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  • 1
    ISSN: 1432-1076
    Schlagwort(e): Key words Eosinophil cationic protein ; Eosinophils ; Crohn disease ; Ulcerative colitis ; Disease activity indices.
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The aim of this study was to compare in vitro release of eosinophil cationic protein (ECP) from peripheral blood eosinophils during active phases of childhood Crohn disease (CD) and ulcerative colitis with phases of remission. Ten children with CD and nine children with ulcerative colitis were investigated during 55 and 56 clinical visits, respectively. Each patient was investigated during at least one phase of clinically active disease and one phase of remission. Disease activity was assessed by means of the Paediatric Crohn Disease Activity Index (PCDAI) in Crohn disease and according to the clinical activity index of Rachmilewitz in ulcerative colitis. On an intra-individual basis, in vitro ECP release was significantly higher (P 〈 0.001) during active phases of CD and ulcerative colitis than in phases of remission (CD:median: 24.5 μg/l, range 16.0–61.2 versus median: 5.7 μg/l, range 2.0–16.7; ulcerative colitis: 14.8 μg/l, 8.3–39.8 versus 4.9 μg/l, 2.0–9.9). On an inter-individual basis, in CD and ulcerative colitis a strong and highly significant correlation was observed between disease activity indices and in vitro release of ECP from peripheral eosinophils (r = 0.89, P 〈 0.0001 and r = 0.82, P 〈 0.0001, respectively). Conclusion These results show that in vitro ECP release from peripheral eosinophils reflects disease activity in both CD and ulcerative colitis and therefore can be used as a new appropriate laboratory parameter for assessment of disease activity in chronic inflammatory bowel disease.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 275 (1997), S. 1018-1026 
    ISSN: 1435-1536
    Schlagwort(e): Key words Water ; desorption ; multilayer adsorption ; water structure ; water cooperativity ; H-bonds ; IR spectroscopy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract  The structure of water adsorbed in cellulose acetate membranes is determined by the fundamental and overtone IR spectra. Water is weakly H-bonded to ester and ether groups of the membrane, at low water contents. With increasing water content, more and more liquid-like water is observed. In addition, a small amount of a third type of water is present. The amounts of these three species are estimated from the spectra. At high water contents, the amount of liquid-like water increases strongly. The H-bond cooperativity of such water may be the cause for this increase and for the common anomalous water adsorption isotherms. The H-bond energy of the first hydration shell is relatively small, contrary to the anomalous large adsorption heats ΔH ad. This could be described by larger van der Waals interactions between this type of water and the membrane groups as a result of a higher coordination number compared with Z=4.4 of liquid-like water. This model is in agreement with the decrease of ΔH ad with increasing water sorption reaching the evaporization enthalpy of pure water at high water contents.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 275 (1997), S. 964-971 
    ISSN: 1435-1536
    Schlagwort(e): Key words Membranes ; water desorption ; desorption heat ; adsorption mechanism ; multilayer adsorption ; partition coefficients ; water cooperativity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract  The water desorption isotherms are determined in three cellulose acetate membranes with different acetyl content as a function of p/p 0 at 10–40 °C. The partition coefficients (adsorbed water over water pressure) show a minimum at p/p 0=0.5–0.6. This indicates a two energy mechanism. The agreement of our results with the BET adsorption isotherms only till p/p 0〈0.3 shows that a two energy adsorption mechanism is valid only for small water contents, probably one hydrate layer and a second more liquid-like water layer. At large p/p 0, the adsorbed water becomes more and more liquid like by polarization of the hydrogen bonds. The heat of desorption is larger than the vaporization heat of water ΔH vap(H2O). It decreases with increasing water content asymptotically to ΔH vap(H2O). The cause may be a larger van der Waals interaction of the hydrate layer due to coordination numbers larger than 4.4 as in liquid water. Additionally, we found a hole adsorption process by sorbing unpolar solvents. The water and methonal adsorption are 100 times larger due to a swelling mechanism depending on the number of acetyl groups in the membranes. The amounts of n-alcohols sorbed decrease with their chain length.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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