Challenging the Macrocycle Paradigm: Four-Arm, High-Denticity Acyclic Chelators for Radiopharmaceuticals Incorporating Actinium and Lanthanides

As an alternative to macrocyclic chelators, a family of high-denticity, acyclic chelating agents based on picolinate arms has been devised with the aim of finding versatile chelating agents for <sup>225</sup>Ac, <sup>161</sup>Tb, and <sup>177</sup>Lu. This family comprises six symmetrical four-arm decadentate chelators that differ in the nature of the backbone spacer, ethylene (H<sub>4</sub><b>tpaen</b>), <i>o</i>-phenylene (H<sub>4</sub><b>tpaopd</b>), 2,3-naphtylene (H<sub>4</sub><b>tpaond</b>), <i>m-</i>xylylene (H<sub>4</sub><b>tpamxd</b>), <i>p</i>-xylylene (H<sub>4</sub><b>tpapxd</b>), and 2-hydroxypropylene (H<sub>4</sub><b>tpadapo</b>), and two dissymmetrical octadentate ligands, H<sub>3</sub><b>tripaen</b> and H<sub>4</sub><b>asyoctapa</b>, structurally derived from H<sub>4</sub><b>tpaen</b> by the loss of one arm (the first) and the replacement of two vicinal picolinate pendent arms by acetate groups (the second). The coordination chemistry of each chelating ligand with nonradioactive Lu<sup>3+</sup>, Tb<sup>3+</sup>, and La<sup>3+</sup> (the latter as a surrogate for [<sup>225</sup>Ac]Ac<sup>3+</sup>) has been explored to rationalize the findings in radiolabeling and human serum stability studies. With an RCY of 96% at 10<sup>-7</sup> M, which is directly comparable to the gold standard macrocyclic chelators H<sub>2</sub><b>macropa</b> and H<sub>4</sub><b>crown</b>, H<sub>4</sub><b>tpaond</b> is an excellent candidate for the development of radiopharmaceuticals based on <sup>225</sup>Ac. In addition, both H<sub>4</sub><b>tpaen</b> and H<sub>4</sub><b>tpaopd</b> are also an opportunity for the <sup>225</sup>Ac/<sup>155</sup>Tb theranostic pair. Meanwhile, H<sub>4</sub><b>asyoctapa</b> appears to be a great opportunity, not only for developing terbium radiopharmaceuticals, but also for the promising <sup>177</sup>Lu/<sup>155</sup>Tb pair.

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Journal
Inorganic Chemistry
Published
2026-03-17
DOI
https://doi.org/10.1021/acs.inorgchem.6c00216
Primary Topic
Radiopharmaceutical Chemistry and Applications
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article
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article

Challenging the Macrocycle Paradigm: Four-Arm, High-Denticity Acyclic Chelators for Radiopharmaceuticals Incorporating Actinium and Lanthanides

José L. Barriada, Chris Orvig, Daniel Fernández-Pavón, María Martínez-Cabanas et al.
Inorganic Chemistry
Radiopharmaceutical Chemistry and Applications
article

Challenging the Macrocycle Paradigm: Four-Arm, High-Denticity Acyclic Chelators for Radiopharmaceuticals Incorporating Actinium and Lanthanides

José L. Barriada, Chris Orvig, Daniel Fernández-Pavón, María Martínez-Cabanas, François Bénard, Brian O. Patrick, Luke Wharton, Andrés de Blas, Teresa Rodríguez-Blas, María de Guadalupe Jaraquemada-Peláez, Hua Yang
article en

Abstract

As an alternative to macrocyclic chelators, a family of high-denticity, acyclic chelating agents based on picolinate arms has been devised with the aim of finding versatile chelating agents for <sup>225</sup>Ac, <sup>161</sup>Tb, and <sup>177</sup>Lu. This family comprises six symmetrical four-arm decadentate chelators that differ in the nature of the backbone spacer, ethylene (H<sub>4</sub><b>tpaen</b>), <i>o</i>-phenylene (H<sub>4</sub><b>tpaopd</b>), 2,3-naphtylene (H<sub>4</sub><b>tpaond</b>), <i>m-</i>xylylene (H<sub>4</sub><b>tpamxd</b>), <i>p</i>-xylylene (H<sub>4</sub><b>tpapxd</b>), and 2-hydroxypropylene (H<sub>4</sub><b>tpadapo</b>), and two dissymmetrical octadentate ligands, H<sub>3</sub><b>tripaen</b> and H<sub>4</sub><b>asyoctapa</b>, structurally derived from H<sub>4</sub><b>tpaen</b> by the loss of one arm (the first) and the replacement of two vicinal picolinate pendent arms by acetate groups (the second). The coordination chemistry of each chelating ligand with nonradioactive Lu<sup>3+</sup>, Tb<sup>3+</sup>, and La<sup>3+</sup> (the latter as a surrogate for [<sup>225</sup>Ac]Ac<sup>3+</sup>) has been explored to rationalize the findings in radiolabeling and human serum stability studies. With an RCY of 96% at 10<sup>-7</sup> M, which is directly comparable to the gold standard macrocyclic chelators H<sub>2</sub><b>macropa</b> and H<sub>4</sub><b>crown</b>, H<sub>4</sub><b>tpaond</b> is an excellent candidate for the development of radiopharmaceuticals based on <sup>225</sup>Ac. In addition, both H<sub>4</sub><b>tpaen</b> and H<sub>4</sub><b>tpaopd</b> are also an opportunity for the <sup>225</sup>Ac/<sup>155</sup>Tb theranostic pair. Meanwhile, H<sub>4</sub><b>asyoctapa</b> appears to be a great opportunity, not only for developing terbium radiopharmaceuticals, but also for the promising <sup>177</sup>Lu/<sup>155</sup>Tb pair.

Inorganic Chemistry
Universidade da Coruña (ES), TRIUMF (CA), University of British Columbia (CA), Institute of Inorganic Chemistry of the Slovak Academy of Sciences (SK)
Openalex Percentile: Top 20%
Radiopharmaceutical Chemistry and Applications
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