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Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface
Lipids and amphiphilic block copolymers spontaneously self-assemble in water to form a plethora of micelles and vesicles. They are typically fluidic in nature and often mechanically weak for applications such as drug delivery and gene therapeutics. Mechanical properties of polymeric materials could...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742919/ https://www.ncbi.nlm.nih.gov/pubmed/26837260 http://dx.doi.org/10.1038/ncomms10599 |
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author | Wang, Wenda Qi, Hao Zhou, Tian Mei, Shan Han, Lin Higuchi, Takeshi Jinnai, Hiroshi Li, Christopher Y. |
author_facet | Wang, Wenda Qi, Hao Zhou, Tian Mei, Shan Han, Lin Higuchi, Takeshi Jinnai, Hiroshi Li, Christopher Y. |
author_sort | Wang, Wenda |
collection | PubMed |
description | Lipids and amphiphilic block copolymers spontaneously self-assemble in water to form a plethora of micelles and vesicles. They are typically fluidic in nature and often mechanically weak for applications such as drug delivery and gene therapeutics. Mechanical properties of polymeric materials could be improved by forming crystalline structures. However, most of the self-assembled micelles and vesicles have curved surfaces and precisely tuning crystallization within a nanoscale curved space is challenging, as the curved geometry is incommensurate with crystals having three-dimensional translational symmetry. Herein, we report using a miniemulsion crystallization method to grow nanosized, polymer single-crystal-like capsules. We coin the name crystalsome to describe this unique structure, because they are formed by polymer lamellar crystals and their structure mimics liposomes and polymersomes. Using poly(L-lactic acid) (PLLA) as the model polymer, we show that curved water/p-xylene interface formed by the miniemulsion process can guide the growth of PLLA single crystals. Crystalsomes with the size ranging from ∼148 nm to over 1 μm have been formed. Atomic force microscopy measurement demonstrate a two to three orders of magnitude increase in bending modulus compared with conventional polymersomes. We envisage that this novel structure could shed light on investigating spherical crystallography and drug delivery. |
format | Online Article Text |
id | pubmed-4742919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47429192016-03-04 Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface Wang, Wenda Qi, Hao Zhou, Tian Mei, Shan Han, Lin Higuchi, Takeshi Jinnai, Hiroshi Li, Christopher Y. Nat Commun Article Lipids and amphiphilic block copolymers spontaneously self-assemble in water to form a plethora of micelles and vesicles. They are typically fluidic in nature and often mechanically weak for applications such as drug delivery and gene therapeutics. Mechanical properties of polymeric materials could be improved by forming crystalline structures. However, most of the self-assembled micelles and vesicles have curved surfaces and precisely tuning crystallization within a nanoscale curved space is challenging, as the curved geometry is incommensurate with crystals having three-dimensional translational symmetry. Herein, we report using a miniemulsion crystallization method to grow nanosized, polymer single-crystal-like capsules. We coin the name crystalsome to describe this unique structure, because they are formed by polymer lamellar crystals and their structure mimics liposomes and polymersomes. Using poly(L-lactic acid) (PLLA) as the model polymer, we show that curved water/p-xylene interface formed by the miniemulsion process can guide the growth of PLLA single crystals. Crystalsomes with the size ranging from ∼148 nm to over 1 μm have been formed. Atomic force microscopy measurement demonstrate a two to three orders of magnitude increase in bending modulus compared with conventional polymersomes. We envisage that this novel structure could shed light on investigating spherical crystallography and drug delivery. Nature Publishing Group 2016-02-03 /pmc/articles/PMC4742919/ /pubmed/26837260 http://dx.doi.org/10.1038/ncomms10599 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Wenda Qi, Hao Zhou, Tian Mei, Shan Han, Lin Higuchi, Takeshi Jinnai, Hiroshi Li, Christopher Y. Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
title | Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
title_full | Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
title_fullStr | Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
title_full_unstemmed | Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
title_short | Highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
title_sort | highly robust crystalsome via directed polymer crystallization at curved liquid/liquid interface |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742919/ https://www.ncbi.nlm.nih.gov/pubmed/26837260 http://dx.doi.org/10.1038/ncomms10599 |
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