Analysis of silibinin in rat plasma and bile for hepatobiliary excretion and oral bioavailability application

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• 作者：Jhy-Wen Wu ; Lie-Chwen Lin ; Shih-Chieh Hung ; Chin-Wen Chi ; Tung-Hu Tsai
• 关键词：Bioavailability ; Herbal medicine ; Milk thistle ; Silybum marianum ; Silymarin
• 刊名：Journal of Pharmaceutical and Biomedical Analysis
• 出版年：2007
• 出版时间：30 November 2007
• 年：2007
• 卷：45
• 期：4
• 页码：635-641
• 全文大小：379 K

文摘

Silibinin is an herbal ingredient isolated from milk thistle. The aim of this study was to develop a simple liquid chromatographic system to assay silibinin in plasma and bile for pharmacokinetic study. Silibinin was given oral and intravenously. The plasma sample (25 μL) was vortex-mixed with 50 μL of internal standard solution (naringenin 10 μg/mL in acetonitrile) to achieve protein precipitation. Silibinin in the rat plasma and bile was separated using a reversed-phase C18 column (250 mm × 4.6 mm, 5 μm) with a mobile phase of acetonitrile −10 mM monosodium phosphate (pH 5.45 adjusted with orthophosphoric acid) (50:50, v/v) and the flow-rate of 1 mL/min. The UV detection wavelength was 288 nm. The concentration–response relationship from the present method indicated linearity over a concentration range of 0.5–100 μg/mL. Intra- and inter-assay precision and accuracy of silibinin fell well within the predefined limits of acceptability (<15 % ). An ultrafiltration method was used in this experiment and the protein binding of silibinin was 70.3 ± 4.6 % . After silibinin administration in rats, the disposition of silibinin in the plasma and bile fluid was due to rapid distribution and equilibration between the blood and hepatobiliary system, and the bile levels of unconjugated silibinin and total silibinin were greater than those in the plasma. The oral bioavailability of silibinin in rats was estimated to be 0.73 % .