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pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes

[Image: see text] We report the first example of reversible encapsulation of micron-sized particles by oppositely charged submicron smaller colloids. The reversibility of this encapsulation process is regulated by pH-responsive poly(acrylic acid) (PAA) present in solution. The competitive adsorption...

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Autores principales: Guo, Yong, van Ravensteijn, Bas G. P., Evers, Chris H. J., Kegel, Willem K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427486/
https://www.ncbi.nlm.nih.gov/pubmed/28419800
http://dx.doi.org/10.1021/acs.langmuir.7b00845
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author Guo, Yong
van Ravensteijn, Bas G. P.
Evers, Chris H. J.
Kegel, Willem K.
author_facet Guo, Yong
van Ravensteijn, Bas G. P.
Evers, Chris H. J.
Kegel, Willem K.
author_sort Guo, Yong
collection PubMed
description [Image: see text] We report the first example of reversible encapsulation of micron-sized particles by oppositely charged submicron smaller colloids. The reversibility of this encapsulation process is regulated by pH-responsive poly(acrylic acid) (PAA) present in solution. The competitive adsorption between the small colloids and the poly(acrylic acid) on the surface of the large colloids plays a key role in the encapsulation behavior of the system. pH offers an experimental knob to tune the electrostatic interactions between the two oppositely charged particle species via regulation of the charge density of the poly(acrylic acid). This results in an increased surface coverage of the large colloids by the smaller colloids when decreasing pH. Furthermore, the poly(acrylic acid) also acts as a steric barrier limiting the strength of the attractive forces between the oppositely charged particle species, thereby enabling detachment of the smaller colloids. Finally, based on the pH tunability of the encapsulation behavior and the ability of the small colloids to detach, reversible encapsulation is achieved by cycling pH in the presence of the PAA polyelectrolytes. The role of polyelectrolytes revealed in this work provides a new and facile strategy to control heteroaggregation behavior between oppositely charged colloids, paving the way to prepare sophisticated hierarchical assemblies.
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spelling pubmed-54274862017-05-15 pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes Guo, Yong van Ravensteijn, Bas G. P. Evers, Chris H. J. Kegel, Willem K. Langmuir [Image: see text] We report the first example of reversible encapsulation of micron-sized particles by oppositely charged submicron smaller colloids. The reversibility of this encapsulation process is regulated by pH-responsive poly(acrylic acid) (PAA) present in solution. The competitive adsorption between the small colloids and the poly(acrylic acid) on the surface of the large colloids plays a key role in the encapsulation behavior of the system. pH offers an experimental knob to tune the electrostatic interactions between the two oppositely charged particle species via regulation of the charge density of the poly(acrylic acid). This results in an increased surface coverage of the large colloids by the smaller colloids when decreasing pH. Furthermore, the poly(acrylic acid) also acts as a steric barrier limiting the strength of the attractive forces between the oppositely charged particle species, thereby enabling detachment of the smaller colloids. Finally, based on the pH tunability of the encapsulation behavior and the ability of the small colloids to detach, reversible encapsulation is achieved by cycling pH in the presence of the PAA polyelectrolytes. The role of polyelectrolytes revealed in this work provides a new and facile strategy to control heteroaggregation behavior between oppositely charged colloids, paving the way to prepare sophisticated hierarchical assemblies. American Chemical Society 2017-04-18 2017-05-09 /pmc/articles/PMC5427486/ /pubmed/28419800 http://dx.doi.org/10.1021/acs.langmuir.7b00845 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Guo, Yong
van Ravensteijn, Bas G. P.
Evers, Chris H. J.
Kegel, Willem K.
pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes
title pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes
title_full pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes
title_fullStr pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes
title_full_unstemmed pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes
title_short pH Reversible Encapsulation of Oppositely Charged Colloids Mediated by Polyelectrolytes
title_sort ph reversible encapsulation of oppositely charged colloids mediated by polyelectrolytes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427486/
https://www.ncbi.nlm.nih.gov/pubmed/28419800
http://dx.doi.org/10.1021/acs.langmuir.7b00845
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