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Production of Ac-225 from Th-229 for targeted alpha therapy
C Apostolidis1, R Molinet, G Rasmussen
1European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe, Germany.
Analytical Chemistry
|October 1, 2005
Summary
This study presents a novel method for purifying Actinium-225 (Ac-225) from Thorium-229 (Th-229) sources. The efficient process yields high-purity Ac-225 for targeted alpha therapy applications.
Area of Science:
- Radiochemistry
- Nuclear Medicine
- Chemical Separation Science
Background:
- Actinium-225 (Ac-225) is a critical radionuclide for targeted alpha therapy (TAT).
- Efficient separation of Ac-225 from its parent isotope Thorium-229 (Th-229) is essential for clinical applications.
- Current purification methods require optimization for yield and purity.
Purpose of the Study:
- To develop and validate a robust method for Ac-225 separation and purification from Th-229.
- To achieve clinical-grade, carrier-free Ac-225 with high overall yield.
- To enable the production of Ac-225/Bismuth-213 (Bi-213) radionuclide generators for cancer therapy research.
Main Methods:
- Combined ion exchange and extraction chromatography in nitric acid media.
- Radiometric analysis including alpha and gamma spectrometry for quality control.
- Mass spectrometry for product characterization and purity assessment.
Main Results:
- Achieved separation and purification of Ac-225 from Th-229.
- Prepared carrier-free, clinical-grade Ac-225 with an overall yield exceeding 95%.
- Validated product quality using multiple analytical techniques.
Conclusions:
- The developed method provides a highly efficient route to clinical-grade Ac-225.
- The purified Ac-225 is suitable for loading onto radionuclide generators for Bi-213 production.
- This advancement supports preclinical and clinical studies in targeted alpha therapy for cancer and infectious diseases.

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