Pharmacokinetics of DA-7867, a new oxazolidinone, after intravenous or oral administration to rats: Intestinal first-pass effect

被引:21
|
作者
Bae, SK
Chung, WS
Kim, EJ
Rhee, JK
Kwon, JW
Kim, WB
Lee, MG
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul 151742, South Korea
[3] Dong A Pharmaceut Co Ltd, Res Lab, Yongin 449900, Kyunggi Do, South Korea
关键词
D O I
10.1128/AAC.48.2.659-662.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pharmacokinetic parameters of DA-7867 were dose independent after both intravenous administration and oral administration (at doses of 1 to 20 mg/kg of body weight) to rats. After oral administration of DA-7867 to rats at a dose of 10 mg/kg, approximately 8.27% of oral dose was not absorbed from the gastrointestinal tract, F was 70.8%, and approximately 21.8% of the oral dose was eliminated by the intestine (intestinal first-pass effect).
引用
收藏
页码:659 / 662
页数:4
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