807 research outputs found

    Diagnostic biologique des candidoses

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    Candidiasis is the most common fungal infection in humans. Conventional techniques are usually sufficient for the diagnosis of superficial candidiasis. For deep-seated or systemic candidiasis, blood cultures still represent the “gold standard”, although their sensitivity can be overtaken. In recent decades, numerous alternative tests have been developed to overcome this lack of sensitivity. These techniques allow the detection of antibodies, antigens, metabolites or nucleic acids. In most cases, serological results have to be interpretated according to the immune status of patients. Detection of antibodies alone is often poorly contributive to the diagnosis, except when this is associated with the detection of circulating antigens. Thus, the detection of circulating mannans is useful in the diagnosis of infections caused by the most frequent Candida species; the sensitivity of this test increases with the repetition of samplings and the joint detection of anti-mannan antibodies. Besides, detection of β(1.3)-D glucans, alone or in association with the detection of mannans, may be useful for early diagnosis of deep-seated candidiasis. Molecular biology helps us to diagnose deep-seated candidiasis without referring to the patient\u27s immune status. With the newly commercialized kits, molecular detection of Candida should expand in laboratories. In the same way, proteomic analysis by MALDI-TOF allows to substantially shorten the time for identification of isolated yeasts. Modern methods of molecular typing, which are based on the analysis of genome variability, replaced phenotypic techniques. Although insufficiently standardized, they represent a powerful tool to better understand the epidemiology of Candida infections

    In situ cleaning of diagnostic first mirrors: An experimental comparison between plasma and laser cleaning in ITER-relevant conditions

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    This paper presents an experimental comparison between the plasma cleaning and the laser cleaning techniques of diagnostic first mirrors (FMs). The re-deposition of contaminants sputtered from a tokamak first wall onto FMs could dramatically decrease their reflectance in an unacceptable way for the proper functioning of plasma diagnostic systems. Therefore, suitable in situ cleaning solutions will be required to recover the FMs reflectance in ITER. Currently, plasma cleaning and laser cleaning are considered the most promising solutions. In this work, a set of ITER-like rhodium mirrors contaminated with materials tailored to reproduce tokamak redeposits is employed to experimentally compare plasma and laser cleaning against different criteria (reflectance recovery, mirror integrity, time requirement). We show that the two techniques present different complementary features that can be exploited for the cleaning of ITER FMs. In particular, plasma cleaning ensures an excellent reflectance recovery in the case of compact contaminants, while laser cleaning is faster, gentler, and more effective in the case of porous contaminant. In addition, we demonstrate the potential benefits of a synergistic solution which combines plasma and laser cleaning to exploit the best features of each technique

    Surface chemistry of rare-earth oxide surfaces at ambient conditions: reactions with water and hydrocarbons

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    Rare-earth (RE) oxide surfaces are of significant importance for catalysis and were recently reported to possess intrinsic hydrophobicity. The surface chemistry of these oxides in the low temperature regime, however, remains to a large extent unexplored. The reactions occurring at RE surfaces at room temperature (RT) in real air environment, in particular, in presence of polycyclic aromatic hydrocarbons (PAHs), were not addressed until now. Discovering these reactions would shed light onto intermediate steps occurring in automotive exhaust catalysts before reaching the final high operational temperature and full conversion of organics. Here we first address physical properties of the RE oxide, nitride and fluoride surfaces modified by exposure to ambient air and then we report a room temperature reaction between PAH and RE oxide surfaces, exemplified by tetracene (C18H12) on a Gd2O3. Our study evidences a novel effect-oxidation of higher hydrocarbons at significantly lower temperatures (similar to 300 K) than previously reported (>500 K). The evolution of the surface chemical composition of RE compounds in ambient air is investigated and correlated with the surface wetting. Our surprising results reveal the complex behavior of RE surfaces and motivate follow-up studies of reactions between PAH and catalytic surfaces at the single molecule level
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