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Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction
Particle adhesion onto hydrogels has recently attracted considerable attention because of the potential biomedical applications of the resultant materials. A variety of interactions have been taken advantage of for adsorption, including electrostatic forces, hydrophobic interactions and hydrogen bon...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522479/ https://www.ncbi.nlm.nih.gov/pubmed/28733639 http://dx.doi.org/10.1038/s41598-017-06257-1 |
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author | Sato, Naoko Aoyama, Yurina Yamanaka, Junpei Toyotama, Akiko Okuzono, Tohru |
author_facet | Sato, Naoko Aoyama, Yurina Yamanaka, Junpei Toyotama, Akiko Okuzono, Tohru |
author_sort | Sato, Naoko |
collection | PubMed |
description | Particle adhesion onto hydrogels has recently attracted considerable attention because of the potential biomedical applications of the resultant materials. A variety of interactions have been taken advantage of for adsorption, including electrostatic forces, hydrophobic interactions and hydrogen bonding. In this study, we report significant adsorption of submicron-sized silica particles onto hydrogel surfaces in water, purely by van der Waals (vdW) attraction. The vdW forces enabled strong adhesions between dielectric materials in air. However, because the Hamaker constant decreases in water typically by a factor of approximately 1/100, it is not clear whether vdW attraction is the major driving force in aqueous settings. We investigated the adsorption of silica particles (diameter = 25–600 nm) on poly(acrylamide) and poly(dimethylacrylamide) gels using optical microscopy, under conditions where chemical and electrostatic adsorption is negligible. The quantity of adsorbed particles decreased on decreasing the Hamaker constant by varying the refractive indices of the particles and medium (ethyleneglycol/water), indicating that the adsorption is because of the vdW forces. The adsorption isotherm was discussed based on the adhesive contact model in consideration of the deformation of the gel surface. The present findings will advance the elucidation and development of adsorption in various types of soft materials. |
format | Online Article Text |
id | pubmed-5522479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55224792017-07-26 Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction Sato, Naoko Aoyama, Yurina Yamanaka, Junpei Toyotama, Akiko Okuzono, Tohru Sci Rep Article Particle adhesion onto hydrogels has recently attracted considerable attention because of the potential biomedical applications of the resultant materials. A variety of interactions have been taken advantage of for adsorption, including electrostatic forces, hydrophobic interactions and hydrogen bonding. In this study, we report significant adsorption of submicron-sized silica particles onto hydrogel surfaces in water, purely by van der Waals (vdW) attraction. The vdW forces enabled strong adhesions between dielectric materials in air. However, because the Hamaker constant decreases in water typically by a factor of approximately 1/100, it is not clear whether vdW attraction is the major driving force in aqueous settings. We investigated the adsorption of silica particles (diameter = 25–600 nm) on poly(acrylamide) and poly(dimethylacrylamide) gels using optical microscopy, under conditions where chemical and electrostatic adsorption is negligible. The quantity of adsorbed particles decreased on decreasing the Hamaker constant by varying the refractive indices of the particles and medium (ethyleneglycol/water), indicating that the adsorption is because of the vdW forces. The adsorption isotherm was discussed based on the adhesive contact model in consideration of the deformation of the gel surface. The present findings will advance the elucidation and development of adsorption in various types of soft materials. Nature Publishing Group UK 2017-07-21 /pmc/articles/PMC5522479/ /pubmed/28733639 http://dx.doi.org/10.1038/s41598-017-06257-1 Text en © The Author(s) 2017 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 Sato, Naoko Aoyama, Yurina Yamanaka, Junpei Toyotama, Akiko Okuzono, Tohru Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction |
title | Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction |
title_full | Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction |
title_fullStr | Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction |
title_full_unstemmed | Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction |
title_short | Particle Adsorption on Hydrogel Surfaces in Aqueous Media due to van der Waals Attraction |
title_sort | particle adsorption on hydrogel surfaces in aqueous media due to van der waals attraction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522479/ https://www.ncbi.nlm.nih.gov/pubmed/28733639 http://dx.doi.org/10.1038/s41598-017-06257-1 |
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