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  • Chemistry  (4,109)
  • Analytical Chemistry and Spectroscopy  (753)
  • 2020-2022  (33)
  • 1980-1984  (2,398)
  • 1970-1974  (1,678)
  • 11
    Electronic Resource
    Electronic Resource
    Blood-materials interactions: The minimum interfacial free energy and the optimum polar/apolar ratio hypotheses (1982)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 16 (1982), S. 381-398 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Numerous hypotheses exist to explain observed blood-materials interactions. It is the purpose of this article to test two popular hypotheses, namely, the minimum interfacial free energy hypothesis and the optimum polar/apolar ratio hypothesis. Methacrylate polymers and copolymers were characterized using the captive bubble underwater contact angle method; bulk water content was determined by gravimetric methods; streaming potential measurements were made; and surface roughness and possible particulate contamination were evaluated by reflected light microscopy. In vitro blood tests include whole blood clotting time measurements on polymer-coated tubes; centrifugal force platelet adhesion on polymer-coated coverslips; and a measure of the partial thromboplastin time, Russell's viper venom time (Stypven time), and the prothrombin time of native whole blood exposed to polymer-coated microscope slides. Results suggest that platelet adhesion correlates in the opposite direction of whole blood clotting time and partial thromboplastin time, emphasizing the need for a multiparameter approach to blood-materials testing. Based on these tests the minimum interfacial free energy hypothesis is not supported. In fact, the data suggest the opposite to be true. It is apparent that platelet adhesion can be a misleading indicator of blood compatibility. Neither hypotheses can explain the apparent conflict between the platelet adhesion data and the coagulation time data.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820160407
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  • 12
    Electronic Resource
    Electronic Resource
    Heparin sorptivity and blood compatibility of carbon surfaces (1970)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 4 (1970), S. 145-187 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The influences of the conditioning treatments, surface topography, and crystal structure of carbonaceous surfaces on their ability to sorb heparin and their in vivo compatibility with blood were investigated. The results of the sorption studies indicated that the adsorption of heparin on the surfaces of turbostratic and graphitic materials is not crystallographically selective and that the amount adsorbed on relatively smooth surfaces is near the amount expected for monolayer formation. Although the adsorption of heparin on relatively smooth carbon surfaces is not influenced by the presence of benzalkonium chloride, the sorption of heparin in porous carbons can be greatly increased by a pretreatment with benzalkonium chloride. This increase was found to be due to the formation and entrapment of the insoluble heparin-benzalkonium complex in the accessible porosity. Since the heparin sorptions in Dag-154 coatings were found to be enhanced by a pretreatment with benzalkonium chloride, it was inferred that these coatings contain accessible porosity and that their initial thromboresistance depends on the formation of the benzalkonium-heparin complex in pores. In vivo tests showed that polished and outgassed, impermeable isotropic carbons deposited at low temperatures were significantly thromboresistant without the exogenous application of heparin. There was no relationship between the amount of heparin sorbed on these materials and their compatibility with blood. Polishing, for example, which reduced heparin sorption, enhanced the thromboresistance of these carbons, and while chemisorption of oxygen markedly reduced their thromboresistance, it did not influence the amount of heparin that could be sorbed. Although the heparin-benzalkonium complex sorbed in a porous carbon conferred excellent thromoboresistance in a 2-hr test, the long-tern (14-day) compatibility was not as good as for carbon surfaces that were deposited at low temperatures and then polished and outgassed prior to implanting. In vivo tests of HTI carbon structures and annealed LTI carbons indicate that the blood compatibility of a turbostratic carbon is not significantly dependent on crystallite size, Le. Limited tests of surfaces that had a preponderance of c-faces oriented parallel to the blood-carbon interface at the surface suggest that orientations of this sort are better than others.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820040202
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  • 13
    Electronic Resource
    Electronic Resource
    Fracture of porous polyethylene-bone composite (1983)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 17 (1983), S. 59-70 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Porous high-density polyethylene specimens were implanted in the femurs of mongrel canines. At the end of the residency period (3 or 6 months), the animals were sacrificed and the implants were retrieved. The work-of-fracture of the implant specimens was then determined using the technique of Tattersall and Tappin. The work required to fracture a specimen in three-point bending by controlled crack propagation through a triangular cross section was obtained directly from the load-deflection curve. The area of the resulting fracture surface was measured by macro-photographic techniques, and the work-of-fracture was calculated as work per unit area. The implants were subsequently sectioned and examined microradiographically to determine the extent of bone ingrowth. Bone specimens adjacent to the implants and porous high-density polyethylene controls (no ingrowth) were also tested to determine their work-of-fracture. The results showed that bone adjacent to the implant specimens had a higher work-of-fracture than normal medial, canine femoral bone and was not appreciably different from the composite. The work-of-fracture of porous high-density polyethylene was not significantly increased by an increase in bone infiltration, and this anomalous behavior was attributed to a degradation of the polyethylene during implant residence. Control studies supported this hypothesis.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820170106
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  • 14
    Electronic Resource
    Electronic Resource
    The electroinitiated polymerization of N-vinylcarbazole with zinc bromide, IIPart I: cf.12.. Kinetics of polymerization (1973)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 169 (1973), S. 177-189 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die elektroinitiierte Polymerisation von N-Vinylcarbazol (VCZ) wurde in Aceton bei 25°C mit Zinkbromid als Katalysator unter Verwendung von Platinelektroden eingehend untersucht. Die Polymerisationsgeschwindigkeit erwies sich als direkt abhängig von der Stromstärke, der Zinkbromid-Konzentration und dem anfänglichen Wassergehalt des Solvens.Die Molekulargewichte der entstandenen Polymeren (1000-6000) sind unabhängig von der Stromstärke, der Zinkbromid-Konzentration und dem Umsetzungsgrad des Monomeren zum Polymeren, werden jedoch beeinflußt durch Wasser, die Monomerkonzentration und das Elektrodenmaterial. Die chemische Zusammensetzung der Polymeren ändert sich nicht mit der Stromstärke, der Zinkbromid-Konzentration, dem Umsetzungsgrad und dem Elektrodenmaterial. Sie ändert sich jedoch ein wenig mit dem Wassergehalt des Acetons.
    Notes: The electroinitiated polymerization of N-vinylcarbazole (VCZ) in acetone solvent at 25°C with zinc bromide, as catalyst, and platinum electrodes was investigated in detail. The polymerization rate was found to be directly dependent on current strength, zinc bromide concentration and the initial water content of the solvent.The molecular weights of the formed polymers (1000-6000) are independent of current strength, zinc bromide concentration and degree of conversion of monomer to polymer, but are affected by water, monomer concentration, and by the type of electrodes used. The chemical composition of the polymer is invariant with current strength, zinc bromide concentration, degree of conversion, and electrode material but does vary slightly with the water content of acetone.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1973.021690117
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  • 15
    Electronic Resource
    Electronic Resource
    Infrared spectroscopy of human amyloid fibrils and immunogolbulin proteinsFor reprints, write to : Dr. J. D. Termine, Labortory of Biological Structure, National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland 20014. (1972)
    New York : Wiley-Blackwell
    Biopolymers 11 (1972), S. 1103-1113 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The presence of the antiparallel-β-pleated sheet coformation io isolated human amyloid protein fibrils has been confirmed by infrared spectroscopy. In most amyloid samples, this conformation was enhanced by acidic solution conditions. Infrared spectroscopy (Amide I and Amide V absorption bands) and x-ray diffraction methods were also used to examine the immunoglobulin molecule for solid state-β-structure. It was found that both heavy chains and Bence Jones proteins exhibited some β-pleated sheet content upon acid and/or heat treatment. Furthermore, pepsin digests comprising either the variable-rich region (Fd′) of the immunloglobulin heavy chain or in particular, filamentous variable segments of κ and λ Bence Jones proteins were, as isolated, very similar to amyloid in β-structure content. Data from other immunoglobulin-derived sample did not exhibit extensive β-pleated sheet content. On the other hand, most amyliod and immunoglobulin-derived samples did display some β-structure when cast from 50% HCOOH solution. Under these conditions, however, filamentous light chain-variable segments exhibited well-defined infrared patterns rich in antiparallel-β-pleated sheet structure and gave a “cross-β” x-ray diffraction pattern.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1972.360110512
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  • 16
    Electronic Resource
    Electronic Resource
    High performance liquid chromatography (HPLC) of natural products part VI.For part V, see [1] Sulfoxides of penicillin N and cephalosporin c and their role in biosynthesis of β-lactam antibiotics (1984)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 67 (1984), S. 876-884 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pure pencillin N α-sulfoxide (1) and penicillin N β-sulfoxide (2) were obtained by HPLC and tested as substrates for deacetoxycephalosporin C synthetase (DXCS). Neither one of the sulfoxides was utilized under conditions of conversion of penicillin N (8) to deacetoxycephalosporin C (9). The cephalosporin C α and β-sulfoxides (3 and 4, resp.) were also prepared. Relative stabilities of the sulfoxides 3 and 4 are discussed by interpretation of the 13C-NMR spectra.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19840670329
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  • 17
    Electronic Resource
    Electronic Resource
    Mean free path for inelastic scattering of 1.2 kev electrons in thin poly(methylmethacrylate) films (1980)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 2 (1980), S. 5-10 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Mean free paths for inelastic scattering (λ) of low energy electrons in poly(methylmethacrylate) (PMMA) have been determined by measuring Al Kα excited C 1s and Si 2s photoelectron signal intensities as a function of ellipsometrically determined thicknesses of PMMA overlayers on silicon substrates. The λ values obtained are 29 ± 4 Å for 1196 eV electrons and 33 ± 5 Å for 1328 eV electrons. These data are necessary for the quantitative analysis of the surface region of PMMA and similar polymers by X-ray photoelectron spectroscopy (XPS). The magnitude of the λ values determined indicates that XPS measurements can provide chemical information about the surface region of polymers, such as PMMA, in the depth range of ∼6 to 100 Å. The results of this study are compared and discussed with respect to λ values determined for other organic compounds.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/sia.740020103
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  • 18
    Electronic Resource
    Electronic Resource
    NQR investigations of 35Cl in crystalline 2,5-dichloro-4-nitroaniline (1981)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 16 (1981), S. 123-125 
    Details
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two NQR lines were observed for 35Cl in 2,5-dichloro-4-nitroaniline at room temperature, using a self-quenched super-regenerative spectrometer. Analysis of the Zeeman effect on the two lines using a cylindrical single crystal reveals that the crystal belongs to the monoclinic system. The principal field gradient Z axes enclose an angle of 35° and 28° in the cases of the low and high frequency resonance lines, respectively. The b axis is parallel to 81°, 280°. The unit cell contains either two or a multiple of two molecules. The molecules in the crystal can be arranged into two sets, with the molecular planes in each set being parallel among each other. The angle subtended between the two planes is 159° and each of the planes is inclined to the b axis at an angle of 79.5°. There is an in-plane bending of the two C—Cl bonds by 5.5°. The ionic, single bond and double bond characters of the C—Cl bonds for both chlorines are almost equal, and are in the ratio 24:73:3.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1270160212
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  • 19
    Electronic Resource
    Electronic Resource
    15N and 13C NMR study of the effects of hydrogen bonding and protonation in linear schiff bases: Models for structural studies of rhodopsin and bacteriorhodopsinPart 4 of the series ‘Spectral Studies of Visual Pigments and Related Systems.’ For part 5, see Ref. 9. Dedicated to the memory of Professor Margaret Avram. (1984)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 22 (1984), S. 121-124 
    Details
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of protonation and hydrogen bonding in linear Schiff bases obtained from n-butylamine with butyraldehyde, crotonaldehyde, sorbaldehyde and all-trans-retinal were studied by means of 15N and 13C NMR. The protonation-induced chemical shifts (Δδ) are an order of magnitude larger for 15N than for 13C. For 15N, this effect was found to increase with the extent of conjugation, culminating in the retinylideneimine (Δδ = -146 ppm), which constitutes a model for the study of the structure of the Schiff base linkage in visual pigments and related systems. Theoretical calculations of protonation-induced Δδ values based on MINDO/ 3 are in agreement with experimental results.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1270220214
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  • 20
    Electronic Resource
    Electronic Resource
    Proposed recommended practice for gel permeation chromatography terms and relationshipsThis report is a proposed recommended practice published for information only. It was prepared by a Task Force of the authors under the auspices of ASTM D-20.70. Although the paper has passed subcommittee ballot comments are solicited and should be sent to author number one. (1971)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 9 (1971), S. 401-411 
    Details
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1971.110090601
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