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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    International journal of cosmetic science 26 (2004), S. 0 
    ISSN: 1468-2494
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: To show the benefits of retinol encapsulation in cosmetic industry, we compared the diffusion of two different retinol preparations through skin:oil-in-water (o/w) emulsions of retinol, also called ‘free retinol’, and suspension of Cylasphere® including retinol, also called ‘encapsulated retinol’. Two methods were used: Franz cell elucidated retinol release and storage in a hairless mouse skin according to time for the two types of preparations. The dosage of retinol by high performance liquid chromatography (HPLC) showed that encapsulated retinol was maintained into the skin for a longer time than free retinol. Raman microspectrometry measurements established a spectral image of the skin and determined the localization of retinol. Maps were collected according to time. They detailed the shifts of free and encapsulated retinol in the epidermis of a human biopsy. Spheres were smaller than droplets and they moved two times faster at this level of the skin.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : American Institute of Physics (AIP)
    Physics of Fluids 4 (1992), S. 1909-1919 
    ISSN: 1089-7666
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Magnetic compression heating experiments at the 1 GW level on field-reversed configuration (FRC) compact toroid plasmas are reported. FRC's formed in a tapered theta-pinch coil have been translated into a single-turn compression coil, where the external magnetic field is slowly raised up to seven times its initial value. Significant electron and ion heating consistent with the expected B4/5 adiabatic scaling is observed, despite significant particle diffusion, which is enhanced during compression. The n=2 rotational instability is enhanced during compression, but has been controlled to an extent by the application of an external quadrupole field. The particle and flux confinement times, τN and τφ, remain approximately equal and decrease roughly with the square of the plasma radius R during compression, implying a constant nonclassical field-null resistivity. The observed τN and τφ magnitudes and scalings are compared with classical and anomalous transport theories, and existing empirical models. Particle diffusion dominates the energy confinement, accounting for three-fourths of the total losses. Upper bounds on the electron thermal diffusivities are estimated.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1089-7666
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Data from an array of external probes provide the first clear evidence for the n=1 rotational instability in field-reversed configurations. The time evolution and the axial structure of this instability are clarified.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1089-7666
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The poloidal magnetic flux φ in large field-reversed configuration plasmas is examined experimentally. A wide range of initial equilibrium conditions, with 1≤φ≤8 mWb, is produced by varying the reverse bias magnetic field strength. The flux confinement time τφ at first improves with bias, albeit with field-null resistivities an order of magnitude larger than classical. A further increase in bias results in a reduction of τφ, which is inconsistent with either classical or anomalous diffusion theory. The data suggest the importance of nondiffusive processes such as instabilities or formation dynamics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics 176 (1993), S. 249-278 
    ISSN: 0301-0104
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1075-4261
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Surface-enhanced Raman spectra (SERS at Creighton colloidal silver) and UV/visible spectra have been recorded for an antimicrobial agent (pefloxacin) at a biologically active concentration (ca. 10-6 mol/L-1). The adsorption of pefloxacin on the silver surface occurs both via the carboxylate group and the carbonyl of the pyridinone ring. The conjugated part of the molecule is tilted and gives rise to a charge transfer between the drug and the plasmon surface. However the orientation of the drug on the colloid varies with the concentration of pefloxacin, salt addition, and pH. Adsorption via only the carboxylate is privileged in presence of strongly competitive anions such as C1-. Thus the carbonyl of the pyridinone ring is desorbed, and the charge transfer is not detected. In basic medium the competitive OH- ion leads to similar orientation changes. For acidic pHs few residual molecules having a carboxylate function, or few carboxylic species bonded via the pyridinone C=O group, remain adsorbed on the aggregated and unstable silver surface. The spectroscopic analyses and the measurements of the particle size of the colloid show that added salt increases the aggregation and enhances the pefloxacin SERS signals if the anion is not competitive. In the presence of NaNO3 an increase of the plasmon oscillations of the metal and a larger number of adsorption sites could explain the SERS amplitude. The competitive anions C1- and OH- to a lesser extent limit the colloid aggregation, pefloxacin adsorption, and SERS enhancement. The influence of the charge transfer on the Raman intensity appears to be weak. © 1995 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biospectroscopy 2 (1996), S. 101-111 
    ISSN: 1075-4261
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Although reversed-phase liquid chromatography has been widely used to separate proteins, the retention mechanisms remain often unpredictable. To evidence the influence of the protein structure on these mechanisms, the conformations, of the recombinant human interferon γ (25ASN) and one of its analogues (Analogue II 25ASP), were studied in relation with their chromatographic behavior. Despite their closely related primary structures, these molecules can be separated by gradient elution in acidic medium. For the solutions, but also when the proteins are adsorbed on a reversed phase RP-C6 support, the present FTIR study delivers an estimation of their secondary structures and also information on the capacity for solvent molecules to accede to the corresponding polypeptide backbones. During the chromatographic procedure, the acetonitrile in solution and the solid phase upon adsorption, induce different structural changes for the r-hu IFNγ and Analogue II. This should generate their different retention times. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biospectroscopy 3 (1997), S. 31-45 
    ISSN: 1075-4261
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The interactions between pefloxacin (antimicrobial agent), magnesium, and DNA single or double strand are studied by UV/Vis and surface-enhanced Raman spectroscopies at biological active concentrations: pefloxacin 2 × 10-6, DNA 2 × 10-5, and Mg2+ 10-3M. Pefloxacin interacts with Mg2+ via its carboxylate and pyridinone C4=O groups. In presence of the colloid, with nitrate salts, Mg2+ is positioned near the C4=O and the drug is bound to the Ag surface via the carboxylate. The conjugated rings are tilted over the colloidal particles and a charge transfer from the plasmon of the surface to the pefloxacin occurs, as in absence of salts or in presence of sodium nitrate. With MgCl2, pefloxacin/Mg2+ species are also adsorbed onto the colloid but essentially via the C4=O of the pyridinone ring, the carboxylate being partly bound to Mg2+. The charge transfer is canceled as occurring with NaCl. Magnesium interacts with DNA single or double strand via the phosphodiester groups and amino bases are oriented toward the colloidal surface. Chlorides specifically favor the fixation of the adenine NH2 substituent. At low DNA concentration and in presence of Mg2+, the adsorbed bases are tilted over the Ag surface, more for double- than for single-strand DNA. Ternary pefloxacin-Mg2+-DNA complexes are adsorbed onto the silver surface, via the amino group of the DNA bases and via one carboxylate oxygen of the drug. The ternary complex formed with Mg2+ (nitrate) and DNA modifies the charge transfer from the plasmon of the surface to the drug. © 1997 John Wiley & Sons, Inc. Biospect 3: 31-45, 1997
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An ir-absorption and Raman-scattering study, in the solid state, has been carried out on monodispersed, N- and C-protected homooligopeptides (number of residues, n, from 2 to 7) of L-valine, L-isoleucine, and L-phenylalanine. The amide I, II, III, V, and vNH regions have been examined. Some deuterated (ND) samples have been examined to complete the assignments. L-Phenylalanine dipeptide displays spectral characteristics compatible with the parallel β-structure; L-isoleucine and L-valine dipeptides are probably in a distorted structure. A mixture of parallel and antiparallel extended chains cannot be excluded for the peptides with n = 3. In the amide I region the spectra of peptides with n ≥ 4 show the existence of the β-conformation. The problem of chain orientation within the pleated-sheet structure is discussed on the basis of a recent theoretical treatment of vibrational interactions of the amide I mode.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monodisperesed, N-and C-Protected homo-oligopeptides [number (n) of resides from 2 to 5] of L-valine, L-isoleucine, and L-phenylalnine were studied by ir absorption spectroscopy between 1200 and 350 cm-1 at various solvents. The solvents and chain-length effects were examined for non-hydrogen-bonded peptide groups. The frequencies of the self-associated species are consistent with a model derived from the amide data. Self-association species are consistent with a model derived from the amide data. Self-association is favored by higher values of n = 2, the peptide is insoluble when more than two chains are bonded. For n = 3, 4, several chains may be associated by sliding along one another and remain soluble. For n = 2, the peptide is insoluble when more than two chains are bonded. For n = 3, 4, several chains may be associated by sliding along one another and remain slouble. For n = 5, the effect of n is to favour a model in which two chains exactly face each other so that the peptide precipitates at relatively low concentration.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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