An Organic Afterglow Protheranostic Nanoassembly

© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 31(2019), 32 vom: 06. Aug., Seite e1902672
1. Verfasser: He, Shasha (VerfasserIn)
Weitere Verfasser: Xie, Chen, Jiang, Yuyan, Pu, Kanyi
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2019
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article activatable probes cancer theranostics optical imaging organic nanoparticles Antineoplastic Agents Luminescent Agents Prodrugs Floxuridine 039LU44I5M mehr... Polyethylene Glycols 3WJQ0SDW1A Hydrogen Peroxide BBX060AN9V doxifluridine V1JK16Y2JP Uridine WHI7HQ7H85
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520 |a Cancer theranostics holds potential promise for precision medicine; however, most existing theranostic nanoagents are simply developed by doping both therapeutic agents and imaging agent into one particle entity, and thus have an "always-on" pharmaceutical effect and imaging signals regardless of their in vivo location. Herein, the development of an organic afterglow protheranostic nanoassembly (APtN) that specifically activates both the pharmaceutical effect and diagnostic signals in response to a tumor-associated chemical mediator (hydrogen peroxide, H2 O2 ) is reported. APtN comprises an amphiphilic macromolecule and a near-infrared (NIR) dye acting as the H2 O2 -responsive afterglow prodrug and the afterglow initiator, respectively. Such a molecular architecture allows APtN to passively target tumors in living mice, specifically release the anticancer drug in the tumor, and spontaneously generate the uncaged afterglow substrate. Upon NIR light preirradiation, the afterglow initiator generates singlet oxygen to react and subsequently transform the uncaged afterglow substrate into an active self-luminescent form. Thus, the intensity of generated afterglow luminescence is correlated with the drug release status, permitting real-time in vivo monitoring of prodrug activation. This study proposes a background-free design strategy toward activatable cancer theranostics 
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650 4 |a activatable probes 
650 4 |a cancer theranostics 
650 4 |a optical imaging 
650 4 |a organic nanoparticles 
650 7 |a Antineoplastic Agents  |2 NLM 
650 7 |a Luminescent Agents  |2 NLM 
650 7 |a Prodrugs  |2 NLM 
650 7 |a Floxuridine  |2 NLM 
650 7 |a 039LU44I5M  |2 NLM 
650 7 |a Polyethylene Glycols  |2 NLM 
650 7 |a 3WJQ0SDW1A  |2 NLM 
650 7 |a Hydrogen Peroxide  |2 NLM 
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650 7 |a WHI7HQ7H85  |2 NLM 
700 1 |a Xie, Chen  |e verfasserin  |4 aut 
700 1 |a Jiang, Yuyan  |e verfasserin  |4 aut 
700 1 |a Pu, Kanyi  |e verfasserin  |4 aut 
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773 1 8 |g volume:31  |g year:2019  |g number:32  |g day:06  |g month:08  |g pages:e1902672 
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