Synthesis and Preclinical Characterization of [¹⁸F]FPBZA: A Novel PET Probe for Melanoma

Figure 4

(a) Inhibition of [¹⁸F]FPBZA uptake in B16F0 cells by the pretreatment with various concentration of NB-DNJ for 48 h. The results were expressed in percentage of administered radioactivity per million cells and presented as mean ± SD (). , compared with the corresponding untreated group. (b) Photos of B16F0 cell pellets with and without NB-DNJ pretreatment (untreated cells were used as control).

(a)

(b)