Near-Infrared-Emitting Nanoparticles for Lifetime-Based Multiplexed Analysis and Imaging of Living Cells

被引:62
作者
Hoffmann, Katrin [1 ]
Behnke, Thomas [1 ]
Drescher, Daniela [1 ,2 ]
Kneipp, Janina [1 ,2 ]
Resch-Genger, Ute [1 ]
机构
[1] BAM Fed Inst Mat Res & Testing, D-12489 Berlin, Germany
[2] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
关键词
fluorescence lifetime imaging microscopy; FLIM; lifetime multiplexing; near-infrared; NIR; cell imaging; nanoparticles; FLUORESCENT SILICA NANOPARTICLES; QUANTUM DOTS; PARTICLES; FLUOROPHORES; DYES; BEADS; SIZE;
D O I
10.1021/nn4029458
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The increase in information content from bioassays and bioimaging requires robust and efficient strategies for the detection of multiple analytes or targets in a single measurement, thereby addressing current health and security concerns. For fluorescence techniques, an attractive alternative to commonly performed spectral or color multiplexing presents lifetime multiplexing and the discrimination between different fluorophores based on their fluorescence decay kinetics. This strategy relies on fluorescent labels with sufficiently different lifetimes that are excitable at the same wave: length and detectable within the same spectral window. Here, we report on lifetime multiplexing and discrimination with a set of nanometer-sized particles loaded with near infrared emissive organic fluorophores chosen to display very similar absorption and emission spectra, yet different fluorescence decay kinetics In suspension. Furthermore, as a first proof-of-concept we describe bioimaging studies with 3T3 fibroblasts and J774 macrophages, incubated with mixtures of these reporters employing fluorescence lifetime imaging microscopy. These proof-of-concept measurements underline the potential of fluorescent nanoparticle reporters in fluorescence lifetime multiplexing, barcoding, and imaging for cellular studies, cell based assays, and molecular imaging.
引用
收藏
页码:6674 / 6684
页数:11
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