| Literature DB >> 31598059 |
Claudio Vinegoni1, Paolo Fumene Feruglio2, Ralph Weissleder1.
Abstract
Fluorescence acquisition and image display over a high dynamic range is highly desirable. However, the limited dynamic range of current photodetectors and imaging CCDs impose a limit on the fluorescence intensities that can be simultaneously captured during a single image acquisition. This is particularly troublesome when imaging biological samples, where protein expression fluctuates considerably. As a result, biological images will often contain regions with signal that is either saturated or hidden within background noise, causing information loss. In this manuscript we summarize recent work from our group and others, to extended conventional to high dynamic range fluorescence imaging. These strategies have many biological applications, such as mapping of neural connections, vascular imaging, bio-distribution studies or pharmacologic imaging at the single cell and organ level.Entities:
Keywords: Intravital microscopy; drug imaging; high dynamic range; in vivo imaging; optical imaging
Year: 2018 PMID: 31598059 PMCID: PMC6785194 DOI: 10.1109/JSTQE.2018.2881608
Source DB: PubMed Journal: IEEE J Sel Top Quantum Electron ISSN: 1077-260X Impact factor: 4.544