6533b82afe1ef96bd128cc43

RESEARCH PRODUCT

Amide-to-triazole switch vs. in vivo NEP-inhibition approaches to promote radiopeptide targeting of GRPR-positive tumors

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Abstract Introduction Radiolabeled bombesin (BBN)-analogs have been proposed for diagnosis and therapy of gastrin-releasing peptide receptor (GRPR)-expressing tumors, such as prostate, breast and lung cancer. Metabolic stability represents a crucial factor for the success of this approach by ensuring sufficient delivery of circulating radioligand to tumor sites. The amide-to-triazole switch on the backbone of DOTA-PEG 4 -[Nle 14 ]BBN(7–14) ( 1 ) was reported to improve the in vitro stability of resulting 177 Lu-radioligands. On the other hand, in-situ inhibition of neutral endopeptidase (NEP) by coinjection of phosphoramidon (PA) was shown to significantly improve the in vivo stability and tumor uptake of biodegradable radiopeptides. We herein compare the impact of the two methods on the bioavailability and localization of 177 Lu-DOTA-PEG 4 -[Nle 14 ]BBN(7–14) analogs in GRPR-positive tumors in mice. Methods The 1,4-disubstituted [1–3]-triazole was used to replace one ( 2 : Gly 11 -His 12 ; 3 : Ala 9 -Val 10 ) or two ( 4 : Ala 9 -Val 10 and Gly 11 -His 12 ) peptide bonds in 1 (reference) and all compounds were labeled with 177 Lu. Each of [ 177 Lu] 1 –[ 177 Lu] 4 was injected without (control) or with PA in healthy mice. Blood samples collected 5min post-injection (pi) were analyzed by HPLC. Biodistribution of [ 177 Lu] 1 –[ 177 Lu] 4 was conducted in SCID mice bearing human prostate adenocarcinoma PC-3 xenografts at 4h pi. Groups of 4 animals were injected with radioligand, alone (controls), or with coinjection of PA, or of a mixture of PA and excess and [Tyr 4 ]BBN to determine GRPR-specificity of uptake (Block). Results The in vivo stability of the radioligands was: [ 177 Lu] 1 (25% intact), [ 177 Lu] 2 (45% intact), [ 177 Lu] 3 (30% intact) and [ 177 Lu] 4 (40% intact). By PA-coinjection these values notably increased to 90%–93%. Moreover, treatment with PA induced an impressive and GRPR-specific uptake of all radioligands in the PC-3 xenografts at 4h pi: [ 177 Lu] 1 : 4.7±0.4 to 24.8±4.9%ID/g; [ 177 Lu] 2 : 8.3±1.2 to 26.0±1.1%ID/g; [ 177 Lu] 3 : 6.6±0.4 to 21.3±4.4%ID/g; and [ 177 Lu] 4 : 4.8±1.6 to 13.7±3.8%ID/g. Conclusions This study has shown that amide-to-triazole substitutions in 177 Lu-DOTA-PEG 4 -[Nle 14 ]BBN(7–14) induced minor effects on bioavailability and tumor uptake in mice models, whereas in-situ NEP-inhibition(s) by PA impressively improved in vivo profiles.