Drug Metabolism and Pharmacokinetics
Online ISSN : 1880-0920
Print ISSN : 1347-4367
ISSN-L : 1347-4367
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Quantitative Prediction of Intestinal Glucuronidation of Drugs in Rats Using In Vitro Metabolic Clearance Data
Takako FURUKAWAFumihiro NAKAMORIKazuhiro TETSUKAYoichi NARITOMIHiroyuki MORIGUCHIKatsuhiro YAMANOShigeyuki TERASHITAToshio TERAMURA
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2012 Volume 27 Issue 2 Pages 171-180

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Abstract

  UDP-glucuronosyltransferase (UGT) is highly expressed in the small intestine and catalyzes the glucuronidation of small molecules, which may affect the oral bioavailability of drugs. However, no method of predicting the in vivo observed fraction of absorbed drug (FaFg) affected by UGT has yet been established. Here, we investigated the relationship between FaFg and in vitro clearance of nine UGT substrates (ketoprofen, tolcapone, telmisartan, raloxifene, entacapone, resveratrol, buprenorphine, quercetin, and ezetimibe) via UGT in intestinal microsomes (CLint, UGT) in rats. FaFg was calculated from pharmacokinetic parameters after intravenous and oral administration or using the portal-systemic concentration difference method, with values ranging from 0.027 (ezetimibe) to 1 (tolcapone). Glucuronides of model compounds were observed in the portal plasma after oral administration, with CLint, UGT values ranging from 57.8 (tolcapone) to 19,200 µL/min/mg (resveratrol). An inverse correlation between FaFg and CLint, UGT was observed for most compounds and was described using a simplified intestinal availability model reported previously. This model gave accurate predictions of FaFg values for three in-house compounds. Our results show that FaFg in rats is affected by UGT and can be predicted using CLint, UGT. This work should hasten the development of a method to predict FaFg in humans.

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© 2012 by The Japanese Society for the Study of Xenobiotics
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