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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 43 (1992), S. 389-392 
    ISSN: 1432-1041
    Keywords: Phenytoin, Pregnancy ; metabolism, p-HPPH pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The steady-state 72 h urinary excretion of various phenytoin metabolites has been measured in 10 epileptic women, whose plasma phenytoin concentrations relative to the phenytoin dose fell during pregnancy and rose again post-partum. In later pregnancy and post parturn, a mean of 61.3 % and 48.9 %, respectively, of the total daily phenytoin dose was eliminated as 5-(4-hydroxyphenyl)-5-phenylhydantoin (p-HPPH). Even thoughp-HPPH accounts for not much more than half the total daily phenytoin dose, increased excretion of this metabolite sufficed to account for the elimination of the entire increase in the dose of phenytoin required during pregnancy. There was no definite increase in the excretion of any other (minor) metabolite measured. Thus pregnancy seems not to enhance uniformly the capacity of the various metabolic pathways of phenytoin.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 27 (1984), S. 105-110 
    ISSN: 1432-1041
    Keywords: phenytoin ; epileptic women ; pharmacokinetics ; bioavailability ; pregnancy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Five epileptic women needing to commence phenytoin therapy during pregnancy received a single intravenous and a single oral dose of phenytoin several days apart before starting regular intake of the drug. Plasma phenytoin concentration — time data were analysed by three different pharmacokinetic techniques. However assessed, the mean oral bioavailability of the drug proved to be about 90% of the intravenous bioavailability. This finding makes it unlikely that impaired bioavailability accounts for the increase in oral phenytoin dosage necessary in pregnancy to maintain plasma phenytoin concentrations at pre-pregnancy values. Phenytoin clearance in the pregnant subjects was approximately double the published values for phenytoin clearance in nonpregnant persons. This suggests that increased (metabolic) clearance accounts for the increased phenytoin dosage requirement of pregnancy.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 451-456 
    ISSN: 1432-1041
    Keywords: Bioavailability ; carbamazepine ; elimination ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The time-courses of plasma carbamazepine concentrations were followed in six apparently healthy adult subjects who, at different times, took single oral drug doses of 200, 400, 500, 600, 700, 800 and 900 mg. There were some suggestions of impaired bioavailability of the drug when given in tablet form. The following values were obtained for various pharmacokinetic parameters:k abs =0.176±0.209 h−1;k=0.0203±0.0055 h−1; T1/2=37.5±13.1 h; VD=0.825±0.1041 · kg−1; Clearance=0.0163±0.0061 l · kg−1. The elimination rate constant showed a statistically significant increase with increasing drug dose. This may help explain the clinical observation that the rate of rise of steady state plasma carbamazepine concentrations tends to decrease with dose increase in patients taking carbamazepine alone.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 27 (1984), S. 105-110 
    ISSN: 1432-1041
    Keywords: phenytoin ; epileptic women ; pharmacokinetics ; bioavailability ; pregnancy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Five epileptic women needing to commence phenytoin therapy during pregnancy received a single intravenous and a single oral dose of phenytoin several days apart before starting regular intake of the drug. Plasma phenytoin concentration — time data were analysed by three different pharmacokinetic techniques. However assessed, the mean oral bioavailability of the drug proved to be about 90% of the intravenous bioavailability. This finding makes it unlikely that impaired bioavailability accounts for the increase in oral phenytoin dosage necessary in pregnancy to maintain plasma phenytoin concentrations at pre-pregnancy values. Phenytoin clearance in the pregnant subjects was approximately double the published values for phenytoin clearance in nonpregnant persons. This suggests that increased (metabolic) clearance accounts for the increased phenytoin dosage requirement of pregnancy.
    Type of Medium: Electronic Resource
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  • 5
    Publication Date: 2017-09-06
    Description: Pyroxene minerals are a significant component of Shergottite-Nakhlite-Chassignite (SNC) meteorites (e.g., Velbel 2012 ) and detected across large areas of Mars’ surface (e.g., Mustard et al. 2005 ). These minerals are associated with chloride, sulfate, and perchlorate salts that may represent briny waters present in Mars’ history. Previous textural analyses by Velbel and Losiak (2010) comparing pyroxenes and amphiboles from various natural weathering environments showed no correlation between apparent apical angles (describing the morphology of denticular weathering textures) and mineralogy or aqueous alteration history in relatively dilute solutions. However, high-salinity brines preferentially dissolve surface species, potentially leading to different textures dependent on the brine chemistry. In this study, we performed controlled pyroxene dissolution experiments in the laboratory on a well-characterized diopside to determine if aqueous alteration in different high-salinity brines, representative of potential weathering fluids on Mars, produce unique textural signatures. Following two months of dissolution in batch reactors, we observed denticles on etch pit margins and pyroxene chip boundaries in all of the solutions investigated: ultrapure water (18 M cm –1 ; a H 2 O = 1); low-salinity solutions containing 0.35 M NaCl ( a H 2 O = 0.99), 0.35 M Na 2 SO 4 ( a H 2 O = 0.98), and 2 M NaClO 4 ( a H 2 O = 0.9); and near-saturated brines containing 1.7 M Na 2 SO 4 ( a H 2 O = 0.95), 3 M NaCl ( a H 2 O = 0.75), and 4.5 M CaCl 2 ( a H 2 O = 0.35). No systematic change in denticle length or apical angle was observed between any of the solutions investigated, even when altered in brines with significantly different salinity, activity of water, and anion composition. Based on these and previous results from natural systems, apical angle measurements are not a useful proxy for determining the extent or nature of aqueous alteration. However, since denticles form relatively slowly during weathering at circum-neutral pH, denticle length may be a useful proxy for chemical weathering duration. All of the experimental solutions produced median denticle lengths ≤1 μm, likely due to the brief weathering experiments. However, perchlorate brines produced a significantly wider range of denticle lengths than those observed in all the other experimental solutions tested. Since perchlorate is likely a common constituent in martian soils ( Glotch et al. 2016 ), denticle length measurements should be used cautiously as proxies for extent of aqueous alteration on Mars, particularly in samples that also contain perchlorate.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 6
    Publication Date: 1977-01-01
    Print ISSN: 0031-6970
    Electronic ISSN: 1432-1041
    Topics: Chemistry and Pharmacology , Medicine
    Published by Springer
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  • 7
    Publication Date: 1984-09-01
    Print ISSN: 0031-6970
    Electronic ISSN: 1432-1041
    Topics: Chemistry and Pharmacology , Medicine
    Published by Springer
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  • 8
    Publication Date: 1992-10-01
    Print ISSN: 0031-6970
    Electronic ISSN: 1432-1041
    Topics: Chemistry and Pharmacology , Medicine
    Published by Springer
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