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  • Polymer and Materials Science  (18)
  • Wiley-Blackwell  (18)
  • EDP Sciences
  • Nature Publishing Group
  • Springer Nature
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  • Wiley-Blackwell  (18)
  • EDP Sciences
  • Nature Publishing Group
  • Springer Nature
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 3241-3241 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 2557-2568 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: To determine the scope of the grafting reaction, over 30 monomers were grafted to steer hide collagen and collagen films using ceric ammonium nitrate as initiator. High yields of apparent graft polymer were obtained with most acrylate and methacrylate esters. Yields were not changed greatly by employing the higher homologues. Moreover, monomers containing such diverse substituents as hydroxy, cyano, chloro, trifluoroethyl, or glycidyl groups may be grafted onto collagen. The presence of these functional groups in the products provides potential reaction centers to further modify the collagenous surface. Presence of vinyl polymer was confirmed by IR spectra. The large number of monomers of varying polarity which were found to undergo apparent grafting makes it possible to vary widely the surface properties of collagen. It was shown that certain monomers impart water and oil repellency to collagenous surfaces, whereas others increased the hydrophilicity or oleophilicity of the substrate. Thus, by proper selection of monomers, the desired degree of hydrophilic to hydrophobic or oleophilic to oleophobic balance of the collagen surface to suit specific applications can be obtained.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 9 (1975), S. 105-117 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A proposed specification covering handling characteristics and physical and chemical properties of bone cement composed primarily of methyl methacrylate has been prepared on the basis of data from the authors' studies and from various other sources. Under handling characteristics, requirements included relate to dough, handling and setting time, proper plasticity for insertion and temperature rise on setting. Mechanical properties specified include compressive strength and indentation and recovery characteristics. Maximum limits are proposed for water sorption and solubility. Suggested packaging requirements are also included.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 11 (1977), S. 577-607 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Rapid and reliable methods for the characterization and quantitative determination of ingredients usually present in self-curing methacrylate bone cements were developed using spectrophotometric, gas chromatographic (GC), and conventional gravimetric procedures. These procedures are applicable to non-crosslinked methacrylate resins. In the presence of some copolymers, polymer blends or crosslinking agents, or other ingredients which will result in the formation of insoluble methacrylate resins, some modification of the identification procedures and quantitative estimation of the resin components will be required. Molecular weight and molecular weight distribution of the powder and cured cement were obtained from viscosity and gel-permeation measurements. Residual low molecular weight materials in the cured cement were determined for various storage times. Residual and water-leachable monomer and residual dimethyl-p-toluidine (DMPT) were measured by GC. In air, the monomer content of the cured resin decreased from 3.3% after 1 hr to 2.4% after 215 days. When stored in water at 37°C, over 65% of the extractable monomer is leached out within 10 min. After 6 hr, the rate of diffusion of monomer into the aqueous phase is low. The cured cement contains as much as 0.6% DMPT, which does not leach out. Residual peroxide, estimated spectrophotometrically, amounts to 0.8%, but decreases to 0.14% after 15 months in water at 37°C. A semiquantitative colorimetric test indicated that the hydroquinone content of specimens analyzed within 24 hr after curing amounted to 9 ppm.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 8 (1974), S. 451-470 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: This paper describes a novel approach for obtaining covalent bonding to tissues by chemical grafting of polymeric side chains to the collagenous backbone. Soft tissues such as calfskin or ratskin can be modified by acrylic, methacrylic, or vinyl monomers containing a variety of functional groups using ceric ions, persulfate-bisulfite or comonomers forming donor-acceptor complexes as initiators. Reactions take place within 20 min to 3 hr under experimental condition which, with suitable changes, might be tolerated clinically. The resulting products are insoluble in solvents for the respective homopolymers. It is likely that the polymeric side chain is attached chemically to the collagenous backbone. With ratskin, the grafting takes place mainly at the surface, resulting in a change in wettability and water sorption of the substrate. Modified hydrophilic, hydrophobic or even oil repellent surfaces can be prepared by judicious choice of monomer used. Thus, hydrophobic, oleophobic subdermal ratskin surfaces are obtained on reaction with flourinated monomers. Treated ratskins appear more resistant to fungal attack than the original substrate. It is conceivable that the polymeric side chains can serve as adhesive liners since the modified surface may improve the ability of the substrate to adhere to restorative materials.
    Additional Material: 5 Tab.
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  • 6
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Vanillate esters with multifunctional groups that react with metal oxides to give chainextended molecules have been synthesized. Divanillates were obtained from vanillic acid and the corresponding polymethylenediols. Methacryloylethyl vanillate (MEV) and vanillyl methacrylates were prepared respectively from hydroxyethyl vanillate or vanillyl alcohol and methacryloyl chloride. The properties of cements prepared with liquids incorporating these compounds were determined. Liquids containing divanillates dissolved in the reactive chelating agent o-ethoxybenzoic acid (EBA) when mixed with zinc oxide powders harden within a few minutes. The resulting cements have a tensile strength much higher than the commonly used zinc oxide-eugenol cements, have low solubility, do not inhibit polymerization, and adhere well to metallic substrates. Similarly, liquids with MEV as an ingredient yield cements with excellent strength and good adhesion to stainless steel and composites. Their brittleness can be overcome by addition of an oligomeric methacryloylethyl vanillate to the liquid or silanized glass to the powder ingredient. These cements, subject to their biocompatibility to oral tissues, could be most useful for a number of dental applications.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 23 (1989), S. 295-309 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A series of methacrylate oligomers containing pendant isocyanate groups were synthesized by reacting 2-isocyanatoethyl methacrylate (IEM) and/or m-isopropenyl- α, α-dimethylbenzyl isocyanate (TMI) in ethoxyethyl acetate with methacrylates ranging from methyl to stearyl methacrylate or allyl-, cyclohexyl-, glycidyl-, i-bornyl-, or dicyclopentenyloxyethyl methacrylate. The oligomers which are stable at room temperature were characterized by IR for NCO, ester, and C = C groups and by their refractive indices. They have a small number of residual double bonds and a molecular weight low enough so that the compounds are liquids at room temperature and dissolve readily in esters and chlorinated hydrocarbons. HPLC showed no residual monomer. GPC and intrinsic viscosity of selected oligomers indicated a molecular weight range from 1400 to 2600. Isocyanate groups were determined titrimetrically and ranged from 15.9% to 5.1%. Concurrent studies have demonstrated that these oligomers bond strongly to hard and soft tissues. Thus, subject to their biocompatibility they could find many applications as tissue adhesives.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 13 (1979), S. 593-606 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The durability of the bond strength developed between 2-cyanoacrylate esters and bone has been determined by aging specimens in water. One-day bond strength of the isobutyl and isomeric amyl 2-cyanoacrylates varied from 6.2 to 7.2 MPa. The strength of the bond decreased on storage or on thermocycling in water. Hydrolytic stability increased with increasing length of the alkyl ester group. After a six-month storage in water the various amyl 2-cyanoacrylates retained from 70% to 73% of their one-day bond strength. Pretreatment of the bone surface prior to application of the adhesive did not prove beneficial. The cured 2-cyanoacrylate can be removed from the substrate surface by appropriate solvents. Thus, it is not bonded covalently to bone. The bond strength, especially of the isobutyl and amyl 2-cyanoacrylates to bone in an aqueous environment, appears to be superior to other adhesives. Provided these monomers are biocompatible, they may be useful clinically where an intermediate-term adhesion is desired.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 20 (1986), S. 839-852 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Commercial bone cements usually contain hydroquinone as the polymerization inhibitor and N,N-dimethyl-p-toluidine as the accelerator in the benzoyl peroxide-initiated redox polymerization. The former compounds have certain shortcomings in their biocompatibility profile. Measurements of the setting times, polymerization exotherms, and postpolymerization strengths of the cured monomer-polymer compositions show that the hydroquinone can be replaced by food grade di-tert-butyl-p-cresol (BHT). The more reactive 4-N,N-(dimethylamino)phenethanol can replace 4-N,N-dimethyl-p-toluidine, yielding cements with shorter setting times and increased strengths. Excessive heat liberated on polymerization can be reduced by partial substitution of higher-molecular-weight methacrylates, e.g., dicyclopentenyloxyethyl methacrylate for methyl methacrylate, but there is a decrease in strength of the resulting polymer. More successful has been the addition to the monomer of 1% or 2% of the chain transfer agent pentaerythritol tetra(3-mercapto-propionate), which lowers the peak temperature without changing the physical properties of the cement. Compositions with short curing times, lower exotherms, and mechanical properties that exceed those of a commercial material have been formulated.
    Additional Material: 2 Ill.
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  • 10
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The adhesive properties of a series of oligomers prepared from 2-isocyanatoethyl methacrylates (IEM) and/or m-iso-propenyl-α,α-dimethylbenzyl isocyanate (TMI) and various acrylates or methacrylates were studied. The bond strength of bone, dentin, or soft tissue specimens joined with these oligomers respectively to bone, dental composite restorative, or denture base resin were determined by tensile adhesion or shear tests. These oligomers are more effective in forming stronger bonds to bone than are other tissue adhesives. Fracture occurs cohesively, usually within the bone. Thermocycling in water for 1 week between 5°C and 55°C did not decrease adhesion indicating that exposure to water or thermal shock produced no deterioration of the bond. Tensile adhesion of bovine or human dentin joined to composite restorative resin by means of the oligomers is similar to that of the best dental bonding agents such as Gluma (glutaraldehyde and 2-hydroxyethyl methacrylate) or ferric oxalate + Nphenylglycine + dimethylacryloxyethyl-pyromellitate. These oligomers also strongly bond soft tissues and calfskin and to acrylic resins and composites.
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