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Review
. 2023 Mar 23;8(1):6.
doi: 10.1186/s41181-023-00192-5.

Highlight selection of radiochemistry and radiopharmacy developments by editorial board

Oliver C Kiss  1 , Peter J H Scott  2 , Martin Behe  3 , Ivan Penuelas  4 , Jan Passchier  5 , Ana Rey  6 , Marianne Patt  7 , Silvio Aime  8 , Amir Jalilian  9 , Peter Laverman  10 , Zhen Cheng  11 , Alain Faivre Chauvet  12 , Jonathan Engle  13 , Frederik Cleeren  14 , Hua Zhu  15 , Johnny Vercouillie  16 , Michael van Dam  17 , Ming Rong Zhang  18 , Lars Perk  10 , Benjamin Guillet  19 , Francisco Alves  20
Affiliations
Review

Highlight selection of radiochemistry and radiopharmacy developments by editorial board

Oliver C Kiss et al. EJNMMI Radiopharm Chem. .

Abstract

Background: The Editorial Board of EJNMMI Radiopharmacy and Chemistry releases a biannual highlight commentary to update the readership on trends in the field of radiopharmaceutical development.

Main body: This selection of highlights provides commentary on 21 different topics selected by each coauthoring Editorial Board member addressing a variety of aspects ranging from novel radiochemistry to first-in-human application of novel radiopharmaceuticals.

Conclusion: Trends in radiochemistry and radiopharmacy are highlighted. Hot topics cover the entire scope of EJNMMI Radiopharmacy and Chemistry, demonstrating the progress in the research field, and include new PET-labelling methods for 11C and 18F, the importance of choosing the proper chelator for a given radioactive metal ion, implications of total body PET on use of radiopharmaceuticals, legislation issues and radionuclide therapy including the emerging role of 161Tb.

Keywords: Highlight articles; Nuclear medicine; Radiochemistry; Radiopharmaceutical Sciences; Radiopharmacy; Trends in radiopharmaceutical sciences.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Synthetic scheme for synthesis of 11C-amino acids through isotopic exchange catalyzed by benzaldehyde
Fig. 2
Fig. 2
AR42J tumor cell viability (MTT assay) and Kaplan–Meier plot (2 × 10 MBq; 0.2 nmol) for 161Tb- and 177Lu-labeled SSTR agonists (DOTATOC) and antagonists (DOTA-LM3) in AR42J tumor-bearing mice. (adapted from Borgna et al. 2022)
Fig. 3
Fig. 3
Overview of use of new H2BZmacropa chelator, its conjugation to an antibody and biodistribution results. (from Bioconjugate Chem. 2022;33, 6, 1222–1231)
Fig. 4
Fig. 4
A 68Ga-DOTANOC and B 18 F-AlF-OC images (from top to bottom: maximum-intensity projection PET, transversal PET and fused PET/CT images, respectively) of a seventy-year old male patient with an intestinal neuroendocrine tumor with multiple liver metastases and one involved lymph node. 18 F-AlF-OC detected an additional bone lesion (blue arrow) that was confirmed by C follow-up 68Ga-DOTANOC imaging 6 months later. Lookup tables apply to PET images (SUV). (From Pauwels et al. 2022)
Fig. 5
Fig. 5
Schematic overview of preclinical experiments to evaluate 99mTc labelled EGFR imaging agents. (from Kiritsis et al. 2022)
Fig. 6
Fig. 6
Schematic overview of [18F]difluorocarbene precursors obtained through a halogen exchange 18F/Br of (bromofluoromethyl)(4-chlorophenyl)sulfane starting material, followed by an oxidation step. Examples of produced 18F-radioligands are presented
Fig. 7
Fig. 7
Structure of [18F]8
See this image and copyright information in PMC

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