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Biomedical nanoparticle design: What we can learn from viruses
Viruses are nanomaterials with a number of properties that surpass those of many synthetic nanoparticles (NPs) for biomedical applications. They possess a rigorously ordered structure, come in a variety of shapes, and present unique surface elements, such as spikes. These attributes facilitate propi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525328/ https://www.ncbi.nlm.nih.gov/pubmed/33007365 http://dx.doi.org/10.1016/j.jconrel.2020.09.045 |
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author | Maslanka Figueroa, Sara Fleischmann, Daniel Goepferich, Achim |
author_facet | Maslanka Figueroa, Sara Fleischmann, Daniel Goepferich, Achim |
author_sort | Maslanka Figueroa, Sara |
collection | PubMed |
description | Viruses are nanomaterials with a number of properties that surpass those of many synthetic nanoparticles (NPs) for biomedical applications. They possess a rigorously ordered structure, come in a variety of shapes, and present unique surface elements, such as spikes. These attributes facilitate propitious biodistribution, the crossing of complex biological barriers and a minutely coordinated interaction with cells. Due to the orchestrated sequence of interactions of their stringently arranged particle corona with cellular surface receptors they effectively identify and infect their host cells with utmost specificity, while evading the immune system at the same time. Furthermore, their efficacy is enhanced by their response to stimuli and the ability to spread from cell to cell. Over the years, great efforts have been made to mimic distinct viral traits to improve biomedical nanomaterial performance. However, a closer look at the literature reveals that no comprehensive evaluation of the benefit of virus-mimetic material design on the targeting efficiency of nanomaterials exists. In this review we, therefore, elucidate the impact that viral properties had on fundamental advances in outfitting nanomaterials with the ability to interact specifically with their target cells. We give a comprehensive overview of the diverse design strategies and identify critical steps on the way to reducing them to practice. More so, we discuss the advantages and future perspectives of a virus-mimetic nanomaterial design and try to elucidate if viral mimicry holds the key for better NP targeting. |
format | Online Article Text |
id | pubmed-7525328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75253282020-09-30 Biomedical nanoparticle design: What we can learn from viruses Maslanka Figueroa, Sara Fleischmann, Daniel Goepferich, Achim J Control Release Review Article Viruses are nanomaterials with a number of properties that surpass those of many synthetic nanoparticles (NPs) for biomedical applications. They possess a rigorously ordered structure, come in a variety of shapes, and present unique surface elements, such as spikes. These attributes facilitate propitious biodistribution, the crossing of complex biological barriers and a minutely coordinated interaction with cells. Due to the orchestrated sequence of interactions of their stringently arranged particle corona with cellular surface receptors they effectively identify and infect their host cells with utmost specificity, while evading the immune system at the same time. Furthermore, their efficacy is enhanced by their response to stimuli and the ability to spread from cell to cell. Over the years, great efforts have been made to mimic distinct viral traits to improve biomedical nanomaterial performance. However, a closer look at the literature reveals that no comprehensive evaluation of the benefit of virus-mimetic material design on the targeting efficiency of nanomaterials exists. In this review we, therefore, elucidate the impact that viral properties had on fundamental advances in outfitting nanomaterials with the ability to interact specifically with their target cells. We give a comprehensive overview of the diverse design strategies and identify critical steps on the way to reducing them to practice. More so, we discuss the advantages and future perspectives of a virus-mimetic nanomaterial design and try to elucidate if viral mimicry holds the key for better NP targeting. Elsevier B.V. 2021-01-10 2020-09-30 /pmc/articles/PMC7525328/ /pubmed/33007365 http://dx.doi.org/10.1016/j.jconrel.2020.09.045 Text en © 2020 Elsevier B.V. All rights reserved. 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 | Review Article Maslanka Figueroa, Sara Fleischmann, Daniel Goepferich, Achim Biomedical nanoparticle design: What we can learn from viruses |
title | Biomedical nanoparticle design: What we can learn from viruses |
title_full | Biomedical nanoparticle design: What we can learn from viruses |
title_fullStr | Biomedical nanoparticle design: What we can learn from viruses |
title_full_unstemmed | Biomedical nanoparticle design: What we can learn from viruses |
title_short | Biomedical nanoparticle design: What we can learn from viruses |
title_sort | biomedical nanoparticle design: what we can learn from viruses |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525328/ https://www.ncbi.nlm.nih.gov/pubmed/33007365 http://dx.doi.org/10.1016/j.jconrel.2020.09.045 |
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