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  • pharmacokinetics  (2)
  • Dehydration measurement  (1)
  • Polymeremulsion  (1)
  • General Physics: Statistical and Quantum Mechanics, Quantum Information, etc.
  • Photosystem II
  • 1985-1989  (4)
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Keywords
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Year
  • 1
    ISSN: 1432-1041
    Keywords: famotidine ; renal failure ; H2-receptor antagonist ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of a new, potent H2-receptor antagonist, famotidine, 20 mg i.v. was studied in 7 subjects with normal renal function and in 24 patients with varying degrees of renal impairment. The volume of distribution at steady state was 1.14 l/kg in normal subjects and was not altered in renal failure. The half-life of elimination was 2.59 h in normal subjects and was unchanged in mild renal failure (creatinine clearance, CLCR 90–60 ml/min/1.48 m2) but was increased to 4.72 h in moderate renal failure (CLCR 60–30 ml/min/1.48 m2), and to 12.07 h in severe renal failure (CLCR below 30 ml/min/1.48 m2). The cumulative urinary excretion and renal clearance of famotidine were correspondingly reduced in patients with impaired kidney function. In normal subjects and in patients with mild to moderate renal failure, about 70% of famotidine was excreted through the kidney, mainly by tubular secretion. In patients with a CLCR above 60 ml/min/1.48 m2 the normal daily dose of famotidine can be employed, but in those with a CLCR between 60 and 30 ml/min/1.48 m2 the dose should be reduced by half, and in patients with a CLCR below 30 ml/min/1.48 m2 a reduction by three quarters of the normal dose is recommended.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1041
    Keywords: TZU-0460 ; renal failure ; H2-receptor antagonist ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary We have studied pharmacokinetics of a new H2-receptor antagonist, TZU-0460, in patients with varying degrees of renal impairment. The apparent volume of distribution at steady-state was 1.70 l/kg, and the plasma protein binding of TZU-0460 or its active metabolite, desacetyl TZU-0460 was less than 10% in normal subjects. These variables were not altered with renal impairment. Sixty percent of TZU-0460 given orally was excreted via the kidney, mainly by tubular secretion. The half-time of elimination was 3.94 h in normal subjects, and was prolonged to 12.13 h in severe renal failure (creatinine clearance below 30 ml/min/1.48 m2). Dosage adjustment of TZU-0460 is necessary in renal failure.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1536
    Keywords: Polymeremulsion ; polymermicrosphere ; XPSanalysis ; styrene ; 2-hydroxyethylmethacrylate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polymer microspheres composed of various compositions of styrene and 2-hydroxyethyl methacrylate (HEMA) were produced by batch emulsifier-free emulsion polymerization. The HEMA content at the surface, [HEMA] s , of the microspheres powdered by freeze-drying was determined by both quantitativeC 1s /O 1s analysis andC 1s peak shape analysis of the x-ray photoelectron spectroscopic spectra. When the HEMA content in the microsphere, [HEMA] p , was less than about 5 mole%, the [HEMA] s values determined by the two different methods showed good agreement. At [HEMA]p above 5 mole %, [HEMA]s values determined by the first method were about 15 mole % greater than those determined by the second. They both showed a similar tendency with the [HEMA] s being higher than the [HEMA] p , e.g., when [HEMA] p was 1 mole %, [HEMA] s was 11 mole %. The intensity of the satellite peak due to theπ→π * transition of the benzene ring of the styrene component decreased with an increase in [HEMA] p , to zero at 5 mole % of [HEMA] p . These results indicate that the HEMA component is localized at the surface.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 24 (1986), S. 71-77 
    ISSN: 1741-0444
    Keywords: Bioimpedance ; Dehydration measurement ; Skin admittance ; Skin moisturisation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The properties of skin adminttance were investigated with the intention of applying them to skin moisturisation measurement. Skin admittance is determined by measuring relative permittivity and the resistivity of the stratum corneum, and by contact ratio between dry electrode and stratum corneum. It was found, however, that the contact ratio is the predominant factor producing the change of skin admittance induced by changes in the water content of skin. To measure skin admittance, the following conditions were found to be approriate: (a) frequency of about 100 kHz; (b) concentric electrodes, the diameter of the measuring (inner) electrode being about 5 mm, and (c) an electrode pressure of about 100 g cm−2. Based on these optimal conditions, a system for measuring skin admittance was constructed. All measuring procedures were automated. Experimental observations made with this system have indicated its usefulness for the measurement of skin moisturisation.
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