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Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery

Nanotubes are emerging as promising materials for healthcare applications but the selection of clinically relevant starting materials for their synthesis remains largely unexplored. Here we present, for the first time, the synthesis of poly(ethylene glycol) (PEG) based nanotubes via the photopolymer...

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Detalles Bibliográficos
Autores principales: Newland, B., Taplan, C., Pette, D., Friedrichs, J., Steinhart, M., Wang, W., Voit, B., Seib, F. P., Werner, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944428/
https://www.ncbi.nlm.nih.gov/pubmed/29714385
http://dx.doi.org/10.1039/c8nr00603b
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author Newland, B.
Taplan, C.
Pette, D.
Friedrichs, J.
Steinhart, M.
Wang, W.
Voit, B.
Seib, F. P.
Werner, C.
author_facet Newland, B.
Taplan, C.
Pette, D.
Friedrichs, J.
Steinhart, M.
Wang, W.
Voit, B.
Seib, F. P.
Werner, C.
author_sort Newland, B.
collection PubMed
description Nanotubes are emerging as promising materials for healthcare applications but the selection of clinically relevant starting materials for their synthesis remains largely unexplored. Here we present, for the first time, the synthesis of poly(ethylene glycol) (PEG) based nanotubes via the photopolymerization of poly(ethylene glycol) diacrylate and other diacrylate derivatives within the pores of anodized aluminum oxide templates. Template-assisted synthesis allowed the manufacture of a diverse set of polymeric nanotubes with tunable physical characteristics including diameter (∼200–400 nm) and stiffness (405–902 kPa). PEG nanotubes were subjected to cytotoxicty assessment in cell lines and primary stem cells and showed excellent cytocompatability (IC(50) > 120 μg ml(–1)). Nanotubes were readily drug loaded but released the majority of the drug over 5 days. Direct administration of drug loaded nanotubes to human orthotopic breast tumors substantially reduced tumor growth and metastasis and outperformed i.v. administration at the equivalent dose. Overall, this nanotube templating platform is emerging as a facile route for the manufacture of poly(ethylene glycol) nanotubes.
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spelling pubmed-59444282018-05-18 Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery Newland, B. Taplan, C. Pette, D. Friedrichs, J. Steinhart, M. Wang, W. Voit, B. Seib, F. P. Werner, C. Nanoscale Chemistry Nanotubes are emerging as promising materials for healthcare applications but the selection of clinically relevant starting materials for their synthesis remains largely unexplored. Here we present, for the first time, the synthesis of poly(ethylene glycol) (PEG) based nanotubes via the photopolymerization of poly(ethylene glycol) diacrylate and other diacrylate derivatives within the pores of anodized aluminum oxide templates. Template-assisted synthesis allowed the manufacture of a diverse set of polymeric nanotubes with tunable physical characteristics including diameter (∼200–400 nm) and stiffness (405–902 kPa). PEG nanotubes were subjected to cytotoxicty assessment in cell lines and primary stem cells and showed excellent cytocompatability (IC(50) > 120 μg ml(–1)). Nanotubes were readily drug loaded but released the majority of the drug over 5 days. Direct administration of drug loaded nanotubes to human orthotopic breast tumors substantially reduced tumor growth and metastasis and outperformed i.v. administration at the equivalent dose. Overall, this nanotube templating platform is emerging as a facile route for the manufacture of poly(ethylene glycol) nanotubes. Royal Society of Chemistry 2018-05-14 2018-05-01 /pmc/articles/PMC5944428/ /pubmed/29714385 http://dx.doi.org/10.1039/c8nr00603b Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Newland, B.
Taplan, C.
Pette, D.
Friedrichs, J.
Steinhart, M.
Wang, W.
Voit, B.
Seib, F. P.
Werner, C.
Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
title Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
title_full Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
title_fullStr Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
title_full_unstemmed Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
title_short Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
title_sort soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944428/
https://www.ncbi.nlm.nih.gov/pubmed/29714385
http://dx.doi.org/10.1039/c8nr00603b
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