house-sharing outside of decennial census years. This abstract discusses the purpose and derivation methodology of the MHI, before illustrating how it can be used and outlining some future research and policy applications

    Pixel sensitivity variation in a CdTe-Medipix2 detector using poly-energetic x-rays

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    We have a 1-mm-thick cadmium telluride (CdTe) sensor bump-bonded to a Medipix2 readout chip. This detector has been characterized using a poly-energetic x-ray beam. Open beam images (i.e. without an attenuating specimen between the x-ray source and the detector) have been acquired at room temperature using the MARS-CT system. Profiles of various rows and columns were analyzed for one hundred, 35-ms exposures taken with a bias voltage of -300 V (operating in electron collection mode). A region of increased sensitivity is observed around the edges of the detector. A reasonably periodic, repeatable variation in pixel sensitivity is observed. Some small regions with very low sensitivity and others with zero signals are also observed. Surrounding these regions are circular rings of pixels with higher counts. At higher flux (higher tube current in the x-ray source) there is evidence of saturation of the detector assembly. In this paper we present our understanding of the origin of these features and demonstrate the improved image quality obtained after correcting for these variations

    Design, Implementation and First Measurements with the Medipix Neutron Camera in CMS

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    The Medipix detector is the first device dedicated to measuring mixed-field radiation in the CMS cavern and able to distinguish between different particle types. Medipix2-MXR chips bump bonded to silicon sensors with various neutron conversion layers developed by the IEAP CTU in Prague were successfully installed for the 2008 LHC start-up in the CMS experimental and services caverns to measure the flux of various particle types, in particular neutrons. They have operated almost continuously during the 2010 run period, and the results shown here are from the proton run between the beginning of July and the end of October 2010. Clear signals are seen and different particle types have been observed during regular LHC luminosity running, and an agreement in the measured flux rate is found with the simulations. These initial results are promising, and indicate that these devices have the potential for further and future LHC and high energy physics applications as radiation monitoring devices for mixed field environments, including neutron flux monitoring. Further extensions are foreseen in the near future to increase the performance of the detector and its coverage for monitoring in CMS.Comment: 15 pages, 16 figures, submitted to JINS

    Perspectives from those involved in healthy stadia

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    Healthy stadia is a growing agenda across industry and in turn academia. In this era of growth, much of the research literature is primarily sourced from academics with little contribution from applied and industry stakeholders. As such, the editors have sought to offer practitioners a platform to share novel projects, perspectives and preliminary intervention evaluation findings. This applied article intends to share evaluation and insight from applied practice, to encourage closer debate between the academic community and applied industry

    Sprinting with an amputation: Some race-based lower-limb step observations.

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    BACKGROUND: T44 sprinting with an amputation is still in a state of relative infancy. Future scope for athletic training and prosthetic limb development may be assisted with a better understanding of information derived from T44 athletes when under race-based conditions. OBJECTIVES: To investigate the behaviour of step count and step frequency when under competitive conditions. STUDY DESIGN: The study comprises two elements: (1) a video-based analysis of race-based limb-to-limb symmetry and (2) a video-based analysis of race-based step count. METHODS: Video analysis of several major events from 1996-2012 are assessed for step count and step limb-to-limb symmetry characteristics. RESULTS: The video analysis highlights limb-to-limb imbalances greater than those indicated in the previous literature. A low step count is determined to be desirable for success in the 100-m event. CONCLUSION: Future analysis of athletes with a lower-limb amputation would be worthwhile when placed under race-based conditions as the limb-to-limb behaviour is more exaggerated than those seen in typical studies held within a laboratory setting. The within-event behaviour of step counts requires further investigation to establish where these take place or whether it is a cumulative step length issue. CLINICAL RELEVANCE: This article increases the understanding of the race-based behaviour of amputee athletes and provides more information to contribute to any discussions on the performance of lower-limb prostheses

    How can we optimise inhaled beta2 agonist dose as ā€˜relieverā€™ medicine for wheezy pre-school children? Study protocol for a randomised controlled trial

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    Background: Asthma is a common problem in children and, if inadequately controlled, may seriously diminish their quality of life. Inhaled short-acting beta2 agonists such as salbutamol are usually prescribed as ā€˜relieverā€™ medication to help control day-to-day symptoms such as wheeze. As with many medications currently prescribed for younger children (defined as those aged 2 years 6 months to 6 years 11 months), there has been no pre-licensing age-specific pharmacological testing; consequently, the doses currently prescribed (200ā€“1000 Ī¼g) may be ineffective or likely to induce unnecessary side effects. We plan to use the interrupter technique to measure airway resistance in this age group, allowing us for the first time to correlate inhaled salbutamol dose with changes in clinical response. We will measure urinary salbutamol levels 30 min after dosing as an estimate of salbutamol doses in the lungs, and also look for genetic polymorphisms linked to poor responses to inhaled salbutamol. Methods: This is a phase IV, randomised, controlled, observer-blinded, single-centre trial with four parallel groups (based on a sparse sampling approach) and a primary endpoint of the immediate bronchodilator response to salbutamol so that we can determine the most appropriate dose for an individual younger child. Simple randomisation will be used with a 1:1:1:1 allocation. Discussion: The proposed research will exploit simple, non-invasive and inexpensive tests that can mostly be performed in an outpatient setting in order to help develop the evidence for the correct dose of salbutamol in younger children with recurrent wheeze who have been prescribed salbutamol by their doctor. Trial registration: EudraCT2014-001978-33, ISRCTN15513131. Registered on 8 April 2015

    Dissolution of ionizable water-insoluble drugs: The combined effect of pH and surfactant

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    This study reports the results of the combined effect of pH and surfactant on the dissolution of piroxicam (PX), an ionizable water-insoluble drug in physiological pH. The intrinsic dissolution rate ( J total ) of PX was measured in the pH range from 4.0 to 7.8 with 0%, 0.5%, and 2.0% sodium lauryl sulfate (SLS) using the rotating disk apparatus. Solubility ( c total ) was also measured in the same pH and SLS concentration ranges. A simple additive model including an ionization (PX ā†” H + + PX āˆ’ ) and two micellar solubilization equilibria (PX + micelle ā†” [PX] micelle , PX āˆ’ + micelle ā†” [PX āˆ’ ] micelle ) were considered in the convective diffusion reaction model. J total and c total of PX increased with increasing pH and SLS concentration in an approximately additive manner. Nonlinear regression analysis showed that observed experimental data were well described with the proposed model ( r 2 = 0.86, P < 0.001 for J total and r 2 = 0.98, P < 0.001 for c total ). The p K a value of 5.63 Ā± 0.02 estimated from c total agreed well with the reported value. The micellar solubilization equilibrium coefficient for the unionized drug was estimated to be 348 Ā± 77 L/mol, while the value for the ionized drug was nearly equal to zero. The diffusion coefficients of the species PX, PX āˆ’ , and [PX] micelle were estimated from the experimental results as (0.93 Ā± 0.35) Ɨ 10 āˆ’5 , (1.4 Ā± 0.30) Ɨ 10 āˆ’5 , and (0.59 Ā± 0.21) Ɨ 10 āˆ’5 cm 2 /s, respectively. The total flux enhancement is less than the total solubility enhancement due to the smaller diffusion coefficients of the micellar species. This model may be useful in predicting the dissolution of an ionizable water insoluble drug as a function of pH and surfactant and for establishing in vitro ā€“ in vivo correlations, IVIVC, for maintaining bioequivalence of drug products. Ā© 2000 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 89: 268ā€“274, 2000Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/34499/1/14_ftp.pd

    PPARĪ± and PPARĪ³ activation is associated with pleural mesothelioma invasion but therapeutic inhibition is ineffective

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    Mesothelioma is a cancer that typically originates in the pleura of the lungs. It rapidly invades the surrounding tissues, causing pain and shortness of breath. We compared cell lines injected either subcutaneously or intrapleurally and found that only the latter resulted in invasive and rapid growth. Pleural tumors displayed a transcriptional signature consistent with increased activity of nuclear receptors PPARĪ± and PPARĪ³ and with an increased abundance of endogenous PPAR-activating ligands. We found that chemical probe GW6471 is a potent, dual PPARĪ±/Ī³ antagonist with anti-invasive and anti-proliferative activity in vitro. However, administration of GW6471 at doses that provided sustained plasma exposure levels sufficient for inhibition of PPARĪ±/Ī³ transcriptional activity did not result in significant anti-mesothelioma activity in mice. Lastly, we demonstrate that the in vitro anti-tumor effect of GW6471 is off-target. We conclude that dual PPARĪ±/Ī³ antagonism alone is not a viable treatment modality for mesothelioma
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