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Line-scanning confocal microscopy for high-resolution imaging of upconverting rare-earth-based contrast agents
Journal article   Open access   Peer reviewed

Line-scanning confocal microscopy for high-resolution imaging of upconverting rare-earth-based contrast agents

Laura M Higgins, Margot Zevon, Vidya Ganapathy, Yang Sheng, Mei Chee Tan, Richard E Riman, Charles M Roth, Prabhas V Moghe and Mark C Pierce
Journal of biomedical optics, Vol.20(11), pp.110506-110506
01/11/2015
PMID: 26603495

Abstract

Cell Line, Tumor - chemistry Cell Line, Tumor - ultrastructure Contrast Media - chemistry Equipment Design Equipment Failure Analysis Humans Image Enhancement - instrumentation Metals, Rare Earth Microscopy, Fluorescence - instrumentation Molecular Imaging - methods Nanoparticles - chemistry Nanoparticles - ultrastructure Reproducibility of Results Sensitivity and Specificity
Rare-earth (RE) doped nanocomposites emit visible luminescence when illuminated with continuous wave near-infrared light, making them appealing candidates for use as contrast agents in biomedical imaging. However, the emission lifetime of these materials is much longer than the pixel dwell times used in scanning intravital microscopy. To overcome this limitation, we have developed a line-scanning confocal microscope for high-resolution, optically sectioned imaging of samples labeled with RE-based nanomaterials. Instrument performance is quantified using calibrated test objects. NaYF4 : Er,Yb nanocomposites are imaged in vitro, and in ex vivo tissue specimens, with direct comparison to point-scanning confocal microscopy. We demonstrate that the extended pixel dwell time of line-scanning confocal microscopy enables subcellular-level imaging of these nanomaterials while maintaining optical sectioning. The line-scanning approach thus enables microscopic imaging of this emerging class of contrast agents for preclinical studies, with the potential to be adapted for real-time in vivo imaging in the clinic.
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https://doi.org/10.1117/1.JBO.20.11.110506View
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