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  • 1
    Electronic Resource
    Electronic Resource
    Disposition kinetics, urinary excretion and dosage regimen of kanamycin in buffalo calves following single intravenous administration (1993)
    Springer
    Veterinary research communications 17 (1993), S. 219-225 
    Details
    ISSN: 1573-7446
    Keywords: buffalo ; disposition ; dose ; kanamycin ; pharmacokinetics ; serum ; urine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The disposition kinetics and appropriate dosage regimen for kanamycin were investigated in buffalo calves following a single intravenous dose of 10 mg/kg body weight. The distribution and elimination half-lives were 0.12±0.01 h and 1.94±0.11 h, respectively. The apparent volume of distribution and total body clearance were 0.2±0.01 L/kg and 92.9±3.69 ml/kg/h, respectively. About 74% of the administered dose was excreted in urine in 24 h. A suitable dosage regimen for the intravenous administration of kanamycin was also calculated.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01839170
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Pharmacokinetics and dosage regimen of cephalexin in buffalo calves (Bubalus bubalis) following single intravenous and intramuscular administration (1990)
    Springer
    Veterinary research communications 14 (1990), S. 59-62 
    Details
    ISSN: 1573-7446
    Keywords: buffalo ; cephalexin ; pharmacokinetics ; treatment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00346385
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    p-acetyl benzylidene triphenylarsonium ylide initiated radical terpolymerization of styrene, acrylonitrile and copper acrylate: synthesis, characterization and properties (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 407-412 
    Details
    ISSN: 0959-8103
    Keywords: terpolymerization ; kinetics ; thermal properties ; arsonium ylide ; styrene ; acrylonitrile ; copper acrylate ; 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: Solution terpolymerization of styrene (Sty), acrylonitrile (AN) and copper acrylate (CuA) has been carried out in dimethylformamide at 90°C for 4 h using p-acetyl benzylidene triphenylarsonium ylide as radical initiator. 1H nuclear magnetic resonance (NMR), IR and elemental analysis have been used to characterized the terpolymer. Analysis of kinetic data indicates the following rate equation: $$R_{\rm p} \propto \left[ {{\rm ylide}} \right]^{0.5} \left[ {{\rm Sty}} \right]\left[ {{\rm AN}} \right]{1 \over {\left[ {{\rm CuA}} \right]}}$$ The overall activation energy is 38 kJ mol-1. The composition of terpolymer calculated from NMR and elemental analysis has been used to evaluate reactivity ratios as r1(Sty) = 5 ± 2 and r2(AN + CuA) = 0.4 ± 0.02 employing the Finemann-Ross method, which confirms its random origin. The terpolymer was thermally stable up to 2007deg;C.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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    Paper (German National Licenses)
  • 4
    Electronic Resource
    Electronic Resource
    Copolymerization of zinc acrylate with acrylonitrile initiated by As2S3-styrene complex (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 34 (1994), S. 105-109 
    Details
    ISSN: 0959-8103
    Keywords: Zinc acrylate ; acrylonitrile ; As2S3-styrene complex ; copolymerization ; dilatometry ; kinetics ; 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: Radical copolymerization of zinc acrylate (ZnA2) with acrylonitrile (AN), initiated by As2S3-styrene complex(I), in dimethyl Sulphoxide (DMSO) at 90 ± 0.1°C for 1.0h under inert atmosphere, yields non-alternating copolymers. The kinetic expression is Rp ∝ [I]0.33 [ZnA2]0.25 [AN]0.44, i.e. the system follows non-ideal kinetics, which is due to primary radical termination as well as degradative chain transfer reactions. The values for activation energy (E) and k2p/kt are 128kJ mol-1 and 8.57 × 10-7 litre mol-1 s-1, respectively. Thermal stability, solubility in different solvents, and IR and NMR spectra have been evaluated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pi.1994.210340114
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    Paper (German National Licenses)
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