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The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes

Polymersomes are being widely explored as synthetic analogs of lipid vesicles based on their enhanced stability and potential uses in a wide variety of applications in (e.g., drug delivery, cell analogs, etc.). Controlled formation of giant polymersomes for use in membrane studies and cell mimetic s...

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Autores principales: Greene, Adrienne C., Henderson, Ian M., Gomez, Andrew, Paxton, Walter F., VanDelinder, Virginia, Bachand, George D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943728/
https://www.ncbi.nlm.nih.gov/pubmed/27410487
http://dx.doi.org/10.1371/journal.pone.0158729
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author Greene, Adrienne C.
Henderson, Ian M.
Gomez, Andrew
Paxton, Walter F.
VanDelinder, Virginia
Bachand, George D.
author_facet Greene, Adrienne C.
Henderson, Ian M.
Gomez, Andrew
Paxton, Walter F.
VanDelinder, Virginia
Bachand, George D.
author_sort Greene, Adrienne C.
collection PubMed
description Polymersomes are being widely explored as synthetic analogs of lipid vesicles based on their enhanced stability and potential uses in a wide variety of applications in (e.g., drug delivery, cell analogs, etc.). Controlled formation of giant polymersomes for use in membrane studies and cell mimetic systems, however, is currently limited by low-yield production methodologies. Here, we describe for the first time, how the size distribution of giant poly(ethylene glycol)-poly(butadiene) (PEO-PBD) polymersomes formed by gel-assisted rehydration may be controlled based on membrane fluidization. We first show that the average diameter and size distribution of PEO-PBD polymersomes may be readily increased by increasing the temperature of the rehydration solution. Further, we describe a correlative relationship between polymersome size and membrane fluidization through the addition of sucrose during rehydration, enabling the formation of PEO-PBD polymersomes with a range of diameters, including giant-sized vesicles (>100 μm). This correlative relationship suggests that sucrose may function as a small molecule fluidizer during rehydration, enhancing polymer diffusivity during formation and increasing polymersome size. Overall the ability to easily regulate the size of PEO-PBD polymersomes based on membrane fluidity, either through temperature or fluidizers, has broadly applicability in areas including targeted therapeutic delivery and synthetic biology.
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spelling pubmed-49437282016-08-01 The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes Greene, Adrienne C. Henderson, Ian M. Gomez, Andrew Paxton, Walter F. VanDelinder, Virginia Bachand, George D. PLoS One Research Article Polymersomes are being widely explored as synthetic analogs of lipid vesicles based on their enhanced stability and potential uses in a wide variety of applications in (e.g., drug delivery, cell analogs, etc.). Controlled formation of giant polymersomes for use in membrane studies and cell mimetic systems, however, is currently limited by low-yield production methodologies. Here, we describe for the first time, how the size distribution of giant poly(ethylene glycol)-poly(butadiene) (PEO-PBD) polymersomes formed by gel-assisted rehydration may be controlled based on membrane fluidization. We first show that the average diameter and size distribution of PEO-PBD polymersomes may be readily increased by increasing the temperature of the rehydration solution. Further, we describe a correlative relationship between polymersome size and membrane fluidization through the addition of sucrose during rehydration, enabling the formation of PEO-PBD polymersomes with a range of diameters, including giant-sized vesicles (>100 μm). This correlative relationship suggests that sucrose may function as a small molecule fluidizer during rehydration, enhancing polymer diffusivity during formation and increasing polymersome size. Overall the ability to easily regulate the size of PEO-PBD polymersomes based on membrane fluidity, either through temperature or fluidizers, has broadly applicability in areas including targeted therapeutic delivery and synthetic biology. Public Library of Science 2016-07-13 /pmc/articles/PMC4943728/ /pubmed/27410487 http://dx.doi.org/10.1371/journal.pone.0158729 Text en © 2016 Greene et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Greene, Adrienne C.
Henderson, Ian M.
Gomez, Andrew
Paxton, Walter F.
VanDelinder, Virginia
Bachand, George D.
The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes
title The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes
title_full The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes
title_fullStr The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes
title_full_unstemmed The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes
title_short The Role of Membrane Fluidization in the Gel-Assisted Formation of Giant Polymersomes
title_sort role of membrane fluidization in the gel-assisted formation of giant polymersomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943728/
https://www.ncbi.nlm.nih.gov/pubmed/27410487
http://dx.doi.org/10.1371/journal.pone.0158729
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