Title : Understanding hepatitis B virus inhibitor, Clevudine transport in human blood circulation: An in vitro albumin binding study
Abstract:
Hepatitis B, a viral infection that can cause both acute and chronic hepatitis, cirrhosis and hepatocellular carcinoma, is a major global health issue. Hepatocellular carcinoma is one of the most common types of cancer, accounting for roughly 90% of all primary liver tumours. The virus replication is through reverse transcription and most antiviral drugs are nucleoside/nucleotide analogues. Clevudine, a nucleoside analogue licenced in Korea in 2006 has been found effective in controlling HBV infection. Interaction between a dug and the plasma protein is of pharmacological significance as this interaction could affect drug absorption, distribution, metabolism and excretion in the body as well as the physiological activity of the protein. Understanding such interactions offer information about drug-drug interaction, and drug-protein resistance and is helpful to predict potential drug dosages and adverse effects. Serum albumin, a 585 residue-long protein encompassing three domains, I, II and III with their divisions into two subdomains, A and B, is the main drug transporter in blood circulation. It possesses two well-defined drug-binding sites, namely, Site I (subdomain IIA) and Site II (subdomain IIIA). This talk will highlight the interaction results between clevudine and human serum albumin using a variety of spectroscopic techniques i.e., absorption, fluorescence, circular dichroism and atomic force microscopy along with molecular docking.