Diagnosis of Melanoma with 61Cu-Labeled PET Tracer

Until the recent years, substances containing radioactive 61Cu were strongly considered as potential positron-emitting radiopharmaceuticals for use in positron emission tomography (PET) applications; however, due to their suitably long half-life, and generator-independent and cost-effective producti...

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Veröffentlicht in:Journal of medicinal chemistry 2024-06, Vol.67 (11), p.9342-9354
Hauptverfasser: Bunda, Szilvia, Kálmán-Szabó, Ibolya, Lihi, Norbert, Képes, Zita, Szikra, Dezső, Peline Szabo, Judit, Timári, István, Szücs, Dániel, May, Nóra V., Papp, Gábor, Trencsényi, György, Kálmán, Ferenc K.
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Sprache:eng
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Zusammenfassung:Until the recent years, substances containing radioactive 61Cu were strongly considered as potential positron-emitting radiopharmaceuticals for use in positron emission tomography (PET) applications; however, due to their suitably long half-life, and generator-independent and cost-effective production, they seem to be economically viable for human imaging. Since malignant melanoma (MM) is a major public health problem, its early diagnosis is a crucial contributor to long-term survival, which can be achieved using radiolabeled α-melanocyte-stimulating hormone analog NAPamide derivatives. Here, we report on the physicochemical features of a new CB-15aneN5-based Cu­(II) complex ([Cu­(KFTGdiac)]−) and the ex vivo and in vivo characterization of its NAPamide conjugate. The rigid chelate possesses prompt complex formation and suitable inertness (t 1/2 = 18.4 min in 5.0 M HCl at 50 °C), as well as excellent features in the diagnosis of B16–F10 melanoma tumors (T/M­(SUVs) (in vivo): 12.7, %ID/g: 6.6 ± 0.3, T/M (ex vivo): 22).
ISSN:0022-2623
1520-4804
1520-4804
DOI:10.1021/acs.jmedchem.4c00479