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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 73 (2000), S. 570-574 
    ISSN: 1432-1246
    Keywords: Key words Toluene diisocyanate ; Sampling efficiency ; Closed-face cassette ; Open-face cassette
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objectives: A modified closed-face cassette was developed for sampling and derivatizing airborne toluene diisocyanate (TDI). Methods: The cassette was assembled as a regular two-piece cassette sampler except that the whole inner surface of the sampler was loaded with coated filters to ensure that all of the aspirated TDI react with 1-(2-pyridyl) piperazine (1-2pp). Results: A test atmosphere study showed that the sampling efficiencies were 89.4% and 94.3% for 2,4-TDI and 2,6-TDI. One-third of the 2,4-TDI and 2,6-TDI mass was constantly collected on the top and middle-rim filters. A polyurethane (PU)-manufacturing plant study revealed an average of 35% and 33% of both isomer masses collected on the top and middle-rim filters. The 2,4-TDI collection of the closed-face cassette sampling was 21% higher than that of open-face sampling. Furthermore, consistent isomeric compositions of airborne 2,4-/2,6- TDI obtained from both types of samplers validated the use of the modified cassette sampler. Conclusions: The closed-face cassette sampler is capable of a higher collection of airborne TDI and the technique involved is as simple and feasible as that of the open-face sampler.
    Type of Medium: Electronic Resource
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  • 2
    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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