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Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications
Biomimicking native tissues and organs require the development of advanced hydrogels. The patterning of hydrogel surfaces may enhance the cellular functionality and therapeutic efficacy of implants. For example, nanopatterning of the intraocular lens (IOL) surface can suppress the upregulation of cy...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411613/ https://www.ncbi.nlm.nih.gov/pubmed/36008433 http://dx.doi.org/10.1038/s41598-022-18564-3 |
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author | Krajňák, Tomáš Černá, Eva Šuráňová, Markéta Šamořil, Tomáš Zicha, Daniel Vojtová, Lucy Čechal, Jan |
author_facet | Krajňák, Tomáš Černá, Eva Šuráňová, Markéta Šamořil, Tomáš Zicha, Daniel Vojtová, Lucy Čechal, Jan |
author_sort | Krajňák, Tomáš |
collection | PubMed |
description | Biomimicking native tissues and organs require the development of advanced hydrogels. The patterning of hydrogel surfaces may enhance the cellular functionality and therapeutic efficacy of implants. For example, nanopatterning of the intraocular lens (IOL) surface can suppress the upregulation of cytoskeleton proteins (actin and actinin) within the cells in contact with the IOL surface and, hence, prevent secondary cataracts causing blurry or opaque vision. Here we introduce a fast and efficient method for fabricating arrays consisting of millions of individual nanostructures on the hydrogel surface. In particular, we have prepared the randomly distributed nanopillars on poly(2-hydroxyethyl methacrylate) hydrogel using replica molding and show that the number, shape, and arrangement of nanostructures are fully adjustable. Characterization by atomic force microscopy revealed that all nanopillars were of similar shape, narrow size distribution, and without significant defects. In imprint lithography, choosing the appropriate hydrogel composition is critical. As hydrogels with imprinted nanostructures mimic the natural cell environment, they can find applications in fundamental cell biology research, e.g., they can tune cell attachment and inhibit or promote cell clustering by a specific arrangement of protrusive nanostructures on the hydrogel surface. |
format | Online Article Text |
id | pubmed-9411613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94116132022-08-27 Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications Krajňák, Tomáš Černá, Eva Šuráňová, Markéta Šamořil, Tomáš Zicha, Daniel Vojtová, Lucy Čechal, Jan Sci Rep Article Biomimicking native tissues and organs require the development of advanced hydrogels. The patterning of hydrogel surfaces may enhance the cellular functionality and therapeutic efficacy of implants. For example, nanopatterning of the intraocular lens (IOL) surface can suppress the upregulation of cytoskeleton proteins (actin and actinin) within the cells in contact with the IOL surface and, hence, prevent secondary cataracts causing blurry or opaque vision. Here we introduce a fast and efficient method for fabricating arrays consisting of millions of individual nanostructures on the hydrogel surface. In particular, we have prepared the randomly distributed nanopillars on poly(2-hydroxyethyl methacrylate) hydrogel using replica molding and show that the number, shape, and arrangement of nanostructures are fully adjustable. Characterization by atomic force microscopy revealed that all nanopillars were of similar shape, narrow size distribution, and without significant defects. In imprint lithography, choosing the appropriate hydrogel composition is critical. As hydrogels with imprinted nanostructures mimic the natural cell environment, they can find applications in fundamental cell biology research, e.g., they can tune cell attachment and inhibit or promote cell clustering by a specific arrangement of protrusive nanostructures on the hydrogel surface. Nature Publishing Group UK 2022-08-25 /pmc/articles/PMC9411613/ /pubmed/36008433 http://dx.doi.org/10.1038/s41598-022-18564-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Krajňák, Tomáš Černá, Eva Šuráňová, Markéta Šamořil, Tomáš Zicha, Daniel Vojtová, Lucy Čechal, Jan Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications |
title | Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications |
title_full | Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications |
title_fullStr | Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications |
title_full_unstemmed | Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications |
title_short | Replica-mold nanopatterned PHEMA hydrogel surfaces for ophthalmic applications |
title_sort | replica-mold nanopatterned phema hydrogel surfaces for ophthalmic applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411613/ https://www.ncbi.nlm.nih.gov/pubmed/36008433 http://dx.doi.org/10.1038/s41598-022-18564-3 |
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