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  • 1
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    Unknown
    Berlin : Periodicals Archive Online (PAO)
    Kant-Studien. 76:1 (1985) 114 
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 43 (1987), S. 401-405 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The microabsorption of X-rays diffracted from planar granular powder specimens is caused by bulk porosity and surface roughness of the material. Methods of stochastic geometry are used to describe the geometrical characteristics of powder by volume fraction, mean chord length of powder particles, and density-density correlation function (covariance). Towards the surface of the specimen, the volume fraction of powder particles decays continuously from the bulk value to zero. Within the framework of the kinematic theory, analytical expressions are derived for both bulk and surface contributions to the microabsorption of symmetrically diffracted X-rays in randomly packed powder specimens with particles of irregular shape. Previous theoretical estimates and empirical formulae are discussed as limiting cases of the present more general results.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-7241
    Keywords: diltiazem ; nifedipine ; verapamil ; infarct size ; pigs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of intracoronary (IC) pretreatment with different calcium antagonists (diltiazem, nifedipine, verapamil) on the development of infarcts was investigated in two experimental series including 35 open-chest pigs. The left anterior descending coronary artery (LAD) was distally ligated for 75 minutes (series A) or for 45 minutes (series B) and was reperfused for 24 hours. Infarct size was determined as the ratio of infarcted myocardium (tetrazolium stain) to the risk region (dye technique). In series A, 20 pigs were pretreated immediately before occlusion with either IC diltiazem (n=5, 4 mg/2 min), IC nifedipine (n=5, 0.4 mg/2 min), IC verapamil (n=5, 1 mg/2 min), or isotonic sodium chloride solution (n=5). In series B, IC diltiazem (n=5, 4 mg/2 min), IC verapamil (n=5, 1 mg/2 min), or isotonic saline solution (n=5) were administered 8 minutes prior to ischemia. The IC infusion of all calcium antagonists (series A) depressed left ventricular peak pressure, diastolic blood pressure, and dp/dt max and increased heart rate and coronary venous oxygen saturation. The development of infarcts was significantly delayed by IC diltiazem and IC verapamil. Mean infarct sizes (series A) amounted to 62% in the diltiazem group, 88% in the nifedipine group, 40% in the verapamil group, and 94% in the control group. In series B, where a time period of 8 minutes elapsed between pretreatment and induction of ischemia, mean infarct sizes after 45 minutes of ischemia and 24 hours of reperfusion amounted to 47% in the diltiazem group, 4% in the verapamil group, and 76% in control experiments. The better protection of verapamil in series B can mainly be ascribed to its longer lasting regional depression compared to diltiazem. In conclusion, at the given drug concentrations, IC verapamil and IC diltiazem enhanced the ischemic tolerance to a greater extent than IC nifedipine (series A). When a time period of 8 minutes had elapsed between IC treatment and the onset of ischemia (series B), verapamil still exhibited a protective effect on the treated myocardium, which can mainly be ascribed to its long-lasting negative inotropic action.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Biologie in unserer Zeit 17 (1987), S. 27-29 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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