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  • 1
    Electronic Resource
    Electronic Resource
    Oxford UK : Blackwell Science Ltd
    Alimentary pharmacology & therapeutics 15 (2001), S. 0 
    ISSN: 1365-2036
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Drug hepatotoxicity is a potentially serious adverse reaction of antiretroviral therapy in human immunodeficiency virus-infected patients. The impact of this problem in the routine treatment of patients with human immunodeficiency virus infection is poorly defined.〈section xml:id="abs1-2"〉〈title type="main"〉Objectives:Our aim was to determine what clinical features are associated with hepatotoxicity in human immunodeficiency virus-infected patients receiving antiretroviral therapy.〈section xml:id="abs1-3"〉〈title type="main"〉Methods:Consecutive patients in a primary care-based human immunodeficiency virus clinic were evaluated for hepatotoxicity. Clinic records were used to obtain patient characteristics, as well as independent variables including CD4+ count, coexisting hepatitis C and current alcohol use.〈section xml:id="abs1-4"〉〈title type="main"〉Results:Sixty-five patients taking antiretroviral therapy were evaluated. Twenty-four were identified to have antiretroviral hepatotoxicity. An age over 40 years (P=0.019), an absolute CD4+ count of less than 310 cells/mL (P=0.002) and coexisting hepatitis C infection (P=0.035) were significantly associated with hepatotoxicity. Patients older than 40 years had a sevenfold increased risk (risk ratio, 6.9; 95% confidence interval, 1.7–27.3) and those with an absolute CD4+ count of less than 310 cells/mL had a tenfold increased risk (risk ratio, 10.2; 95% confidence interval, 2.5–41.9) for antiretroviral hepatotoxicity, in comparison with those who were younger or who had a greater absolute CD4+ count. Of the eight patients documented to have coexisting hepatitis C infection, six (75%) were in the antiretroviral hepatotoxicity group.〈section xml:id="abs1-5"〉〈title type="main"〉Conclusions:An age older than 40 years and an absolute CD4+ count of less than 310 cells/mL were significantly associated with antiretroviral-induced hepatotoxicity. The majority of our patients with chronic hepatitis C had hepatotoxicity from antiretroviral therapy.
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 202 (1964), S. 1005-1005 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Over the limited range of concentrations investigated, the rate of polymerization, Rp, was found to be independent, within the limits of experimental error, of the concentration of ferric chloride present as shown in Table 1. These results indicate that the rate of initiation itself is directly ...
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 119 (1968), S. 153-160 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kinetik der dutch Azoisobuttersäuredinitril initiierten radikalischen Polymerisation von N-tert-butylacrylamid wurde in Methanol als Lösungmittel untersacht. Es wurde festgestellt, daß die Bruttoreaktionsgeschwindigkeit proportional der Monomerenkonzentration und proportional der Wurzel aus der Initiatorkonzentration ist. Das Verhältnis kpk1/2t wurde aus den ermittelten Polymerisationsgeschwindigkeiten berechnet und ein Wert von 0,63 ll/2·mole-1/2sec-1/2 bei 25°C gefanden. Aus der bestilimmung des Polymerisationsgrades ergibt sich, daß unter den angewandten Versuchsbedingungen wahrscheinlich Kettenübertragung stattfindet.
    Notes: The kinetics of the radical polymerisation of N-tert-butylacrylamide have been investigated in methanol solution with azo-bis-isobutyronitrile as initiator. It has been found that the overall rate of reaction is proportional to the concentration of monomer and to the square root of the concentration of initiator. The ratio kp/k1/2t has been calculated from the rates of polymerisation determined, the value found being 0.63 1.1/2·mole-1/2sec-1/2 at 25°C. Determinations of the degree of polymerisation indicate that chain transfer probably occurs under the experimental conditions employed.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 73 (1964), S. 145-153 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kinetik der durch γ-Azo-bis-γ-cyan-n-valeriansäure initiierten radikalischen Polymerisation wurde am Acrylamid in Gegenwart von Ferri-perchlorat im Temperaturbereich von 15-25°C untersucht. Die Polymerisationsgeschwindigkeiten in Gegenwart von Ferri-chlorid und Ferri-sulfat bei 25°C wurden ebenfalls gemessen. Zwischen der Bruttoreaktionsgeschwindigkeit und dem Reziprokwert der Ferri-salzkonzentration besteht ein linearer Zusammenhang. Die Polymerisationsgeschwindigkeit ist proportional der Initiatorkonzentration. Aus den ermittelten Polymerisationsgeschwindigkeiten wurde der Häufigkeitsfaktor und die Aktivierungsenergie der Startreaktion berechnet und Werte von 5,64.1012/sec und 26,05 kcal/Mol gefunden.
    Notes: The kinetics of the radical polymerisation of acrylamide in the presence of ferric perchlorate and with 4,4′-azo-bis-4-cyanopentanoic acid as initiator, have been investigated over a range of 15-25°C. Rates of polymerisation at 25°C. have also been measured in the presence of ferric chloride and ferric sulphate. A linear relation exists between the overall rate of reaction and the reciprocal of the concentration of the ferric salt and the rate of polymerisation is proportional to the concentration of the initiator. The pre-exponential factor and energy of activation of the initiation reaction have been calculated from the rates of polymerisation determined and the values found were 5.64.1012/sec. and 26.05 kcal./mole respectively.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 3615-3622 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Viscosity and light-scattering measurements have been made on five samples of poly-N-tert-butylacrylamide in methanol, for which brief preparative details are given. Specific viscosities ηsp have been determined at 25°C. with two U-tube viscometers, No. 0 and No. 1, over a range of concentrations c. The mean flow gradients lie in the range 360-750 sec.-1 for No. 0 and 535-940 sec.-1 for No. 1. Graphs of ηsp/C against c are linear for concentrations between 0.18 and 1.0 g./dl. at all gradients less than about 640 sec.-1 with samples having weight-average molecular weights of 24.5, 5.46, 4.04, 3.79, and 1.65 × 105. At lower concentrations, which give correspondingly higher gradients, the linear relation ceases. Possible reasons for this are suggested. By extrapolation of the linear portions of the appropriate curves to zero concentration, apparent limiting viscosity numbers \documentclass{article}\pagestyle{empty}\begin{document}$[\eta ]_{\begin{array}{*{20}c} {c = 0} \\ {G = 760} \\ \end{array}} $\end{document} have been obtained, where the value G = 760 sec.-1 is the gradient for pure methanol. Light-scattering data have been employed to obtain the molecular weights of the samples using the Zimm technique. Depolarization ratios, determined for different concentrations at wavelengths 4358 and 5461 A. and extrapolated to zero concentration, were negligible. The constants k1 and α in the expression \documentclass{article}\pagestyle{empty}\begin{document}$[\eta ]_{\begin{array}{*{20}c} {c = 0} \\ {G = 760} \\ \end{array}} $\end{document} =k1Mwα have the values 8.87 ± 0.44 × 10-4 and 0.525 ± 0.026, respectively.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 541-550 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The initiation of the polymerization of acrylamide by 4-4′-dicyano-4-4′-azopentanoic acid in aqueous solution has been studied kinetically at 25°C. Ferric chloride and ferric sulfate were used to terminate polymerization so that rates of initiation could be calculated from the rates of production of ferrous iron. Velocity coefficients at 25°C. for the initiation reaction were found to be (25.7 ± 2.8) × 10-7 sec.-1 for the ferric chloride terminated reaction and (73.6 ± 0.6) × 10-7 sec.-1 for the ferric sulfate-terminated polymerization. The value reported for the initiation reaction when acrylamide is polymerized in the absence of metal salts is 1.29 × 10-7 sec.-1. Velocity coefficients for the termination reaction have been calculated from the overall rates of polymerization obtained with ferric salts present. In the case of the ferric chloride-terminated reaction, it has been shown that the rate of polymerization is reduced by increasing the total concentration of chloride ions. Termination velocity coefficients at 25°C. for the inner sphere complexes FeCl2+·5H2O and FeSO4+·4H2O have been calculated to be 18.9 × 104 and 7.98 × 104 l./mole-sec., respectively. The dependence on the concentration of ferric chloride of the molecular weights of the polymers produced has also been considered.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 1307-1314 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of ferric chloride on the kinetics of the radical polymerization of N-tert-butylacrylamide has been investigated in methanol solution at 25°C, with the use of 4,4′-dicyano-4,4′-azodipentanoic acid as initiator. A shrinkage factor of 0.193 mmole polymerized for 1 mm contraction in a capillary of 1 mm diameter has been obtained from density measurements. In the absence of ferric chloride, rates of polymerization were found to be proportional to the concentration of monomer and to the square root of the initiator concentration. With ferric chloride present, the rate of polymerization becomes directly proportional to the initiator concentration and inversely proportional to the concentration of ferric salt. From measurements of the rates of production of ferrous iron, the specific rate constant of the initiation reaction has been found to be (1.8 ± 0.4) × 10-6sec-1 at 25°C, compared with a value of 7.63 × 10-8 sec-1 calculated from the kinetic data obtained with no ferric salt present. The value of the ratio kp/k4. where kp is the propagation coefficient and k4 is the velocity coefficient for termination by ferric chloride, has been calculated to be 6.0 × 10-4 at 25°C, which is considerably smaller than the value found for the ferric chloride-terminated polymerization of acrylamide in water. This markedly lower value of kp/k4 has been attributed principally to the steric effect of the tert-butyl group on the magnitude of kp.
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