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Iodine-124: A Promising Positron Emitter for Organic PET Chemistry

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TLDR
The present review gives a survey on the use of 124I as promising PET radionuclide for molecular imaging and an outlook on the future prospective of using the long-lived positron emitter 124I in the field of organic PET chemistry and molecular imaging.
Abstract
The use of radiopharmaceuticals for molecular imaging of biochemical and physiological processes in vivo has evolved into an important diagnostic tool in modern nuclear medicine and medical research. Positron emission tomography (PET) is currently the most sophisticated molecular imaging methodology, mainly due to the unrivalled high sensitivity which allows for the studying of biochemistry in vivo on the molecular level. The most frequently used radionuclides for PET have relatively short half-lives (e.g. 11C: 20.4 min; 18F: 109.8 min) which may limit both the synthesis procedures and the time frame of PET studies. Iodine-124 (124I, t1/2 = 4.2 d) is an alternative long-lived PET radionuclide attracting increasing interest for long term clinical and small animal PET studies. The present review gives a survey on the use of 124I as promising PET radionuclide for molecular imaging. The first part describes the production of 124I. The second part covers basic radiochemistry with 124I focused on the synthesis of 124I-labeled compounds for molecular imaging purposes. The review concludes with a summary and an outlook on the future prospective of using the long-lived positron emitter 124I in the field of organic PET chemistry and molecular imaging.

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Matching chelators to radiometals for radiopharmaceuticals.

TL;DR: This article is a guide for selecting the optimal match between chelator and radiometal for use in these systems, and a large selection of the most common and most promising chelators are evaluated and discussed for their potential use with a variety of radiometals.
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Radiopharmaceutical chemistry for positron emission tomography.

TL;DR: An overview of the most common chemical approaches for the synthesis of PET-labeled molecules is provided and the most recent developments and trends are highlighted.
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PET tracers based on Zirconium-89.

TL;DR: With well-developed radiochemistry, commercial availability of chelating agents for (89)Zr labeling, increasingly widely available isotope supply, as well as successful proof-of-principle in pilot human studies, it is expected that PET imaging with (89]Zr-based tracers will be a constantly evolving and highly vibrant field in the near future.
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The Next Generation of Positron Emission Tomography Radiopharmaceuticals in Oncology

TL;DR: The topics covered in this review include labeling methods, biological targets, and the most recent preclinical or clinical data of some of the next generation of PET radiopharmaceuticals.
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Radiolabeling of Nanoparticles and Polymers for PET Imaging

TL;DR: Various approaches and methods for the labeling of potential drug delivery systems using positron emitters are described and discussed to provide the radiolabeled analog.
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PET: The Merging of Biology and Imaging into Molecular Imaging

TL;DR: PET and SPECT are molecular imaging techniques that use radiolabeled molecules to image molecular interactions of biological processes in vivo as discussed by the authors, which can be used to titrate drugs to their sites of action within organ systems in vivo and to assay biological outcomes of the processes being modified in the mouse and the patient.
Journal ArticleDOI

Discovery of a potent and selective inhibitor of cyclin-dependent kinase 4/6.

TL;DR: It is demonstrated that the modification of pyrido[2,3-d]pyrimidin-7-ones to include a 2-aminopyridine side chain at the C2-position provides inhibitors with exquisite selectivity for Cdk4/6 in vitro.
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