Literature DB >> 15646644

Remofovir mesylate: a prodrug of PMEA with improved liver-targeting and safety in rats and monkeys.

Chin-Chung Lin1, Li-Tain Yeh, Domenico Vitarella, Zhi Hong, Mark D Erion.   

Abstract

Adefovir dipivoxil (Hepsera), a first-line therapy for chronic hepatitis B, is an esterase-activated prodrug of PMEA. Dose-limiting nephrotoxicity necessitates suboptimal dosing at 10 mg/day. Remofovir mesylate (MB06866Q) (Hepavir B) is a CYP3A4-activated prodrug of PMEA based on the HepDirect technology that targets PMEA to the liver. In a whole body autoradiography study in rats after oral dosing (30 mg/kg) of [14C]adefovir dipivoxil or [14C]remofovir mesylate, remofovir yielded 15 times higher concentrations of radioactivity in the liver than adefovir dipivoxil, but only one-third of the concentrations in the kidney. After oral dosing (4 mg/kg) of the same radiolabelled agents in cynomolgus monkeys, remofovir mesylate yielded 60 times higher levels of total radioactivity in the liver, but only two-thirds of total radioactivity levels in the kidney. Thus, remofovir mesylate may provide better efficacy and reduced nephrotoxicity. In portal vein-cannulated rats (30 mg/kg) after a single oral dose of [14C]adefovir dipivoxil or [14C]remofovir mesylate, no PMEA was detectable in rat portal plasma early after dosing, indicating that intestinal CYP3A4 does not play a role in conversion of remofovir mesylate to PMEA. The portal/systemic extraction ratio was quite high in both models, suggesting good liver-targeting properties. Portal and systemic remofovir/PMEA ratio indicates that the liver is the site of conversion of remofovir to PMEA. 28-Day toxicity studies demonstrated renal toxicity in rats at doses of 100 mg/kg or higher with no safety concerns at 30 mg/kg and acceptable safety in monkeys at doses up to 60 mg/kg. Thus, in rats and non-human primates, remofovir mesylate has liver-targeting properties and is safer than adefovir dipivoxil.

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Year:  2004        PMID: 15646644     DOI: 10.1177/095632020401500603

Source DB:  PubMed          Journal:  Antivir Chem Chemother        ISSN: 0956-3202


  6 in total

1.  Metabolic activation of pradefovir by CYP3A4 and its potential as an inhibitor or inducer.

Authors:  Chin-chung Lin; Che Fang; Salete Benetton; Gui-fen Xu; Li-Tain Yeh
Journal:  Antimicrob Agents Chemother       Date:  2006-09       Impact factor: 5.191

2.  Single-dose pharmacokinetics and metabolism of [14C]remofovir in rats and cynomolgus monkeys.

Authors:  Chin-Chung Lin; Christine Xu; Nanqun Zhu; David Lourenco; Li-Tain Yeh
Journal:  Antimicrob Agents Chemother       Date:  2005-03       Impact factor: 5.191

Review 3.  Synthesis of nucleoside phosphate and phosphonate prodrugs.

Authors:  Ugo Pradere; Ethel C Garnier-Amblard; Steven J Coats; Franck Amblard; Raymond F Schinazi
Journal:  Chem Rev       Date:  2014-08-21       Impact factor: 60.622

4.  Safety, pharmacokinetics and pharmacogenetics of a single ascending dose of pradefovir, a novel liver-targeting, anti-hepatitis B virus drug, in healthy Chinese subjects.

Authors:  Yanhua Ding; Hong Zhang; Xiaojiao Li; Cuiyun Li; Guiling Chen; Hong Chen; Min Wu; Junqi Niu
Journal:  Hepatol Int       Date:  2017-05-30       Impact factor: 6.047

5.  Development and Validation of a Sensitive LC-MS-MS Method for the Determination of Adefovir in Human Serum and Urine: Application to a Clinical Pharmacokinetic Study.

Authors:  Ye Zhang; Lu Shen; Ying Zhan; Qing-Qing Xiao; Jin Yang
Journal:  J Chromatogr Sci       Date:  2015-12-10       Impact factor: 1.618

6.  The treatment of chronic hepatitis B: Focus on adefovir-like antivirals.

Authors:  Hans Ludger Tillmann
Journal:  Ther Clin Risk Manag       Date:  2008-08       Impact factor: 2.423

  6 in total

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