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Timed-kill curve tests

The second most common method to determine the effects of antibiotic combinations is an adaptation of timed-kill curve tests. Two antibiotics are added to the same test tube at fixed concentration fractions of the MIC for each drug, and killing is quantified. With this method, synergism is defined as a 100-fold decrease in viable organisms at 24 hours for the combination as compared with the most potent antibiotic tested alone. Antagonism is defined as a 100-fold or greater increase in viable organism count (Fig. 103-9). It is... [Pg.1903]

Considering all the above data, the U.S. EPA (1991) selected the unit risk of 8.5 x 10 per pg/m, derived from the Weibull time-to-tumor model, as the recommended upper bound estimate of the carcinogenic potency of sulfur mustard for a lifetime exposure to HD vapors. However, U.S. EPA (1991) stated that "depending on the unknown true shape of the dose-response curve at low doses, actual risks may be anywhere from this upper bound down to zero". The Weibull model was considered to be the most suitable because the exposures used were long-term, the effect of killing the test animals before a full lifetime was adjusted for, and the sample size was the largest obtainable from the McNamara et al. (1975) data. [Pg.279]

FIGURE 103-7. Killing curve depicting the effect of concentration on antibiotic bactericidal activity. CPU = colony-forming units MIC = minimal Inhibitory concentration. 0.25-64 times the MIC the organism tested was P. aeruginosa ATCC 27853. (From ref 51.)... [Pg.1902]


See other pages where Timed-kill curve tests is mentioned: [Pg.1902]    [Pg.1902]    [Pg.1902]    [Pg.1902]    [Pg.73]    [Pg.463]    [Pg.189]    [Pg.19]    [Pg.359]    [Pg.312]    [Pg.434]    [Pg.354]    [Pg.176]    [Pg.356]   
See also in sourсe #XX -- [ Pg.1902 , Pg.1902 ]




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