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Fig. 6 | EJNMMI Radiopharmacy and Chemistry

Fig. 6

From: Design of PSMA ligands with modifications at the inhibitor part: an approach to reduce the salivary gland uptake of radiolabeled PSMA inhibitors?

Fig. 6

Maximum intensity projections (MIPs) of μSPECT/CT scans in LNCaP xenograft-bearing mice, acquired 24 h p.i. of (a) [177Lu]Lu-3 (carbamate I) (3.2 MBq) (b) [177Lu]Lu-6 (proinhibitor II) (5.3 MBq) (c) [177Lu]Lu-7 (proinhibitor III) (4.5 MBq) (d) [177Lu]Lu-10 (alkyne) (9.7 MBq) (e) [177Lu]Lu-11 (tetrazole) (7.0 MBq) (f) [177Lu]Lu-PSMA-10 (1) (2.8 MBq). For clear comparison, all images were scaled to the same maximum uptake value (2.5% ID/mL). Arrows indicate apparent tumor uptake in (a), (e) and (f). No μSPECT/CT image is displayed for [177Lu]Lu-5 (proinhibitor I), as ingestion of radioactive animal feed led to putative high activities in stomach and intestine. Therefore, all values of this mouse (= mouse 3) from the respective biodistribution study and also its μSPECT/CT image were excluded. Static images were acquired post mortem (CO2 asphyxiation and cervical dislocation) and after cardiac puncture with an acquisition time of 45 min. Further biodistribution studies were performed after the scan and included in the calculation of % ID/g values provided by Figs. 3 and 4 within this manuscript and Table 3 in the supporting information

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