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  • 1990-1994
  • 1970-1974  (2)
  • 4‴-Methyldigoxin  (1)
  • Digoxin and Derivatives  (1)
Materialart
Erscheinungszeitraum
  • 1990-1994
  • 1970-1974  (2)
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 274 (1972), S. 171-181 
    ISSN: 1432-1912
    Schlagwort(e): Digoxin ; 4‴-Acetyldigoxin ; 4‴-Methyldigoxin ; Absorption Velocities ; Blood Level ; Biliar Excretion
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The kinetics of absorption, of changes in blood concentration, and of biliary excretion after the i.v. and i.d. administration of 40 μCi each, of digoxin, 4‴-acetyldigoxin and 4‴-methyldigoxin were studied in biliary fistula rats. The highest blood concentrations were found after the i.v. administration of 4‴-methyldigoxin, which decline with a half life time of 10 h, compared with 5.6 and 4.5 h for 4‴-acetyldigoxin and digoxin respectively. 71%, 55% and 17% of the dose were excreted in the bile within 12 h after the i.v. administration of digoxin, 4‴-acetyldigoxin and 4‴-methyldigoxin. The blood concentrations observed after the i.d. administration of digoxin and 4‴-acetyldigoxin show almost identical pharmacokinetics with respect to height and elimination velocity (half life 7.0 h for digoxin and 7.5 h for 4‴-acetyldigoxin). In contrast, following the i.d.administration of 4‴-methyldigoxin, blood concentrations, which were twice as high, were observed and declined with the same half life as after the i.v. administration. Determination of the disappearance rates of these glycosides from the intestinal lumen reveals a biphasic course of absorption. A first phase, with k values of 0.4, 0.5, 1.2 for digoxin, 4‴-acetyldigoxin and 4‴-methyldigoxin respectively is followed by a second phase with k values of 0.04, 0.04, 0.001 for digoxin, 4‴-acetyldigoxin and 4‴-methyldigoxin. Thus, 4‴-methyldigoxin is almost completely absorbed within the first two hours, while digoxin and 4‴-acetyldigoxin continue to be absorbed during the following hours. The absorption velocity of digoxin from the ileum was found to be one half of that seen in the duodenum. But this slow absorption, as well, follows a biphasic course. The data indicate that 4‴-methyldigoxin is absorbed at a distinctly higher rate than 4‴-acetyldigoxin and digoxin. Acetylation in 4‴ position evidently provides no important advantage with respect to absorption. While this study allows the determination of absorption and excretion velocities, no account of absorption quotes is given.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 273 (1972), S. 154-167 
    ISSN: 1432-1912
    Schlagwort(e): Digoxin and Derivatives ; Bis- and Monodigitoxosides ; Biliary Excretion ; Renal Excretion
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The metabolism of digoxin (D), 4‴-acetyldigoxin (AD) and 4″-methyldigoxin (MD) was studied in biliary fistula rats by quantitative analysis of the excretion of these glycosides after intraduodenal administration. The total activity excreted within 12 h in bile amounts to 45.1; 40.5; 21.3 and in urine to 11.6; 14.3; 17.6% of the dose of D, AD and MD respectively. AD undergoes a rapid, but incomplete desacetylation in the organism. The highest desacetylation activities were found in liver, in intestinal mucosa and in kidney. Yet considerable amounts of unchanged AD were found in portal vein blood and still another 1–2% of the dose in bile and urine. In contrast MD is very slowly demethylated. 15 min after intraduodenal administration portal vein blood contains almost exclusively MD. A stepwise cleavage of digitoxoses from D as well as of AD and MD is indicated. The absolute amounts of digoxigenin-bis-digitoxoside (4–8% of the dose), digoxigenin-mono-digitoxoside (2.5–8.5%) excreted in bile and urine were in the same range for all three glycosides examined, although the relative amounts of these metabolites in bile and urine were much higher after administration of MD than of the two other glycosides. In addition a water-soluble fraction could be detected in bile and urine after administration of D, AD and MD. The absolute quantities of polar metabolites (4.5–7.0%) excreted in bile and urine were identical for all three glycosides.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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