Recently developed radiopharmaceuticals for bacterial infection imaging

dc.contributor.authorKahts, Maryke
dc.contributor.authorSummers, Beverley
dc.contributor.authorGutta, Aadil
dc.contributor.authorPilloy, Wilfrid
dc.contributor.authorEbenhan, Thomas
dc.date.accessioned2025-01-17T11:31:48Z
dc.date.available2025-01-17T11:31:48Z
dc.date.issued2024
dc.description.abstractInfection remains a major cause of morbidity and mortality, regardless of advances in antimicrobial therapy and improved knowledge of microorganisms. With the major global threat posed by antimicrobial resistance, fast and accurate diagnosis of infections, and the reliable identification of intractable infection, are becoming more crucial for effective treatment and the application of antibiotic stewardship. Molecular imaging with the use of nuclear medicine allows early detection and localisation of infection and infammatory processes, as well as accurate monitoring of treatment response. There has been a continuous search for more specific radiopharmaceuticals to be utilised for infection imaging. This review summarises the most prominent discoveries in specifically bacterial infection imaging agents over the last five years, since 2019. MAIN BODY: Some promising new radiopharmaceuticals evaluated in patient studies are reported here, including radiolabelled bacterial siderophores like [ 68Ga]Ga-DFO-B, radiolabelled antimicrobial peptide/peptide fragments like [ 68Ga]Ga-NOTA-UBI29-41, and agents that target bacterial synthesis pathways (folic acid and peptidoglycan) like [ 11C]para-aminobenzoic acid and D-methyl-[11C]-methionine, with clinical trials underway for [ 18F]fuorodeoxy-sorbitol, as well as for 11C- and 18F-labelled trimethoprim. CONCLUSION: It is evident that a great deal of effort has gone into the development of new radiopharmaceuticals for infection imaging over the last few years, with remarkable progress in preclinical investigations. However, translation to clinical trials, and eventually clinical Nuclear Medicine practice, is apparently slow. It is the authors’ opinion that a more structured and harmonised preclinical setting and well-designed clinical investigations are the key to reliably evaluate the true potential of the newly proposed infection imaging agents.en_US
dc.description.departmentNuclear Medicineen_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.sdgSDG-09: Industry, innovation and infrastructureen_US
dc.description.urihttp://ejnmmipharmchem.springeropen.com/en_US
dc.identifier.citationKahts, M., Summers, B., Gutta, A. et al. Recently developed radiopharmaceuticals for bacterial infection imaging. EJNMMI Radiopharmacy and Chemistry 9, 49 (2024). https://doi.org/10.1186/s41181-024-00279-7.en_US
dc.identifier.issn2365-421X (online)
dc.identifier.other10.1186/s41181-024-00279-7
dc.identifier.urihttp://hdl.handle.net/2263/100157
dc.language.isoenen_US
dc.publisherSpringerOpenen_US
dc.rights© The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License.en_US
dc.subjectBacterial infection imagingen_US
dc.subjectRadiolabelled bacterial siderophoresen_US
dc.subjectRadiolabelled antimicrobial peptidesen_US
dc.subjectRadiolabelled antibioticsen_US
dc.subjectRadiolabelled sugar moleculesen_US
dc.subjectTargeting bacterial nitroen_US
dc.subjectReductaseen_US
dc.subjectTargeting bacterial synthesis pathwaysen_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.subjectSDG-09: Industry, innovation and infrastructureen_US
dc.titleRecently developed radiopharmaceuticals for bacterial infection imagingen_US
dc.typeArticleen_US

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