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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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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. |
format | Online Article Text |
id | pubmed-6332336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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