Background\r\nPhenoxodiol is a novel isoflavone currently being studied in clinical trials for the treatment of cancer. This study reports the pharmacokinetics of phenoxodiol in patients with cancer.\r\nMethods\r\nThe pharmacokinetics of phenoxodiol was studied following a single intravenous (iv) bolus dose and during a continuous intravenous infusion. Three men with prostate cancer and 3 women with breast cancer received IV bolus phenoxodiol (5 mg/kg) and plasma was sampled for free and total phenoxodiol levels. On a separate occasion 5 of the same patients received a continuous intravenous infusion of phenoxodiol (2 mg/kg/h) and plasma was again sampled for free and total phenoxodiol levels. Phenoxodiol was measured using gradient HPLC with ultraviolet detection.\r\nResults\r\nFollowing bolus injection, free and total phenoxodiol appeared to follow first order pharmacokinetics. The elimination half-lives for free and total phenoxodiol were 0.67 �± 0.53 h and 3.19 �± 1.93 h, respectively, while the total plasma clearance rates were 2.48 �± 2.33 L/h and 0.15 �± 0.08 L/h, respectively. The respective apparent volumes of distribution were 1.55 �± 0.69 L/kg and 0.64 �± 0.51 L/kg. During continuous intravenous infusion, free phenoxodiol accumulated rapidly to reach a mean concentration at steady state of 0.79 �± 0.14 �µg/ml after 0.87 �± 0.18 h. The apparent accumulation half-life of free phenoxodiol was 0.17 �± 0.04 h while the plasma clearance during continuous infusion was 1.29 �± 0.23 L/h.\r\nConclusions\r\nPhenoxodiol has a short plasma half-life, particularly in the free form, leading to a rapid attainment of steady state levels during continuous intravenous infusion.
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