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Introduction of a SiFA Moiety into the D-Glutamate Chain of DOTA-PP-F11N Results in Radiohybrid-Based CCK-2R-Targeted Compounds with Improved Pharmacokinetics In Vivo

ORCID
0000-0001-8258-3526
Affiliation
Pharmaceutical Radiochemistry, Technical University of Munich, 85748 Garching, Germany
Holzleitner, Nadine;
ORCID
0000-0002-7412-0297
Affiliation
Pharmaceutical Radiochemistry, Technical University of Munich, 85748 Garching, Germany
Günther, Thomas;
Affiliation
Pharmaceutical Radiochemistry, Technical University of Munich, 85748 Garching, Germany
Beck, Roswitha;
ORCID
0000-0001-7536-2207
Affiliation
Nuclear Medicine, Faculty of Medicine, University of Augsburg, 86156 Augsburg, Germany
Lapa, Constantin;
Affiliation
Pharmaceutical Radiochemistry, Technical University of Munich, 85748 Garching, Germany
Wester, Hans-Jürgen

In order to enable 18 F- and 177 Lu-labelling within the same molecule, we introduced a silicon-based fluoride acceptor (SiFA) into the hexa-D-glutamate chain of DOTA-PP-F11N. In addition, minigastrin analogues with a prolonged as well as γ -linked D-glutamate chain were synthesised and evaluated. CCK-2R affinity ( IC 50 , AR42J cells) and lipophilicity (log D 7.4 ) were determined. Biodistribution studies at 24 h post-injection (p.i.) and µ SPECT/CT imaging at 1, 4 and 24 h p.i. were carried out in AR42J tumour-bearing CB17-SCID mice. CCK-2R affinity of ( R )-DOTAGA-rhCCK-1 to 18 was enhanced with increasing distance between the SiFA building block and the binding motif. Lipophilicity of [ 177 Lu]Lu-( R )-DOTAGA-rhCCK-1 to 18 was higher compared to that of [ 177 Lu]Lu-DOTA-PP-F11N and [ 177 Lu]Lu-CP04. The respective α - and γ -linked rhCCK derivatives revealing the highest CCK-2R affinity were further evaluated in vivo. In comparison with [ 177 Lu]Lu-DOTA-PP-F11N, [ 177 Lu-]Lu-( R )-DOTAGA-rhCCK-9 and -16 exhibited three- to eight-fold increased activity levels in the tumour at 24 h p.i. However, activity levels in the kidneys were elevated as well. We could show that the introduction of a lipophilic SiFA moiety into the hydrophilic backbone of [ 177 Lu]Lu-DOTA-PP-F11N led to a decelerated blood clearance and thus improved tumour retention. However, elevated kidney retention has to be addressed in future studies.

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