Neuromelanin-hedefli ⁇ sup>18 ⁇ /sup>F-P3BZA PET/MR substantia nigra rhesus macaques içinde görüntüleme.

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BackgroundNeuromelanin is mostly located in dopaminergic neurons in the substantia nigra (SN) pars compacta, and can be detected by magnetic resonance imaging (MRI). It is a promising imaging-base biomarker for neurological diseases. We previously developed a melanin-specific probe N-(2-(diethylamino)-ethyl)-18F-5-fluoropicolinamide (18F-P3BZA), which was initially developed for the imaging of melanoma. 18F-P3BZA exhibited high levels of binding to the melanin in vitro and in vivo with high retention and favorable pharmacokinetics. In this study we further investigated whether 18F-P3BZA could be used to quantitatively detect neuromelanin in the SN in healthy rhesus macaques.Results18F-P3BZA exhibited desired hydrophobicity with estimated log K ow 5.08 and log D7.4 1.68. 18F-P3BZA readily crossed the blood-brain barrier with brain transport coefficients (Kin) of 40 ± 8 µL g-1s-1. 18F-P3BZA accumulated specifically in neuromelanotic PC12 cells, melanin-rich melanoma cells, and melanoma xenografts. 18F-P3BZA binding was significantly higher in B16F10 cells vs. amelanotic SKOV3 cells (6.17 ± 0.53%IA vs. 0.24 ± 0.05%IA) and in pigmented PC12 cells vs. non-pigmented PC12 cells(7.09 ± 0.15%IA and 0.29 ± 0.05%IA).In the biodistribution study, 18F-P3BZA had higher accumulation in B16F10 tumors (6.31 ± 0.99%IA/g) than in SKOV3 tumors (0.25 ± 0.09%IA/g). Meanwhile, 18F-P3BZA uptake in B16F10 tumors could be blocked by excess cold 19F-P3BZA (0.81 ± 0.02%IA/g, 88% inhibition, p 18F-P3BZA provided clear visualization of neuromelanin-rich SN at 30-60 min after injection in healthy macaques. The SN to cerebella ratios were 2.7 and 2.4 times higher at 30 and 60 min after injection. In vitro autoradiography studies 18F-P3BZA exhibited high levels of binding to the SN of healthy human and almost no binding to the SN of Parkinson's disease patient.Conclusion18F-P3BZA PET/MRI clearly images neuromelanin in the SN, and may assist in the early diagnosis of neurological diseases associated with abnormal neuromelanin expression.

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