| Literature DB >> 32483892 |
Charlotte Allard1, Léonard Schué2, Frédéric Fossard3, Gaëlle Recher4,5, Rafaella Nascimento2, Emmanuel Flahaut6, Annick Loiseau3, Patrick Desjardins1, Richard Martel2, Etienne Gaufrès3,4,5.
Abstract
Fluorescence is ubiquitous in life science and used in many fields of research ranging from ecology to medicine. Among the most common fluorogenic compounds, dyes are being exploited in bioimaging for their outstanding optical properties from UV down to the near IR (NIR). However, dye molecules are often toxic to living organisms and photodegradable, which limits the time window for in vivo experiments. Here, it is demonstrated that organic dye molecules are passivated and photostable when they are encapsulated inside a boron nitride nanotube (dyes@BNNT). The results show that the BNNTs drive an aggregation of the encapsulated dyes, which induces a redshifted fluorescence from visible to NIR-II. The fluorescence remains strong and stable, exempt of bleaching and blinking, over a time scale longer than that of free dyes by more than 104 . This passivation also reduces the toxicity of the dyes and induces exceptional chemical robustness, even in harsh conditions. These properties are highlighted in bioimaging where the dyes@BNNT nanohybrids are used as fluorescent nanoprobes for in vivo monitoring of Daphnia Pulex microorganisms and for diffusion tracking on human hepatoblastoma cells with two-photon imaging.Entities:
Keywords: NIR-II fluorescence; bio-imaging; molecular aggregation; nanotube heterostructure; photostable fluorescence
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Year: 2020 PMID: 32483892 DOI: 10.1002/adma.202001429
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849