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  • Articles  (30)
  • 1980-1984  (28)
  • 1950-1954  (2)
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  • Articles  (30)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 1 (1953), S. 172-177 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 22 (1982), S. 117-122 
    ISSN: 1432-1041
    Keywords: digoxin ; quinidine ; sparteine ; inotropic effect ; plasma levels ; systolic time intervals ; drug interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The influence of single doses of quinidine sulphate (Q) 0.5 g, sparteine sulphate (SP) 0.2 g, and placebo (PL) on heart rate-corrected systolic time intervals (STI) (QS2c, PEPc, LVETc) and on QTc duration was studied 2 and 4 h after treatment of six healthy volunteers. All measurements were done twice in a double blind fashion, once under digoxin (D) steady state (β-methyl digoxin 0.3 mg daily) and once after an equally prolonged basic treatment period with PL. All basic treatment periods and single dose periods were randomized. Drug effects were estimated by comparison with the results obtained after administration of the corresponding placebo. The data were analyzed by two-factorial multivariate analysis of variance. Steady state digoxin serum concentrations averaged 1.3 µg/l and there was no significant change following antiarrhythmic drugs compared to PL. Single oral doses of Q and SP resulted in mean serum concentrations of about 1.8 mg/l and 0.25 mg/l, respectively. In non-digitalized subjects Q 0.5 g resulted in a lengthening of QS2c (+15 ms), LVETc (+13 ms) and QTc (+65 ms). With SP 0.2 g similar but smaller effects were seen. D alone resulted in shortening of QS2c (−21 ms), LVETc (−14 ms), and QTc (−32 ms). Pretreatment with D did not influence the effects of Q on the various parameters. However, corresponding to the D-induced changes in STI, a parallel shift of the curve was observed. The effects of sparteine were somewhat reduced by D. Most of the effects of Q compared to PL and SP were statistically significant (p〈0.05) during both basic treatments, and the D basic treatment had a statistically significant effect for all treatment regimens, but there was no significant interaction between them. In contrast to others, the present results indicate that the positive inotropic effect of D persists in the presence of Q and SP, and that the antiarrhythmic drugs induce negative inotropic effects independent of basic treatment with D. Under the conditions of this experiment, each drug maintains its negative or positive effect on inotropy, thus resulting in an almost arithmetical superposition of the separate drug effects.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 26 (1984), S. 287-292 
    ISSN: 1432-1041
    Keywords: ouabain ; nitroglycerin ; cardiac glycosides ; impedance cardiography ; systolic time intervals ; echocardiography ; cardiac load changes ; pharmacodynamic effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary In this intraindividual, placebo-controlled, double blind study the dynamic effects of single doses of ouabain 0.5 mg i.v. and 12 mg sublingual were compared with those of the vasodilator sublingual nitroglycerin 0.8 mg. In 12 (sublingual) and 6 (i.v.) healthy volunteers, respectively, cardiac performance was assessed for 60 min after administration, using systolic time intervals (QS2c, PEPc, PEP/LVET), electrical impedance cardiography ((dZ/dt)/RZ index) and echocardiography (EDD, ESD, FS). After i.v. ouabain the typical positive inotropic glycoside effects appeared (shortening of QS2c, PEPc, and PEP/LVET, increase of (dZ/dt)/RZ and FS, decrease of EDD and ESD). With nitroglycerin preload reduction diminished cardiac performance, as shown by a rise in PEPc and PEP/LVET and depression of (dZ/dt)/RZ. In addition, EDD (not significant) and ESD were somewhat reduced, FS was enhanced, and QS2c tended to shorten. Following sublingual ouabain, QS2c was unchanged, there was an increase in PEPc and PEP/LVET, a decrease in (dZ/dt)/RZ and FS, EDD was unchanged, and ESD rose. By this route the absolute magnitude of the effects was about 1/3 that of the i.v. drug action. The spectrum of effects of sublingual ouabain indicates a reduction in cardiac performance without any detectable inotropic action. The effects seem to be induced by load changes, with an indication of an increase in afterload although an additional preload reduction cannot be excluded. This dose of the drug given by the sublingual route appears, therefore, to alter cardiac function via an effect on the peripheral circulation, although the final mechanism has not yet been elucidated. It is not known whether these biological effects in healthy subjects may have any clinical significance in patients with cardiac disorders.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 22 (1982), S. 265-272 
    ISSN: 1432-1041
    Keywords: pharmacokinetics ; variation of absorption ratios ; bioavailability ; dissection of variation due to absorption and intermediate processes ; oral drug application
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Differences in the plasma concentrations of drugs after oral administration are caused by two main factors: variation in absorption ratios and in the distribution processes in the body. A new method for the dissection of both types of factors is discussed. The method uses a reference regression of the AUC-values to the corresponding values after intravenous infusion of graded doses. The reference regression is estimated from an appropriate trial. Deviation of the determined AUC-values from the regression curve afford an estimate of the residual variance due to varying distribution volumes or similar random biological effects. For the estimation of absorption ratios after oral administration the drug is given orally to another sample of subjects and their AUC-values are calculated. The deviation of these AUC values due to the above mentioned random effects are simulated using the residual variance of the reference regression, and are subtracted from the observed AUC-values. Then, the differences in the corresponding absorbed doses are transformed by inverting the reference regression. From these doses the empirical distribution function and statistical parameters (e.g. quantiles) are determined. The method has the advantage that no restrictive assumptions are required, such as first order processes, dose linearity, homogeneity of variance or normal distribution of absorption ratios. Its applicability to substances with qualitative differences in their pharmacokinetics is demonstrated by appropriate examples.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 258 (1980), S. 621-625 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Zusammenfassung Stereokomplexe von isotaktischem (i) und syndiotaktischem (s) Polymethylmethacrylat (PMMA), mit verschiedener Stereoregularität ders-PMMA Komponente, in C6D6 und CD3CN Lösung, wurden durch1H NMR Spektra mit Magisch-Winkel-Rotation (MAR-NMR), durch Breitband (BL) NMR Spektra und durch13C NMR Spektra mit starker Protonenentkopplung untersucht. Es wurde herausgefunden, daß in assoziierten Segmenten des Stereokomplexes mitp = 30–40% (p ist der Bruchteil der assoziierten Monomereinheiten) dieα-CH3 und CH2-Gruppen die gleiche Beweglichkeit wie in Lösungen von nur s oder nuri-PMMA ausweisen, aber infolge der Wechselwirkung der Estergruppen sind diese Bewegungen raumbehindert. In Komplexen mit einem hohen Grad von Wechselwirkungen (p ≥ 75%) ist die Beweglichkeit derα-CH3 und CH2-Gruppen in assoziierten Segmenten verzögert. Das Netzwerkmodell des Stereokomplexes, sowohl als auch die Möglichkeit einer Doppelhelixform, werden diskutiert.
    Notes: Summary Stereocomplexes of isotactic (i) and syndiotactic (s) poly(methyl methacrylate)(PMMA), with different stereoregularity of thes-PMMA component, in C6D6 and CD3CN solution were investigated by means of1H NMR spectra measured with magic angle spinning (MAR-NMR), broadline (BL) NMR spectra and13C NMR spectra measured with strong proton decoupling. This study has shown that in associated segments of the stereocomplexes withp= 30–40% (p is the fraction of associated monomer units) theα-CH3 and CH2 groups exhibit equal mobility as in solutions of onlyi ors PMMA, but in consequence of interaction of the ester groups these motions are restricted in space. In complexes with high density of interactions (p ≥ 75%) the motion ofα-CH3 and CH2 groups in associated segments is retarded. The network model of the stereocomplex, and the possibility of the formation of a double helix are discussed.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Solutions of syndiotactic (s) poly (methyl methacrylate) (PMMA) and samples of solid s-PMMA prepared from these solutions were studied by NMR and infrared (IR) spectroscopy and by wide-angle X-ray scattering (WAXS). IR spectra of s-PMMA films obtained from o-dichlorobenzene solutions by evaporation of solvent at room temperature have shown that the ordering of polymer chains which exists in aggregates of s-PMMA in o-dichlorobenzene is preserved in the solid state. s-PMMA prepared in this way is characterized as partly crystalline by WAXS. When o-dichlorobenzene is evaporated at elevated temperatures at which the aggregates of s-PMMA are decomposed, or if solid s-PMMA is obtained from solutions in which aggregation does not take place, the obtained solid polymer is amorphous.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 481 (1981), S. 107-116 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Electrochemical Syntheses. VIII. Preparation of π-Cyclopentadienyl Metal CompoundsThe electrochemical synthesis of π-cyclopentadienyl metal compounds M(π-Cp)2 (M = Fe, Co, Ni) and of cyclopentadienyl carbonyl derivatives (π-Cp)nM(CO)m(M = Fe, Co, Ni, Ti, V) has been investigated. Most of the complexes can be prepared directly from the corresponding metal anodes, monomeric cyclopentadiene (and CO) in moderate or good yields.
    Notes: Die elektrochemische Synthese von π-Cyclopentadienylmetallverbindungen M(π-Cp)2 (M = Fe, Co, Ni) und von Cyclopentadienylcarbonyl-Derivaten des Typs (π-Cp)n-M(CO)m (M = Fe, Co, Ni, Ti, V) wurde näher untersucht. Die Mehrzahl der Komplexe läßt sich direkt aus den entsprechenden Metallanoden, monomerem Cyclopentadien (und CO) in mäßigen bis guten Ausbeuten darstellen.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 1623-1632 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Association of syndiotactic (s) poly(methyl methacrylates) (PMMAs) in toluene, benzene, and acetonitrile has been studied by NMR spectroscopy, osmometry, and viscometry. It was found that in solutions of highly syndiotactic PMMA in toluene, most of the polymer exists in the associated state. Association takes place by means of stereospecific intermolecular and intramolecular interactions of long parallel syndiotactic sequences. The minimum length of syndiotactic sequences necessary for association of s-PMMA in toluene is 7-8 monomer units. Viscosity data indicate that in dilute solutions the associated structures appear as large formations which do not have the character of compact particles. The formation of the aggregates of PMMA is a relatively slow process. A model of the structure of the aggregates of s-PMMA in toluene is proposed. As compared with that in toluene, the tendency to aggregation in benzene and acetonitrile is negligible. Integral parameters currently used for the characterization of polymer-solvent interaction, like “good” or θ solvent, are not suitable for predicting the tendency of s-PMMA to aggregation. The formation of aggregates evidently has some connection with the effect of the solvent upon the conformational structure of syndiotactic sequences.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 617-635 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: From analysis of infrared spectra it was found that in syndiotactic (s) poly(methyl methacrylate) (PMMA) in solution, long s sequences contain an increased population of diads with a skeletal conformation tt (in the staggered approximation). Self-aggregation of s-PMMA in solution leads to a further increase of the fraction of long s sequences in the extended chain conformation, and to an ordering of easter groups. When solid s-PMMA is isolated from a solution in which it exists in the aggregated state, these characteristics are preserved in the solid. The polymer appears partially crystalline by x-ray scattering, and it exhibits fibrillar morphology under the electron microscope. Ordered structures of s-PMMA melt at temperatures about 150°C, while the presence of residual solvent decreases the temperature of melting. Solid s-PMMA obtained from solutions in which aggregation of the polymer does not take place, like s-PMMA which did not come into contact with solvent, contains a higher proportion of syndiotactic diads with a skeletal conformation tg; these samples are amorphous and morphologically structureless. Analogies between the structure of ordered s-PMMA and the structure of the PMMA stereocomplex are also discussed.
    Additional Material: 10 Ill.
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  • 10
    Publication Date: 1982-12-01
    Print ISSN: 1435-9529
    Electronic ISSN: 1435-9537
    Topics: Geosciences
    Published by Springer
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