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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1990), S. 176-178 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies of protein metabolism with stable isotopes require determination of the ‘natural’ isotopic enrichment in tissues. This has previously been determined by taking a pre-test muscle biopsy or by using the isotopic enrichment of a separate control group of subjects. In this study we have measured and compared the “natural” 13C enrichment of leucine in plasma protein and muscle protein in 14 subjects. The mean enrichment of leucine (δ13CPDB) in muscle protein, -26.627, was not significantly different from that in plasma protein, -27.152. The data indicate that the 13C enrichment of leucine in plasma protein reflects that of muscle protein and provides an attractive alternative to an additional muscle biopsy in studies of protein metabolism with stable isotopes.
    Additional Material: 1 Tab.
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  • 2
    ISSN: 0959-8103
    Keywords: poly(p-phenylene-α,α′-diphenyl vinylene) ; poly(p-phenylene-α-phenyl vinylene) ; calcium ; interface ; photoemission spectroscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: We have investigated the interface formation of Ca with poly(p-phenylene α,α′-diphenyl vinylene) (PPV-DP) and poly(p-phenylene α-phenyl vinylene) (PPV-P) using X-ray photoemission spectroscopy (XPS). Similarly to our earlier findings in metal/PPV interface formation, the O 1s peak shifted toward a lower binding energy as soon as Ca was deposited on to the polymers. This was accompanied by the formation of Ca—O, suggesting a chemical origin for the O 1s shift. By contrast, the C 1s peak shift toward a lower binding energy was observed relatively later, after about 4 Å of Ca deposition. At the same time, a new C 1s component became noticable at about -1.5 eV relative to the initial C 1s peak. This component signifies the possibility of polymer disruption by the Ca atoms to form Ca—C species. The C 1s peak shift is attributed to Ca induced surface band bending and barrier formation as in the case of metal/PPV interface formation. The disruption of the polymer may also induce changes in the interface electronic states and contribute to the C 1s peak shift. From the intensity attenuation analysis, we conclude that the initial 15 Å of Ca overlayer is contaminated by the Ca—O and Ca—C species and the overlayer is pure beyond 15 Å of Ca coverage.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 25 (1991), S. 407-420 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Albumin and fibrinogen were competitively adsorbed onto dimethyldichlorosilane-coated glass (DDS-glass) and platelet activation was examined as a function of the surface fibrinogen concentration. The weight ratio of albumin to fibrinogen in the adsorption solution was varied from 10 to 700. Platelet activation was quantitated by the area and circularity of spread platelets. When the DDS-glass was coated with albumin alone, platelets were only contact adherent and could not spread at all. After competitive adsorption of fibrinogen and albumin, however, platelets were able to spread on the surface. Platelet activation increased linearly as the surface fibrinogen concentration increased up to 0.02 μg/cm2. Platelets were able to activate fully if the surface fibrinogen concentration was 0.02 μg/cm2 or higher, even though the surface was dominated by albumin. It appears that platelets can activate fully as long as only a small fraction (2-15%) of the surface is covered with tightly bound fibrinogen.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 26 (1992), S. 373-391 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Photoreactive poly(ethy1ene glycol) (PEG) was synthesized by reacting 4-fluoro- 3-nitrophenyl azide (FNPA) with sodium salt of PEG. The synthesized 4-azido-2- nitrophenyl PEG (ANP-PEG) was charac- terized by 1H-NMR, IR, and UV spectro- scopy. ANP-PEG was grafted to dimethyldichlorosilane-coated glass (DDS-glass) by photolysis without any premodification of the surface. The effects of various grafting factors, such as the polymer adsorption time, concentration of ANP-PEG, and UV irradiation time, on the PEG grafting efficiency were examined. The PEG-grafted DDS-glass was characterized by measuring surface free energies, surface-induced platelet activation, and the relative amount of PEG grafted on the surface using electron spectroscopy for chemical analysis (ESCA). Platelet adhesion and activation was analyzed by measuring the number and spread area of adherent platelets. The results showed that ANP-PEG had to be adsorbed onto DDS-glass for at least 12 h before photolysis for the maximum grafting efficiency. No platelets could adhere to the PEG-grafted DDS-glass, if the bulk concentration of ANP-PEG in the adsorption solution was between 1 mg/mL and 10 mg/mL. Above 10 mg/mL, platelet activation gradually increased and reached the maximum at 30 mg/mL. Our data indicate that the grafting of ANP-PEG requires careful control of the grafting conditions and that the grafted PEG can prevent surface-induced platelet activation.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 89-98 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: We report on our recent x-ray photoemission spectroscopy investigations of the interface formation of metals with poly(p-phenylene vinylene) (PPV) prepared under various conditions. We have found that during deposition the metal reacts with residual hydroxyl groups in the polymer. In addition, we have found that Schottky barrier formation and the associated band bending depend strongly on surface preparation. In the case of Al deposition, samples converted in situ, containing 5% surface oxygen, show band bending that depends on the thickness of the metal overlayer, with effects arising after as little as 1 Å of metal. On the other hand, a sample converted ex situ, with 10% surface oxygen, is insensitive to aluminium deposition. We feel that surface impurities and adsorbed species may delay Schottky barrier formation by acting as a buffer layer that prevents the PPV substrate from interacting with the growing layer of Al. By contrast, the Ca/PPV surface exhibits delayed band bending, with strong interactions between surface oxygen and Ca. Our results indicate that band bending at the metal/PPV interface is governed by the metallicity of the metal overlayer, which itself is influenced by the interface reaction of the deposited metal with the PPV substrate or the surface residual impurities. Finally, the degree of band bending observed did not correlate directly with the differences in work functions between the metals and PPV.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 831-832 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H NMR spectra of 1,3-benzodithiole and eight derivatives have been analysed. Signals of the protons in positions 4 and 7 are shifted downfield compared with those for the protons in positions 5 and 6. The inter-ring proton-proton couplings have been determined.
    Additional Material: 2 Tab.
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