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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Main Authors: Sabine Szunerits, Alexandre Barras, Manakamana Khanal, Quentin Pagneux, Rabah Boukherroub
Format: Article
Language:English
Published: MDPI AG 2015-08-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/20/8/14051
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spelling doaj-41d3e9511d694019b9027c07da142ed82020-11-24T23:49:36ZengMDPI AGMolecules1420-30492015-08-01208140511408110.3390/molecules200814051molecules200814051Nanostructures for the Inhibition of Viral InfectionsSabine Szunerits0Alexandre Barras1Manakamana Khanal2Quentin Pagneux3Rabah Boukherroub4Institute of Electronics, Microelectronics and Nanotechnology (IEMN), UMR 8520 CNRS, Lille1 University, Avenue Poincaré—BP 60069, 59652 Villeneuve d\'Ascq, FranceInstitute of Electronics, Microelectronics and Nanotechnology (IEMN), UMR 8520 CNRS, Lille1 University, Avenue Poincaré—BP 60069, 59652 Villeneuve d\'Ascq, FranceInstitute of Electronics, Microelectronics and Nanotechnology (IEMN), UMR 8520 CNRS, Lille1 University, Avenue Poincaré—BP 60069, 59652 Villeneuve d\'Ascq, FranceInstitute of Electronics, Microelectronics and Nanotechnology (IEMN), UMR 8520 CNRS, Lille1 University, Avenue Poincaré—BP 60069, 59652 Villeneuve d\'Ascq, FranceInstitute of Electronics, Microelectronics and Nanotechnology (IEMN), UMR 8520 CNRS, Lille1 University, Avenue Poincaré—BP 60069, 59652 Villeneuve d\'Ascq, FranceMultivalent 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.http://www.mdpi.com/1420-3049/20/8/14051viral infectionsantiviral therapynanomaterials
collection DOAJ
language English
format Article
sources DOAJ
author Sabine Szunerits
Alexandre Barras
Manakamana Khanal
Quentin Pagneux
Rabah Boukherroub
spellingShingle Sabine Szunerits
Alexandre Barras
Manakamana Khanal
Quentin Pagneux
Rabah Boukherroub
Nanostructures for the Inhibition of Viral Infections
Molecules
viral infections
antiviral therapy
nanomaterials
author_facet Sabine Szunerits
Alexandre Barras
Manakamana Khanal
Quentin Pagneux
Rabah Boukherroub
author_sort Sabine Szunerits
title Nanostructures for the Inhibition of Viral Infections
title_short 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_sort nanostructures for the inhibition of viral infections
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2015-08-01
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.
topic viral infections
antiviral therapy
nanomaterials
url http://www.mdpi.com/1420-3049/20/8/14051
work_keys_str_mv AT sabineszunerits nanostructuresfortheinhibitionofviralinfections
AT alexandrebarras nanostructuresfortheinhibitionofviralinfections
AT manakamanakhanal nanostructuresfortheinhibitionofviralinfections
AT quentinpagneux nanostructuresfortheinhibitionofviralinfections
AT rabahboukherroub nanostructuresfortheinhibitionofviralinfections
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