Simultaneous pharmacokinetics assessment of caffeine, warfarin, omeprazole, metoprolol, and midazolam intravenously or orally administered to Microminipigs-Reference-Cited by-同舟云学术

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Simultaneous pharmacokinetics assessment of caffeine, warfarin, omeprazole, metoprolol, and midazolam intravenously or orally administered to Microminipigs

Published:2012 Issue:6 Volume:37 Page:1157-1164
ISSN:0388-1350
Container-title:The Journal of Toxicological Sciences
language:en
Short-container-title:J. Toxicol. Sci.

Author:

Mogi Masayuki¹,Toda Akiko¹,Iwasaki Kazuhide¹,Kusumoto Shogo²,Takehara Hiromi³,Shimizu Makiko³,Murayama Norie³,Izumi Hiroyuki²,Utoh Masahiro¹,Yamazaki Hiroshi³

Affiliation:

1. Pharmacokinetics and Bioanalysis Center, Shin Nippon Biomedical Laboratories, Ltd.

2. Drug Safety Research Laboratories, Shin Nippon Biomedical Laboratories, Ltd.

3. Laboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical University

Publisher

Japanese Society of Toxicology

Subject

Toxicology

Link

https://www.jstage.jst.go.jp/article/jts/37/6/37_1157/_pdf

Reference21 articles.

1. Achour, B., Barber, J. and Rostami-Hodjegan, A. (2011): Cytochrome P450 Pig liver pie: determination of individual cytochrome P450 isoform contents in microsomes from two pig livers using liquid chromatography in conjunction with mass spectrometry. Drug Metab. Dispos., 39, 2130-2134.

2. Andersson, T., Miners, J.O., Veronese, M.E., Tassaneeyakul, W., Tassaneeyakul, W., Meyer, U.A. and Birkett, D.J. (1993): Identification of human liver cytochrome P450 isoforms mediating omeprazole metabolism. Br. J. Clin. Pharmacol., 36, 521-530.

3. Anzenbacher, P., Anzenbacherova, E., Zuber, R., Soucek, P. and Guengerich, F.P. (2002): Pig and minipig cytochromes P450. Drug Metab. Dispos., 30, 100-102.

4. Baranova, J., Anzenbacherova, E., Anzenbacher, P. and Soucek, P. (2005): Minipig cytochrome P450 2E1: Comparison with human enzyme. Drug Metab. Dispos., 33, 862-865.

5. Bertz, R.J. and Granneman, G.R. (1997): Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin. Pharmacokinet., 32, 210-258.

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