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Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol)
Nano-sized metal particles are attracting much interest in industrial and biomedical applications due to the recent progress and development of nanotechnology, and the surface-modifications by appropriate polymers are key techniques to stably express their characteristics. Herein, we applied cyclic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705015/ https://www.ncbi.nlm.nih.gov/pubmed/33257670 http://dx.doi.org/10.1038/s41467-020-19947-8 |
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author | Wang, Yubo Quinsaat, Jose Enrico Q. Ono, Tomoko Maeki, Masatoshi Tokeshi, Manabu Isono, Takuya Tajima, Kenji Satoh, Toshifumi Sato, Shin-ichiro Miura, Yutaka Yamamoto, Takuya |
author_facet | Wang, Yubo Quinsaat, Jose Enrico Q. Ono, Tomoko Maeki, Masatoshi Tokeshi, Manabu Isono, Takuya Tajima, Kenji Satoh, Toshifumi Sato, Shin-ichiro Miura, Yutaka Yamamoto, Takuya |
author_sort | Wang, Yubo |
collection | PubMed |
description | Nano-sized metal particles are attracting much interest in industrial and biomedical applications due to the recent progress and development of nanotechnology, and the surface-modifications by appropriate polymers are key techniques to stably express their characteristics. Herein, we applied cyclic poly(ethylene glycol) (c-PEG), having no chemical inhomogeneity, to provide a polymer topology-dependent stabilization for the surface-modification of gold nanoparticles (AuNPs) through physisorption. By simply mixing c-PEG, but not linear counterparts, enables AuNPs to maintain dispersibility through freezing, lyophilization, or heating. Surprisingly, c-PEG endowed AuNPs with even better dispersion stability than thiolated PEG (HS–PEG–OMe). The stronger affinity of c-PEG was confirmed by DLS, ζ-potential, and FT-IR. Furthermore, the c-PEG system exhibited prolonged blood circulation and enhanced tumor accumulation in mice. Our data suggests that c-PEG induces physisorption on AuNPs, supplying sufficient stability toward bio-medical applications, and would be an alternative approach to the gold–sulfur chemisorption. |
format | Online Article Text |
id | pubmed-7705015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77050152020-12-03 Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) Wang, Yubo Quinsaat, Jose Enrico Q. Ono, Tomoko Maeki, Masatoshi Tokeshi, Manabu Isono, Takuya Tajima, Kenji Satoh, Toshifumi Sato, Shin-ichiro Miura, Yutaka Yamamoto, Takuya Nat Commun Article Nano-sized metal particles are attracting much interest in industrial and biomedical applications due to the recent progress and development of nanotechnology, and the surface-modifications by appropriate polymers are key techniques to stably express their characteristics. Herein, we applied cyclic poly(ethylene glycol) (c-PEG), having no chemical inhomogeneity, to provide a polymer topology-dependent stabilization for the surface-modification of gold nanoparticles (AuNPs) through physisorption. By simply mixing c-PEG, but not linear counterparts, enables AuNPs to maintain dispersibility through freezing, lyophilization, or heating. Surprisingly, c-PEG endowed AuNPs with even better dispersion stability than thiolated PEG (HS–PEG–OMe). The stronger affinity of c-PEG was confirmed by DLS, ζ-potential, and FT-IR. Furthermore, the c-PEG system exhibited prolonged blood circulation and enhanced tumor accumulation in mice. Our data suggests that c-PEG induces physisorption on AuNPs, supplying sufficient stability toward bio-medical applications, and would be an alternative approach to the gold–sulfur chemisorption. Nature Publishing Group UK 2020-11-30 /pmc/articles/PMC7705015/ /pubmed/33257670 http://dx.doi.org/10.1038/s41467-020-19947-8 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Yubo Quinsaat, Jose Enrico Q. Ono, Tomoko Maeki, Masatoshi Tokeshi, Manabu Isono, Takuya Tajima, Kenji Satoh, Toshifumi Sato, Shin-ichiro Miura, Yutaka Yamamoto, Takuya Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
title | Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
title_full | Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
title_fullStr | Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
title_full_unstemmed | Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
title_short | Enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
title_sort | enhanced dispersion stability of gold nanoparticles by the physisorption of cyclic poly(ethylene glycol) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705015/ https://www.ncbi.nlm.nih.gov/pubmed/33257670 http://dx.doi.org/10.1038/s41467-020-19947-8 |
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