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Upconversion superballs for programmable photoactivation of therapeutics
Upconversion nanoparticles (UCNPs) are the preferred choice for deep-tissue photoactivation, owing to their unique capability of converting deep tissue-penetrating near-infrared light to UV/visible light for photoactivation. Programmed photoactivation of multiple molecules is critical for controllin...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783568/ https://www.ncbi.nlm.nih.gov/pubmed/31594932 http://dx.doi.org/10.1038/s41467-019-12506-w |
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author | Zhang, Zhen Jayakumar, Muthu Kumara Gnanasammandhan Zheng, Xiang Shikha, Swati Zhang, Yi Bansal, Akshaya Poon, Dennis J. J. Chu, Pek Lim Yeo, Eugenia L. L. Chua, Melvin L. K. Chee, Soo Khee Zhang, Yong |
author_facet | Zhang, Zhen Jayakumar, Muthu Kumara Gnanasammandhan Zheng, Xiang Shikha, Swati Zhang, Yi Bansal, Akshaya Poon, Dennis J. J. Chu, Pek Lim Yeo, Eugenia L. L. Chua, Melvin L. K. Chee, Soo Khee Zhang, Yong |
author_sort | Zhang, Zhen |
collection | PubMed |
description | Upconversion nanoparticles (UCNPs) are the preferred choice for deep-tissue photoactivation, owing to their unique capability of converting deep tissue-penetrating near-infrared light to UV/visible light for photoactivation. Programmed photoactivation of multiple molecules is critical for controlling many biological processes. However, syntheses of such UCNPs require epitaxial growth of multiple shells on the core nanocrystals and are highly complex/time-consuming. To overcome this bottleneck, we have modularly assembled two distinct UCNPs which can individually be excited by 980/808 nm light, but not both. These orthogonal photoactivable UCNPs superballs are used for programmed photoactivation of multiple therapeutic processes for enhanced efficacy. These include sequential activation of endosomal escape through photochemical-internalization for enhanced cellular uptake, followed by photocontrolled gene knockdown of superoxide dismutase-1 to increase sensitivity to reactive oxygen species and finally, photodynamic therapy under these favorable conditions. Such programmed activation translated to significantly higher therapeutic efficacy in vitro and in vivo in comparison to conventional, non-programmed activation. |
format | Online Article Text |
id | pubmed-6783568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67835682019-10-10 Upconversion superballs for programmable photoactivation of therapeutics Zhang, Zhen Jayakumar, Muthu Kumara Gnanasammandhan Zheng, Xiang Shikha, Swati Zhang, Yi Bansal, Akshaya Poon, Dennis J. J. Chu, Pek Lim Yeo, Eugenia L. L. Chua, Melvin L. K. Chee, Soo Khee Zhang, Yong Nat Commun Article Upconversion nanoparticles (UCNPs) are the preferred choice for deep-tissue photoactivation, owing to their unique capability of converting deep tissue-penetrating near-infrared light to UV/visible light for photoactivation. Programmed photoactivation of multiple molecules is critical for controlling many biological processes. However, syntheses of such UCNPs require epitaxial growth of multiple shells on the core nanocrystals and are highly complex/time-consuming. To overcome this bottleneck, we have modularly assembled two distinct UCNPs which can individually be excited by 980/808 nm light, but not both. These orthogonal photoactivable UCNPs superballs are used for programmed photoactivation of multiple therapeutic processes for enhanced efficacy. These include sequential activation of endosomal escape through photochemical-internalization for enhanced cellular uptake, followed by photocontrolled gene knockdown of superoxide dismutase-1 to increase sensitivity to reactive oxygen species and finally, photodynamic therapy under these favorable conditions. Such programmed activation translated to significantly higher therapeutic efficacy in vitro and in vivo in comparison to conventional, non-programmed activation. Nature Publishing Group UK 2019-10-08 /pmc/articles/PMC6783568/ /pubmed/31594932 http://dx.doi.org/10.1038/s41467-019-12506-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Zhen Jayakumar, Muthu Kumara Gnanasammandhan Zheng, Xiang Shikha, Swati Zhang, Yi Bansal, Akshaya Poon, Dennis J. J. Chu, Pek Lim Yeo, Eugenia L. L. Chua, Melvin L. K. Chee, Soo Khee Zhang, Yong Upconversion superballs for programmable photoactivation of therapeutics |
title | Upconversion superballs for programmable photoactivation of therapeutics |
title_full | Upconversion superballs for programmable photoactivation of therapeutics |
title_fullStr | Upconversion superballs for programmable photoactivation of therapeutics |
title_full_unstemmed | Upconversion superballs for programmable photoactivation of therapeutics |
title_short | Upconversion superballs for programmable photoactivation of therapeutics |
title_sort | upconversion superballs for programmable photoactivation of therapeutics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783568/ https://www.ncbi.nlm.nih.gov/pubmed/31594932 http://dx.doi.org/10.1038/s41467-019-12506-w |
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