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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 275 (1972), S. 251-261 
    ISSN: 1432-1912
    Keywords: Tritium-Labelled Hexamethonium Derivatives ; Whole Body Autoradiography ; Distribution ; Accumulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary On each nitrogen atom of 3H-hexamethonium one methyl group was replaced either by a n-propyl, N-n-propylphthalimide or n-nonyl group. By means of whole-body autoradiography the influence of the different substituents on the distribution pattern was studied in mice after i.v. or s.c. injection. Increasing the chain length of the substituents caused an enhanced accumulation of the respective compounds into secreting tissues, heart muscle, and liver, and an augmentation of biliary excretion. The affinity of the bis-quaternary ammonium compounds for cartilaginous tissues was also altered. The physiological “barriers” between blood and brain or blood and the aqueous humor of the eye, were highly effective against the compounds studied, whereas the placenta could be penetreted by these derivatives.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 270 (1971), S. 419-427 
    ISSN: 1432-1912
    Keywords: Tritium Labelled Hexamethonium ; Whole Body Autoradiography ; Distribution ; Accumulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Distribution and accumulation of intravenously and subcutaneously injected tritium-labelled hexamethonium has been studied in mice using autoradiography of whole body sections. The bis-quaternary ammonium compound is rapidly distributed over the organism and excreted mainly by the kidneys, less with the bile. Due to its affinity to “negative binding sites” it combines with acid mucopolysaccharides and is accumulated therefore considerably in connective and cartilaginous tissues. 30 min after either injection route the general distribution pattern of hexamethonium in the organism is characterized as follows (decreasing order): Kidneys, urinary tract, cartilage and connective tissue ≫ lungs 〉 blood, liver 〉 heart and skeletal muscle, gastric and intestinal wall 〉 spleen 〉 adipose tissue, brain and spinal cord.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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