Production of Ac-225 from Th-229 for Targeted α Therapy
Abstract
This work describes a method for the separation and purification of Ac-225 from a Th-229 source. The procedure is based on the combination of ion exchange and extraction chromatographic methods in nitric acid media and allows the preparation of carrier-free, clinical grade Ac-225 with an overall yield exceeding 95%. Quality control of the product is performed using radiometric (alpha, gamma spectrometry) and mass spectrometric methods. The Ac-225 product can be loaded on a radionuclide generator for the preparation of Bi-213 for preclinical and clinical studies of targeted alpha therapy of cancer and infectious diseases.
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The Joint Research Centre in Karlsruhe, Germany, has produced approximately 13 GBq 225Ac annually since the 1990s.
“The Directorate for Nuclear Safety and Security of the Joint Research Centre (JRC) of the European Commission in Karlsruhe, Germany, the first laboratory to prepare 225Ac/213Bi, has produced approximately 13 GBq 225Ac annually since the 1990s for their center and a wide network of clinical collaborators (89, 90).”
From Alpha-peptide receptor radionuclide therapy using actinium-225 labeled somatostatin receptor agonists and antagonists (2022) · cites this paper as [89]
For more than two decades, radiochemical extraction from 229Th, which originated from the decay of the fissile isotope 233U, has been the most utilized strategy for the production of 225Ac and its daughter 213Bi.
“For more than two decades, the radiochemical extraction from 229Th, which is originated from the decay of the fissile isotope 233U (Figure 4), has been the most utilized strategy for the production of 225Ac and its daughter 213Bi (88, 89).”
From Alpha-peptide receptor radionuclide therapy using actinium-225 labeled somatostatin receptor agonists and antagonists (2022) · cites this paper as [89]
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Self-citationThe feasibility of 225 Ac as a source of ??-particles in radioimmunotherapy
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An Improved Method for the Production of Ac-225/Bi-213 from Th-229 for Targeted Alpha Therapy.
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- Authors
- Apostolidis, C., Molinet, R., Rasmussen, G., & Morgenstern, A.
- Affiliations
- Joint Research Centre (DE)
- Venue
- Analytical Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 2005-09-02
- Volume
- 77
- Issue
- 19
- Pages
- 6288-6291
- ISSN
- 0003-2700 (ISSN-L)
- 1520-6882
- OpenAlex
- W2071761375
- Cited by
- 215
- References
- 7
- Citations by year
- 2026: 8 · 2025: 10 · 2024: 20 · 2023: 11 · 2022: 8 · 2021: 13 · 2020: 18 · 2019: 10 · 2018: 20 · 2017: 11 · 2016: 9 · 2015: 6 · 2014: 11 · 2013: 11 · 2012: 10
- FWCI
- 4.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Analytical Chemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Radiopharmaceutical Chemistry and Applications
- Physical Sciences › Chemistry › Inorganic Chemistry › Radioactive element chemistry and processing
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Chemical Reactions and Isotopes
- Keywords
- actinium-225, thorium-229, targeted alpha therapy, radionuclide separation, ion exchange, extraction chromatography, nitric acid medium, carrier-free radionuclides, bismuth-213, radionuclide generator, alpha spectrometry, mass spectrometry, radiopharmaceutical production
- MeSH terms
- Actinium, Anions, Radioisotopes, Thallium
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