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Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography
With the development and progress of nanotechnology, the prospect of using nanorobots to achieve targeted drug delivery is becoming possible. Although nanorobots can potentially improve nano-drug delivery systems, there remains a significant challenge to fabricating magnetically controllable nanorob...
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/PMC9338296/ https://www.ncbi.nlm.nih.gov/pubmed/35906371 http://dx.doi.org/10.1038/s41598-022-17053-x |
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author | Jiang, Teng Song, Xiaoxia Mu, Xueliang Cheang, U. Kei |
author_facet | Jiang, Teng Song, Xiaoxia Mu, Xueliang Cheang, U. Kei |
author_sort | Jiang, Teng |
collection | PubMed |
description | With the development and progress of nanotechnology, the prospect of using nanorobots to achieve targeted drug delivery is becoming possible. Although nanorobots can potentially improve nano-drug delivery systems, there remains a significant challenge to fabricating magnetically controllable nanorobots with a size suitable for drug delivery in complex in vivo environments. Most of the current research focused on the preparation and functionalization of microscale and milliscale robots due to the relative difficulties in fabricating nanoscale robots. To address this problem and move towards in vivo applications, this study uses electron beam lithography to fabricate achiral planar L-shaped nanorobots that are biocompatible with immune cells. Their minimal planar geometry enabled nanolithography to fabricate nanorobots with a minimum feature size down to 400 nm. Using an integrated imaging and control system, the locomotive behavior of the L-shaped nanorobots in a fluidic environment was studied by examining their velocity profiles and trajectories. Furthermore, the nanorobots exhibit excellent cell compatibility with various types of cells, including macrophage cells. Finally, the long-term cell culture medium immersion test demonstrated that the L-shaped nanorobots have robust stability. This work will demonstrate the potential to use these nanorobots to operate in vivo without triggering immune cell responses. |
format | Online Article Text |
id | pubmed-9338296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93382962022-07-31 Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography Jiang, Teng Song, Xiaoxia Mu, Xueliang Cheang, U. Kei Sci Rep Article With the development and progress of nanotechnology, the prospect of using nanorobots to achieve targeted drug delivery is becoming possible. Although nanorobots can potentially improve nano-drug delivery systems, there remains a significant challenge to fabricating magnetically controllable nanorobots with a size suitable for drug delivery in complex in vivo environments. Most of the current research focused on the preparation and functionalization of microscale and milliscale robots due to the relative difficulties in fabricating nanoscale robots. To address this problem and move towards in vivo applications, this study uses electron beam lithography to fabricate achiral planar L-shaped nanorobots that are biocompatible with immune cells. Their minimal planar geometry enabled nanolithography to fabricate nanorobots with a minimum feature size down to 400 nm. Using an integrated imaging and control system, the locomotive behavior of the L-shaped nanorobots in a fluidic environment was studied by examining their velocity profiles and trajectories. Furthermore, the nanorobots exhibit excellent cell compatibility with various types of cells, including macrophage cells. Finally, the long-term cell culture medium immersion test demonstrated that the L-shaped nanorobots have robust stability. This work will demonstrate the potential to use these nanorobots to operate in vivo without triggering immune cell responses. Nature Publishing Group UK 2022-07-29 /pmc/articles/PMC9338296/ /pubmed/35906371 http://dx.doi.org/10.1038/s41598-022-17053-x 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 Jiang, Teng Song, Xiaoxia Mu, Xueliang Cheang, U. Kei Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
title | Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
title_full | Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
title_fullStr | Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
title_full_unstemmed | Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
title_short | Macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
title_sort | macrophage-compatible magnetic achiral nanorobots fabricated by electron beam lithography |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338296/ https://www.ncbi.nlm.nih.gov/pubmed/35906371 http://dx.doi.org/10.1038/s41598-022-17053-x |
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