Figure 2. Effect of P450 3A4 activity on alfentanil disposition. (Left) Alfentanil plasma concentrations in a typical participant. Disposition of alfentanil (20 micro gram/kg given intravenously) is shown for the control (no treatment; triangles), rifampin treatment (squares), and troleandomycin treatment (circles). Symbols depict measured concentrations, and lines represent predicted concentrations using microconstant parameters derived from a three-compartment model. (Right) Average (+/- SE) alfentanil plasma concentrations for all nine men. Table 2shows the average pharmacokinetic parameters for all nine men.

Figure 2. Effect of P450 3A4 activity on alfentanil disposition. (Left) Alfentanil plasma concentrations in a typical participant. Disposition of alfentanil (20 micro gram/kg given intravenously) is shown for the control (no treatment; triangles), rifampin treatment (squares), and troleandomycin treatment (circles). Symbols depict measured concentrations, and lines represent predicted concentrations using microconstant parameters derived from a three-compartment model. (Right) Average (+/- SE) alfentanil plasma concentrations for all nine men. Table 2shows the average pharmacokinetic parameters for all nine men.

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