Year: 2025
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Radioligands with albumin-binding moieties exhibit a great potential for the treatment of tumor diseases owing to the general finding of an increased integral tumor uptake compared to radioligands without such moieties. However, the reasons for this pharmacokinetic behavior are less explored. Herein, we focused on identifying potential mechanisms for our previously developed heterobivalent (SST 2 /albumin) [ 64 Cu]Cu-NODAGA-cLAB-TATEs . For this purpose, we designed two novel derivatives that show either negligible binding to albumin or lack the SST 2 -targeting capability. Based on the in vivo results, we hypothesize that binding of the albumin-bound radioligand to SST 2 in addition to that of the free radioligand causes the increased tumor uptake. This is supported by saturation binding analyses in the presence of albumin and compartment modeling considerations. Overall, the results of this study provide a first tentative explanation for the phenomenon of increased tumor uptake for albumin-binding radioligands, which may support the prospective design of such radioligands.
Source: Journal of Medicinal Chemistry
Language: English
Subfield: Radiology, Nuclear Medicine and Imaging
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4410528505