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Multivalent nanomedicines to treat COVID-19: A slow train coming
The high transmission rate and serious consequences of the unprecedented COVID-19 pandemic make it challenging and urgent to identify viral pathogens and understand their intrinsic resistance mechanisms, to pave the way for new approaches to combat severe acute respiratory syndrome coronavirus-2 (SA...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473256/ https://www.ncbi.nlm.nih.gov/pubmed/32922510 http://dx.doi.org/10.1016/j.nantod.2020.100962 |
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author | Tabish, Tanveer A. Hamblin, Michael R. |
author_facet | Tabish, Tanveer A. Hamblin, Michael R. |
author_sort | Tabish, Tanveer A. |
collection | PubMed |
description | The high transmission rate and serious consequences of the unprecedented COVID-19 pandemic make it challenging and urgent to identify viral pathogens and understand their intrinsic resistance mechanisms, to pave the way for new approaches to combat severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Multivalent interactions are responsible for performing a broad range of biological functions in normal cells, such as cell-cell communication and adhesion. Multivalency underlies the reversibility of ligand-receptor interactions during infections. Previous studies into multivalent nanomedicines used against viruses, have revealed their ability, not only to probe the molecular processes of viral infections, but also to target pathogen-host cell binding with minimal collateral damage to normal cells. Nanomedicines are comparable in size to viruses and to cell receptor complexes (that mediate viral uptake), and can function as safe and accurate armoured vehicles to facilitate the transport of anti-viral drugs. Multivalent nanomedicines can be designed to avoid binding to extracellular serum proteins, and ultimately lead to destruction of the viruses. This brief perspective highlights the potential of innovative smart and safe multivalent nanomedicines that could target multiple viral factors involved in infections at cellular levels. For instance it is possible to target viral spike protein mediated entry pathways, as well as viral replication and cell lysis. Nanomedicine-based approaches could open new opportunities for anti-coronavirus therapies. |
format | Online Article Text |
id | pubmed-7473256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74732562020-09-08 Multivalent nanomedicines to treat COVID-19: A slow train coming Tabish, Tanveer A. Hamblin, Michael R. Nano Today News and Opinions The high transmission rate and serious consequences of the unprecedented COVID-19 pandemic make it challenging and urgent to identify viral pathogens and understand their intrinsic resistance mechanisms, to pave the way for new approaches to combat severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Multivalent interactions are responsible for performing a broad range of biological functions in normal cells, such as cell-cell communication and adhesion. Multivalency underlies the reversibility of ligand-receptor interactions during infections. Previous studies into multivalent nanomedicines used against viruses, have revealed their ability, not only to probe the molecular processes of viral infections, but also to target pathogen-host cell binding with minimal collateral damage to normal cells. Nanomedicines are comparable in size to viruses and to cell receptor complexes (that mediate viral uptake), and can function as safe and accurate armoured vehicles to facilitate the transport of anti-viral drugs. Multivalent nanomedicines can be designed to avoid binding to extracellular serum proteins, and ultimately lead to destruction of the viruses. This brief perspective highlights the potential of innovative smart and safe multivalent nanomedicines that could target multiple viral factors involved in infections at cellular levels. For instance it is possible to target viral spike protein mediated entry pathways, as well as viral replication and cell lysis. Nanomedicine-based approaches could open new opportunities for anti-coronavirus therapies. Published by Elsevier Ltd. 2020-12 2020-09-04 /pmc/articles/PMC7473256/ /pubmed/32922510 http://dx.doi.org/10.1016/j.nantod.2020.100962 Text en © 2020 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | News and Opinions Tabish, Tanveer A. Hamblin, Michael R. Multivalent nanomedicines to treat COVID-19: A slow train coming |
title | Multivalent nanomedicines to treat COVID-19: A slow train coming |
title_full | Multivalent nanomedicines to treat COVID-19: A slow train coming |
title_fullStr | Multivalent nanomedicines to treat COVID-19: A slow train coming |
title_full_unstemmed | Multivalent nanomedicines to treat COVID-19: A slow train coming |
title_short | Multivalent nanomedicines to treat COVID-19: A slow train coming |
title_sort | multivalent nanomedicines to treat covid-19: a slow train coming |
topic | News and Opinions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473256/ https://www.ncbi.nlm.nih.gov/pubmed/32922510 http://dx.doi.org/10.1016/j.nantod.2020.100962 |
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