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Bottlebrush Bridge between Soft Gels and Firm Tissues
[Image: see text] Softness and firmness are seemingly incompatible traits that synergize to create the unique soft-yet-firm tactility of living tissues pursued in soft robotics, wearable electronics, and plastic surgery. This dichotomy is particularly pronounced in tissues such as fat that are known...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099586/ https://www.ncbi.nlm.nih.gov/pubmed/32232141 http://dx.doi.org/10.1021/acscentsci.9b01216 |
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author | Keith, Andrew N. Vatankhah-Varnosfaderani, Mohammad Clair, Charles Fahimipour, Farahnaz Dashtimoghadam, Erfan Lallam, Abdelaziz Sztucki, Michael Ivanov, Dimitri A. Liang, Heyi Dobrynin, Andrey V. Sheiko, Sergei S. |
author_facet | Keith, Andrew N. Vatankhah-Varnosfaderani, Mohammad Clair, Charles Fahimipour, Farahnaz Dashtimoghadam, Erfan Lallam, Abdelaziz Sztucki, Michael Ivanov, Dimitri A. Liang, Heyi Dobrynin, Andrey V. Sheiko, Sergei S. |
author_sort | Keith, Andrew N. |
collection | PubMed |
description | [Image: see text] Softness and firmness are seemingly incompatible traits that synergize to create the unique soft-yet-firm tactility of living tissues pursued in soft robotics, wearable electronics, and plastic surgery. This dichotomy is particularly pronounced in tissues such as fat that are known to be both ultrasoft and ultrafirm. However, synthetically replicating this mechanical response remains elusive since ubiquitously employed soft gels are unable to concurrently reproduce tissue firmness. We have addressed the tissue challenge through the self-assembly of linear–bottlebrush–linear (LBL) block copolymers into thermoplastic elastomers. This hybrid molecular architecture delivers a hierarchical network organization with a cascade of deformation mechanisms responsible for initially low moduli followed by intense strain-stiffening. By bridging the firmness gap between gels and tissues, we have replicated the mechanics of fat, fetal membrane, spinal cord, and brain tissues. These solvent-free, nonleachable, and tissue-mimetic elastomers also show enhanced biocompatibility as demonstrated by cell proliferation studies, all of which are vital for the safety and longevity of future biomedical devices. |
format | Online Article Text |
id | pubmed-7099586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70995862020-03-30 Bottlebrush Bridge between Soft Gels and Firm Tissues Keith, Andrew N. Vatankhah-Varnosfaderani, Mohammad Clair, Charles Fahimipour, Farahnaz Dashtimoghadam, Erfan Lallam, Abdelaziz Sztucki, Michael Ivanov, Dimitri A. Liang, Heyi Dobrynin, Andrey V. Sheiko, Sergei S. ACS Cent Sci [Image: see text] Softness and firmness are seemingly incompatible traits that synergize to create the unique soft-yet-firm tactility of living tissues pursued in soft robotics, wearable electronics, and plastic surgery. This dichotomy is particularly pronounced in tissues such as fat that are known to be both ultrasoft and ultrafirm. However, synthetically replicating this mechanical response remains elusive since ubiquitously employed soft gels are unable to concurrently reproduce tissue firmness. We have addressed the tissue challenge through the self-assembly of linear–bottlebrush–linear (LBL) block copolymers into thermoplastic elastomers. This hybrid molecular architecture delivers a hierarchical network organization with a cascade of deformation mechanisms responsible for initially low moduli followed by intense strain-stiffening. By bridging the firmness gap between gels and tissues, we have replicated the mechanics of fat, fetal membrane, spinal cord, and brain tissues. These solvent-free, nonleachable, and tissue-mimetic elastomers also show enhanced biocompatibility as demonstrated by cell proliferation studies, all of which are vital for the safety and longevity of future biomedical devices. American Chemical Society 2020-01-22 2020-03-25 /pmc/articles/PMC7099586/ /pubmed/32232141 http://dx.doi.org/10.1021/acscentsci.9b01216 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Keith, Andrew N. Vatankhah-Varnosfaderani, Mohammad Clair, Charles Fahimipour, Farahnaz Dashtimoghadam, Erfan Lallam, Abdelaziz Sztucki, Michael Ivanov, Dimitri A. Liang, Heyi Dobrynin, Andrey V. Sheiko, Sergei S. Bottlebrush Bridge between Soft Gels and Firm Tissues |
title | Bottlebrush Bridge between Soft Gels and Firm Tissues |
title_full | Bottlebrush Bridge between Soft Gels and Firm Tissues |
title_fullStr | Bottlebrush Bridge between Soft Gels and Firm Tissues |
title_full_unstemmed | Bottlebrush Bridge between Soft Gels and Firm Tissues |
title_short | Bottlebrush Bridge between Soft Gels and Firm Tissues |
title_sort | bottlebrush bridge between soft gels and firm tissues |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099586/ https://www.ncbi.nlm.nih.gov/pubmed/32232141 http://dx.doi.org/10.1021/acscentsci.9b01216 |
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