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Updated: Feb 13, 2026

High-resolution Live Imaging of Cell Behavior in the Developing Neuroepithelium
Published on: April 12, 2012
Development and characterization of a scintillating cell imaging dish for radioluminescence microscopy
Debanti Sengupta1, Tae Jin Kim1, Sepideh Almasi1
1Radiation Oncology, Stanford University, 300 Pasteur Dr, Stanford, California, USA. pratx@stanford.edu.
Abstract:
Radioluminescence microscopy is an emerging modality that can be used to image radionuclide probes with micron-scale resolution. This technique is particularly useful as a way to probe the metabolic behavior of single cells and to screen and characterize radiopharmaceuticals, but the quality of the images is critically dependent on the scintillator material used to image the cells. In this paper, we detail the development of a microscopy dish made of a thin-film scintillating material, Lu2O3:Eu, that could be used as the blueprint for a future consumable product. After developing a simple quality control method based on long-lived alpha and beta sources, we characterize the radioluminescence properties of various thin-film scintillator samples. We find consistent performance for most samples, but also identify a few samples that do not meet the specifications, thus stressing the need for routine quality control prior to biological experiments. In addition, we test and quantify the transparency of the material, and demonstrate that transparency correlates with thickness. Finally, we evaluate the biocompatibility of the material and show that the microscopy dish can produce radioluminescent images of live single cells.
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