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Hydrogel-Coated Near Infrared Absorbing Nanoshells as Light-Responsive Drug Delivery Vehicles
[Image: see text] Nanoparticle drug delivery carriers that can modulate drug release based on an exogenous signal, such as light, are of great interest, especially for improving cancer therapy. A light-activated delivery vehicle was fabricated by synthesizing a thin, thermally responsive poly(N-isop...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565577/ https://www.ncbi.nlm.nih.gov/pubmed/26366438 http://dx.doi.org/10.1021/acsbiomaterials.5b00111 |
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author | Strong, Laura E. West, Jennifer L. |
author_facet | Strong, Laura E. West, Jennifer L. |
author_sort | Strong, Laura E. |
collection | PubMed |
description | [Image: see text] Nanoparticle drug delivery carriers that can modulate drug release based on an exogenous signal, such as light, are of great interest, especially for improving cancer therapy. A light-activated delivery vehicle was fabricated by synthesizing a thin, thermally responsive poly(N-isopropylacrylamide-co-acrylamide) hydrogel coating directly onto the surfaces of individual near-infrared (NIR) absorbing gold-silica nanoshells. This hydrogel was designed to be in a swollen state under physiological conditions and expel large amounts of water, along with any entrapped drug, at elevated temperatures. The required temperature change can be achieved via NIR absorption by the nanoshell, allowing the hydrogel phase change to be triggered by light, which was observed by monitoring changes in particle sizes as water was expelled from the hydrogel network. The phase change was reversible and repeatable. As a model drug, the chemotherapeutic doxorubicin was loaded into this delivery vehicle, and rapid release of doxorubicin occurred upon NIR exposure. Further, colon carcinoma cells exposed to the irradiated platform displayed nearly 3 times as much doxorubicin uptake as cells exposed to nonirradiated particles or free drug, which in turn resulted in a higher loss of cell viability. We hypothesize these effects are because the NIR-mediated heating results in a transient increase in cell membrane permeability, thus aiding in cellular uptake of the drug. |
format | Online Article Text |
id | pubmed-4565577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45655772015-09-11 Hydrogel-Coated Near Infrared Absorbing Nanoshells as Light-Responsive Drug Delivery Vehicles Strong, Laura E. West, Jennifer L. ACS Biomater Sci Eng [Image: see text] Nanoparticle drug delivery carriers that can modulate drug release based on an exogenous signal, such as light, are of great interest, especially for improving cancer therapy. A light-activated delivery vehicle was fabricated by synthesizing a thin, thermally responsive poly(N-isopropylacrylamide-co-acrylamide) hydrogel coating directly onto the surfaces of individual near-infrared (NIR) absorbing gold-silica nanoshells. This hydrogel was designed to be in a swollen state under physiological conditions and expel large amounts of water, along with any entrapped drug, at elevated temperatures. The required temperature change can be achieved via NIR absorption by the nanoshell, allowing the hydrogel phase change to be triggered by light, which was observed by monitoring changes in particle sizes as water was expelled from the hydrogel network. The phase change was reversible and repeatable. As a model drug, the chemotherapeutic doxorubicin was loaded into this delivery vehicle, and rapid release of doxorubicin occurred upon NIR exposure. Further, colon carcinoma cells exposed to the irradiated platform displayed nearly 3 times as much doxorubicin uptake as cells exposed to nonirradiated particles or free drug, which in turn resulted in a higher loss of cell viability. We hypothesize these effects are because the NIR-mediated heating results in a transient increase in cell membrane permeability, thus aiding in cellular uptake of the drug. American Chemical Society 2015-06-10 2015-08-10 /pmc/articles/PMC4565577/ /pubmed/26366438 http://dx.doi.org/10.1021/acsbiomaterials.5b00111 Text en Copyright © 2015 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 | Strong, Laura E. West, Jennifer L. Hydrogel-Coated Near Infrared Absorbing Nanoshells as Light-Responsive Drug Delivery Vehicles |
title | Hydrogel-Coated Near Infrared Absorbing Nanoshells
as Light-Responsive Drug Delivery Vehicles |
title_full | Hydrogel-Coated Near Infrared Absorbing Nanoshells
as Light-Responsive Drug Delivery Vehicles |
title_fullStr | Hydrogel-Coated Near Infrared Absorbing Nanoshells
as Light-Responsive Drug Delivery Vehicles |
title_full_unstemmed | Hydrogel-Coated Near Infrared Absorbing Nanoshells
as Light-Responsive Drug Delivery Vehicles |
title_short | Hydrogel-Coated Near Infrared Absorbing Nanoshells
as Light-Responsive Drug Delivery Vehicles |
title_sort | hydrogel-coated near infrared absorbing nanoshells
as light-responsive drug delivery vehicles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565577/ https://www.ncbi.nlm.nih.gov/pubmed/26366438 http://dx.doi.org/10.1021/acsbiomaterials.5b00111 |
work_keys_str_mv | AT stronglaurae hydrogelcoatednearinfraredabsorbingnanoshellsaslightresponsivedrugdeliveryvehicles AT westjenniferl hydrogelcoatednearinfraredabsorbingnanoshellsaslightresponsivedrugdeliveryvehicles |