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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-5944428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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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
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title_short | Soft and flexible poly(ethylene glycol) nanotubes for local drug delivery
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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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