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  • Flow injection  (1)
  • Infinitesimal Perturbation Analysis  (1)
  • MIC  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Analytica Chimica Acta 266 (1992), S. 325-329 
    ISSN: 0003-2670
    Keywords: Chemiluminescence ; Enzymatic methods ; Ethanol ; Fibre-optic sensor ; Flow injection ; Wines
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Discrete event dynamic systems 6 (1996), S. 221-239 
    ISSN: 1573-7594
    Keywords: Stochastic Timed Event Graphs ; Discrete Event Dynamic Systems ; Marking Optimization ; Infinitesimal Perturbation Analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract This paper addresses the marking optimization of stochastic timed event graphs, where the transition firing times are generated by random variables with general distributions. The marking optimization problem consists of obtaining a given cycle time while minimizing a p-invariant criterion. We propose two heuristic algorithms, both starting from the optimal solution to the associated deterministic problem and iteratively adding tokens to adequate places as long as the given cycle time is not obtained. Infinitesimal perturbation analysis of the average cycle time with respect to the transition firing times is used to identify the appropriate places in which new tokens are added at each iteration. Numerical results show that the heuristic algorithms provide solutions better than the ones obtained by the existing methods.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1437-7780
    Keywords: Key words Cefpiramide ; Cephalosporin ; Clinical strains ; MIC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The in-vitro antibacterial activity of cefpiramide was compared with those of 15 other broad-spectrum cephalosporins. A total of 440 clinical strains of bacteria, including 9 bacterial species, were isolated from our hospital in 1998. The minimum inhibitory concentrations (MICs) of cefpiramide and five other antibiotics were determined for each species, using the agar-dilution method. The MIC of cefpiramide for Escherichia coli and Klebsiella pneumoniae was higher than those of three other third-generation cephalosporins, (ie, cefoperazone, ceftazidime, and ceftriaxone). Fifty-one percent (26/51) of Enterobacter cloacae isolates were resistant to cefpiramide. Cefoperazone/sulbactam and cefepime had greater activity against E. cloacae (resistance, 3.9% and 19.6%, respectively) than cefpiramide. Cefpiramide was more active against Pseudomonas aeruginosa (resistance rates, 12%) than cefoperazone, ceftazidime, ceftriaxone, aztreonam, and cefepime. Cefpiramide-resistant P. aeruginosa strains were resistant to ceftazidime, but 27% of ceftazidime-resistant strains were susceptible to cefpiramide; 15.3% of cefpiramide-resistant S. maltophilia strains were also susceptible to ceftazidime, but 50% of ceftazidime-resistant strains were still susceptible to cefpiramide. Cefoperazone/sulbactam was the most active agent against Acinetobacter baumannii, showing a resistance rate of 2%. Ampicillin/sulbactam, ceftazidime, and cefpiramide were the second most active agents, and about 50% of the tested strains were susceptible to these three antibiotics. Cefpiramide had an activity comparable to that of all tested β-lactams against oxacillin-susceptible Staphylococcus aureus (MIC90, 2 μg/ml). Against Streptococcus pneumoniae and Haemophilus influenzae, cefpiramide had good activity, with an MIC90 concentration at which 90% of the strain was inhibited of 1 μg/ml and 0.5 μg/ml, respectively. These results indicated that cefpiramide was more active against glucose non-fermenting bacteria than against Enterobacteriaceae, and was very active against oxacillin-susceptible Staphylo-coccus aureus, S. pneumoniae, and H. influenzae. Thus, cefpiramide may be a good choice of drug for the treatment of patients with infections with glucose non-fermenting bacteria and community acquired infections.
    Type of Medium: Electronic Resource
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