Self-Assembled Biocompatible Fluorescent Nanoparticles for Bioimaging

被引:23
|
作者
Caponetti, Valeria [1 ]
Trzcinski, Jakub W. [2 ]
Cantelli, Andrea [1 ]
Tavano, Regina [3 ]
Papini, Emanuele [3 ]
Mancin, Fabrizio [2 ]
Montalti, Marco [1 ]
机构
[1] Univ Bologna, Dipartimento Chim Giacomo Ciamician, Bologna, Italy
[2] Univ Padua, Dipartimento Sci Chim, Padua, Italy
[3] Univ Padua, Dipartimento Sci Biomed, Padua, Italy
来源
FRONTIERS IN CHEMISTRY | 2019年 / 7卷
基金
欧洲研究理事会;
关键词
fluorescence; fluorescent probes; ultra-bright; nanoparticles; nanoprecipitation; tracking; single particle imaging; bioimaging; ORGANIC NANOPARTICLES; SILICA NANOPARTICLES; EMISSION; PROBES; LUMINESCENCE; TRACKING; STRATEGY; DELIVERY; CATIONS; BINDING;
D O I
10.3389/fchem.2019.00168
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fluorescence is a powerful tool for mapping biological events in real-time with high spatial resolution. Ultra-bright probes are needed in order to achieve high sensitivity: these probes are typically obtained by gathering a huge number of fluorophores in a single nanoparticle (NP). Unfortunately this assembly produces quenching of the fluorescence because of short-range intermolecular interactions. Here we demonstrate that rational structural modification of a well-known molecular fluorophore N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) (NBD) produces fluorophores that self-assemble in nanoparticles in the biocompatible environment without any dramatic decrease of the fluorescence quantum yield. Most importantly, the resulting NP show, in an aqueous environment, a brightness which is more than six orders of magnitude higher than the molecular component in the organic solvent. Moreover, the NP are prepared by nanoprecipitation and they are stabilized only via non-covalent interaction, they are surprisingly stable and can be observed as individual bright spots freely diffusing in solution at a concentration as low as 1 nM. The suitability of the NP as biocompatible fluorescent probes was demonstrated in the case of HeLa cells by fluorescence confocal microscopy and MTS assays.
引用
收藏
页数:10
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