Efficient formation of inert Bi-213 chelates by tetraphosphorus acid analogues of DOTA: towards improved alpha-therapeutics
Status PubMed-not-MEDLINE Language English Country Germany Media electronic
Document type Journal Article
Grant support
NO822/4-1
Deutsche Forschungsgemeinschaft
CRC 824
Deutsche Forschungsgemeinschaft
UNCE/SCI/014
Charles University
PubMed
30091088
PubMed Central
PMC6082748
DOI
10.1186/s13550-018-0431-3
PII: 10.1186/s13550-018-0431-3
Knihovny.cz E-resources
- Keywords
- Bismuth, Phosphinic acid, Phosphonic acid, Radiopharmaceuticals, Targeted alpha therapy,
- Publication type
- Journal Article MeSH
BACKGROUND: The recently growing interest in targeted alpha-therapy (TAT) calls for improvement of the labelling chemistry of the corresponding radionuclides. 213BiIII is a short-lived alpha emitter which emits only one alpha particle in its decay chain. Hence, it might be safer in application than other respective nuclides, such as 223Ra or 225Ac, because no alpha-emitting daughters are released upon recoil. We investigated cyclen derivatives with phosphorus-containing pendant arms regarding their suitability for 213Bi labelling. RESULTS: The concentration dependency of 213Bi labelling at 25 °C and 95 °C was determined for DOTP, DOTPH, DOTPEt, and DOTPI, as well as for DOTA and CHX-A"-DTPA for comparison. The labelling efficiency of the phosphorus-containing ligands was at least comparable to CHX-A"-DTPA and exceeded that of DOTA. DOTP was most efficient, requiring chelator concentrations for labelling which were approx. two orders of magnitude lower than those required for CHX-A"-DTPA, both at 25 °C and 95 °C. The 213Bi complexes of phosphorus ligands furthermore showed a higher stability against demetallation (> 96% of intact complex after 120-min incubation in plasma were found for DOTP, DOTPH, and DOTPEt, compared to 85% for DOTA and 76% for CHX-A"-DTPA). CONCLUSION: Cyclen derivatives bearing four N-methylenephosphonic or -phosphinic acid substituents, e.g., DOTP, are capable of complexing the alpha-emitting radionuclide 213BiIII with higher efficiency and in-vitro stability than the current gold standards DOTA and CHX-A"-DTPA.
Department of Inorganic Chemistry Charles University Hlavova 2030 12843 Prague 2 Czech Republic
Present address Isotope Technologies Garching GmbH Garching Germany
See more in PubMed
Seidl C. Radioimmunotherapy with α-particle-emitting radionuclides. Immunotherapy. 2014;6:431–458. doi: 10.2217/imt.14.16. PubMed DOI
Pommé S, Marouli M, Suliman G, Dikmen H, Van Ammel R, Jobbágy V, et al. Measurement of the 225Ac half-life. Appl Radiat Isot. 2012;70:2608–2614. doi: 10.1016/j.apradiso.2012.07.014. PubMed DOI
McDevitt MR, Ma DS, Lai LT, Simon J, Borchardt P, Frank RK, et al. Tumor therapy with targeted atomic nanogenerators. Science. 2001;294:1537–1540. doi: 10.1126/science.1064126. PubMed DOI
Parker C, Nilsson S, Heinrich D, Helle SI, O'Sullivan JM, Fosså SD, et al. Alpha emitter radium-223 and survival in metastatic prostate cancer. New Engl J Med. 2013;369:213–223. doi: 10.1056/NEJMoa1213755. PubMed DOI
Kratochwil C, Bruchertseifer F, Giesel FL, Weis M, Verburg FA, Mottaghy F, et al. 225Ac-PSMA-617 for PSMA-targeted α-radiation therapy of metastatic castration-resistant prostate Cancer. J Nucl Med. 2016;57:1941–1944. doi: 10.2967/jnumed.116.178673. PubMed DOI
Kozempel J, Mokhodoeva O, Vlk M. Progress in targeted alpha-particle therapy. What we learned about recoils release from in vivo generators. Molecules. 2018;23:581. doi: 10.3390/molecules23030581. PubMed DOI PMC
de Kruijff RM, Wolterbeek HT, Denkova AG. A critical review of alpha radionuclide therapy—how to deal with recoiling daughters? Pharmaceuticals. 2015;8:321–336. doi: 10.3390/ph8020321. PubMed DOI PMC
Morgenstern A, Bruchertseifer F, Apostolidis C. Targeted alpha therapy with 213Bi. Curr Radiopharm. 2011;4:295–305. doi: 10.2174/1874471011104040295. PubMed DOI
Morgenstern A, Bruchertseifer F, Apostolidis C. Bismuth-213 and actinium-225—generator performance and evolving therapeutic applications of two generator-derived alpha-emitting radioisotopes. Curr Radiopharm. 2012;5:221–227. doi: 10.2174/1874471011205030221. PubMed DOI
Kratochwil C, Giesel FL, Bruchertseifer F, Mier W, Apostolidis C, Boll R, et al. 213Bi-DOTATOC receptor-targeted alpha-radionuclide therapy induces remission in neuroendocrine tumours refractory to beta radiation: a first-in-human experience. Eur J Nucl Med Mol Imaging. 2014;41:2106–2119. doi: 10.1007/s00259-014-2857-9. PubMed DOI PMC
Allen BJ, Singla AA, Rizvi SM, Graham P, Bruchertseifer F, Apostolidis C, et al. Analysis of patient survival in a phase I trial of systemic targeted α-therapy for metastatic melanoma. Immunotherapy. 2011;3:1041–1050. doi: 10.2217/imt.11.97. PubMed DOI
Cordier D, Forrer F, Bruchertseifer F, Morgenstern A, Apostolidis C, Good S, et al. Targeted alpha-radionuclide therapy of functionally critically located gliomas with 213Bi-DOTA-[Thi8,Met(O2)11]-substance P: a pilot trial. Eur J Nucl Med Mol Imaging. 2010;37:1335–1344. doi: 10.1007/s00259-010-1385-5. PubMed DOI
Notni J, Wester HJ. Re-thinking the role of radiometal isotopes: towards a future concept for theranostic radiopharmaceuticals. J Label Compd Radiopharm. 2018;61:141–153. doi: 10.1002/jlcr.3582. PubMed DOI
Šimeček J, Hermann P, Havlíčková J, Herdtweck E, Kapp TG, Engelbogen N, et al. A cyclen-based tetraphosphinate chelator for preparation of radiolabeled tetrameric bioconjugates. Chem Eur J. 2013;19:7748–7757. doi: 10.1002/chem.201300338. PubMed DOI
Kotková Z, Pereira GA, Djanashvili K, Kotek J, Rudovský J, Hermann P, et al. Lanthanide(III) complexes of phosphorus acid analogues of H4DOTA as model compounds for the evaluation of the second-sphere hydration. Eur J Inorg Chem. 2009:119–36.
Apostolidis C, Molinet R, Rasmussen G, Morgenstern A. Production of Ac-225 from Th-229 for targeted alpha therapy. Anal Chem. 2005;77:6289–91. PubMed
Brechbiel MW, Gansow OA. Synthesis of C-functionalized trans-cyclohexyldiethylenetriaminepenta-acetic acids for labelling of monoclonal antibodies with the bismuth-212 α-particle emitter. J Chem Soc Perkin Trans 1. 1992:1173–8.
Stasiuk GJ, Long NJ. The ubiquitous DOTA and its derivatives: the impact of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid on biomedical imaging. Chem Commun. 2013;49:2732–2746. doi: 10.1039/c3cc38507h. PubMed DOI
Notni J, Šimeček J, Wester HJ. Phosphinic acid functionalized polyazacycloalkane chelators for radiodiagnostics and radiotherapeutics: unique characteristics and applications. ChemMedChem. 2014;9:1107–1115. doi: 10.1002/cmdc.201400055. PubMed DOI
Notni J. With Gallium-68 into a new era? Nachr Chem. 2012;60:645–649. doi: 10.1002/nadc.201290233. DOI
Rösch F. Past, present and future of 68Ge/68Ga generators. Appl Rad Isot. 2013;76:24–30. doi: 10.1016/j.apradiso.2012.10.012. PubMed DOI
Hama H, Takamoto S. Polarographic determination of stability constants of divalent metal chelates of 1,4,7-triazacyclononane-N,N',N''-triacetic acid. Nippon Kagaku Kaishi. 1975:1182–5.
Kabachnik MI, Medved TY, Belskii FI, Pisareva SA. Izv Akad Nauk SSSR Ser Khim. 1988;37:1886–1890.
Geraldes CFCG, Sherry AD, Lázár I, Miseta A, Bogner P, Berenyi E, et al. Relaxometry, animal biodistribution, and magnetic resonance imaging studies of some new gadolinium (III) macrocyclic phosphinate and phosphonate monoester complexes. Magn Reson Med. 1993;30:696–703. doi: 10.1002/mrm.1910300607. PubMed DOI
Bazakas K, Lukeš I. Synthesis and complexing properties of polyazamacrocycles with pendant N-methylenephosphinic acid. J Chem Soc Dalton Trans. 1995:1133–7.
Stetter H, Frank W. Complex formation with tetraazacycloalkane-N,N',N",N'"-tetraacetic acids as a function of ring size. Angew Chem Int Ed Engl. 1976;15:686. doi: 10.1002/anie.197606861. DOI
Wu C, Kobayashi H, Sun B, Yoo TM, Paik CH, Gansow OA, et al. Stereochemical influence on the stability of radio-metal complexes in vivo. Synthesis and evaluation of the four stereoisomers of 2-(p-nitrobenzyl)-trans-CyDTPA. Bioorg Med Chem. 1997;5:1925–1934. doi: 10.1016/S0968-0896(97)00130-2. PubMed DOI
Camera L, Kinuya S, Garmestani K, Wu CC, Brechbiel MW, Pai LH, et al. Evaluation of the serum stability and in vivo biodistribution of CHX-DTPA and other ligands for yttrium labeling of monoclonal antibodies. J Nucl Med. 1994;35:882–889. PubMed
Moreau J, Guillon E, Pierrard JC, Rimbault J, Port M, Aplincourt M. Complexing mechanism of the lanthanide cations Eu3+, Gd3+, and Tb3+ with 1,4,7,10-tetrakis(carboxymethyl)-1,4,7,10-tetraazacyclododecane (dota)—characterization of three successive complexing phases: study of the thermodynamic and structural properties of the complexes by potentiometry, luminescence spectroscopy, and EXAFS. Chem Eur J. 2004;10:5218–5232. doi: 10.1002/chem.200400006. PubMed DOI
Ševčík R, Vaněk J, Michalicová R, Lubal P, Hermann P, Santos IC, et al. Formation and decomplexation kinetics of copper(II) complexes with cyclen derivatives having mixed carboxylate and phosphonate pendant arms. Dalton Trans. 2016;45:12723–33. PubMed