ANALYSIS OF TARGETED DELIVERY OF RIBAVIRIN TO HEPATIC CELLS IN TREATMENT OF HEPATO-CELLULAR CARCINOMA
*Karthick Jayaraman, Praveen Kumar Posa Krishnamoorthy, Posa Krishnamoorthy
ABSTRACT
The study is to analyse computationally, the Lipid Bilayer Nano-
Particles or liposomes mediated, targeted delivery of Ribavirin, a drug
used primarily in the treatment of Cholangiocarcinoma, a Hepatomal
disease mainly caused due to infection by liver flukes or by mutation in
epithelial cells. For In-Silico binding studies, 5 different liposomes are
selected and their properties are studied. Based on the feasibility of the
drug-liposome binding that is examined by using MD Simulations,
those that meet the criteria for targeted drug delivery are chosen and
the Binding Aminoacid interactions with the drug and the lipid
nanoparticles are determined. It was seen that the best drug binding
affinity is shown for 1, 2 -Distearoyl- sn -glycero-3-phosphocholine
(DSPC) liposome. Then Liver Receptors, specific to cholesterol and
sterol metabolism are chosen for Binding studies with the above
mentioned liposome (capsulated with the drug) docked using LigandFit
and screened primarily through dock scores using Ligscore module in Discovery Studio. The
study revealed that SREBP-1 Liver Receptor has a greater efficiency in binding with the
drug-liposome complex and hence can be adjudged to be most suited for targeted drug
delivery experiments.
Keywords: Liposomes, Ribavirin, Binding, Receptors, Docking.
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