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Nanostructures for the Inhibition of Viral Infections

Multivalent interactions are omnipresent in biology and confer biological systems with dramatically enhanced affinities towards different receptors. Such multivalent binding interactions have lately been considered for the development of new therapeutic strategies against bacterial and viral infecti...

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Detalles Bibliográficos
Autores principales: Szunerits, Sabine, Barras, Alexandre, Khanal, Manakamana, Pagneux, Quentin, Boukherroub, Rabah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332336/
https://www.ncbi.nlm.nih.gov/pubmed/26247927
http://dx.doi.org/10.3390/molecules200814051
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author Szunerits, Sabine
Barras, Alexandre
Khanal, Manakamana
Pagneux, Quentin
Boukherroub, Rabah
author_facet Szunerits, Sabine
Barras, Alexandre
Khanal, Manakamana
Pagneux, Quentin
Boukherroub, Rabah
author_sort Szunerits, Sabine
collection PubMed
description Multivalent interactions are omnipresent in biology and confer biological systems with dramatically enhanced affinities towards different receptors. Such multivalent binding interactions have lately been considered for the development of new therapeutic strategies against bacterial and viral infections. Multivalent polymers, dendrimers, and liposomes have successfully targeted pathogenic interactions. While a high synthetic effort was often needed for the development of such therapeutics, the integration of multiple ligands onto nanostructures turned to be a viable alternative. Particles modified with multiple ligands have the additional advantage of creating a high local concentration of binding molecules. This review article will summarize the different nanoparticle-based approaches currently available for the treatment of viral infections.
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spelling pubmed-63323362019-01-24 Nanostructures for the Inhibition of Viral Infections Szunerits, Sabine Barras, Alexandre Khanal, Manakamana Pagneux, Quentin Boukherroub, Rabah Molecules Review Multivalent interactions are omnipresent in biology and confer biological systems with dramatically enhanced affinities towards different receptors. Such multivalent binding interactions have lately been considered for the development of new therapeutic strategies against bacterial and viral infections. Multivalent polymers, dendrimers, and liposomes have successfully targeted pathogenic interactions. While a high synthetic effort was often needed for the development of such therapeutics, the integration of multiple ligands onto nanostructures turned to be a viable alternative. Particles modified with multiple ligands have the additional advantage of creating a high local concentration of binding molecules. This review article will summarize the different nanoparticle-based approaches currently available for the treatment of viral infections. MDPI 2015-08-03 /pmc/articles/PMC6332336/ /pubmed/26247927 http://dx.doi.org/10.3390/molecules200814051 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Szunerits, Sabine
Barras, Alexandre
Khanal, Manakamana
Pagneux, Quentin
Boukherroub, Rabah
Nanostructures for the Inhibition of Viral Infections
title Nanostructures for the Inhibition of Viral Infections
title_full Nanostructures for the Inhibition of Viral Infections
title_fullStr Nanostructures for the Inhibition of Viral Infections
title_full_unstemmed Nanostructures for the Inhibition of Viral Infections
title_short Nanostructures for the Inhibition of Viral Infections
title_sort nanostructures for the inhibition of viral infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332336/
https://www.ncbi.nlm.nih.gov/pubmed/26247927
http://dx.doi.org/10.3390/molecules200814051
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