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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 9 (1993), S. 1-3 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1807
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 5087-5098 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We construct a free-energy density-functional approximation for the primitive model of the electrical double layer. The hard-sphere term of the free-energy functional is based on a nonlocal generic model functional proposed by Percus. This latter model functional, which is a generalization of the exact solution for the nonuniform hard-rod model, requires as input the free energy of a homogeneous hard-sphere mixture. We choose the extension of the Carnahan–Starling equation of state to mixtures. The electrostatic part of the nonuniform fluid ion–ion correlations present in the interface is approximated by that of a homogeneous bulk electrolyte. Using the mean spherical approximation for a neutral electrolyte, we apply the theory to symmetrical 1:1 and 2:2 salts in the restricted primitive model. We present comparisons of density profiles and diffuse layer potentials with Gouy–Chapman theory and Monte Carlo data. We also compare our results with data from other recent theories of the double layer. For highly charged surfaces, the profiles show the layering of counterions and charge inversion effects, in agreement with Monte Carlo data.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 625 (1991), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Neurochemical research 14 (1989), S. 963-969 
    ISSN: 1573-6903
    Keywords: Iodide ; chloride ; astrocytes ; neurons ; thiocyanate ; furosemide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Primary cultures of both mouse astrocytes and neurons accumulate more125I− than36Cl− from the medium. The average cell/medium ratio of125I− of astrocytes (1.01) is greater than that of neurons (0.74), whereas the ratio of36Cl− of neurons (0.47) is greater than that of astrocytes (0.25). The equilibrium potentials of both125I− and36Cl− calculated from the cell/medium ratios in astrocytes and neurons are significantly lower than their corresponding resting transmembrane potentials which suggest that both iodide and chloride are actively transported into both cell types. With respect to different transport inhibitors, thiocyanate is more effective in inhibiting125I− uptake whereas furosemide is more effective in inhibiting36Cl− uptake. Radioiodide uptake by mouse astrocytes was directly proportional to the [Na+]o but was not significantly affected by changes of [Cl−]o or [HCO 3 − ]o, except that it is low in bicarbonate-free medium. Radiochloride uptake by astrocytes was inversely related to [Cl−]o and [HCO 3 − ]o and was not affected [Na+]o, except that it was low in sodium-free medium. Radioiodide uptake by neurons was directly related to [Na+]o between 60 and 140 mM and inversely related to [HCO 3 − ]o between 10 and 40 mM, but it was not affected by [Cl−]o. Radiochloride uptake by neurons was directly related to [Cl−]o and to [Na+]o between 60 and 140 mM and was not affected by [HCO 3 − ]o. However, in sodium-free medium both125I− and36Cl− uptakes into neurons were higher than those in [Na+]o between 5 and 60 mM. These results indicate that uptake of125I− and36Cl− into astrocytes and neurons are different in their ion dependence and that they are under separate regulation.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1590-3478
    Keywords: maximal electroshock ; pentilenetetrazol ; anticonvulsant drugs ; animal models of epilepsy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Numerosi modelli animali di crisi epilettiche sono stati impiegati per ricercare nuovi farmaci antiepilettici utili per il trattamento delle epilessie umane. Attualmente nessuno dei tests di laboratorio è in grado, da solo, di stabilire il valore entiepilettico di una determinata sostanza, o di predirne l'utilità clinica. Tra i molti modelli animali disponibili quelli più comunemente impiegati per selezionare nuovi farmaci antiepilettici sono il test di risposta all'elettroshock massimale (MES) e alla somministrazione subcutanea di pentilenetetrazolo (scPTZ). Il presente capitolo passa in rassegna la metodologia dei due tests, le loro limitazioni e il contributo che essi hanno formito in passato e tutt'ora forniscono alla scoperta di nuovi farmaci antiepilettici.
    Notes: Abstract A number of widely different animal seizure models have been employed in the search for new and novel anticonvulsant drugs useful for the tratment of human epilepsy. At present, no single laboratory test will, in itself, establish the presence or absence of anticonvulsant activity or fully predict the clinical potential of a test substance. Of the many available animal models, the maximal electroshock (MES) and subcutaneous pentylenetetrazol (scPTZ) tests still represent the most commonly employed models for the routine screening and identification of new, anticonvulsant drugs. This chapter will briefly describe how these two tests are conducted, their limitations and how they have contributed in the past and to the present day anticonvulsant drug discovery process.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-6903
    Keywords: Astrocytes ; neurons ; potassium and cations ; potassium and anions ; pHi and potassium ; membrane potential and potassium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Inastrocytes, as [K+]o was increased from 1.2 to 10 mM, [K+]i and [Cl−]i were increased, whereas [Na+]i was decreased. As [K+]o was increased from 10 to 60 mM, intracellular concentration of these three ions showed no significant change. When [K+]o was increased from 60 to 122 mM, an increase in [K+]i and [Cl−]i and a decrease in [Na+]i were observed.Inneurons, as [K+]o was increased from 1.2 to 2.8 mM, [Na+]i and [Cl−]i were decreased, whereas [K+]i was increased. As [K+]o was increased from 2.8 to 30 mM, [K+]i, [Na+]i and [Cl−]i showed no significant change. When [K+]o was increased from 30 to 122 mM, [K+]i and [Cl−]i were increased, whereas [Na+]i was decreased. Inastrocytes, pHi increased when [K+]o was increased. Inneurons, there was a biphasic change in pHi. In lower [K+]o (1.2–2.8 mM) pHi decreased as [K+]o increased, whereas in higher [K+]o (2.8–122 mM) pHi was directly related to [K+]o. In bothastrocytes andneurons, changes in [K+]o did not affect the extracellular water content, whereas the intracellular water content increased as the [K+]o increased. Transmembrane potential (Em) as measured with Tl-204 was inversely related to [K+]o between 1.2 and 90 mM, a ten-fold increase in [K+]o depolarized the astrocytes by about 56 mV and the neurons about 52 mV. The Em values measured with Tl-204 were close to the potassium equilibrium potential (Ek) except those in neurons at lower [K+]o. However, they were not equal to the chloride equilibrium potential (ECl) at [K+]o lower than 30 mM in both astrocytes and neurons. Results of this study demonstrate that alteration of [K+]o produced different changes in [K+]i, [Na+]i, [Cl−]i, and pHi in astrocytes and neurons. The data show that astrocytes can adapt to alterations in [K+]o, in such a way to maintain a more suitable environment for neurons.
    Type of Medium: Electronic Resource
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