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Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility
Multiphoton microscopy is an exciting tool for biomedical research because it can be used to image single cells in vivo due to its greater penetration depth, lower phototoxicity and higher resolution when compared to confocal laser scanning microscopy. This helps researchers understand how certain c...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618339/ https://www.ncbi.nlm.nih.gov/pubmed/28970884 http://dx.doi.org/10.1039/c7sc00908a |
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author | Nicol, Alexander Qin, Wei Kwok, Ryan T. K. Burkhartsmeyer, Jeffrey Mark Zhu, Zhenfeng Su, Huifang Luo, Wenwen Lam, Jacky W. Y. Qian, Jun Wong, Kam Sing Tang, Ben Zhong |
author_facet | Nicol, Alexander Qin, Wei Kwok, Ryan T. K. Burkhartsmeyer, Jeffrey Mark Zhu, Zhenfeng Su, Huifang Luo, Wenwen Lam, Jacky W. Y. Qian, Jun Wong, Kam Sing Tang, Ben Zhong |
author_sort | Nicol, Alexander |
collection | PubMed |
description | Multiphoton microscopy is an exciting tool for biomedical research because it can be used to image single cells in vivo due to its greater penetration depth, lower phototoxicity and higher resolution when compared to confocal laser scanning microscopy. This helps researchers understand how certain cells change over time and evaluate the efficacy of different therapies. Herein, we report a new AIE luminogen (AIEgen), abbreviated as TPE-TETRAD, with a favorable absorption and efficient deep-red emission in the solid state. TPE-TETRAD possesses a high two-photon absorption cross-section (313 MG at 830 nm) and a rich array of non-linear optical properties including aggregation-induced three-photon luminescence. Biotinylated TPE-TETRAD nanoparticles are also fabricated and applied to stain mitochondria in live cancer cells with high specificity. The purpose of this study is to characterize a novel deep-red AIEgen and fabricate biotinylated nanoparticles for applications as (1) biocompatible and photostable AIE probes for specific mitochondria imaging and (2) multiphoton imaging probes suitable for two/three-photon fluorescence microscopy. |
format | Online Article Text |
id | pubmed-5618339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56183392017-10-02 Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility Nicol, Alexander Qin, Wei Kwok, Ryan T. K. Burkhartsmeyer, Jeffrey Mark Zhu, Zhenfeng Su, Huifang Luo, Wenwen Lam, Jacky W. Y. Qian, Jun Wong, Kam Sing Tang, Ben Zhong Chem Sci Chemistry Multiphoton microscopy is an exciting tool for biomedical research because it can be used to image single cells in vivo due to its greater penetration depth, lower phototoxicity and higher resolution when compared to confocal laser scanning microscopy. This helps researchers understand how certain cells change over time and evaluate the efficacy of different therapies. Herein, we report a new AIE luminogen (AIEgen), abbreviated as TPE-TETRAD, with a favorable absorption and efficient deep-red emission in the solid state. TPE-TETRAD possesses a high two-photon absorption cross-section (313 MG at 830 nm) and a rich array of non-linear optical properties including aggregation-induced three-photon luminescence. Biotinylated TPE-TETRAD nanoparticles are also fabricated and applied to stain mitochondria in live cancer cells with high specificity. The purpose of this study is to characterize a novel deep-red AIEgen and fabricate biotinylated nanoparticles for applications as (1) biocompatible and photostable AIE probes for specific mitochondria imaging and (2) multiphoton imaging probes suitable for two/three-photon fluorescence microscopy. Royal Society of Chemistry 2017-06-01 2017-05-09 /pmc/articles/PMC5618339/ /pubmed/28970884 http://dx.doi.org/10.1039/c7sc00908a Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Nicol, Alexander Qin, Wei Kwok, Ryan T. K. Burkhartsmeyer, Jeffrey Mark Zhu, Zhenfeng Su, Huifang Luo, Wenwen Lam, Jacky W. Y. Qian, Jun Wong, Kam Sing Tang, Ben Zhong Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility |
title | Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility
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title_full | Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility
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title_fullStr | Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility
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title_full_unstemmed | Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility
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title_short | Functionalized AIE nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility
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title_sort | functionalized aie nanoparticles with efficient deep-red emission, mitochondrial specificity, cancer cell selectivity and multiphoton susceptibility |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618339/ https://www.ncbi.nlm.nih.gov/pubmed/28970884 http://dx.doi.org/10.1039/c7sc00908a |
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