Towards 213Bi alpha-therapeutics and beyond: unravelling the foundations of efficient BiIII complexation by DOTP

Author:

Horváth Dávid1234ORCID,Travagin Fabio5678ORCID,Guidolin Nicol910118ORCID,Buonsanti Federica910118,Tircsó Gyula1234ORCID,Tóth Imre123412ORCID,Bruchertseifer Frank13141516,Morgenstern Alfred13141516,Notni Johannes1718192016ORCID,Giovenzana Giovanni B.567821ORCID,Baranyai Zsolt910118ORCID

Affiliation:

1. Department of Physical Chemistry

2. University of Debrecen

3. Debrecen

4. Hungary

5. Dipartimento di Scienze del Farmaco

6. Università del Piemonte Orientale “A. Avogadro” Largo Donegani 2/3

7. Novara

8. Italy

9. Bracco Research Center

10. Bracco Imaging SpA

11. 10010 Colleretto Giacosa (TO)

12. Department of Inorganic and Analytical Chemistry

13. European Commission

14. Joint Research Centre (JRC)

15. Karlsruhe

16. Germany

17. Institute of Pathology

18. Klinikum rechts der Isar

19. Technische Universität München

20. 81675 München

21. CAGE Chemicals

Abstract

BiIII-DOTP complex is characterised by a fast formation kinetics, an outstanding thermodynamic stability and an impressive kinetic interness, making BiIII-DOTP an optimal model for the development of targeted α-therapy (TAT) radiopharmaceuticals.

Funder

National Research, Development and Innovation Office

Università degli Studi del Piemonte Orientale

European Regional Development Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

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