Fig. 5. (  A ) Graphs of the ratio of measured to predicted drug concentrations  versus time relations for  S -(+)- and  R -(−)-ketamine in all five dogs. Predicted concentrations are from the ketamine models in which ClEis modeled from the arterial sampling site (central) and all distribution parameters are adjusted independently (model 1). (  B ) Graphs of the ratio of measured to predicted drug concentrations  versus time relations for  S -(+)- and  R -(−)-ketamine in all five dogs. Predicted concentrations are from the ketamine models in which ClEis modeled from the rapidly equilibrating peripheral tissue compartment (peripheral) and all distribution parameters are adjusted such that they are the same for the  S -(+)- and  R -(−)-enantiomers (model 4). 

Fig. 5. (  A ) Graphs of the ratio of measured to predicted drug concentrations  versus time relations for  S -(+)- and  R -(−)-ketamine in all five dogs. Predicted concentrations are from the ketamine models in which ClEis modeled from the arterial sampling site (central) and all distribution parameters are adjusted independently (model 1). (  B ) Graphs of the ratio of measured to predicted drug concentrations  versus time relations for  S -(+)- and  R -(−)-ketamine in all five dogs. Predicted concentrations are from the ketamine models in which ClEis modeled from the rapidly equilibrating peripheral tissue compartment (peripheral) and all distribution parameters are adjusted such that they are the same for the  S -(+)- and  R -(−)-enantiomers (model 4). 

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