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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    European journal of clinical pharmacology 32 (1987), S. 625-629 
    ISSN: 1432-1041
    Schlagwort(e): disopyramide ; bioavailability ; saturable binding ; pharmacokinetics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Medizin
    Notizen: Summary The pharmacokinetics of disopyramide were determined in 10 healthy volunteers after a 300 mg oral dose and again after a 2mg/kg i.v. dose. The unbound clearance was 599 ml/min and the unbound renal clearance 310 ml/min. The terminal elimination rate constant of unbound drug was 0.180 h−1 after the i.v. dose and 0.203 h−1 after the oral dose. The absorption rate constant was 0.53−1 and the maximum peak concentration occurred after 3.2 h. The bioavailability was 0.809 using the area under the unbound plasma concentration time curve. Although a saturable plasma protein binding was found in all subjects the bioavailability using the total concentration, in contrast to theoretical expectations, showed the same value (0.813) as the unbound concentrations.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    European journal of clinical pharmacology 35 (1988), S. 313-317 
    ISSN: 1432-1041
    Schlagwort(e): disopyramide ; alpha1-acid glycoprotein ; renal dysfunction ; pharmacokinetics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Medizin
    Notizen: Summary The pharmacokinetics of disopyramide was studied in 15 patients with renal dysfunction (4 with pyelonephritis, 7 with glomerular nephritis and 4 with interstitial nephritis). The elimination rate constant of unbound disopyramide was 0.094 h−1 and CLu/f (unbound clearance divided by bioavailability) was 245 ml/min. Both the unbound renal clearance (CLR) and CLu/f were highly correlated with the creatinine clearance (CLCR). The apparent unbound metabolic clearance in the patients was approximately two-fold lower than that previously reported in normal subjects. The estimated unbound metabolic clearance in the renal dysfunction patients showed a significant negative correlation with the α1-acid glycoprotein (AAG) concentration and only a weak, non-significant correlation with CLCR. As AAG in the renal dysfunction subjects was increased in comparison with normal values, it is possible that AAG is a factor in the decrease in the apparent unbound metabolic clearance.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    European journal of clinical pharmacology 31 (1987), S. 711-714 
    ISSN: 1432-1041
    Schlagwort(e): flecainide ; pharmacokinetics ; moderate renal failure ; variability of elimination half-time
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Medizin
    Notizen: Summary We have studied the pharmacokinetics of flecainide after the oral administration of 100 mg to 8 patients without renal impairment and 8 patients with mild to moderate renal failure. Both groups gave comparable results with respect to the peak plasma concentrations and the time to peak. There was a significant correlation between renal flecainide clearance and endogenous creatinine clearance. The elimination half-time in the patients with impaired renal function was significantly longer (19.9, SD 9.9 h) than that in the patients with normal renal function (11.5, SD 4.2 h), but the variability in the elimination half-time in renal failure could not be explained on the basis of the available results.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    European journal of clinical pharmacology 28 (1985), S. 665-670 
    ISSN: 1432-1041
    Schlagwort(e): tocainide ; renal failure ; pharmacokinetics ; oral dosing ; pharmacodynamics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Medizin
    Notizen: Summary The plasma levels of tocainide have been followed after oral administration of 600 mg p.o. to 20 patients with renal failure due to various causes, and to 8 healthy controls. The peak plasma concentrations in the patients with pyelonephritis (3.80 µg/ml) and interstitial nephritis (3.74 µg/ml) but not in those with glomerulonephritis (3.17 µg/ml) differed from that in healthy volunteers (3.24 µg/ml). The renal clearance of tocainide was well correlated with the endogenous creatinine clearance and was dependent on urine pH. No difference in renal clearance was observed between the patients groups. It is suggested that the changes in plasma levels are a consequence of decreased renal clearance. Creatinine clearance was shown to be a poor estimator of tocainide clearance, which suggests that extrarenal clearance plays an important role in the handling of the drug in the body. The findings are used to suggest a safe dosage regimen.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    ISSN: 1434-6036
    Schlagwort(e): 71.10.+x ; 71.28.+d ; 79.20.Fv
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Due to their sensitivity to electron-correlation effects,CVV Auger-electron (AES) and appearance-potential spectroscopy (APS) can provide useful information on the electronic structure of solids. Correlations among the valence-band electrons (VV correlations) as well as correlations between the valence-band and the core electrons (CV correlations) are responsible for a variety of effects. StrongVV correlations are well known to give rise to sharp satellites in the spectra, which are related to localized two-hole (electron) final states. On the other hand, the screening of the core-hole potential in the initial state for AES, the sudden response of the valence-band electrons after the destruction of the core hole, and, for APS, the scattering of the valence-band electrons at the core hole are all consequences ofCV correlations. Up to now, however, little is known about the combined influence of both types of correlations on the spectra. We present a new theoretical approach that refers to the general case of a model system with arbitrary band-filling and arbitrary strengths ofVV as well asCV correlations. Remaining restrictions and simplifications concerning the degeneracy of the valence band, the transition matrix elements, etc. can be improved systematically. Of course, this generality can only be achieved at the expense of inevitable approximations in the theoretical formulation. The AES and APS intensities are given by properly defined three-particle Green functions, which are determined by use of a diagrammatic vertex-correction method that is based on the three-particle ladder approximation, which is the main idea of our approach. It is a direct generalization of the two-particle ladder approximation, which in the past has been applied for the calculation of two-particle Green functions that are related to the AES and APS intensities, ifCV correlations can be neglected.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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