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Xenobiotica
the fate of foreign compounds in biological systems
Volume 46, 2016 - Issue 10
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Animal Pharmacokinetics and Metabolism

Factors limiting the extent of absolute bioavailability of pradefovir in rat

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Pages 913-921 | Received 23 Sep 2015, Accepted 15 Dec 2015, Published online: 05 Feb 2016
 

Abstract

1. Pradefovir was designed as an oral liver target prodrug of 9-(2-phosphonylmethoxyethyl) adenine (PMEA). Liver targeting arises through first pass hepatic metabolism by cytochrome P-450 3A4 (CYP3A4). For CYP3A4 primarily exists in intestines and liver, intestinal metabolism may impair its liver selectivity and oral bioavailability, and then impair its efficacy and safety. It was important to reveal details of the disposition of pradefovir in intestines and liver in a preclinical study.

2. The absolute bioavailability of pradefovir was 4.75% based on the intravenous and oral AUC0–24 h in rats. Pradefovir was stable in intestinal segments and microsomes. The fractions of the dose absorbed from the GI tract were 20.3% and 15.3% from intravenous and oral administration of pradefovir in rats and portal vein-cannulated rat models, respectively. The liver extraction ratio was predicted to be 49.2% from liver microsomes system, based on the monitoring substrate loss rate. Rat intestines’ Ussing chamber experiment indicated that P-glycoprotein (P-gp) transporter and paracellular pathway may involve in intestinal transportation.

3. Activation of pradefovir mainly occurs in the liver. Low intestinal absorption was the main reason of low bioavailability of pradefovir in rats. The result was suggestive for the disposition of pradefovir in human intestine and liver.

Declaration of interest

The authors have no conflicts of interest to declare.

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