The peroral (po) bioavailability of nifedipine is reported to range from about 45 to 58% in the rat; this compares favourably to human beings. The metabolism of nifedipine is similar in rats and humans (oxidation of the dihydropyridine ring), with the liver believed to be solely responsible for the
โฆ LIBER โฆ
Intestinal First-Pass Metabolism of Eperisone in the Rat
โ Scribed by Kiyoshi Mihara; Mina Matsumura; Eiji Yoshioka; Kazuhiko Hanada; Hiromitsu Nakasa; Shigeru Ohmori; Mitsukazu Kitada; Hiroyasu Ogata
- Book ID
- 110295645
- Publisher
- Springer US
- Year
- 2001
- Tongue
- English
- Weight
- 154 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0724-8741
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