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Molecular afterglow imaging with bright, biodegradable polymer nanoparticles
Ultra-high signal-to-background in vivo imaging is enabled by biocompatible semiconducting polymer nanoparticles. Afterglow optical agents, which emit light long after cessation of excitation, hold promise for ultrasensitive in vivo imaging because they eliminate tissue autofluorescence. However, af...
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Published in: | Nature biotechnology 2017-11, Vol.35 (11), p.1102-1110 |
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creator | Miao, Qingqing Xie, Chen Zhen, Xu Lyu, Yan Duan, Hongwei Liu, Xiaogang Jokerst, Jesse V Pu, Kanyi |
description | Ultra-high signal-to-background
in vivo
imaging is enabled by biocompatible semiconducting polymer nanoparticles.
Afterglow optical agents, which emit light long after cessation of excitation, hold promise for ultrasensitive
in vivo
imaging because they eliminate tissue autofluorescence. However, afterglow imaging has been limited by its reliance on inorganic nanoparticles with relatively low brightness and short-near-infrared (NIR) emission. Here we present semiconducting polymer nanoparticles (SPNs) |
doi_str_mv | 10.1038/nbt.3987 |
format | article |
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in vivo
imaging is enabled by biocompatible semiconducting polymer nanoparticles.
Afterglow optical agents, which emit light long after cessation of excitation, hold promise for ultrasensitive
in vivo
imaging because they eliminate tissue autofluorescence. However, afterglow imaging has been limited by its reliance on inorganic nanoparticles with relatively low brightness and short-near-infrared (NIR) emission. Here we present semiconducting polymer nanoparticles (SPNs) <40 nm in diameter that store photon energy via chemical defects and emit long-NIR afterglow luminescence at 780 nm with a half-life of ∼6 min.
In vivo
, the afterglow intensity of SPNs is more than 100-fold brighter than that of inorganic afterglow agents, and the signal is detectable through the body of a live mouse. High-contrast lymph node and tumor imaging in living mice is demonstrated with a signal-to-background ratio up to 127-times higher than that obtained by NIR fluorescence imaging. Moreover, we developed an afterglow probe, activated only in the presence of biothiols, for early detection of drug-induced hepatotoxicity in living mice.</description><identifier>ISSN: 1087-0156</identifier><identifier>EISSN: 1546-1696</identifier><identifier>DOI: 10.1038/nbt.3987</identifier><identifier>PMID: 29035373</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>14/33 ; 14/34 ; 14/5 ; 639/301/357/354 ; 639/925/350/59 ; 639/925/352/2734 ; 64/60 ; 9/10 ; Agriculture ; Animals ; Biodegradability ; Biodegradable Plastics ; Biodegradation ; Bioinformatics ; Biomedical Engineering/Biotechnology ; Biomedicine ; Biopolymers ; Biotechnology ; Defects ; Diagnostic Imaging ; Fluorescence ; HeLa Cells ; Hepatotoxicity ; Humans ; I.R. radiation ; Imaging ; Life Sciences ; Light ; Luminescent Agents ; Lymph nodes ; Mice ; Mice, Nude ; Nanoparticles ; Near infrared radiation ; Neoplasms, Experimental ; Optical properties ; Polymers ; Quantum Dots - chemistry</subject><ispartof>Nature biotechnology, 2017-11, Vol.35 (11), p.1102-1110</ispartof><rights>Springer Nature America, Inc. 2017</rights><rights>COPYRIGHT 2017 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Nov 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-2d08e5ce970bbfefa53db50ed2f187981d5b805e78d55ec7bece4623c7feb9073</citedby><cites>FETCH-LOGICAL-c551t-2d08e5ce970bbfefa53db50ed2f187981d5b805e78d55ec7bece4623c7feb9073</cites><orcidid>0000-0002-8064-6009</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29035373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miao, Qingqing</creatorcontrib><creatorcontrib>Xie, Chen</creatorcontrib><creatorcontrib>Zhen, Xu</creatorcontrib><creatorcontrib>Lyu, Yan</creatorcontrib><creatorcontrib>Duan, Hongwei</creatorcontrib><creatorcontrib>Liu, Xiaogang</creatorcontrib><creatorcontrib>Jokerst, Jesse V</creatorcontrib><creatorcontrib>Pu, Kanyi</creatorcontrib><title>Molecular afterglow imaging with bright, biodegradable polymer nanoparticles</title><title>Nature biotechnology</title><addtitle>Nat Biotechnol</addtitle><addtitle>Nat Biotechnol</addtitle><description>Ultra-high signal-to-background
in vivo
imaging is enabled by biocompatible semiconducting polymer nanoparticles.
Afterglow optical agents, which emit light long after cessation of excitation, hold promise for ultrasensitive
in vivo
imaging because they eliminate tissue autofluorescence. However, afterglow imaging has been limited by its reliance on inorganic nanoparticles with relatively low brightness and short-near-infrared (NIR) emission. Here we present semiconducting polymer nanoparticles (SPNs) <40 nm in diameter that store photon energy via chemical defects and emit long-NIR afterglow luminescence at 780 nm with a half-life of ∼6 min.
In vivo
, the afterglow intensity of SPNs is more than 100-fold brighter than that of inorganic afterglow agents, and the signal is detectable through the body of a live mouse. High-contrast lymph node and tumor imaging in living mice is demonstrated with a signal-to-background ratio up to 127-times higher than that obtained by NIR fluorescence imaging. Moreover, we developed an afterglow probe, activated only in the presence of biothiols, for early detection of drug-induced hepatotoxicity in living mice.</description><subject>14/33</subject><subject>14/34</subject><subject>14/5</subject><subject>639/301/357/354</subject><subject>639/925/350/59</subject><subject>639/925/352/2734</subject><subject>64/60</subject><subject>9/10</subject><subject>Agriculture</subject><subject>Animals</subject><subject>Biodegradability</subject><subject>Biodegradable Plastics</subject><subject>Biodegradation</subject><subject>Bioinformatics</subject><subject>Biomedical Engineering/Biotechnology</subject><subject>Biomedicine</subject><subject>Biopolymers</subject><subject>Biotechnology</subject><subject>Defects</subject><subject>Diagnostic Imaging</subject><subject>Fluorescence</subject><subject>HeLa Cells</subject><subject>Hepatotoxicity</subject><subject>Humans</subject><subject>I.R. radiation</subject><subject>Imaging</subject><subject>Life Sciences</subject><subject>Light</subject><subject>Luminescent Agents</subject><subject>Lymph nodes</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Nanoparticles</subject><subject>Near infrared radiation</subject><subject>Neoplasms, Experimental</subject><subject>Optical properties</subject><subject>Polymers</subject><subject>Quantum Dots - 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Academic</collection><jtitle>Nature biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miao, Qingqing</au><au>Xie, Chen</au><au>Zhen, Xu</au><au>Lyu, Yan</au><au>Duan, Hongwei</au><au>Liu, Xiaogang</au><au>Jokerst, Jesse V</au><au>Pu, Kanyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular afterglow imaging with bright, biodegradable polymer nanoparticles</atitle><jtitle>Nature biotechnology</jtitle><stitle>Nat Biotechnol</stitle><addtitle>Nat Biotechnol</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>35</volume><issue>11</issue><spage>1102</spage><epage>1110</epage><pages>1102-1110</pages><issn>1087-0156</issn><eissn>1546-1696</eissn><abstract>Ultra-high signal-to-background
in vivo
imaging is enabled by biocompatible semiconducting polymer nanoparticles.
Afterglow optical agents, which emit light long after cessation of excitation, hold promise for ultrasensitive
in vivo
imaging because they eliminate tissue autofluorescence. However, afterglow imaging has been limited by its reliance on inorganic nanoparticles with relatively low brightness and short-near-infrared (NIR) emission. Here we present semiconducting polymer nanoparticles (SPNs) <40 nm in diameter that store photon energy via chemical defects and emit long-NIR afterglow luminescence at 780 nm with a half-life of ∼6 min.
In vivo
, the afterglow intensity of SPNs is more than 100-fold brighter than that of inorganic afterglow agents, and the signal is detectable through the body of a live mouse. High-contrast lymph node and tumor imaging in living mice is demonstrated with a signal-to-background ratio up to 127-times higher than that obtained by NIR fluorescence imaging. Moreover, we developed an afterglow probe, activated only in the presence of biothiols, for early detection of drug-induced hepatotoxicity in living mice.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>29035373</pmid><doi>10.1038/nbt.3987</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-8064-6009</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 14/33 14/34 14/5 639/301/357/354 639/925/350/59 639/925/352/2734 64/60 9/10 Agriculture Animals Biodegradability Biodegradable Plastics Biodegradation Bioinformatics Biomedical Engineering/Biotechnology Biomedicine Biopolymers Biotechnology Defects Diagnostic Imaging Fluorescence HeLa Cells Hepatotoxicity Humans I.R. radiation Imaging Life Sciences Light Luminescent Agents Lymph nodes Mice Mice, Nude Nanoparticles Near infrared radiation Neoplasms, Experimental Optical properties Polymers Quantum Dots - chemistry |
title | Molecular afterglow imaging with bright, biodegradable polymer nanoparticles |
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