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KMID : 0043320100330060933
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Archives of Pharmacal Research
2010 Volume.33 No. 6 p.933 ~ p.938
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Pharmacokinetics of Magnolin in Rats
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Lee Hye-Suk
Kim Nam-Jin
Song Won-Young
Yoo Sun-Dong
Lee Hyeong-Kyu
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Abstract
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This study was first conducted to characterize the intravenous and oral pharmacokinetics of magnolin, a major pharmacologically active ingredient of Magnolia fargesii, at various doses in rats. Magnolin was administered to rats by intravenous injection (0.5, 1 and 2 mg/kg doses) and oral administration (1, 2 and 4 mg/kg doses), and serial plasma and urine samples were harvested. Magnolin concentrations were determined by a validated LC/MS/MS assay. After both intravenous and oral administration, the AUCs were linearly increased as the dose increased. Other pharmacokinetic parameters of magnolin (except the Vss after the intravenous administration) were also independent of the doses. The extent of absolute oral bioavailability ranged from 54.3-76.4% for the oral doses examined. Magnolin was considerably bound to rat plasma proteins and the binding value was constant (71.3-80.5%) over a concentration ranging from 500 to 10000 ng/mL. The pharmacokinetic parameters of magnolin were doseindependent after both intravenous and oral administration. When given orally, magnolin was rapidly absorbed.
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KEYWORD
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Magnolia fargesii, Magnolin, Pharmacokinetics, Plasma protein binding, Rats
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