Tributyltin(IV)[3‐(3′,5′‐dimethylphenylamido)propanoate] as a potent HCV inhibitor, its delivery study, controlled release and binding sites using CTAB as a standard cell membrane

Abstract

Gaussia luciferase assay was used to measure the anti‐hepatitis C (anti‐HCV) potency of tributyltin(IV)[3‐(3′,5′‐dimethylphenylamido)propanoate] in infected Huh 7.5 cells (human hepatocellular cell). Interaction of the organotin(IV) complex with cetyl N,N,N‐trimethylammonium bromide (CTAB) micelles was studied using UV–visible and steady‐state florescence spectroscopy. The anti‐HCV study showed a log IC50 value of 0.96 nm for the complex. The complex–CTAB interaction parameter showed that partition of the complex from bulk water to the CTAB micelle was a spontaneous process, and the red shift in visible spectra of the complex confirmed its increased solubility into micelles. Copyright © 2013 John Wiley & Sons, Ltd.