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  • Polymer and Materials Science  (2)
  • Membrane  (1)
  • PACS. 34.20.-b Interatomic and intermolecular potentials and forces, potential energy surfaces for collisions – 34.20.Gj Intermolecular and atom-molecule potentials and forces – 34.50.-s Scattering of atoms and molecules  (1)
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Years
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 1153 (1993), S. 143-154 
    ISSN: 0005-2736
    Keywords: (Mammal) ; Cholesterol ; Fluidity ; Fluorescence ; Generalized polarization ; Laurdan ; Membrane
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 15 (2001), S. 321-329 
    ISSN: 1434-6079
    Keywords: PACS. 34.20.-b Interatomic and intermolecular potentials and forces, potential energy surfaces for collisions – 34.20.Gj Intermolecular and atom-molecule potentials and forces – 34.50.-s Scattering of atoms and molecules
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: The interaction between LiH and H has been calculated using a Coupled Cluster approach in view of examining the strength of the coupling between the impinging atom and the rovibrational LiH states in low energy collision regimes. The potential energy surface was thus obtained by considering not only the angular anisotropy but also the dependence of the interaction energy on the vibrational motion of the LiH molecule, hence producing the strength of the vibrational coupling. The main objective is that of gaining a realistic description of the interaction in the sub-reactive region. The results of our calculations show here that this interaction should be used in conjunction with that of the reactive configurational space because of the strong coupling between the non-reactive and the reactive channels in the present system makes the full reactive scattering calculations a more reliable way to obtain realistic cross-sections also for inelastic relaxation and excitation processes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 28 (1994), S. 1157-1163 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A commercial polyester acrylate prepolymer, to which a 2:3 wt/wt ratio of tripropyleneglycol diacrylate was added to increase photopolymerization rate, was employed as photochemical conjugating agent, through photografting. 1,2-Diphenyl,2,2-dimethoxyethanone was added as standard photoinitiator (7.0 wt/wt%), together with varying amounts (0.003-4.0 wt/wt%) of some proprietary photocatalytic systems, based on the following photocataiysts: m̈-peroxobis [N,N′-ethylene-bis(salicylideneiminato)cobalt](III) (I), vanadium (V) triethoxide (II), and a synergic mixture of vanadium (V) tri-t-butoxide and tri-i-propoxide (III). A homogeneous suspension containing (10 ± 2) × 105 human thyroid follicular cells per milliliter of photochemically reacting medium was photografted, at a surface density of 6.5 ± 0.7 mg · cm -2 of diacrylate prepolymer mixture, onto polystyrene plates or onto commercial microfiltration and ultrafiltration membranes consisting of nonwoven cellulose tissues with known porosities varying between 5 and 30 m̈m and in photografted polyester acrylate-based membranes with a cutoff of 50 ± 5 KD. Bioconjugation yields, as a function of photografting time, were measured gravimetrically and by multiple internal reflection IR spectroscopy. Three series of experiments were performed: (1) measurements of graft yields of the prepolymer, and of the parallel disappearance of double bonds, in the absence of mammalian cells; (2) the same as (1), in the presence of thyroid follicular cells; (3) the same as (2), but with the photoinitiating system formed by the standard photoinitiator alone, with no photocatalyst. Results show that if a suitable photocatalyst is not added, no practical conjugation is possible. An appropriate choice of the photocatalytic system and of its concentration allows reduction of irradiation times (e. g., by a factor of about 2 × 104 calculated as the mean lifetime ratio, between the uncatalyzed system and that with 0.1 wt% of [III]), thus minimizing cell inactivation and/or improving responsiveness to the bioassay. From this point of view, photoactivity of (III) is outstanding. The very small, but clearly perceptible, influence of polymeric support on bioconjugation is also commented upon. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 29 (1995), S. 59-63 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The release behavior of typical commercial tissue expanders has been examined by carrying out two kinds of experiments: (1) Determination of chemical nature and its modification after in vivo use by X-ray photoelectron spectroscopy for chemical analysis. This study has been parallelled by scanning electron microscopy with associated energy dispersive X-ray analysis of surface, as well as by silicon compounds analysis of tissues around implants. (2) Kinetic examination of silicon compounds released by the biomaterial in physiologic solution at 36 ± 0.3°C. Results of these investigations have shown independently that the starting material was not a filler-free, pure polymer, but a composite, reinforced elastomer, with the reinforcing agent most seemingly represented by silicon dioxide. Release of latter, with a relatively fast kinetics, is compatible with data of the simulating laboratory runs in the physiologic solution. All these facts seem to rule out any hypothesis of a prevailing siloxane oligomer migration. The correlation of kinetic and physicochemical tests with the in vivo behavior is discussed. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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