Rapid thermodynamically stable complex formation of [nat/111In]In3+, [nat/90Y]Y3+, and [nat/177 Lu]Lu 3+ with H 6 dappa

A phosphinate-bearing picolinic acid-based chelating ligand (H6dappa) was synthesized and characterized to assess its potential as a bifunctional chelator (BFC) for inorganic radiopharmaceuticals. Nuclear magnetic resonance (NMR) spectroscopy was employed to investigate the chelator coordination che...

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Hauptverfasser: Kostelnik, Thomas I. (VerfasserIn) , Wang, Xiaozhu (VerfasserIn) , Southcott, Lily (VerfasserIn) , Wagner, Hannah (VerfasserIn) , Kubeil, Manja (VerfasserIn) , Stephan, Holger (VerfasserIn) , Jaraquemada-Peláez, María de Guadalupe (VerfasserIn) , Orvig, Chris (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: April 27, 2020
In: Inorganic chemistry
Year: 2020, Jahrgang: 59, Heft: 10, Pages: 7238-7251
ISSN:1520-510X
DOI:10.1021/acs.inorgchem.0c00671
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.inorgchem.0c00671
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Verfasserangaben:Thomas I. Kostelnik, Xiaozhu Wang, Lily Southcott, Hannah K. Wagner, Manja Kubeil, Holger Stephan, María de Guadalupe Jaraquemada-Peláez, and Chris Orvig

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245 1 0 |a Rapid thermodynamically stable complex formation of [nat/111In]In3+, [nat/90Y]Y3+, and [nat/177 Lu]Lu 3+ with H 6 dappa  |c Thomas I. Kostelnik, Xiaozhu Wang, Lily Southcott, Hannah K. Wagner, Manja Kubeil, Holger Stephan, María de Guadalupe Jaraquemada-Peláez, and Chris Orvig 
246 3 3 |a Rapid thermodynamically stable complex formation of [nat/111In]In three plus, [nat/90Y]Y three plus, and [nat/177Lu]Lu three plus with H six dappa 
246 3 3 |a Rapid thermodynamically stable complex formation of [nat/111 In]In 3+, [nat/90 Y]Y 3+, and [nat/177Lu]Lu3+ with H6dappa 
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520 |a A phosphinate-bearing picolinic acid-based chelating ligand (H6dappa) was synthesized and characterized to assess its potential as a bifunctional chelator (BFC) for inorganic radiopharmaceuticals. Nuclear magnetic resonance (NMR) spectroscopy was employed to investigate the chelator coordination chemistry with a variety of nonradioactive trivalent metal ions (In3+, Lu3+, Y3+, Sc3+, La3+, Bi3+). Density functional theory (DFT) calculations explored the coordination environments of aforementioned metal complexes. The thermodynamic stability of H6dappa with four metal ions (In3+, Lu3+, Y3+, Sc3+) was deeply investigated via potentiometric and spectrophotometric (UV-vis) titrations, employing a combination of acidic in-batch, joint potentiometric/spectrophotometric, and ligand-ligand competition titrations; high stability constants and pM values were calculated for all four metal complexes. Radiolabeling conditions for three clinically relevant radiometal ions were optimized ([111In]In3+, [177Lu]Lu3+, [90Y]Y3+), and the serum stability of [111In][In(dappa)]3- was studied. Through concentration-, time-, temperature-, and pH-dependent labeling experiments, it was determined that H6dappa radiolabels most effectively at near-physiological pH for all radiometal ions. Furthermore, very rapid radiolabeling at ambient temperature was observed, as maximal radiolabeling was achieved in less than 1 min. Molar activities of 29.8 GBq/μmol and 28.2 GBq/μmol were achieved for [111In]In3+ and [177Lu]Lu3+, respectively. For H6dappa, high thermodynamic stability did not correlate with kinetic inertness—lability was observed in serum stability studies, suggesting that its metal complexes might not be suitable as a BFC in radiopharmaceuticals. 
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700 1 |a Southcott, Lily  |e VerfasserIn  |4 aut 
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700 1 |a Jaraquemada-Peláez, María de Guadalupe  |e VerfasserIn  |4 aut 
700 1 |a Orvig, Chris  |e VerfasserIn  |4 aut 
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