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  • Exercise test  (1)
  • Lansoprazole  (1)
  • Separations  (1)
  • Springer  (3)
  • 1995-1999  (1)
  • 1985-1989  (2)
  • 1975-1979
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 48 (1995), S. 391-395 
    ISSN: 1432-1041
    Keywords: Lansoprazole ; Theophylline ; proton pump inhibitor ; theophylline metabolism ; cytochrome P-450 ; drug interaction ; enzyme induction ; human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract The effect of the new substituted benzimidazole proton pump inhibitor, lansoprazole, on pharmacokinetics and metabolism of theophylline has been studied in healthy adults given oral lansoprazole 30 mg once daily for 11 days. On Days 4 and 11 of 300 mg aminophylline was simultaneously administered orally and blood samples for theophylline analysis were taken over 24 h. Urine samples were collected for up to 24 h and were assayed for theophylline and its major metabolites 1,3-dimethyluric acid (1,3-DMU), 1-methyluric acid (1-MU) and 3-methylxanthine (3-MX). The pharmacokinetic parameters of theophylline were determined, and the urinary recovery of unchanged theophylline and its major metabolites were calculated. After administration of lansoprazole for 4 days, no significant alteration in the terminal elimination half-life (t 1/2β) or the mean residence time (MRT) was detected. However, there was a significant decrease of about 13% in the area under the plasma concentration-time curve (AUC) and a significant increase of about 19% in the apparent clearance (CLapp). Lansoprazole treatment for 11 days caused a significant decrease of approximately 12% in t 1/2β and about 10% in the MRT of theophylline, although neither AUC nor CLapp showed a significant alteration. The excretion of 3-MX in the urine was significantly increased by about 20% after lansoprazole treatment for 4 and 11 days, although there was no significant alteration in the excretion of unchanged theophylline, 1,3-DMU or 1-MU. The results indicate that repeated administration of lansoprazole to humans induces the hepatic microsomal P-450-dependent drug oxidation system that mediates N-1-demethylation of theophylline, consequently increasing its metabolism.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 23 (1985), S. 482-486 
    ISSN: 1741-0444
    Keywords: Children ; Exercise test ; Heart rate ; Oxygen uptake ; Physical activity rate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1612-1112
    Keywords: Thin-layer chromatography (TLC) ; Polyethyleneimine (PEI) cellulose ; Sulfuric acid — organic solvent ; Inorganic ions ; Separations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Thin-layer chromatographic behavior of 49 inorganic ions has been systematically studied on polyethyleneimine (PEI) cellulose with solvent mixtures consisting of sulfuric acid and either methanol or acetone. The sorption of most ions on the cellulose increases with increasing methanol content in the solvent. The feature is noticeable for some ions which form sulfato complexes. The Rf values of Re(VII) slightly increase with increasing methanol content. Ba(II), Hg(II), Pb(II), Pd(II), Au(III), Bi(III), Ru(III), Sb(III), Pt(IV), Mo(VI) and W(VI) are strongly retained on the layer in methanol media. The behavior of most ions in the acetone system does not appreciably differ from that in the methanol system, but their Rf values are somewhat higher in acetone than in methanol. There are marked differences in the behavior og Hg(II), Au(III), Ru(III) and Re(VII) between the two systems. Feasibilities for the separation of many ions of analytical interest are also demonstrated in these systems.
    Type of Medium: Electronic Resource
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