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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 12 (1964), S. 131-138 
    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
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 13 (1965), S. 438-442 
    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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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of natural products 49 (1986), S. 318-320 
    ISSN: 1520-6025
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1420-908X
    Keywords: Key words: ABT-299 — Platelet activating factor (PAF) —β-thromboglobulin — Platelet — Degranulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Objective and Design: ABT-299 is a prodrug that is converted by serum esterase to a potent platelet activating factor (PAF) antagonist (A-85783). In order to evaluate the pharmacological activity of this antagonist in man the effect of ABT-299 given to healthy volunteers on ex vivo PAF-induced β-thromboglobulin (β-TG) release in blood was assessed.¶Subjects: 37 healthy male volunteers, age 18 to 40 (mean age of 23.6 years) and free of medication, participated in the study.¶Treatment: Subjects were administered intravenously 0.8 mg, 2 mg, or 70 mg doses of ABT-299 (6–7 subjects per group) or placebo (9 subjects, pooled).¶Methods: Peripheral blood taken over 12 h after dosing was used for ex vivo β-TG release and, in the case of the 70 mg dose, measurement of plasma drug concentration. Data were compared by Student's t-test.¶Results: All three doses produced highly significant inhibition (p 〈0.005 compared to predose values) of PAF-induced β-TG release (units/ml plasma±SEM) 12 h after drug administration (54±14 vs. 405±51, n=8; 79±23 vs. 480±127, n=7; 21±10 vs. 327±72, n=6, respectively) whereas there was no significant difference in β-TG release in the placebo group (449±90 vs. 307±49, n=9). Inhibition was associated with the rapid appearance in plasma of A-85783 and the pyridine N-oxide metabolite of A-85783. Within 2 h, the plasma concentration of the metabolite exceeded that of the parent drug. Both the parent drug and the metabolite exhibited potent in vitro inhibition of PAF-induced β-TG release (A2 values of 4 and 1 nM respectively).¶Conclusions: These studies are the first to illustrate the utility of the β-TG release assay for assessing ex vivo activity of PAF antagonists. These studies also demonstrate that the administration of ABT-299 to man results in potent, long lasting inhibition of PAF-mediated platelet activation, due in part to the pyridine-N-oxide metabolite, and support the potential therapeutic utility of this prodrug in treating PAF-mediated diseases.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1238
    Keywords: Bronchodilators ; Mechanical ventilation ; COPD
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective To compare the bronchodilating effect of a single drug, ipratropium bromide (IBr), with that of its combination with fenoterol (IBr+F). Design The study was triple blind and randomized. Setting Medical-surgical intensive care unit. Patients 12 patients with acute exacerbation of chronic obstructive pulmonary disease (COPD) requiring mechanical ventilation for severe respiratory failure. Interventions Before administering each drug, peak airway pressure (Ppeak), end inspiratory pressure (Pei), resistive pressure (Pres), and auto positive — end expiratory pressure (auto-PEEP) were measured. Inspiratory system resistance (Rins) and dynamic respiratory system compliance (C) were calculated. Arterial pH and blood gas determinations were made. These measurements were repeated 60 min after administration of each therapeutic regimen. For ipratropium bromide alone the dose was 0.04 mg. When the combination of drugs was used, the doses were 0.04 mg for ipratropium bromide and 0.1 mg for fenoterol. Measurements and results With the combination of both drugs, all the pressures in the airway, as well as the auto-PEEP and the Rins were significantly reduced (p〈0.05) with respect to baseline values. With ipratropium bromide alone, no significant changes were observed either in the pressures or in the inspiratory resistance. No significant changes were observed either in the pH or blood gases with any of the treatments. The combination of both drugs produced significantly reduction in Pei and auto-PEEP when compared with ipratropium bromide alone. Conclusions The combination of both drugs is more effective than ipratropium bromide alone at the doses used in this study.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1238
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Conclusion Cardiac surgery without blood or blood products can be performed in JW with no increase in ICU or hospital length-of-stay, or perioperative complications.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-1238
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Conclusions 1) Sixty percent of low and moderate risk cardiac surgery patients could be succesfully extubated within 11 h of operation. 2) As a result length-of-stay in ICU was reduced and the percentage of patients discharged within 24 h was increased. 3) There was no increase in postoperative morbidity.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 120 (1998), S. 70-84 
    ISSN: 1432-1106
    Keywords: Key words Neostriatum ; Cable properties ; Dye coupling ; Brain slices ; Potassium blockers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Voltage recordings from neostriatal projection neurons were obtained using in vitro intracellular techniques before and during K+-conductance blockade. Neurons were stained with the biocytin technique. Somatic surface area (A S) was determined by both whole-cell recordings in isolated somata and by measuring stained somata recorded in slices. Dendritic measurements were done in reconstructed neurons. Average determinations of dendritic (A D) and neuronal (A N) surface areas coincided with previously reported anatomical data. Thus: A S≈ 6.5 × 10–6 cm2; A D≈ 1.9 × 10–4 cm2; A N≈A D + A S≈ 2 × 10–4 cm2; A D/A S≈ 30. Measurements were done before and after superfusion with K+-conductance blockers (K+-blockers). Cells whose neuronal morphology was not obviously distorted by K+-blockade were chosen for the present study. Electrotonic transients were matched to a somatic shunt equivalent cylinder model adjusted with the generalized correction factor (F dga) that constrains the parameters for neuronal anatomy. Neuronal input resistance (R N; mean ± SEM) increased when it was corrected for somatic shunt, from 49 ± 2 MΩ (n = 80) to 179 ± 7 MΩ (n = 32). A difference was also obtained between the slowest time constant, τ0 = 16 ± 0.9 ms (n = 49), and the dendritic membrane time constant, τmD = 33 ± 1.6 ms (n = 36). When these electrophysiological measurements were used to calculate A N, the value obtained was similar to the anatomical measurements. Combining anatomical and electrophysiological data, somatic and dendritic input resistances were determined: R D = 182 ± 7 MΩ; R S (with shunt) = 74 ± 4 MΩ (n = 32). The generalized correction factor, F dga = 0.91 ± 0.007 (n = 10), implied a short effective electrotonic length for dendrites: L D = 0.46 ± 0.014 (n = 32). Saturating concentrations of the K+-blockers tetraethylammonium, Cs+, and Ba2+ increased R N and induced charging curves well fitted by single exponential functions in 56% of neostriatal neurons. Ba2+ greatly decreased the somatic shunt (n = 5): (R N = 216 ± 21 MΩ, τ0 = 46 ± 2 ms, R D = 239 ± 25 MΩ, and R S = 3.2 ± 0.5 GΩ), rendering values similar to those obtained with whole-cell recordings (e.g., R N≈ 198 MΩ, RS≈ 2.62 GΩ) (n = 52). Cs+ (n = 5) had less effect on the somatic shunt (R N = 115 ± 19 MΩ, τ0 = 49 ± 13 ms, R S = 161 ± 8 MΩ), although dendritic conductance was equally blocked (R D = 261 ± 16 MΩ). The Cs+-sensitive conductance exhibited inward rectifying properties not displayed by the Ba2+-sensitive conductance, suggesting that Cs+ preferentially acted upon inward rectifier conductances. In contrast, Ba2+ significantly acted upon linear conductances making up the somatic shunt. This suggests a differential action of different K+-blockers on the somato-dendritic membrane, implying a differential distribution of membrane conductances. Another action of K+-blockers, in about 40% of the cells, was to induce dye and probably electrical coupling between neighboring neurons.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    International journal of cosmetic science 27 (2005), S. 0 
    ISSN: 1468-2494
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The objective of the present work was to evaluate the possible use of Myrosma cannifolia starch L.F. Maranthaceae (‘Guapo’), as a raw material in heterogeneous systems or powdered cosmetic and pharmaceutical products formulation. The starch chemical and physical characteristics, physico-chemical properties, and rheological behaviour, previously studied, were considered. Flowing characteristics, particle size distribution, water absorption capacity at 25°C (ambient temperature), and toxicity were assessed. Results showed that Myrosma starch complies with the USP and British pharmacopoeia, and presented a normal particle distribution. More than 25% of the granules had a diameter 〉23.81 μm and the average size of particles was 〉16.92 μm. When compared with talc, ‘guapo’ starch presented higher values for water absorption capacity and flowing characteristics. Starch showed negative local toxicity, and low acute toxicity in vitro on two human dermis cell types. The amylographic study and the difractograms suggest the possible use of this starch in heterogeneous systems. A facial transparent powder was formulated and some of its properties were determined by sensorial analysis. It was concluded that the M. cannifolia starch presents certain characteristics useful in the formulation of new powdered products.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 171 (1953), S. 82-83 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Hydrolysis of hypertensinogen or a second hydrolysis (with pepsin at pH. 2-5) of the extracts which contain pepsitensin produces a substance which lacks any hypertensive effects but shows instead an intense anti-diuretic action in water-loaded rats (Burn's test). The substance shows chemical and ...
    Type of Medium: Electronic Resource
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