Abstract
Dual Positron emission tomography (PET)/optical imaging techniques have captured scientific interest for clinical applications due to their potential as an effective tool for visualizing in vivo information such as disease processes. 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dye has been considered an ideal platform strategy to achieve dual PET/optical imaging due to its photochemical nature and chemical structure. Various radiofluorination methods to prepare [18F]BODIPY dye have been developed and established, ranging from nucleophilic substitution reactions to isotope exchange reactions. In addition, 18F-labelled BODIPY dyes for biologically important targets have been used for in vivo and ex vivo studies. These studies proved the practicality of [18F]BODIPY dyes as a hybrid PET/optical imaging probe. In this review, recent advances in the synthesis and biological evaluation of 18F-labelled BODIPY dyes are described.
| Original language | English |
|---|---|
| Pages (from-to) | 22-36 |
| Number of pages | 15 |
| Journal | Nuclear Medicine and Biology |
| Volume | 93 |
| DOIs | |
| State | Published - 2021.02 |
Keywords
- BODIPY dyes
- Fluorescent
- Molecular imaging
- PET
- Radiofluorination
Quacquarelli Symonds(QS) Subject Topics
- Medicine
- Biological Sciences
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