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Obtained from in vitro time-kill data for <t>florfenicol.</t> Each point represents an experimental value. The curve is the line of best fit based on the sigmoidal Emax equation.
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Obtained from in vitro time-kill data for florfenicol. Each point represents an experimental value. The curve is the line of best fit based on the sigmoidal Emax equation.

Journal: PLoS ONE

Article Title: Pharmacokinetic/pharmacodynamic integration and modelling of florfenicol for the pig pneumonia pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida

doi: 10.1371/journal.pone.0177568

Figure Lengend Snippet: Obtained from in vitro time-kill data for florfenicol. Each point represents an experimental value. The curve is the line of best fit based on the sigmoidal Emax equation.

Article Snippet: Individual animal plasma concentration-time profiles for florfenicol generated in young pigs were obtained for two florfenicol containing products (Nuflor, Merck Animal Health, New Jersey, U.S., and Norfenicol, Norbrook Laboratories, Newry, Northern Ireland).

Techniques: In Vitro

Pharmacokinetic variables (mean, standard deviation, n = 34) for florfenicol.

Journal: PLoS ONE

Article Title: Pharmacokinetic/pharmacodynamic integration and modelling of florfenicol for the pig pneumonia pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida

doi: 10.1371/journal.pone.0177568

Figure Lengend Snippet: Pharmacokinetic variables (mean, standard deviation, n = 34) for florfenicol.

Article Snippet: Individual animal plasma concentration-time profiles for florfenicol generated in young pigs were obtained for two florfenicol containing products (Nuflor, Merck Animal Health, New Jersey, U.S., and Norfenicol, Norbrook Laboratories, Newry, Northern Ireland).

Techniques: Standard Deviation

Integration of pharmacokinetic ( in vivo plasma concentration) and pharmacodynamic (MIC determined in broth and serum) variables for florfenicol (mean and standard deviation).

Journal: PLoS ONE

Article Title: Pharmacokinetic/pharmacodynamic integration and modelling of florfenicol for the pig pneumonia pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida

doi: 10.1371/journal.pone.0177568

Figure Lengend Snippet: Integration of pharmacokinetic ( in vivo plasma concentration) and pharmacodynamic (MIC determined in broth and serum) variables for florfenicol (mean and standard deviation).

Article Snippet: Individual animal plasma concentration-time profiles for florfenicol generated in young pigs were obtained for two florfenicol containing products (Nuflor, Merck Animal Health, New Jersey, U.S., and Norfenicol, Norbrook Laboratories, Newry, Northern Ireland).

Techniques: In Vivo, Clinical Proteomics, Concentration Assay

Integration of pharmacokinetic ( in vivo plasma concentration) and pharmacodynamic (MPC determined in broth and serum) variables for florfenicol (mean and standard deviation).

Journal: PLoS ONE

Article Title: Pharmacokinetic/pharmacodynamic integration and modelling of florfenicol for the pig pneumonia pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida

doi: 10.1371/journal.pone.0177568

Figure Lengend Snippet: Integration of pharmacokinetic ( in vivo plasma concentration) and pharmacodynamic (MPC determined in broth and serum) variables for florfenicol (mean and standard deviation).

Article Snippet: Individual animal plasma concentration-time profiles for florfenicol generated in young pigs were obtained for two florfenicol containing products (Nuflor, Merck Animal Health, New Jersey, U.S., and Norfenicol, Norbrook Laboratories, Newry, Northern Ireland).

Techniques: In Vivo, Clinical Proteomics, Concentration Assay