Abstract
Itraconazole (ITZ) is a potent inhibitor of CYP3A in vivo. However, unbound plasma concentrations of ITZ are much lower than its reported in vitro Ki, and no clinically significant interactions would be expected based on a reversible mechanism of inhibition. The purpose of this study was to evaluate the reasons for the in vitro-in vivo discrepancy. The metabolism of ITZ by CYP3A4 was studied. Three metabolites were detected: hydroxy-itraconazole (OH-ITZ), a known in vivo metabolite of ITZ, and two new metabolites: keto-itraconazole (keto-ITZ) and N-desalkyl-itraconazole (ND-ITZ). OHITZ and keto-ITZ were also substrates of CYP3A4. Using a substrate depletion kinetic approach for parameter determination, ITZ exhibited an unbound Km of 3.9 nM and an intrinsic clearance (CLint) of 69.3 ml·min-1·nmol CYP3A4-1. The respective unbound Km values for OH-ITZ and keto-ITZ were 27 nM and 1.4 nM and the CLint values were 19.8 and 62.5 ml·min-1·nmol CYP3A4-1. Inhibition of CYP3A4 by ITZ, OH-ITZ, keto-ITZ, and ND-ITZ was evaluated using hydroxylation of midazolam as a probe reaction. Both ITZ and OH-ITZ were competitive inhibitors of CYP3A4, with unbound Ki (1.3 nM for ITZ and 14.4 nM for OH-ITZ) close to their respective Km. ITZ, OH-ITZ, keto-ITZ and ND-ITZ exhibited unbound IC50 values of 6.1 nM, 4.6 nM, 7.0 nM, and 0.4 nM, respectively, when coincubated with human liver microsomes and midazolam (substrate concentration < Km). These findings demonstrate that ITZ metabolites are as potent as or more potent CYP3A4 inhibitors than ITZ itself, and thus may contribute to the inhibition of CYP3A4 observed in vivo after ITZ dosing.
Footnotes
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This study was supported in part by National Institutes of Health Grant P01 GM32165.
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doi:10.1124/dmd.104.000315.
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ABBREVIATIONS: ITZ, itraconazole; OH-ITZ, hydroxy-itraconazole; keto-ITZ, keto-itraconazole; ND-ITZ, N-desalkyl-itraconazole; OH-MDZ, 1′-hydroxymidazolam; HLM, human liver microsome; HPLC, high performance liquid chromatography; KPi, monobasic phosphate; MS/MS, tandem mass spectrometry; LC-MS, liquid chromatography-mass spectrometry; P450, cytochrome P450, Km, Michaelis constant; Ki, inhibition constant, CLint, intrinsic clearance; AUC, area under the curve.
- Received April 19, 2004.
- Accepted July 6, 2004.
- The American Society for Pharmacology and Experimental Therapeutics
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