Abstract
Background: A practical, simple, high-performance liquid chromatographic (HPLC) method is needed for the determination of itraconazole in clinical plasma samples. Methods: Itraconazole and bifonazole (internal standard) were extracted from plasma using a C8 bonded solid-phase cartridge, separated by C8 reversed-phase HPLC, and quantified by ultraviolet absorption at 263 nm. Results: This new method enabled the determination of itraconazole in the concentration range of 10.0-500.0 μg/L. The detection limit of itraconazole was 5.0 μg/L The mean recovery of itraconazole added to plasma was more than 89.1%, with a coefficient of variation of less than 6.9%. We applied this method for the determination of plasma itraconazole in volunteers treated daily with a 200 mg oral capsule of itraconazole for four days. We monitored the plasma level of itraconazole for the following 24 h and obtained the mean area under the plasma concentration-time curve from 0 to 24 h (AUC0-24) value of 4358.9 ± 1933.4 μg h/L. Conclusion: Our new method will be clinically useful for accurately monitoring the plasma concentration of itraconazole in patients under treatment. © 2005 The Association of Clinical Biochemists.
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CITATION STYLE
Ohkubo, T., & Osanai, T. (2005). Determination of itraconazole in human plasma by high-performance liquid chromatography with solid-phase extraction. Annals of Clinical Biochemistry, 42(2), 94–98. https://doi.org/10.1258/0004563053492711
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