Open Access
18 July 2018 Enhancing in vivo renal ischemia assessment by high-dynamic-range fluorescence molecular imaging
Yang Gao, Yuan Zhou, Fei Liu, Jianwen Luo
Author Affiliations +
Funded by: National Key R&D Program of China, National Natural Science Foundation of China (NSFC), Fundamental Research Funds for the Central Universities, Fundamental Research Funds for Central Universities
Abstract
Fluorescence imaging has been used to evaluate the physiological features of renal ischemia in animal model. However, the fluorophore distribution details of the ischemia model could not be fully represented due to the limited dynamic range of the charged-couple device. A high-dynamic-range (HDR) strategy was adopted in renal ischemia fluorescence imaging, both ex vivo and in vivo. The HDR strategy successfully combined ischemia relevant biological features that could only be captured with different exposure times, and then presented these features in the HDR results. The HDR results effectively highlighted the renal ischemic areas with relatively better perfusion and diminished the saturation that resulted from long exposure time. The relative fluorescence intensities of the ischemic kidneys and the image entropy values were significantly higher in the HDR images than in the original images, therefore enhancing the visualization of the renal ischemia model. The results suggest that HDR could serve as a postprocessing strategy to enhance the assessment of in vivo renal ischemia, and HDR fluorescence molecular imaging could be a valuable imaging tool for future studies of clinical ischemia detection and evaluation.
© 2018 Society of Photo-Optical Instrumentation Engineers (SPIE) 1083-3668/2018/$25.00 © 2018 SPIE
Yang Gao, Yuan Zhou, Fei Liu, and Jianwen Luo "Enhancing in vivo renal ischemia assessment by high-dynamic-range fluorescence molecular imaging," Journal of Biomedical Optics 23(7), 076009 (18 July 2018). https://doi.org/10.1117/1.JBO.23.7.076009
Received: 7 May 2018; Accepted: 29 June 2018; Published: 18 July 2018
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Cited by 2 scholarly publications.
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KEYWORDS
Luminescence

High dynamic range imaging

Ischemia

Kidney

In vivo imaging

Charge-coupled devices

Molecular imaging

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