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- Title
Human uridine-cytidine kinase phosphorylation of ribavirin: a convenient method for activation of ribavirin for conjugation to proteins.
- Authors
Virovic Jukic, Lucija; Duvnjak, Marko; Wu, Catherine H.; Wu, George Y.
- Abstract
Ribavirin is a synthetic nucleoside analog that is used for the treatment of hepatitis C virus (HCV) infection. Its primary toxicity is hemolytic anemia, which sometimes necessitates dose reduction or discontinuation of therapy. Selective delivery of ribavirin into liver cells would be desirable to enhance its antiviral activity and avoid systemic side effects. One approach to liver-specific targeting is conjugation of the ribavirin with asialoglycoprotein that is taken up specifically by liver cells. Human uridine-cytidine kinase-1 (UCK-1) was used for ribavirin phosphorylation to its monophosphate form. 1-Ethyl-3-diisopropylaminocarbodiimide (EDC) was used as a coupling agent. The best results were obtained using direct conjugation protocol with a molar ratio of 6.5 ribavirin monophosphate (RMP) molecules per one asialoorosomucoid (AsOR) molecule. Our findings show that ribavirin is a potential substrate of UCK-1, and RMP formed could be chemically coupled to AsOR to form a conjugate for liver specific targeting.
- Subjects
RIBAVIRIN; URIDINE; AZARIBINE; PHOSPHORYLATION; CHEMICAL reactions; HEPATITIS C treatment
- Publication
Journal of Biomedical Science, 2008, Vol 15, Issue 2, p205
- ISSN
1021-7770
- Publication type
Article
- DOI
10.1007/s11373-007-9224-9