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Bioorg Med Chem Lett ; 20(9): 2718-21, 2010 May 01.
Article in English | MEDLINE | ID: mdl-20382017

ABSTRACT

Gold nanoparticles coated with multiple copies of an amphiphilic sulfate-ended ligand are able to bind the HIV envelope glycoprotein gp120 as measured by surface plasmon resonance (SPR) and inhibit in vitro the HIV infection of T-cells at nanomolar concentrations. A 50% density of sulfated ligands on approximately 2 nm nanoparticles (the other ligands being inert glucose derivatives) is enough to achieve high anti-HIV activities. This result opens up the possibility of tailoring both sulfated ligands and other anti-HIV molecules on the same gold cluster, thus contributing to the development of non-cocktail based multifunctional anti-HIV systems.


Subject(s)
Anti-HIV Agents/chemistry , Gold/chemistry , Ligands , Metal Nanoparticles/chemistry , Sulfates/chemistry , Anti-HIV Agents/administration & dosage , Anti-HIV Agents/chemical synthesis , Cell Line , Drug Carriers , HIV Envelope Protein gp120/chemistry , HIV Envelope Protein gp120/metabolism , HIV Infections/prevention & control , Humans , Surface Plasmon Resonance
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