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  • 11
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 2785-2788 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 2824-2829 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 2113-2119 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Cancer chemotherapy and pharmacology 14 (1985), S. 15-20 
    ISSN: 1432-0843
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The metabolism of bisantrene, a new anthracene anticancer agent active in the treatment of disseminated breast cancer, was studied in vitro using rat liver S9 preparations and in vivo in patients receiving the drug as treatment for their cancers.14C-ring labeled bisantrene (248 mCi/40 mg) plus cold bisantrene were administered IV to cancer patients (260–340 mg/m2). Fractional urine samples were collected at various time intervals up to 120 h after drug administration and analyzed by HPLC. The percent of total14C excreted as unchanged parent drug per ml urine ranged from 37 to 79% in the 0 to 24 h samples. The remainder of the radioactivity appeared chromatographically just prior to the bisantrene peak, indicating that compounds more polar than the parent were present as transformation products. Metabolism of bisantrene was also studied in vitro under oxic (O2) and hypoxic (N2) conditions, using commercially available Aroclor 1254 induced rat liver S9 preparations. Following N2 incubation at 37° C for 1 h there was no evidence of metabolism, whereas there was more than 50% decrease in parent drug within 1 h following O2 incubation in the presence of NADPH generating system, suggesting that the metabolic process involves an oxidative reduction. HPLC chromatogram profiles of the mixtures exposed to the activated S9 system indicated that there were at least 3 polar metabolites. In vitro human tumor clonogenic assay showed that the biological activity of bisantrene decreased greater than 4-fold when the drug was incubated with S9 preparations in the presence of NADPH and O2, indicating that the transformation process leads to relatively inactive bisantrene metabolites.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Diseases of the colon & rectum 38 (1995), S. 670-670 
    ISSN: 1530-0358
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 859-878 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The behavior of catalytic chain transfer in semi-batch emulsion polymerization has been studied for two monomers, viz, methyl and n-butyl methacrylate. Two different catalytic chain transfer reagents were used with different water solubilities: cobaloxime boron fluoride (COBF), which was found to partition approximately equally between organic and aqueous phases, and tetra-phenyl cobaloxime boron fluoride (COPhBF), which was found to reside predominantly in the organic phase. The difference in hydrophilicity between the two transfer agents was found to affect the polymerization mechanism. COBF exhibited superior transfer behavior in all cases, whereas the restricted mobility of the COPhBF had a deleterious effect on the efficiency of the transfer mechanism. The best results were achieved under monomer flooded conditions using COBF. MALDI-TOF mass spectrometry analysis shows catalytic chain transfer to be the dominant mechanism initiating and stopping chain growth as none of the chains appear to have initiator fragment end groups. Analysis of copolymers by MALDI-TOF mass spectrometry reveals both molecular weight and composition data. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 859-878, 1997
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 181-185 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2097-2106 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The propagation kinetics for the copolymerization of 4-methoxystyrene with methyl methacrylate and 4-methoxystyrene with styrene have been investigated using a pulsed laser technique. The dependence of the copolymerization propagation rate constant on the monomer feed ratio shows a diviation from classic Mayo-Lewis model kinetics for 4-methoxystyrene with methyl methacrylate but not for 4-methoxystyrene with styrene. These results have been interpreted to indicate that a penultimate effect is apparent in the first monomer pair but not in the second. With r1r2 = 0.092 for the copolymerization of 4-methoxystyrene with methyl methacrylate and r1r2 = 0.95 for 4-methoxystyrene with styrene, it is suggested that a deviation of the product of the coplymerization reactivity ratios from unity may be an indication of the presence of a penultimate effect.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2311-2321 
    ISSN: 0887-624X
    Keywords: styrene ; methyl methacrylate ; pulsed-laser polymerization ; “living” free radical ; propagation rate coefficient ; solvent effects ; benzyl alcohol ; N-methyl pyrrolidinone ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The free radical propagation rate coefficients of both Methyl Methacrylate (MMA) and Styrene (STY) have been measured using Pulsed-Laser Polymerization. The effect of solvents on the propagation rate coefficient, kp, is reported for several solvents, namely, bromobenzene, chlorobenzene, dimethyl sulphoxide, diethyl malonate, diethyl phthalate, benzonitrile, and benzyl alcohol, at 26.5°C. This preliminary data indicated that benzyl alcohol (BzA) had a large effect on the MMA propagation reaction. As earlier work indicated that N-methyl pyrrolidinone (NMP) would also have a large effect on the kp of MMA, Arrhenius parameters were evaluated for both MMA and STY at two different concentrations of monomer in BzA and NMP. BzA had a significant effect (at 95% confidence) increasing both the activation energy (Ea) and the preexponential factor (A) for MMA and STY. In NMP, a similar trend is observed for MMA polymerization; however, while a solvent effect on STY was observed, the effect on Ea and A was too small to discern with confidence. A series of additional experiments was performed to evaluate the influence of camphorsulfonic acid (CSA) as an additive in STY polymerization. There was no effect of CSA on kp, confirming that the strong effect CSA has on “living” radical polymerization of styrene does not originate from complexation leading to an accelerated propagation step but rather by altering the ratio of active-to-dormant chains in the reaction. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2311-2321, 1997
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 36 (1995), S. 219-226 
    ISSN: 0959-8103
    Keywords: microemulsion ; hydrogel ; poly(2-hydroxyethyl methacrylate) ; equilibrium water content ; oxygen permeability ; scanning electron microscopy ; 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: A series of microemulsions have been formulated, with 2-hydroxyethyl methacrylate (HEMA) or HEMA/water/propanol mixtures as the continuous phase and methylcyclohexane as the discontinuous phase. The effect of surfactant type was investigated with the utilization of both anionic and nonionic surfactants. The microemulsion continuous phase was polymerized by UV radiation and a thermal post-cure. The resultant polymers were extracted to remove the discontinuous phase and the surfactant. On swelling, the majority of the polymers became opaque, although transparent PHEMA hydrogels were synthesized with an improved equilibrium water content (EWC). The cause of opacity was shown by field emission scanning electron microscopy (FESEM). The breakdown in the microemulsion on polymerization is caused by unfavourable interactions between the PHEMA and the stabilizing surfactants causing agglomerization of the discontinuous phase. All the hydrogels were found to have higher water retention than PHEMA, with EWCs of up to 70%. The modified polymers also demonstrated an increased rate of water diffusion into the matrix. A preliminary study of oxygen permability revealed that a significant improvement had been made over standard PHEMA membranes. The porous structure of the PHEMA gels has been shown to be dependent on the type of surfactant used during synthesis.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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