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Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects
The newly emerged ribonucleic acid (RNA) enveloped human beta-coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection caused the COVID-19 pandemic, severely affects the respiratory system, and may lead to death. Lacking effective diagnostics and therapies made this pandem...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837559/ https://www.ncbi.nlm.nih.gov/pubmed/33519200 http://dx.doi.org/10.2147/IJN.S283686 |
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author | Varahachalam, Sree Pooja Lahooti, Behnaz Chamaneh, Masoumeh Bagchi, Sounak Chhibber, Tanya Morris, Kevin Bolanos, Joe F Kim, Nam-Young Kaushik, Ajeet |
author_facet | Varahachalam, Sree Pooja Lahooti, Behnaz Chamaneh, Masoumeh Bagchi, Sounak Chhibber, Tanya Morris, Kevin Bolanos, Joe F Kim, Nam-Young Kaushik, Ajeet |
author_sort | Varahachalam, Sree Pooja |
collection | PubMed |
description | The newly emerged ribonucleic acid (RNA) enveloped human beta-coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection caused the COVID-19 pandemic, severely affects the respiratory system, and may lead to death. Lacking effective diagnostics and therapies made this pandemic challenging to manage since the SARS-CoV-2 transmits via human-to-human, enters via ACE2 and TMPSSR2 receptors, and damages organs rich in host cells, spreads via symptomatic carriers and is prominent in an immune-compromised population. New SARS-CoV-2 informatics (structure, strains, like-cycles, functional sites) motivated bio-pharma experts to investigate novel therapeutic agents that act to recognize, inhibit, and knockdown combinations of drugs, vaccines, and antibodies, have been optimized to manage COVID-19. However, successful targeted delivery of these agents to avoid off-targeting and unnecessary drug ingestion is very challenging. To overcome these obstacles, this mini-review projects nanomedicine technology, a pharmacologically relevant cargo of size within 10 to 200 nm, for site-specific delivery of a therapeutic agent to recognize and eradicate the SARS-CoV-2, and improving the human immune system. Such combinational therapy based on compartmentalization controls the delivery and releases of a drug optimized based on patient genomic profile and medical history. Nanotechnology could help combat COVID-19 via various methods such as avoiding viral contamination and spraying by developing personal protective equipment (PPE) to increase the protection of healthcare workers and produce effective antiviral disinfectants surface coatings capable of inactivating and preventing the virus from spreading. To quickly recognize the infection or immunological response, design highly accurate and sensitive nano-based sensors. Development of new drugs with improved activity, reduced toxicity, and sustained release to the lungs, as well as tissue targets; and development of nano-based immunizations to improve humoral and cellular immune responses. The desired and controlled features of suggested personalized therapeutics, nanomedicine, is a potential therapy to manage COVID-19 successfully. The state-of-the-art nanomedicine, challenges, and prospects of nanomedicine are carefully and critically discussed in this report, which may serve as a key platform for scholars to investigate the role of nanomedicine for higher efficacy to manage the COVID-19 pandemic. |
format | Online Article Text |
id | pubmed-7837559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-78375592021-01-28 Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects Varahachalam, Sree Pooja Lahooti, Behnaz Chamaneh, Masoumeh Bagchi, Sounak Chhibber, Tanya Morris, Kevin Bolanos, Joe F Kim, Nam-Young Kaushik, Ajeet Int J Nanomedicine Review The newly emerged ribonucleic acid (RNA) enveloped human beta-coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection caused the COVID-19 pandemic, severely affects the respiratory system, and may lead to death. Lacking effective diagnostics and therapies made this pandemic challenging to manage since the SARS-CoV-2 transmits via human-to-human, enters via ACE2 and TMPSSR2 receptors, and damages organs rich in host cells, spreads via symptomatic carriers and is prominent in an immune-compromised population. New SARS-CoV-2 informatics (structure, strains, like-cycles, functional sites) motivated bio-pharma experts to investigate novel therapeutic agents that act to recognize, inhibit, and knockdown combinations of drugs, vaccines, and antibodies, have been optimized to manage COVID-19. However, successful targeted delivery of these agents to avoid off-targeting and unnecessary drug ingestion is very challenging. To overcome these obstacles, this mini-review projects nanomedicine technology, a pharmacologically relevant cargo of size within 10 to 200 nm, for site-specific delivery of a therapeutic agent to recognize and eradicate the SARS-CoV-2, and improving the human immune system. Such combinational therapy based on compartmentalization controls the delivery and releases of a drug optimized based on patient genomic profile and medical history. Nanotechnology could help combat COVID-19 via various methods such as avoiding viral contamination and spraying by developing personal protective equipment (PPE) to increase the protection of healthcare workers and produce effective antiviral disinfectants surface coatings capable of inactivating and preventing the virus from spreading. To quickly recognize the infection or immunological response, design highly accurate and sensitive nano-based sensors. Development of new drugs with improved activity, reduced toxicity, and sustained release to the lungs, as well as tissue targets; and development of nano-based immunizations to improve humoral and cellular immune responses. The desired and controlled features of suggested personalized therapeutics, nanomedicine, is a potential therapy to manage COVID-19 successfully. The state-of-the-art nanomedicine, challenges, and prospects of nanomedicine are carefully and critically discussed in this report, which may serve as a key platform for scholars to investigate the role of nanomedicine for higher efficacy to manage the COVID-19 pandemic. Dove 2021-01-22 /pmc/articles/PMC7837559/ /pubmed/33519200 http://dx.doi.org/10.2147/IJN.S283686 Text en © 2021 Varahachalam et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Varahachalam, Sree Pooja Lahooti, Behnaz Chamaneh, Masoumeh Bagchi, Sounak Chhibber, Tanya Morris, Kevin Bolanos, Joe F Kim, Nam-Young Kaushik, Ajeet Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects |
title | Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects |
title_full | Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects |
title_fullStr | Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects |
title_full_unstemmed | Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects |
title_short | Nanomedicine for the SARS-CoV-2: State-of-the-Art and Future Prospects |
title_sort | nanomedicine for the sars-cov-2: state-of-the-art and future prospects |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837559/ https://www.ncbi.nlm.nih.gov/pubmed/33519200 http://dx.doi.org/10.2147/IJN.S283686 |
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