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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Disposition of perphenazine is related to polymorphic debrisoquin hydroxylation in human beings.

The pharmacokinetics of a single oral dose of 6 mg perphenazine was studied in a group of six slow and six rapid hydroxylators of debrisoquin. Peak serum concentrations of perphenazine were significantly higher in slow hydroxylators than they were in rapid hydroxylators (2.4 +/- 0.6 versus 0.7 +/- 0.3 nmol/L, p less than 0.001). The AUC(0-12) was also higher in slow hydroxylators than it was in rapid hydroxylators (18.5 +/- 6.2 versus 4.5 +/- 2.5 nmol.L-1.hr, p less than 0.001). The data suggest that the disposition of the antipsychotic drug perphenazine covaries with polymorphic debrisoquin hydroxylation.[1]

References

  1. Disposition of perphenazine is related to polymorphic debrisoquin hydroxylation in human beings. Dahl-Puustinen, M.L., Lidén, A., Alm, C., Nordin, C., Bertilsson, L. Clin. Pharmacol. Ther. (1989) [Pubmed]
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