Related Experiment Video
Updated: Aug 27, 2025

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses
Published on: May 5, 2014
[What future for ribavirin beyond hepatitis C therapy?]
H Jeulin1, F Kedzierewicz2, N Grancher3
1Laboratoire de virologie, centre hospitalier universitaire de Nancy, Groupe d'étude des vecteurs supramoléculaires du médicament, faculté de pharmacie, UMR 7565 CNRS-Nancy Université, Adresse actuelle: Laboratoire de virologie, centre hospitalier universitaire de Nancy - EA RHEM 4369, faculté de médecine, Nancy Université.
Abstract:
Most of emerging and re-emerging diseases are due to RNA viruses and available drugs are insufficient. Currently the ribavirin is only licensed for the treatment of chronic hepatitis C infection, whereas this guanosin analogue has a broad-spectrum in vitro activity against many DNA and RNA viruses. It was consequently used as a last resort, in emergency state like avian influenza or in front of new viruses (SARS). The strategies for development of new antiviral drugs are usually based on virus structure and properties. In regard to recent development of chemical vector designed for improving drug bioavailability, use of former drug, like ribavirin, could be reconsidered. For example, complexation of ribavirin with cyclodextrins, cyclic oligosaccharide vectors, can improve its bioavailability in central nervous system and improve encephalitis treatment.
Related Concept Videos
Microorganisms in Medicine and Therapeutics
Retrovirus Life Cycles
Retroviruses
Hepatic Drug Excretion: Influencing Factors
Subviral Agents
Hepatic Drug Excretion: Enterohepatic Cycling
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...

