Multimodal Imaging Probe Development for Pancreatic β Cells: From Fluorescence to PET
- J Am Chem Soc. 2020 Feb 19;142(7):3430-3439. doi: 10.1021/jacs.9b11173.
- 1. Laboratory of Bioimaging Probe Development , Singapore Bioimaging Consortium, Agency for Science, Technology and Research , Singapore 138667 , Singapore.
- 2. New Drug Discovery Center, DGMIF , Daegu 41061 , Republic of Korea.
- 3. Department of Nuclear Medicine , Seoul National University College of Medicine, Seoul National University Bundang Hospital , Seongnam 13620 , Republic of Korea.
- 4. Department of Transdisciplinary Studies, Graduate School of Convergence Science and Technology , Seoul National University , Seoul 08826 , Republic of Korea.
- 5. Department of Bioengineering, College of Engineering, and BK21 PLUS Future Biopharmaceutical Human Resources Training and Research Team, and Institute of Nano Science & Technology (INST) , Hanyang University , Seoul 04763 , Republic of Korea.
- 6. Department of Chemistry , National University of Singapore , Singapore 117543 , Singapore.
- 7. Center for Self-Assembly and Complexity , Institute for Basic Science (IBS) , Pohang 37673 , Republic of Korea.
- 8. Bio &Drug Discovery Division , Korea Research Institute of Chemical Technology Yuseong-Gu , Gajeongro 141 , Daejeon 34114 , Republic of Korea.
- 9. Department of Chemistry , Gwangju Institute of Science and Technology (GIST) , Gwangju 61005 , Republic of Korea.
- 10. Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology (IMCB) , Agency for Science, Technology and Research (A*STAR) , Singapore 138673 , Singapore.
- 11. Department of Biochemistry and Department of Medicine, Yong Loo Lin School of Medicine , National University of Singapore , Singapore 117597 , Singapore.
- 12. Center for Nanomolecular Imaging and Innovative Drug Development , Advanced Institutes of Convergence Technology , Suwon 16229 , Republic of Korea.
Pancreatic β cells are responsible for Insulin secretion and are important for glucose regulation in a healthy body and diabetic disease patient without prelabeling of islets. While the conventional biomarkers for diabetes have been glucose and Insulin concentrations in the blood, the direct determination of the pancreatic β cell mass would provide critical information for the disease status and progression. By combining fluorination and diversity-oriented fluorescence library strategy, we have developed a multimodal pancreatic β cell probe PiF for both fluorescence and for PET (positron emission tomography). By simple tail vein injection, PiF stains pancreatic β cells specifically and allows intraoperative fluorescent imaging of pancreatic islets. PiF-injected pancreatic tissue even facilitated an antibody-free islet analysis within 2 h, dramatically accelerating the day-long histological procedure without any fixing and dehydration step. Not only islets in the pancreas but also the low background of PiF in the liver allowed us to monitor the intraportal transplanted islets, which is the first in vivo visualization of transplanted human islets without a prelabeling of the islets. Finally, we could replace the built-in fluorine atom in PiF with radioactive 18F and successfully demonstrate in situ PET imaging for pancreatic islets.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Fluorescent Dye