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Antimicrobial Agents and Chemotherapy, February 2004, p. 659-662, Vol. 48, No. 2
0066-4804/04/$08.00+0 DOI: 10.1128/AAC.48.2.659-662.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Kwanak-Gu, Seoul 151-742,1 Research Laboratory, Dong-A Pharmaceutical Company, Ltd., Yongin, Kyunggi-Do 449-900, Korea2
Received 31 January 2003/ Returned for modification 12 July 2003/ Accepted 4 October 2003
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).
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