Overall, this improvement is highly significant since it cut the amount of nonradioactive mass dose of the NT160 by >50% thus enabling performing blocking (target engagement) studies in vivo and will likely enable clinical translation of [ 18 F]NT160 by starting with larger amounts of radioactivity (i.e., >3.0 Ci).
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High-Contrast PET Imaging with [<sup>18</sup>F]NT160, a Class-IIa Histone Deacetylase Probe for In Vivo Imaging of Epigenetic Machinery in the Central Nervous System.
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