Efficient Production of the PET Radionuclide

PET actinium-225 lanthanum-133 macropa targeted alpha therapy theranostics

Journal

Pharmaceuticals (Basel, Switzerland)
ISSN: 1424-8247
Titre abrégé: Pharmaceuticals (Basel)
Pays: Switzerland
ID NLM: 101238453

Informations de publication

Date de publication:
21 Sep 2022
Historique:
received: 07 09 2022
revised: 15 09 2022
accepted: 16 09 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 28 10 2022
Statut: epublish

Résumé

Targeted Alpha Therapy is a research field of highest interest in specialized radionuclide therapy. Over the last decades, several alpha-emitting radionuclides have entered and left research topics towards their clinical translation. Especially, 225Ac provides all necessary physical and chemical properties for a successful clinical application, which has already been shown by [225Ac]Ac-PSMA-617. While PSMA-617 carries the DOTA moiety as the complexing agent, the chelator macropa as a macrocyclic alternative provides even more beneficial properties regarding labeling and complex stability in vivo. Lanthanum-133 is an excellent positron-emitting diagnostic lanthanide to radiolabel macropa-functionalized therapeutics since 133La forms a perfectly matched theranostic pair of radionuclides with the therapeutic radionuclide 225Ac, which itself can optimally be complexed by macropa as well. 133La was thus produced by cyclotron-based proton irradiation of an enriched 134Ba target. The target (30 mg of [134Ba]BaCO3) was irradiated for 60 min at 22 MeV and 10−15 µA beam current. Irradiation side products in the raw target solution were identified and quantified: 135La (0.4%), 135mBa (0.03%), 133mBa (0.01%), and 133Ba (0.0004%). The subsequent workup and anion-exchange-based product purification process took approx. 30 min and led to a total amount of (1.2−1.8) GBq (decay-corrected to end of bombardment) of 133La, formulated as [133La]LaCl3. After the complete decay of 133La, a remainder of ca. 4 kBq of long-lived 133Ba per 100 MBq of 133La was detected and rated as uncritical regarding personal dose and waste management. Subsequent radiolabeling was successfully performed with previously published macropa-derived PSMA inhibitors at a micromolar range (quantitative labeling at 1 µM) and evaluated by radio-TLC and radio-HPLC analyses. The scale-up to radioactivity amounts that are needed for clinical application purposes would be easy to achieve by increasing target mass, beam current, and irradiation time to produce 133La of high radionuclide purity (>99.5%) regarding labeling properties and side products.

Identifiants

pubmed: 36297279
pii: ph15101167
doi: 10.3390/ph15101167
pmc: PMC9611457
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Sci Rep. 2019 Jul 23;9(1):10658
pubmed: 31337833
Expert Rev Anticancer Ther. 2020 Oct;20(10):823-829
pubmed: 32820953
Cancer Biother Radiopharm. 2005 Feb;20(1):52-7
pubmed: 15778581
Angew Chem Int Ed Engl. 2017 Nov 13;56(46):14712-14717
pubmed: 28963750
Nucl Med Biol. 2022 Jul-Aug;110-111:59-66
pubmed: 35487834
Diagnostics (Basel). 2021 Oct 03;11(10):
pubmed: 34679525
Pharmaceutics. 2021 Jun 18;13(6):
pubmed: 34207408
J Radioanal Nucl Chem. 2013;295(1):205-209
pubmed: 26224928
ACS Omega. 2020 Oct 06;5(41):26431-26440
pubmed: 33110971
Cancer Biother Radiopharm. 2018 Oct;33(8):336-348
pubmed: 29889562
Cancer Biother Radiopharm. 2020 Aug;35(6):404-417
pubmed: 32552031
Cancers (Basel). 2021 Apr 20;13(8):
pubmed: 33923965
J Nucl Med. 2018 Nov;59(11):1655-1659
pubmed: 30262514
Nucl Med Biol. 2018 Jan;56:10-20
pubmed: 29031230
Appl Radiat Isot. 2020 Jan;155:108936
pubmed: 31655351
Nucl Med Biol. 2007 Oct;34(7):779-85
pubmed: 17921029
J Labelled Comp Radiopharm. 2020 Nov;63(13):553-563
pubmed: 32865290
Cancer Biother Radiopharm. 2020 Aug;35(6):437-445
pubmed: 31967907
J Nucl Med. 2021 Nov;62(11):1495-1503
pubmed: 34301779
J Nucl Med. 2022 Apr;63(4):584-590
pubmed: 34385334
EJNMMI Phys. 2019 Dec 12;6(1):23
pubmed: 31832809
Inorg Chem. 2021 Jan 18;60(2):623-632
pubmed: 33213142
Cancer Biother Radiopharm. 2020 Sep;35(7):497-510
pubmed: 32255671
J Nucl Med. 2016 Dec;57(12):1941-1944
pubmed: 27390158
Curr Radiopharm. 2011 Oct;4(4):283-94
pubmed: 22202151
Clin Cancer Res. 2019 Aug 1;25(15):4723-4734
pubmed: 31064781
Appl Radiat Isot. 2013 Feb;72:169-76
pubmed: 23220029
Eur J Nucl Med Mol Imaging. 2018 May;45(5):824-845
pubmed: 29234845
Curr Radiopharm. 2011 Jul;4(3):177-85
pubmed: 22201707
Pharmaceutics. 2020 Dec 31;13(1):
pubmed: 33396374

Auteurs

Santiago Andrés Brühlmann (SA)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.
Technische Universität Dresden, Faculty of Chemistry and Food Chemistry, D-01062 Dresden, Germany.

Martin Kreller (M)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.

Hans-Jürgen Pietzsch (HJ)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.

Klaus Kopka (K)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.
Technische Universität Dresden, Faculty of Chemistry and Food Chemistry, D-01062 Dresden, Germany.

Constantin Mamat (C)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.
Technische Universität Dresden, Faculty of Chemistry and Food Chemistry, D-01062 Dresden, Germany.

Martin Walther (M)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.

Falco Reissig (F)

Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Bautzner Landstraße 400, D-01328 Dresden, Germany.

Classifications MeSH