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Article

Pharmacokinetics and Excretion Studies on CDRI-85/92, an Antiulcer Proton Pump Inhibitor

by
Pratima SRIVASTAVA
Pharmacokinetics and Drug Metabolism, Central Drug Research Institute, Lucknow, India
Submission received: 6 November 2011 / Accepted: 12 December 2011 / Published: 12 December 2011

Abstract

CDRI 85/92 is an antiulcer pharmacophore and a proton pump inhibitor, which is in an advanced stage of preclinical trials. In view of its importance, pharmacokinetic and excretion were studied in Sprague Dawley rats after administering 20 mg/kg oral and intravenous doses. The compound was detectable in the serum samples as early as 5 min post-oral administration. The compound was eliminated slowly from serum with an elimination half-life of 2.1 h. Following the 20 mg/kg oral dose, maximum serum concentration (Cmax) was found to be 469.28 ± 45.52 ng/ml after 1.0 h. Based on AUC values, the absolute bioavailability of the CDRI 85/92 was 70.5% after oral administration. It was found to be excreted in urine (~15% of the dose) in intravenously treated (bile duct cannulated as well as noncannulated) rats, whereas bile and feces depicted insignificant levels of the compound.
Keywords: CDRI Compound 85/92; Antiulcer pharmacophore; Bioavailability; Pharmacokinetics; Excretion; PPI CDRI Compound 85/92; Antiulcer pharmacophore; Bioavailability; Pharmacokinetics; Excretion; PPI

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MDPI and ACS Style

SRIVASTAVA, P. Pharmacokinetics and Excretion Studies on CDRI-85/92, an Antiulcer Proton Pump Inhibitor. Sci. Pharm. 2012, 80, 167-178. https://0-doi-org.brum.beds.ac.uk/10.3797/scipharm.1111-05

AMA Style

SRIVASTAVA P. Pharmacokinetics and Excretion Studies on CDRI-85/92, an Antiulcer Proton Pump Inhibitor. Scientia Pharmaceutica. 2012; 80(1):167-178. https://0-doi-org.brum.beds.ac.uk/10.3797/scipharm.1111-05

Chicago/Turabian Style

SRIVASTAVA, Pratima. 2012. "Pharmacokinetics and Excretion Studies on CDRI-85/92, an Antiulcer Proton Pump Inhibitor" Scientia Pharmaceutica 80, no. 1: 167-178. https://0-doi-org.brum.beds.ac.uk/10.3797/scipharm.1111-05

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