acute and chronic administrations of rheum palmatum reduced the bioavailability of phenytoin in rats a new herb-drug interaction急性和慢性的政府感冒palmatum苯妥英的生物利用度,减少老鼠一个新的herb-drug交互.pdfVIP

acute and chronic administrations of rheum palmatum reduced the bioavailability of phenytoin in rats a new herb-drug interaction急性和慢性的政府感冒palmatum苯妥英的生物利用度,减少老鼠一个新的herb-drug交互.pdf

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acute and chronic administrations of rheum palmatum reduced the bioavailability of phenytoin in rats a new herb-drug interaction急性和慢性的政府感冒palmatum苯妥英的生物利用度,减少老鼠一个新的herb-drug交互

Hindawi Publishing Corporation Evidence-Based Complementary and Alternative Medicine Volume 2012, Article ID 701205, 9 pages doi:10.1155/2012/701205 Research Article Acute and Chronic Administrations of Rheum palmatum Reduced the Bioavailability of Phenytoin in Rats: A New Herb-Drug Interaction Ying-Chang Chi,1 Shin-Hun Juang,1 Wai Keung Chui,2 Yu-Chi Hou,3, 4 and Pei-Dawn Lee Chao3 1 Institute of Pharmaceutical Chemistry, China Medical University, Taichung 40402, Taiwan 2 Department of Pharmacy, Faculty of Science, National University of Singapore, 18 Science Drive 4, Singapore 117543 3 School of Pharmacy, China Medical University, Taichung 40402, Taiwan 4 Department of Medical Research, China Medical University Hospital, Taichung 40402, Taiwan Correspondence should be addressed to Yu-Chi Hou, hou5133@ and Pei-Dawn Lee Chao, Received 16 March 2012; Revised 23 April 2012; Accepted 27 April 2012 Academic Editor: Paul Siu-Po Ip Copyright © 2012 Ying-Chang Chi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The rhizome of Rheum palmatum (RP) is a commonly used herb in clinical Chinese medicine. Phenytoin (PHT) is an antiepileptic with narrow therapeutic window. This study investigated the acute and chronic effects of RP on the pharmacokinetics of PHT in rat. Rats were orally administered with PHT (200 mg/kg) with and without RP decoction (single dose and seven doses of 2 g/kg) in a crossover design. The serum concentrations of PHT, PHT glucuronide (PHT-G), 4-hydroxyphenytoin (HPPH), and HPPH glucuronide (HPPH-G) were determined by HPLC method. Cell line models were us

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