Multiresolution Localization With Temporal Scanning for Super-Resolution Diffuse Optical Imaging of Fluorescence
Year: 2019
Type: article
Abstract: A super-resolution optical imaging method is presented that relies on the distinct temporal information associated with each fluorescent optical reporter to determine its spatial position to high precision with measurements of heavily scattered light. This multiple-emitter localization approach uses a diffusion equation forward model in a cost function, and has the potential to achieve micron-scale spatial resolution through centimeters of tissue. Utilizing some degree of temporal separation for the reporter emissions, position and emission strength are determined using a computationally efficient time stripping multiresolution algorithm. The approach circumvents the spatial resolution challenges faced by earlier optical imaging approaches using a diffusion equation forward model, and is promising for in vivo applications. For example, in principle, the method could be used to localize individual neurons firing throughout a rodent brain, enabling direct imaging of neural network activity.
Language: English
Subfield: Radiology, Nuclear Medicine and Imaging
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $2,045
Funders: National Science Foundation, U.S. Department of Energy, National Institutes of Health, Directorate for Computer and Information Science and Engineering, National Nuclear Security Administration, National Cancer Institute, National Institute of Neurological Disorders and Stroke, Sandia National Laboratories
Awards: G11630931, In Vivo Optical Imaging of Alpha-Synuclein Aggregation, G1934875286, G2214935549, G3263106614, G413247060, G4771968897, G4903105778, G5339743583, G5767419451, G6338696783, CIF - Small: High Resolution Computational Imaging with Motion in Spatially Varying Fields, Optical Imaging of Targeted Anti-Cancer Drug Delivery Kinetics, G8178004050, G855168022
OpenAlex ID: W2969038981
