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Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies

[Image: see text] The fabrication of monodisperse nanostructures of highly controlled size and morphology with spatially distinct functional regions is a current area of high interest in materials science. Achieving this control directly in a biologically relevant solvent, without affecting cell via...

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Autores principales: Arno, Maria C., Inam, Maria, Coe, Zachary, Cambridge, Graeme, Macdougall, Laura J., Keogh, Robert, Dove, Andrew P., O’Reilly, Rachel K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789388/
https://www.ncbi.nlm.nih.gov/pubmed/29078700
http://dx.doi.org/10.1021/jacs.7b10199
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author Arno, Maria C.
Inam, Maria
Coe, Zachary
Cambridge, Graeme
Macdougall, Laura J.
Keogh, Robert
Dove, Andrew P.
O’Reilly, Rachel K.
author_facet Arno, Maria C.
Inam, Maria
Coe, Zachary
Cambridge, Graeme
Macdougall, Laura J.
Keogh, Robert
Dove, Andrew P.
O’Reilly, Rachel K.
author_sort Arno, Maria C.
collection PubMed
description [Image: see text] The fabrication of monodisperse nanostructures of highly controlled size and morphology with spatially distinct functional regions is a current area of high interest in materials science. Achieving this control directly in a biologically relevant solvent, without affecting cell viability, opens the door to a wide range of biomedical applications, yet this remains a significant challenge. Herein, we report the preparation of biocompatible and biodegradable poly(ε-caprolactone) 1D (cylindrical) and 2D (platelet) micelles in water and alcoholic solvents via crystallization-driven self-assembly. Using epitaxial growth in an alcoholic solvent, we show exquisite control over the dimensions and dispersity of these nanostructures, allowing access to uniform morphologies and predictable dimensions based on the unimer-to-seed ratio. Furthermore, for the first time, we report epitaxial growth in aqueous solvent, achieving precise control over 1D nanostructures in water, an essential feature for any relevant biological application. Exploiting this further, a strong, biocompatible and fluorescent hydrogel was obtained as a result of living epitaxial growth in aqueous solvent and cell culture medium. MC3T3 and A549 cells were successfully encapsulated, demonstrating high viability (>95% after 4 days) in these novel hydrogel materials.
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spelling pubmed-57893882018-01-31 Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies Arno, Maria C. Inam, Maria Coe, Zachary Cambridge, Graeme Macdougall, Laura J. Keogh, Robert Dove, Andrew P. O’Reilly, Rachel K. J Am Chem Soc [Image: see text] The fabrication of monodisperse nanostructures of highly controlled size and morphology with spatially distinct functional regions is a current area of high interest in materials science. Achieving this control directly in a biologically relevant solvent, without affecting cell viability, opens the door to a wide range of biomedical applications, yet this remains a significant challenge. Herein, we report the preparation of biocompatible and biodegradable poly(ε-caprolactone) 1D (cylindrical) and 2D (platelet) micelles in water and alcoholic solvents via crystallization-driven self-assembly. Using epitaxial growth in an alcoholic solvent, we show exquisite control over the dimensions and dispersity of these nanostructures, allowing access to uniform morphologies and predictable dimensions based on the unimer-to-seed ratio. Furthermore, for the first time, we report epitaxial growth in aqueous solvent, achieving precise control over 1D nanostructures in water, an essential feature for any relevant biological application. Exploiting this further, a strong, biocompatible and fluorescent hydrogel was obtained as a result of living epitaxial growth in aqueous solvent and cell culture medium. MC3T3 and A549 cells were successfully encapsulated, demonstrating high viability (>95% after 4 days) in these novel hydrogel materials. American Chemical Society 2017-10-27 2017-11-22 /pmc/articles/PMC5789388/ /pubmed/29078700 http://dx.doi.org/10.1021/jacs.7b10199 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Arno, Maria C.
Inam, Maria
Coe, Zachary
Cambridge, Graeme
Macdougall, Laura J.
Keogh, Robert
Dove, Andrew P.
O’Reilly, Rachel K.
Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies
title Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies
title_full Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies
title_fullStr Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies
title_full_unstemmed Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies
title_short Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies
title_sort precision epitaxy for aqueous 1d and 2d poly(ε-caprolactone) assemblies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789388/
https://www.ncbi.nlm.nih.gov/pubmed/29078700
http://dx.doi.org/10.1021/jacs.7b10199
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