Journal Article (Review Article)

DZNE-2026-00837

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Auger-Emitting Radionuclides in Radiopharmaceutical Research: Decay-Associated Processes, Vector-Dependent Localization, and Translational Perspectives.

Schomäcker, K. ; Sudbrock, F. ; Freifrau von Brandenstein, M. ; Akgül, B. ; Hufbauer, M. ; Fischer, T. ; Sahnoun, S. E. M. ; Dietlein, F. ; Krapf, P. ; Dietlein, M. ; Drzezga, A. (Last author)DZNE*

2026
Molecular Diversity Preservation International Basel

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Please use a persistent id in citations: doi:10.3390/ijms27146445

Abstract: Auger-electron-emitting radionuclides offer a distinctive route toward molecular-scale radiotherapy because their biological effects depend primarily on the nanoscale location of the decay event rather than on long-range tissue penetration. This review examines Auger-emitting radionuclides from a radiopharmaceutical perspective, integrating decay-associated physicochemical processes, cellular dosimetry, subcellular targeting, and translational relevance. We first discuss the physical determinants of Auger radiotoxicity, including Auger and Coster-Kronig electrons, internal-conversion electrons, local ionization density, and possible molecular consequences of highly localized Auger cascades. Cellular S values are used to illustrate how the same radionuclide can produce markedly different absorbed doses depending on whether activity is localized in the nucleus, cytoplasm, cell membrane, or neighboring cells. Iodine-125 incorporated into DNA as [125I]iododeoxyuridine ([125I]IUdR) remains the classical reference model for maximal Auger-mediated radiotoxicity. However, this direct DNA-incorporation model should not be generalized to receptor-targeted radiopharmaceuticals, which usually achieve indirect nuclear, chromatin-associated, perinuclear, membrane-associated, or vesicular localization rather than incorporation into DNA. These alternative source-target geometries may also produce biologically relevant effects, but they are mechanistically distinct from DNA-proximal [125I]IUdR decay. Particular attention is given to iodine-123 versus iodine-125, the influence of physical half-life and specific activity, the interpretation of terbium-161 as a hybrid β-/internal-conversion/Auger emitter, and the overlooked radiobiological relevance of diagnostic Auger emitters such as technetium-99m, indium-111, and gallium-67. We conclude that Auger-emitter radiopharmaceuticals cannot be ranked by electron yield or decay scheme alone. Their therapeutic or toxicological relevance emerges from the integration of decay-associated physicochemical processes, cellular source-target dosimetry, intracellular trafficking, retention, and the temporal realization of dose delivery.

Keyword(s): Auger electrons ; Coster–Kronig electrons ; Coulomb explosion ; DNA damage ; cellular dosimetry ; internal conversion electrons ; radiopharmaceutical therapy ; subcellular localization ; technetium-99m ; terbium-161

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Contributing Institute(s):

1. Positron Emissions Tomography (PET) (AG Boecker)

Research Program(s):

1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Appears in the scientific report 2026

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Database coverage:
; Clarivate Analytics Master Journal List ; Current Contents - Physical, Chemical and Earth Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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