182 research outputs found

    New process for the production of permeate powders without spray dryer

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    An innovative process scheme for the production of dairy permeate powders was tested at the pilot scale. It includes: (i) overconcentration of the permeate concentrate from 60 to 80% w/w dry matter (DM) content; (ii) granulation of the overconcentrate with powder up to 88% DM; and (iii) drying of the granules up to 97% DM.The quality of the resulting powder was comparable to a standard powder produced using conventional technologies. Furthermore, considering energy required for water removal, the new process led to significant savings: they were estimated in the range of 10.7 to 23.5% and up to 32% when taking into account the whole production process or the drying step alone, respectively

    Quantification de l'architecture osseuse par microtomographie 3D utilisant le rayonnement synchrotron

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    Nous présentons un système de microtomographie 3D par rayonnement synchrotron développé à l'ESRF de Grenoble, en vue de l'analyse de la structure trabéculaire osseuse. Ce système permet d'acquérir de façon non destructive des images 3D d'échantillons osseux , ayant des voxels isotrope de 6.65 μm. Afin de caractériser la structure 3D de l'os, des paramètres quantitatifs sont extraits de ces images. Les paramètres morphologiques et topologiques utilisés en histomorphométrie, sont calculés sur les différentes coupes du volume. La variabilité des paramètres dans l'échantillon et la nécessité d'une analyse réellement tridimensionnelle sont soulignés. L'influence de la résolution spatiale sur l'exactitude des paramètres calculés est également examinée

    FAME : A new beamline for X-ray absorption investigations of very-diluted systems of environmental, material and biological interests

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    International audienceFAME is the French Absorption spectroscopy beamline in Material and Environmental sciences at the ESRF (France), operational since September 2002. Technically speaking, the source is a 0.85 T bending magnet and the main optical element is a two-crystals monochromator using either Si(111) or Si(220) monocrystals so that the available energy ranges from 4 to 40 keV. The first crystal is liquid nitrogen cooled in order to avoid a thermal bump and thus preserve the energy resolution. The second crystal is dynamically bent during the energy scan in order to focus the beam in the horizontal plane. Two bendable mirrors are located before and after the monochromator, for beam-collimation (to optimize the energy resolution) and vertical focalization, respectively. During scans, the beam on the sample is kept constant in position and size (around 150 × 200 μm2, V × H). The high flux on the sample combined with the sensitivity of our 30-elements fluorescence detector allow to decrease the detection limit down to 10 ppm or around less than a monolayer. Moreover, quick-EXAFS acquisition is operational: the acquisition time may be reduced down to 30s

    Maintenance of active chromatin states by HMGN2 is required for stem cell identity in a pluripotent stem cell model

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    Background: Members of the HMGN protein family modulate chromatin structure and influence epigenetic modifications. HMGN1 and HMGN2 are highly expressed during early development and in the neural stem/progenitor cells of the developing and adult brain. Here, we investigate whether HMGN proteins contribute to the chromatin plasticity and epigenetic regulation that is essential for maintaining pluripotency in stem cells. Results: We show that loss of Hmgn1 or Hmgn2 in pluripotent embryonal carcinoma cells leads to increased levels of spontaneous neuronal differentiation. This is accompanied by the loss of pluripotency markers Nanog and Ssea1, and increased expression of the pro-neural transcription factors Neurog1 and Ascl1. Neural stem cells derived from these Hmgn-knockout lines also show increased spontaneous neuronal differentiation and Neurog1 expression. The loss of HMGN2 leads to a global reduction in H3K9 acetylation, and disrupts the profile of H3K4me3, H3K9ac, H3K27ac and H3K122ac at the Nanog and Oct4 loci. At endodermal/mesodermal genes, Hmgn2-knockout cells show a switch from a bivalent to a repressive chromatin configuration. However, at neuronal lineage genes whose expression is increased, no epigenetic changes are observed and their bivalent states are retained following the loss of HMGN2. Conclusions: We conclude that HMGN1 and HMGN2 maintain the identity of pluripotent embryonal carcinoma cells by optimising the pluripotency transcription factor network and protecting the cells from precocious differentiation. Our evidence suggests that HMGN2 regulates active and bivalent genes by promoting an epigenetic landscape of active histone modifications at promoters and enhancers

    A low-cost HPV immunochromatographic assay to detect high-grade cervical intraepithelial neoplasia

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    Objective To evaluate the reproducibility and accuracy of the HPV16/18-E6 test. Methods The study population was comprised of 448 women with a previously abnormal Pap who were referred to the Barretos Cancer Hospital (Brazil) for diagnosis and treatment. Two cervical samples were collected immediately before colposcopy, one for the hr-HPV-DNA test and cytology and the other for the HPV16/18-E6 test using high-affinity monoclonal antibodies (mAb). Women with a histologic diagnosis of cervical intraepithelial neoplasia grade 2 or 3 were considered to be positive cases. Different strategies using a combination of screening methods (HPV-DNA) and triage tests (cytology and HPV16/18-E6) were also examined and compared. Results The HPV16/18-E6 test exhibited a lower positivity rate compared with the HPV-DNA test (19.0% vs. 29.3%, p<0.001) and a moderate/high agreement (kappa = 0.68, 95% CI: 0.60-0.75). It also exhibited a significantly lower sensitivity for CIN2+ and CIN3+ detection compared to the HPV-DNA test and a significantly higher specificity. The HPV16/18-E6 test was no different from cytology in terms of sensitivity, but it exhibited a significantly higher specificity in comparison to ASCH+. A triage test after HPV-DNA detection using the HPV16/18-E6 test exhibited a significantly higher specificity compared with a triage test of ASCH+ to CIN2+ (91.8% vs. 87.4%, p = 0.04) and CIN3+ (88.6% vs. 84.0%, p = 0.05). Conclusion The HPV16/18-E6 test exhibited moderate/high agreement with the HPV-DNA test but lower sensitivity and higher specificity for the detection of CIN2+ and CIN3+. In addition, its performance was quite similar to cytology, but because of the structural design addressed for the detection of HPV16/18-E6 protein, the test can miss some CIN2/3+ lesions caused by other high-risk HPV types.Cancer Prevention Department, Center for the Researcher Support and Pathology Department of the Barretos Cancer Hospital. This study was supported by CNPq 573799/2008-3 and FAPESP 2008/57889-1info:eu-repo/semantics/publishedVersio

    The ThomX project status

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    Work supported by the French Agence Nationale de la recherche as part of the program EQUIPEX under reference ANR-10-EQPX-51, the Ile de France region, CNRS-IN2P3 and Université Paris Sud XI - http://accelconf.web.cern.ch/AccelConf/IPAC2014/papers/wepro052.pdfA collaboration of seven research institutes and an industry has been set up for the ThomX project, a compact Compton Backscattering Source (CBS) based in Orsay - France. After a period of study and definition of the machine performance, a full description of all the systems has been provided. The infrastructure work has been started and the main systems are in the call for tender phase. In this paper we will illustrate the definitive machine parameters and components characteristics. We will also update the results of the different technical and experimental activities on optical resonators, RF power supplies and on the electron gun
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