Wide-field time-gated photoluminescence microscopy for fast ultrahigh-sensitivity imaging of photoluminescent probes
| Autor: | Andrei V. Zvyagin, Varun K. A. Sreenivasan, W. A. W. Razali, Mark Connor, Ewa M. Goldys, Carlo Bradac |
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| Rok vydání: | 2016 |
| Předmět: |
Materials science
Photoluminescence Light Luminescent Measurements General Physics and Astronomy 02 engineering and technology 010402 general chemistry 01 natural sciences Signal General Biochemistry Genetics and Molecular Biology law.invention Mice Optics law Cell Line Tumor Microscopy Fluorescence microscope Animals General Materials Science Fluorescent Dyes business.industry Lasers General Engineering General Chemistry 021001 nanoscience & nanotechnology Laser Fluorescence 0104 chemical sciences Autofluorescence Microscopy Fluorescence 0210 nano-technology business |
| Zdroj: | Journal of Biophotonics. 9:848-858 |
| ISSN: | 1864-063X |
| DOI: | 10.1002/jbio.201600050 |
| Popis: | Fluorescence microscopy is a fundamental technique for the life sciences, where biocompatible and photostable photoluminescence probes in combination with fast and sensitive imaging systems are continually transforming this field. A wide-field time-gated photoluminescence microscopy system customised for ultrasensitive imaging of unique nanoruby probes with long photoluminescence lifetime is described. The detection sensitivity derived from the long photoluminescence lifetime of the nanoruby makes it possible to discriminate signals from unwanted autofluorescence background and laser backscatter by employing a time-gated image acquisition mode. This mode enabled several-fold improvement of the photoluminescence imaging contrast of discrete nanorubies dispersed on a coverslip. It enabled recovery of the photoluminescence signal emanating from discrete nanorubies when covered by a layer of an organic fluorescent dye, which were otherwise invisible without the use of spectral filtering approaches. Time-gated imaging also facilitated high sensitivity detection of nanorubies in a biological environment of cultured cells. Finally, we monitor the binding kinetics of nanorubies to a functionalised substrate, which exemplified a real-time assay in biological fluids. 3D-pseudo colour images of nanorubies immersed in a highly fluorescent dye solution. Nanoruby photoluminescence is subdued by that of the dye in continuous excitation/imaging (left), however it can be recovered by time-gated imaging (right). At the bottom is schematic diagram of nanoruby assay in a biological fluid. |
| Databáze: | OpenAIRE |
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