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  • Polymers
  • energy economics
  • environmental policy
  • 1985-1989  (23)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 119 (1988), S. 1125-1141 
    ISSN: 1434-4475
    Keywords: Significant electron structures ; Condensed hydrocarbons ; Polymers ; Stabilization energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Superposition of significant electron structures is used to estimate the mesomerism stabilization of polycyclic benzenoid systems by consideration of the number ofKekulé structures and of benzenoid interactions between them. General formulae and stability rules are given for many classes of cata and pericondensed molecules. The decoupling of large benzenoid systems into isolated subsystems is described. Three distinct types of polymeric benzenoid systems exist: unstable systems with vanishing mesomerism energy per monomeric umit, and stable systems with nonvanishing mesomerism energy, which are or are not decoupled into isolated subsystems.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of statistical physics 53 (1988), S. 1073-1080 
    ISSN: 1572-9613
    Keywords: Polymers ; path integrals ; constraints
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The statistical mechanical properties of plane polymer loops enclosing a constant area are investigated, using a continuous model from the start. For this purpose an analytic expression for the generating functional is obtained, which in turn is used to derive (1) the distribution function for the enclosed area, (2) the average squared distance of a given repeating unit from the origin, and (3) the entropic force on a repeating unit.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 75 (1989), S. 261-270 
    ISSN: 1432-2234
    Keywords: Polymers ; XPS ; ESCA ; Ab initio ; Oxygen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract This letter reports the results of ab initio quantum chemical calculations on the C1s core levels of model systems for a number of oxygen containing polymers. Conformational effects were studied. SCF calculations have been carried out with STO-3G and 4-31G basis sets, and Koopmans' theorem was applied to obtain the core-level binding energies. To evaluate the performance of the procedure ΔSCF calculations were carried out on polyacrylic acid. The existence of oxygen-induced secondary substituent effects in the XPS-(ESCA-)spectra is discussed. A comparison with semi-empirical CNDO/2 results from Clark and Thomas has been made.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pharmacy world & science 8 (1986), S. 165-189 
    ISSN: 1573-739X
    Keywords: Biocompatible materials ; Chemistry, analytical ; Chemistry, physical ; Drug delivery ; Hydrogels ; Polymers ; Release, sustained ; Review ; Structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Hydrogels are widely studied materials for the preparation of sustained release drug dosage forms. Their soft, tissue-like consistency and their high biocompatibility in a number of applications make them promising candidates for this purpose. The water and the polymer in the gel form intricate structures and much research has been devoted to the elucidation of these structures, and of the interactions involved in their formation. Simple, drug-loaded hydrogels normally give a matrix-type delivery profile, in which the release rate is proportional to the square root of time; a number of approaches has been used to change this profile to other types of delivery, for instance to zero-order release. A number ofin vivo tests using hydrogel delivery systems has given favourable results.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 266 (1988), S. 1087-1094 
    ISSN: 1435-1536
    Keywords: Polymers ; shear flow ; crystallization ; induction time ; relaxation ; injection molding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In the presented model elements of polymer melt rheology and polymer crystallization kinetics are combined. In particular, the proneness of the melt to the special type of crystallization which is characteristic for shear treatment is supposed to emerge only gradually during shear flow. Following Avrami's early ideas on crystal growth, an induction time is introduced. In principle, the model can be applied to any flow and temperature history. The special case of isothermal flow at constant shear rate is covered in greater detail: A favorable comparison is made with experimental results, as published by Lagasse and Maxwell [10].
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of statistical physics 38 (1985), S. 531-540 
    ISSN: 1572-9613
    Keywords: Polymers ; lattice model ; gridlock ; melting/crystallization phase transition ; excluded volume interactions ; semiflexible chains
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract It has been suggested that some lattice models of polymers, especially ones that incorporate more realistic excluded volume interactions extending to further neighbors, may be subject to gridlock. A model is defined to have the property of gridlock if it cannot melt at any temperature unless a density decrease is allowed. Classical theories of polymer melting are incompatible with the property of gridlock. This paper proves rigorously that a two-dimensional square-lattice model of polymer chains that have nearest-neighbor excluded volume interactions (called the X1S model) has the gridlock property. The proof uses elementary concepts from graph theory. Also, different interpretations of the X1S model are given in terms of real polymers. This leads to a discussion of a number of different classes of melting depending upon whether the intramolecular rotameric energies and the attractive intermolecular energies are antagonistic to or supportive of the melting transition.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of statistical physics 44 (1986), S. 225-235 
    ISSN: 1572-9613
    Keywords: Polymers ; self-avoiding walks ; transfer matrix
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We develop two independent transfer matrix methods for the determination of the exponentγ in the two-dimensional, self-avoiding walk problem. Our first method is based on the calculation of the correlation length and uses conformal invariance. Our second method is based on the direct calculation of the moments of the order parameter distribution. Our results are in good agreement with the conjectured values.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 11 (1988), S. 46-50 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Dynamic headspace ; Multivariate data analysis ; Pattern recognition ; Polymers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gas chromatographic profiles have been generated from different batches of a polypropylene/polyethylene copolymer. The profiles generated from polymer pellets have been obtained by dynamic headspace/capillary gas chromatography analysis. Initially 10 to 40 peaks were chosen at random from the quantitative reports and transferred to a data table. After appropriate scaling the table has been analyzed by a multivariate statistic program, SIMCA (Soft Independent Modeling of Class Analogy) a pattern recognition technique. The method has been used to differentiate batches according to sensory qualities of the final packaging product and changes in polymer peilet production.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 11 (1988), S. 830-836 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Dynamic headspace ; Mass spectrometry ; Polymers ; Polyolefins ; Quantitative determination ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The possibilities of quantitative dynamic headspace by use of a multiple extraction method and an internal gas standard system for various classes of organic compounds in polyethylene and polypropylene are demonstrated. Numerous compounds can be analyzed over wide ranges of concentration and vapor pressure. However, the present study shows that the precision of the desorption parameters is of critical importance for assuring good quantitative results. The possibilities of using a theoretical model are also described. The recovery may be determined and the use of repeated desorption cycles can be reduced.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 21-37 
    ISSN: 0570-0833
    Keywords: Chirality ; Optical activity ; Polymers ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Main-chain chirality is the optical activity resulting from the configurational or conformational arrangement in the main chain of a polymer. The chirality of the most important types of structures has been investigated on the basis of systematic considerations of symmetry. This has led to the surprising result that even in polymers derived from 1-substituted or nonsymmetric 1,1-disubstituted olefins (the technologically most important polymers) several types of chiral structures exist, which are expected to result in optical activity if a particular enantiomer is favorably formed. By carrying out an asymmetric cyclopolymerization, it has been possible to obtain certain structural types in the form of optically active copolymers or homopolymers (e.g., copolymers of styrene with methyl methacrylate, or even the homopolymer of styrene). Another new group of optically active polymers consists of the atropisomeric helical polyisocyanides, poly(trityl methacrylates), and polychlorals. Optically active polymers are already used as adsorbents for the chromatographic separation of racemic mixtures. Further applications are likely to emerge.
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 1 (1987), S. 319-323 
    ISSN: 0268-2605
    Keywords: Mössbauer ; Dibutyltin dichloride ; PVC ; Polymers ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Variable-temperature Sn-119m Mössbauer studies of tin(IV) chloride (SnCl4) and dibutyltin dichloride (Bu2SnCl2) when dispersed in a poly(vinyl chloride) (PVC) matrix have been interpreted using a Debye model. Recoilless fractions have been determined which indicate that at 80 K the Mössbauer technique is nearly three times as sensitive to the presence of SnCl4 compared with Bu2SnCl2 within the poly(vinyl chloride) matrix. These observations have been explained in terms of structural changes occurring on dispersion in the polymer matrix which result in the tin atom in tin(IV) chloride becoming six-coordinate whereas that in dibutyltin dichloride reduces its coordination to five. The implications of these results for future applications of Mössbauer spectroscopy to the study of organotin compounds present in polymers are considered.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 723-742 
    ISSN: 0570-0833
    Keywords: Transition metals ; Polymers ; Alkene ligands ; Electrocatalysis ; Complexes ; Alkyne ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An unprecedented series of highly reactive alkene-and diene-complexes of the early transition metals (Groups 3A-5A of the periodic system) have been isolated recently. Diene complexes of this sort (M = Ti, Zr, Hf, Nb, Ta) prefer, besides the (η4-s-cis-diene)metal structure, either a novel bent η4-metallacyclo-3-pentene structure or the unique (η4-s-trans-diene)metal structure. In bis(diene)metal complexes of Nb and Ta the η4-s-cis-dienes assume an unusual exo-endo (supine-prone) geometry. The M—C bonds in these diene-metal complexes generally exhibit highly polarized σ-bonding along with π-bonding character. The complexes therefore undergo a variety of regio- and stereoselective carbometalations with substrates containing C—C, C—O, or C—N multiple bonds. Examples of the products that can be obtained include ketones, vinyl ketones, unsaturated primary, secondary, and tertiary alcohols, as well as diols and unsaturated acids. Mechanistic studies on the stoichiometric and catalytic conversions of unsaturated hydrocarbons provides, inter alia, some insights into the course of polymerization reactions.
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 816-824 
    ISSN: 0570-0833
    Keywords: Liquid crystals ; Crystalline polymers ; Polymers ; Optoelectronics ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The liquid crystalline behavior of low molecular weight compounds has been known for more than a century; synthetic polymers have been manufactured on a large scale for several decades, but just recently it was found possible to produce polymers using the structural principles of liquid crystalline compounds. The resulting materials have, as expected, unusual properties. Numerous applications, not only in opto-electronics, are already anticipated for such materials.
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  • 14
    ISSN: 0570-0833
    Keywords: Surface recognition ; Molecular recognition ; Self-assembly ; Biological membranes ; Membranes ; Polymers ; Micelles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Part and the Whole. The principle of self-organization for the creation of functional units is not an invention of modern natural sciences. It was already a basic idea of the ancient philosophies in Asia and Europe: only the mutuality of the parts creates the whole and its ability to function. Translated into the language of chemistry this means: the self-organization of molecules leads to supramolecular systems and is responsible for their functions. Thermotropic and lyotropic liquid crystals are such functional units, formed by self-organization. As highly oriented systems, they exhibit new properties. The importance of lyotropic liquid crystals for the life sciences has been known for a long time. They are a prerequisite for the development of life and the ability of cells to function. In materials sciences this concept of function through organization led to the development of new liquid-crystalline materials. From the point of view of macromolecular chemistry, this review tries to combine these two different fields and especially hopes to stimulate their interaction and joint treatment. To exemplify this, the molecular architecture of polymeric organized systems will be discussed. Polymeric liquid crystals combine the ability to undergo spontaneous self-organization-typical of liquid-crystalline phases-with the polymer-specific property of stabilizing these ordered states. As new materials, polymeric liquid crystals have already been investigated intensively. As model systems for biomembranes as well as for the simulation of biomembrane processes, they so far have been little discussed. The intention of this review article is to show that polymer science is able to contribute to the simulation of cellular processes such as the stabilization of biomembranes, specific surface recognition, or even the “uncorking” of cells. Polymer science, having an old tradition as an inter-disciplinary field, can no longer restrict itself to common plastics. Attempts to reach new horizons have already begun. The borderland between liquid crystals and cells will certainly play an important role. Basic requirements to work in this frontier area between organic chemistry, membrane biology, life science, and materials science will be the delight in scientific adventures as well as the courage to go ahead. The most important prerequisite will be the willingness to cooperate with disciplines which so far have not really accepted each other. From this point of view, this review does not aim at giving defined answers. It wants instead to encourage the scientific venture: too often we cling to painfully acquired knowledge, fearing adventures.
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 1468-1483 
    ISSN: 0570-0833
    Keywords: NMR spectroscopy ; 13C NMR spectroscopy ; Polymers ; Analytical methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Until a few years ago, solid-state nuclear resonance yielded spectra containing broad lines only. Meanwhile, CP/MAS-NMR spectroscopy has provided a method which gives narrow nuclear resonance lines from a solid-state specimen as well. Using this technique, it is now possible to produce spectra of “rare” nuclei (13C, 29Si, 15N etc.) which are resolved in terms of chemical structure. The analytical capabilities of NMR spectroscopy can be applied to the solid state: it may be that it is necessary to identify compounds in the solid state because, for example, a solvent would alter the coordination sphere, or that it is desired to monitor chemical reactions in the solid state, for example the baking of an enamel. Where a substance in the solid state is concerned, high-resolution 13C-NMR spectroscopy provides not only information about the chemical structure, but also about the solid state itself. To mention just a few examples, information on the conformation, crystal structure and molecular dynamics, as well as molecular miscibility is given. This opens up a broad spectrum of applications, from a statement concerning the crystal modification of an active substance in ready-to-use pharmaceutical preparations, e.g. tablets, to the question of whether two polymers are miscible with one another at a molecular level.
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  • 16
    ISSN: 0570-0833
    Keywords: NMR spectroscopy ; NMR spectroscopy ; Polymers ; Analytical methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: NMR spectroscopy is an effective method not only for examining liquid samples but also for characterizing molecular sturcture, order and dynamics in amorphous and ordered solids. Recent developments in the area of solid-state NMR spectroscopy span from model-dependent studies of conventional one-dimensional spectra to the more definitive two-dimensional (2D) spectra which provide more specific information. For example, with 2D-NMR spectroscopy it is possible to determine the orientational distribution functions of molecular segments in drawn polymers and to distinguish different mechanisms of complex molecular motions. Following an introduction to basic NMR spectroscopy, an overview of the current state-of-the-art of 2D methods in solid-state NMR spectroscopy is presented and demonstrated with selected examples.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 1 (1987), S. 311-317 
    ISSN: 0268-2605
    Keywords: Organotin stabilizers ; Dibutyltin ; PVC ; Polymers ; Gamma irradiation ; Degradation ; Dealkylation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organotin stabilizers of the type Bu2SnX2 (X = SCH2CO2C8H17 or O2CCH=CHCO2C8H17) present in poly(vinyl chloride) (PVC) and subjected to varying doses of gamma irradiation in the range 1-200 kGy (0.1-20 Mrad) are shown to suffer degradation with dealkylation to form monobutyltin trichloride and tin(IV) chloride, which have been characterized by a subsequent alkylation procedure followed by gas chromatographic analysis. The extent of degradation of the stabilizers on prolonged gamma irradiation is much more severe than during thermal degradation leading to comparable blackening of the polymer.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 13 (1989), S. 309-334 
    ISSN: 0741-0581
    Keywords: Freeze-fracture ; Electron microscopy ; Rapid freezing ; Dispersions ; Polymers ; Gels ; Liquid crystals ; Emulsions ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Understanding the relationship between the molecular structure and the macroscopic properties of polymer solutions and gels, oil-water-surfactant emulsions, lyotropic and thermotropic liquid crystals, colloidal dispersions, detergents, and other such “microstructured fluids” is essential to the optimal use of these commercially important materials. Modern rapid-freezing methods followed by freeze-fracture replication techniques are ideally suited to allow the direct visualization of the three-dimensional structure of the particles or units that make up the dispersion, while simultaneously revealing their orientation and distribution with molecular resolution. This paper reviews the necessary experimental conditions required to successfully exploit the freeze-fracture technique as it applies to microstructured fluid systems. The benefits and limitations of structural studies by freeze-fracture techniques as opposed to the more commonly used light, X-ray, and neutron-scattering methods are discussed. Freeze-fracture replicas can also be imaged by scanning tunneling microscopy to reveal directly three-dimensional fracture contours with improved resolution.
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 253-267 
    ISSN: 0570-0833
    Keywords: Stiff-chain polymers ; Polymers ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Most of the industrial plastics used up to now consist of flexible macromolecules in which the repeat units are joined together in a nonlinear fashion by rotating bonds. Stiff-chain polymers, which in the ideal case have a rodlike shape, have received much less attention. The reason for this is that such polymers usually exhibit an exceedingly low solubility. Very often, they are absolutely insoluble and do not melt. However, in recent years these polymers have aroused technical interest because high-modulus fibers and moldings can be fabricated from them. These favorable mechanical properties are directly related to the nearly parallel arrangement of the rodlike macromolecules in the solid state which is achieved through spinning or extrusion from a liquid crystalline (nematic) state. It is therefore evident that a thorough understanding of the phase behavior and the structure is required for a universal technical utilization of these materials. The great variety of methods used in polymer science today has led to a deeper understanding of stiff-chain polymers. Experimental results together with theoretical modeling of the phase behavior have direct implications for the practical use of these macromolecular materials.
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  • 20
    Publication Date: 1986-09-05
    Description: The oral administration of peptide drugs is well known to be precluded by their digestion in the stomach and small intestine. As a new approach to oral delivery, peptide drugs were coated with polymers cross-linked with azoaromatic groups to form an impervious film to protect orally administered drugs from digestion in the stomach and small intestine. When the azopolymer-coated drug reached the large intestine, the indigenous microflora reduced the azo bonds, broke the cross-links, and degraded the polymer film, thereby releasing the drug into the lumen of the colon for local action or for absorption. The ability of the azopolymer coating to protect and deliver orally administered peptide drugs was demonstrated in rats with the peptide hormones vasopressin and insulin.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Saffran, M -- Kumar, G S -- Savariar, C -- Burnham, J C -- Williams, F -- Neckers, D C -- AI 18710/AI/NIAID NIH HHS/ -- SO-7-RR05700-15/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1986 Sep 5;233(4768):1081-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3526553" target="_blank"〉PubMed〈/a〉
    Keywords: Administration, Oral ; Animals ; Azo Compounds ; Blood Glucose/metabolism ; Diabetes Mellitus, Experimental/drug therapy ; Enterobacteriaceae/metabolism ; Insulin/*administration & dosage ; Lypressin/administration & dosage ; Peptides/*administration & dosage ; Polymers ; Rats ; *Tablets, Enteric-Coated
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 21
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-09-25
    Description: Biomaterials are being used with increasing frequency for tissue substitution. Complex devices such as total joint replacements and the total artificial heart represent combinations of polymers and metal alloys for system and organ replacement. The major barriers to the extended use of these devices are the possibility of bacterial adhesion to biomaterials, which causes biomaterial-centered infection, and the lack of successful tissue integration or compatibility with biomaterial surfaces. Interactions of biomaterials with bacteria and tissue cells are directed not only by specific receptors and outer membrane molecules on the cell surface, but also by the atomic geometry and electronic state of the biomaterial surface. An understanding of these mechanisms is important to all fields of medicine and is derived from and relevant to studies in microbiology, biochemistry, and physics. Modifications to biomaterial surfaces at an atomic level will allow the programming of cell-to-substratum events, thereby diminishing infection by enhancing tissue compatibility or integration, or by directly inhibiting bacterial adhesion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gristina, A G -- R01AM26957-05/AM/NIADDK NIH HHS/ -- R01GM35939-01/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1987 Sep 25;237(4822):1588-95.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3629258" target="_blank"〉PubMed〈/a〉
    Keywords: *Bacterial Adhesion ; Bacterial Infections/*microbiology ; *Biocompatible Materials ; *Cell Adhesion ; Ceramics ; Chemistry, Physical ; Glass ; Glycoproteins ; Humans ; Ions ; Physicochemical Phenomena ; Polymers ; Solubility
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 22
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-10-30
    Description: F-actin is the major component of muscle thin filaments and, more generally, of the microfilaments of the dynamic, multifunctional cytoskeletal systems of nonmuscle eukaryotic cells. Polymeric F-actin is formed by reversible noncovalent self-association of monomeric G-actin. To understand the dynamics of microfilament systems in cells, the dynamics of polymerization of pure actin must be understood. The following model has emerged from recent work. During the polymerization process, adenosine 5'-triphosphate (ATP) that is bound to G-actin is hydrolyzed to adenosine 5'-diphosphate (ADP) that is bound to F-actin. The hydrolysis reaction occurs on the F-actin subsequent to the polymerization reaction in two steps: cleavage of ATP followed by the slower release of inorganic phosphate (Pi). As a result, at high rates of filament growth a transient cap of ATP-actin subunits exists at the ends of elongating filaments, and at steady state a stabilizing cap of ADP.Pi-actin subunits exists at the barbed ends of filaments. Cleavage of ATP results in a highly stable filament with bound ADP.Pi, and release of Pi destabilizes the filament. Thus these two steps of the hydrolytic reaction provide potential mechanisms for regulating the monomer-polymer transition.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Korn, E D -- Carlier, M F -- Pantaloni, D -- New York, N.Y. -- Science. 1987 Oct 30;238(4827):638-44.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Cell Biology, National Heart, Lung, and Blood Institute, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3672117" target="_blank"〉PubMed〈/a〉
    Keywords: Actin Cytoskeleton/*physiology ; Actins/*physiology ; Adenosine Diphosphate/metabolism ; Adenosine Triphosphate/*metabolism ; Animals ; Cytoskeleton/*physiology ; Humans ; Hydrolysis ; Kinetics ; Polymers ; Protein Binding
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 23
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-09-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1985 Sep 13;229(4718):1109-13.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4035352" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Crystallography ; DNA, Superhelical/analysis ; *Histones ; Models, Structural ; Nucleic Acid Conformation ; *Nucleosomes ; Polymers ; X-Ray Diffraction
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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