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  • 1
    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
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 275 (1972), S. 1-10 
    ISSN: 1432-1912
    Schlagwort(e): Enterohepatic Circulation ; Pharmacokinetics ; Digoxigenin-Bis- and Mono-Digitoxoside ; Polar Conjugates
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary After intraduodenal administration of 3H-digoxin (d) in biliary fistula (b.f.) rats, the total radioactivity in blood and bile is eliminated with t1/2 of 7 h in both fluids. In rats with intact enterohepatic circulation (e.c.), a t1/2 of 13.5 h was observed in blood and of 22 h in bile. To explain the much longer t1/2 in bile than in blood, the pharmacokinetics were studied of all substances, which might participate in e.c. after d administration. E.c. of the water soluble fraction is negligible since almost no absorption was found. Digoxigenin-bis- (b) and monodigitoxoside (m) showed approximately the same absorption kinetics as d. However, the blood levels of radioactivity after i.d. administration of these metabolites in b.f. rats were 5–6 times lower than those after d as a consequence of higher biliary excretion. 90–95% of the absorbed amounts of b and m were extrected in bile within 11 h compared with 61% after d administration. Thus the far longer t1/2 of elimination of radioactivity in bile than in blood after i.d. administration of d in rats with e.c. seemed to be due to a short circuit of b and m between intestine and liver. Evidence for this comes from the chromatographic analysis of the total radioactivity in the bile of these animals which shows that significantly more b is present in the bile of rats with e.c. than b.f. rats. No differences were found in the case of m, which on one hand is formed to a lesser extent and is on the other rapidly converted to polar metabolites, which are not reabsorbed.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 272 (1972), S. 450-453 
    ISSN: 1432-1912
    Schlagwort(e): Urinary Excretion ; Methyldigoxin ; Digoxin ; Metabolites
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary In man the oral or intravenous administration of 4‴-methyldigoxin yields metabolites in urine which are soluble either in chloroform or in water. The chromatographic analysis reveals demethylation as the main metabolic reaction in man. In addition to methyldigoxin and digoxin small amounts of digoxigenin-bisdigitoxoside and digoxigenin-mono-digitoxoside can be detected. The water soluble metabolites represent 7% of the radioactivity excreted in 7 days reaching a maximum within the first 8 h.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 273 (1972), S. 172-174 
    ISSN: 1432-1912
    Schlagwort(e): 4′-Methyldigoxin ; Half Life ; Excretion
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary In 10 patients the time course of specific activity in plasma, and the excretion rates in urine and feces after oral and intravenous administration of 12α-3H-4‴-methyldigoxin were studied. The determined biological half life of radioactivity in plasma averaged 43 h and corresponds with the renal excretion velocity (50 h). 32.5 ± 5.0 and 31.5 ± 6.3% of the dose were found in feces and 59.7 ± 1.3 and 52.9 ± 1.8% were excreted in urine within 7 days after intravenous and oral administration, respectively. These results together with the observed plasma concentrations suggest a rapid and almost complete absorption of 4′-methyldigoxin.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    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
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 250 (1972), S. 1094-1104 
    ISSN: 1435-1536
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Beschreibung / Inhaltsverzeichnis: Summary The relaxation behavior of polyethylene is studied by analyzing the line shape of the NMR-spectra. The broad, medium and narrow components correspond to three kinds of molecular motion: rigid, hindered mobile and liquid like mobile. The line shapes of the components are assumed to be that of a completely crystalline polyethylene sample, a hybrid between aGauβ andLorentz curve, and aLorentz curve, respectively. For a melt crystallized linear polyethylene of density 0,972 gcm−3 it is found that only (25±3)% of the noncrystalline protons are able to participate in the liquid like motion. For solution crystallized polyethylene this fraction is only (3±1)%. By swelling the polyethylene with carbon tetrachloride the mobility of the noncrystalline regions is increased. This is seen by the lowering of the glass transition temperature and a narrowing of the medium and narrow component. Branched polyethylene shows a different relaxation behavior from linear polyethylene, which follows from the disturbance of the polyethylene structure by the branching points.
    Notizen: Zusammenfassung Die Untersuchung des Relaxationsverhaltens von Polyäthylen geschieht durch die Linienformanalyse der NMR-Spektren. Der breiten, mittleren und schmalen Komponente entsprechen drei Arten der Molekularbeweglichkeit: unbeweglich, behindert beweglich und fiüssigkeitsähnlich beweglich. Zur mathematischen Beschreibung der breiten Komponente benutzen wir die an einer hochkristallinen Probe experimentell bestimmte Kurvenform, für die mittlere Komponente eine ausGauss- undLorentz-Kurve gemischte Kurve und für die schmale Komponente eineLorentz-Kurve. Die Wendepunktsbreiten der drei Komponenten betragen 14 bis 16 G, 2 bis 10 G und⩽1G. Es wird gefunden, daß bei schmelzkristallisiertem linearem Polyäthylen der Dichte 0,972 g cm−3 nur (25±3)% aller nichtkristallinen Protonen eine flüssigkeitsähnliche Bewegung ausführen. Bei lösungskristallisiertem linearem Polyäthylen derselben Kristallinität ist der Anteil mit (3 ±1)% noch wesentlich kleiner. Durch die Quellung des Polyäthylens mit Tetrachlorkohlenstoff erhöht sich die Beweglichkeit in den nichtkristallinen Bereichen. Dies äußert sich in der Erniedrigung der Glastemperatur sowie in einer Verschmälerung der mittleren und schmalen Komponente. Verzweigtes Polyäthylen zeigt aufgrund seiner durch die Verzweigungsstellen gestörten Struktur ein von linearem Polyäthylen abweichendes Verhalten.
    Materialart: Digitale Medien
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